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Research Associate I - E&L Chemical Characterization

Baxter Healthcare Round Lake, IL

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives— where your purpose accelerates our mission. Your Role at Baxter This is where your work saves lives. We currently have an opening for a versatile Analytical Chemist who can execute lab experiments and facilitate Operational Excellence in the Medication Delivery R&D chemistry lab in Round Lake, Illinois, as well as: Effectively contribute basic technical knowledge and skills to a variety of projects within relevant discipline. Interact effectively with a variety of disciplines. Conduct routine research and design experiments with some assistance. What you'll be doing: Contribute routine scientific knowledge or expertise to research and development activities for achievement of project goals and solve routine experimental design or research problems with some assistance. Under direction, conduct routine research and/or developmental activities. This may include wet chemistry sample preparation and mass spectrometric analyses. Plan details of assigned tasks within specific parameters. Organize data and prepare relevant documentation for assigned projects. Write and issue reports with minimal guidance. Understand and apply applicable corporate and divisional SOPs. Maintain knowledge of relevant quality and safety requirements. Employ appropriate techniques and methods to successfully conduct specific assignments within negotiated deadlines after receiving general instruction. Demonstrate working knowledge of basic technical theories and principles within area of expertise for routine tasks. Develop knowledge and understanding of GxP and related regulations and guidance. Assess feasibility of simple research and design concepts within area of expertise. What you'll bring: Bachelors degree with 0-1 years of experience. Possess relevant laboratory/technical, writing, and computer skills. Able to work in a team environment appropriately supporting others. Self motivated and takes personal responsibility for getting the job done. Ability to organize and clearly communicate information. Understand importance of project schedules and impact of not achieving milestones. Able to adapt to shifting priorities. Ability to demonstrate critical thinking and problem solving. Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time. US Benefits at Baxter (except for Puerto Rico) This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. #J-18808-Ljbffr

Best Match

Research Associate I - E&L Chemical Characterization,

Baxter International Inc. Round Lake, IL

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives— where your purpose accelerates our mission. Your Role at Baxter This is where your work saves lives. We currently have an opening for a versatile Analytical Chemist who can execute lab experiments and facilitate Operational Excellence in the Medication Delivery R&D chemistry lab in Round Lake, Illinois, as well as: Effectively contribute basic technical knowledge and skills to a variety of projects within relevant discipline. Interact effectively with a variety of disciplines. Conduct routine research and design experiments with some assistance. What you'll be doing: Contribute routine scientific knowledge or expertise to research and development activities for achievement of project goals and solve routine experimental design or research problems with some assistance. Under direction, conduct routine research and/or developmental activities, including wet chemistry sample preparation and mass spectrometric analyses. Organize data and prepare relevant documentation for assigned projects. Write and issue reports with minimal guidance. Understand and apply applicable corporate and divisional SOPs. Maintain knowledge of relevant quality and safety requirements. Employ appropriate techniques and methods to successfully conduct specific assignments within negotiated deadlines after receiving general instruction. Demonstrate working knowledge of basic technical theories and principles within area of expertise for routine tasks. Develop knowledge and understanding of GxP and related regulations and guidance. Assess feasibility of simple research and design concepts within area of expertise. What you'll bring: Bachelors degree with 0-1 years of experience. Possess relevant laboratory/technical, writing, and computer skills. Able to work in a team environment appropriately supporting others. Self motivated and takes personal responsibility for getting the job done. Ability to organize and clearly communicate information. Understand importance of project schedules and impact of not achieving milestones. Able to adapt to shifting priorities. Ability to demonstrate critical thinking and problem solving. Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time. #J-18808-Ljbffr

Work Life Balance

Research Associate I - E&L Chemical Characterization

Baxter International Round Lake, IL

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives— where your purpose accelerates our mission. Your Role at Baxter This is where your work saves lives. We currently have an opening for a versatile Analytical Chemist who can execute lab experiments and facilitate Operational Excellence in the Medication Delivery R&D chemistry lab in Round Lake, Illinois, as well as: Effectively contribute basic technical knowledge and skills to a variety of projects within relevant discipline. Interact effectively with a variety of disciplines. Conduct routine research and design experiments with some assistance. What you'll be doing: Contribute routine scientific knowledge or expertise to research and development activities for achievement of project goals and solve routine experimental design or research problems with some assistance. Under direction, conduct routine research and/or developmental activities. This may include wet chemistry sample preparation and mass spectrometric analyses. Plan details of assigned tasks within specific parameters. Organize data and prepare relevant documentation for assigned projects. Write and issue reports with minimal guidance. Understand and apply applicable corporate and divisional SOPs. Maintain knowledge of relevant quality and safety requirements. Employ appropriate techniques and methods to successfully conduct specific assignments within negotiated deadlines after receiving general instruction. Demonstrate working knowledge of basic technical theories and principles within area of expertise for routine tasks. Develop knowledge and understanding of GxP and related regulations and guidance. Assess feasibility of simple research and design concepts within area of expertise. What you'll bring: Bachelors degree with 0-1 years of experience. Possess relevant laboratory/technical, writing, and computer skills. Able to work in a team environment appropriately supporting others. Self motivated and takes personal responsibility for getting the job done. Ability to organize and clearly communicate information. Understand importance of project schedules and impact of not achieving milestones. Able to adapt to shifting priorities. Ability to demonstrate critical thinking and problem solving. Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a required minimum number of days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $72,000 to $99,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than the anticipated range based upon market data and other factors, all of which are subject to change. Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time. #J-18808-Ljbffr

Wound Care Nurse

Franciscan Ministries Round Lake, Illinois

Overview: Position Summary In this role, you will be responsible for overseeing the treatment of residents with all types of wounds and ulcers and serve as an expert at the community for any skin integrity issues. You may also administer treatments including but not limited to sharp debridement. Hours Monday-Friday: 8:00am to 4:30pm 1055 E. Grand Ave Lindenhurst, IL 60046 Essential Functions, Key Duties, & Responsibilities Oversee and assess all residents with wounds and pressure ulcers. Assess and consult for all residents with skin integrity issues as needed. Collaborate with physicians to develop a plan of treatment. Oversee and complete the administration of wound care treatment to the residents. Assess the effectiveness of treatments, documenting progress and changes in the condition of the residents’ skin. Communicate results and concerns to the physician, Director of Nursing, and any other associates as needed. Establish wound care protocol at the community and identify high-risk residents to promote optimal skin integrity outcomes. Identify and provide associate educational needs pertaining to wound care. Prepare job-related reports to present to the leadership of the department. Perform other duties as assigned. Comply with all policies and procedures and any updates. Position Requirements Education : Associate’s degree or higher in a clinical/nursing area of study required Licenses/Certifications: Licensed Practical Nurse (LPN) or Registered Nurse (RN) license required Experience : 1+ years of experience in a clinical/nursing setting within the geriatric industry Skills & Abilities: Outstanding customer services and bedside manner Travel : N/A #Livingjoyfully Min: USD $33.00/Hr. Max: USD $45.00/Hr.

Licensed Marriage and Family Therapist (LMFT, LPC, LCSW)

LifeStance Health Round Lake, Illinois

At LifeStance Health, we believe in a truly healthy society where mental and physical healthcare are unified to make lives better. Our mission is to help people lead healthier, more fulfilling lives by improving access to trusted, affordable, and personalized mental healthcare. Everywhere. Every day. It’s a lofty goal; we know. But we make it happen with the best team in behavioral health. Thank you for taking the time to explore a career with us. As the fastest growing behavioral health practice group in the country, now is the perfect time to join our clinical team! We are actively looking to hire talented therapists in the area, who are passionate about patient care and committed to clinical excellence. We are currently interviewing! We offer our Therapists: Flexible work schedules: Full-time and part-time (20 hours week+) available - set your own schedule! Hybrid Models (on-site & telehealth) 100% outpatient work. No nights, no hospital calls, no weekends. Compensation with unlimited/uncapped earnings Full benefits package: health, dental, vision, life, 401k (with match), paid parental leave, holidays, EAP and more. Collegial work environment Newly designed and modern offices Full administrative support (scheduling & billing) Latest in digital technology Strong work/life balance! Our Therapists are a critical part of our clinical team. We’re seeking Therapists who are: Fully licensed in Wisconsin LCSW, LPC, or LMFT Child, adolescent, or adult experience. ***$82,000 - $109,000 annually + Sign on bonus (full-time) I'd be glad to set up a call to discuss this opportunity with you and answer any questions! Thank you, Sophie Pelletier Director, Practice Development LifeStance Health, Inc. (e) [email protected] (c) 561-339-4883 About LifeStance Health LifeStance is a national provider of mental healthcare services focused on evidenced-based, medically driven treatment services for children, adolescents and adults suffering from a variety of mental health issues in an outpatient care setting, both in-person at its clinics nationwide and through its digital health telemedicine offering. The company employs psychiatrists, psychologists, psychiatric nurse practitioners, and licensed therapists throughout the US. LifeStance Health is an equal opportunity employer. We celebrate diversity and are fully committed to creating an inclusive work environment for all our employees. Our values: Belonging: We cultivate a space where everyone can show up as their authentic self. Empathy: We seek out diverse perspectives and listen to learn without judgment. Courage: We are all accountable for doing the right thing - even when it's hard - because we know it's worth it. One Team: We realize our full potential when we work together towards our shared purpose.

Receptionist

Franciscan Ministries Round Lake, IL

Overview: Position Summary In this role, you will be responsible for answering the telephone and professionally greeting visitors and assisting residents with their questions or needs while maintaining the residents rights to confidentiality. H ours Needed PRN -As Needed 1055 E Grand Ave Lindenhurst, IL 60046 Essential Functions, Key Duties, & Responsibilities Answer multi-line telephone and transfer calls and messages to appropriate personnel. Monitor the emergency notification system, respond immediately, and direct help to the scene of the emergency. Assist residents, guests, and visitors with questions or concerns. Direct marketing appointments and walk-ins and provide a tour if necessary. Distribute mail and packages to residents and associates. Provide secretarial assistance to Administration as needed. Monitor and prepare visitor sign-in and sign-out logs. Perform other duties as assigned. Comply with all policies and procedures and any updates. Position Requirements Education : High School Diploma/GED Licenses/Certifications: N/A Experience : None required; 1+ years of customer service or administrative/clerical experience preferred Skills & Abilities: Keen attention to detail Excellent organizational and communication skills Min: USD $15.00/Hr. Max: USD $16.50/Hr.

CDL-A Solo & Team Drivers - Earn Up to $100,000/Year - 6 Months Exp.

CFI Round Lake, IL

Job Description CFI is now hiring CDL-A Drivers - She Drives! \n CFI is Proud to Support Women Drivers! \nExcellent Pay and Benefits - Reliable Home Time \n\n Why Drive for CFI: \n\n \n\t Solo drivers: \n\t Earn up to $0.56 per mile \n\t Top drivers earn $100,000+ annually \n\t Team drivers: \n\t Earn up to $0.73 per mile (split) \n\t Each driver is paid their pay rate for all miles the truck runs \n\t Top drivers earn $100,000+ annually (each) \n\t 14% of Our Fleet is Female Drivers! \n\t 90% No-touch freight \n\t Regional and OTR routes available \n\t Top-of-the-line equipment \n \n\n Get Started: \n\n \n\t STEP ONE: Request info by submitting this form \n\t STEP TWO: Complete the CFI online driver application (provided upon completion of STEP ONE) \n\t STEP THREE: Connect with a CFI specialist to discuss available options & routes (we'll contact you at the number provided) \n \n\n Apply Now and Speak to a Recruiter Today! \n\n 14% of our fleet is female drivers! \n\n She Drives CFI means building an environment where women feel safe, supported, and happy in their work environment. We provide opportunities for women to grow within CFI. Our goal is to bring confidence, respect, and equality to our entire CFI team. We are proud to have repeatedly been named a Top Company for Women to Work for in Transportation by Women in Trucking. \n\n When you drive for CFI, you can count on: \n\n \n\t Top drivers earn $100,000+ annually \n\t 401(k) with company match \n\t Health, Dental, and Life Insurance \n\t Practical mile pay \n\t Consistent freight \n\t Stop-off pay, Canadian border pay, local pay, layover pay, & non-customary work pay \n\t Holiday pay \n\t Rider program \n\t Electronic logs (e-logs) used by full fleet \n \n\n Peace of Mind with Layover Pay : At CFI, we strive to provide our CDL-A Drivers with consistent miles. In the rare event of a layover, you'll receive $125 after the first 24 hours and $125 for each additional 24-hour period, ensuring your time is always valued. \n\n Would you like to experience an enhanced sense of pride and build lifelong friendships with those you mentor? CFI has immediate openings for Driver Trainers! Gain the satisfaction of helping someone start a new career and earn a higher level of respect among your peers. Earn an additional $0.23 per mile on all miles and a potential bonus of $500! \n\n Qualifications: \n\n \n\t Valid CDL-A \n\t 6 months minimum Tractor-trailer driving experience \n\t 21 years of age or older \n\t Has the right to work and live in the United States \n\t Be willing to travel throughout all 48 contiguous states for two to three weeks at a time \n\t No BACs, DUIs, DWIs or license suspensions for moving violations in the past five years \n\t Ability to meet work attendance and availability requirements and all applicable legal and DOT regulations to drive a commercial truck in the United States \n\t Ability to pass all applicable CFI certification class testing and requirements \n \n\n CFI is Proud to Support Women Drivers! Apply Now! \n\n It is the policy of CFI to provide equal employment and individual opportunity to all job applicants and employees without regard to race, color, religion, sex, age, national origin, disability, veteran status or any other status as protected by federal, state and local governments.

Home Health Physical Therapist - $43-64 per hour

Advocate Aurora Health Round Lake Beach, IL

Advocate Aurora Health is seeking a Home Health Physical Therapist for a job in Round Lake Beach, Illinois. Job Description & Requirements Specialty: Physical Therapist Discipline: Therapy Duration: Ongoing 40 hours per week Shift: days Employment Type: Staff Major Responsibilities: Assuring and Improving Quality of Care: Facilitates the patient and family's right to receive quality cost-effective care following Advocate's MVP of Stewardship. 1)Utilizes appropriate resources to respond to situations that have the potential to negatively impact outcomes. 2)Adapts practice to the latest standards according to evidence based literature. Utilizes appropriate tests and measures, and interventions to achieve outcomes. 3)Participates in quality/process improvement initiatives. 4)Promotes efforts to reduce risk and improve patient safety. 5)Consistently demonstrates the ability to thoroughly and decisively document to support reimbursement and regulatory requirements. Care and Service Coordination: Practices as an effective member of the patient care team to formulate an integrated approach to care following Advocate's MVP of Partnership. 1)Participates in staff meetings, agency in services, and educational activities to enhance development and support organizational initiatives. 2)Utilizes available resources to maintain current knowledge base relevant to practice. 3)Demonstrates effective communication, feedback, and conflict resolution skills promoting collaboration among healthcare team members. 4)Seeks out opportunities to enhance knowledge, skill, and competency of self and other department members. Leadership/Collaboration/Professional Development: Demonstrates respect and understanding for peers and other clinical disciplines and participates as an effective member of the patient care team to formulate an integrated approach to care following the Advocate MVP of Excellence. 1)Consistently makes sound clinical decisions, demonstrating the ability to care for all patients, including those with complex problems. 2)Recognizes changes in clinical situations. Evaluates and implements changes to the plan of care. 3)Prioritizes and organizes patient care, ensures clear hand-off communication to achieve optimal health outcomes for patients, utilizing excellent communication techniques like SBAR and 5P's. 4)Initiates referrals and discharge planning for assigned patients and actively coordinates care utilizing the interdisciplinary approach. (As appropriate based on employment status). 5)Actively participates in interdisciplinary case conferences. (As appropriate based on employment status). Patient Relationship: Develops and maintains a restorative relationship throughout the healthcare continuum, following Advocate's MVP of Compassion. 1)Provides care that routinely exceeds patients and families expectations, as measured by survey instruments. 2)Promotes patient/family knowledge and confidence to safely manage self-care, disease process, medications, procedures and infection control prevention. 3)Incorporates an individualized approach to the plan of care, which includes assessment of physical, psychosocial, comfort and wellness needs. 4)Incorporates AHHS Standards of Behavior into interactions with patients, other associates, and physicians. 5)Assesses patient and family readiness and involves them in goal setting, planning and implementation of care. Seeks consultation and outside referrals as needed. 6)Demonstrates adaptive communication styles based on individual patient needs. Business Development and Growth: Demonstrates behaviors that enhance productivity and an understanding of financial and economic conditions in the health care environment. 1)Demonstrates adherence to personnel and operational policies. 2)Collaborates and plans patient care with others in organization to maximize efficiencies and conserve resources. 3)Monitors utilization of resources to achieve excellent health outcomes for patients. Patient Education: Demonstrates a commitment to meet the learning needs of patients and their families. Application of a systematic process involving optimal level of self care for patients and optimal quality of life for patient, family and significant others following Advocate's MVP of Equality. 1)Assesses patient and family readiness to learn and modifies approach as necessary. 2)Provides and adapts appropriate resource material to achieve patient education outcomes, employing health literacy assessments and principles. Licensure: Physical Therapist Education/Experience Required: Licensed in the State of Illinois (or eligible for licensure) Able to demonstrate compliance with state continuing education requirements 1 year of clinical experience or demonstration of strong spectrum of clinical affiliation experience Knowledge, Skills & Abilities Required: Basic knowledge of computer use (i.e. Microsoft Word, email access and use) Ability to learn to use computer based scheduling and documentation system Ability to communicate professionally both verbally and through written reports, with strong documentation skills Good interpersonal skills Good time management and self organization skills Proficient use of all home based therapy equipment and assistive devices, (balls, bands, weights, Hoyer lifts, etc) Licensed as Physical Therapist in the State of Illinois. Physicial Requirements and Working Conditions: Extensive travel within geographical boundaries in all extremes of weather and on all types of roads including expressways. Must be able to provide/arrange own transportation to and from patients homes and branch offices. Ability to work rotating weekends and holidays. Requires adherence to scheduled days and hours of work based on commitment to patient/client and work load assigned. Ability to attend mandatory informational/education/branch meetings. Work environment includes patient or family homes, or assisted living facilities. Requires full range of body motion including: a. Bending, sitting and standing b. Climbing stairs while carrying objects c. Pulling, pushing, reaching, carrying and lifting; (must be able to lift/carry at minimum 25 pounds). d. Assisting and maintaining patient's safety with ambulation on flat surfaces and stairs; and transferring patients using standard pivot transfers or with use of transfer board of Hoyer lift e. Providing treatment on standard beds in the home environment. This requirement supersedes any previous lifting requirement effective 08/01/2014. Ability to lift up to 35 pounds without assistance. For patient lifts of over 35 pounds, or when patient is unable to assist with the lift, patient handling equipment is expected to be used, with at least one other associate, when available. Unique patient lifting/movement situations will be assessed on a case-by-case basis. This job description indicates the general nature and level of work expected of the incumbent. It is not designed to cove

Sr Quality Assurance Specialist II - QA Ops (Hiring Immediately)

Takeda Pharmaceutical Round Lake, IL

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role: The QA Specialist II oversees daily activities within Quality Assurance Operations. You will work as part of aa team, providing quality leadership and ensuring product quality and compliance. Main responsibilities include Quality on the Shop Floor (QOTSF), Acceptable Quality Limit (AQL) inspections, incoming raw material release, documentation review (e.g., batch records and electronic batch records), and approvals for investigations and change controls. You will uphold Takeda’s Quality Culture elements of keeping it simple, taking pride in doing it right, ensuring a speak up culture and overseeing and demonstrating commitment to Quality. How you will contribute: Oversee and approve Standard Operating Procedures (SOPs) and other quality documentation relevant to the Quality department and all areas of the plant. Develop, delivers, and approves training materials related to Quality operations, ensuring agreement across all plant areas. Manage a QA Operations team, encouraging continuous development and ensuring the achievement of performance goals. Provide leadership and oversight to quality operations and other responsibilities and escalate. Manage investigations and CAPAs for the Quality department, providing oversight and approvals for compliance across all plant operations. Oversee and approve change controls within the Quality department, ensuring understanding of existing compliance requirements. Provide Quality approval for labeling artwork and packaging material specifications using artwork management software. Lead Quality project teams, presenting project plans, progress, and risks to plant management, and representing the organization to regulatory bodies. Approve documentation following cGMP guidelines, identifying opportunities for process improvements and ensuring compliance on the manufacturing floor. Review and approve raw materials following SOPs, releasing materials for manufacturing use, resolving issues related to materials release, and overseeing preprinted material accountability, material receipt, and JDE inventory management system issues. Be a subject matter expert (SME) during internal and external regulatory audits, presenting Quality operations to auditors. Collaborate with Manufacturing and Engineering teams through Quality on the Shop Floor (QOTSF) programs to lead sound, compliant Quality decisions. Conduct gap assessments and implement global processes to enhance Quality operations. Manage Final Container sampling processes and Quarantine and Reject processes for materials and finished products. Experience with visual inspection and AQL processes related to parenteral drugs. Knowledge of manufacturing processes related to aseptic filling, visual inspection, and packaging. Knowledge of FDA, EMA, CFDA, PDA Regulations, application of Good Data and Documentation Practices (GDDP) and application of current Good Manufacturing Practices (cGMP). What you bring to Takeda: Bachelor's degree in science, engineering, or other related technical field. 6 years of related work experience. Important Considerations At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. You may: You will be asked to not be allergic to Cephalosporin drugs. Ability to walk 1-3 miles and lift 10 lbs. during a workday is required. Indoor working conditions. May work around moving equipment and machinery. Some Clean Room and cool/hot storage conditions. May work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas. Will need to remove all make-up, jewelry, contact lenses, nail polish and artificial fingernails while in the manufacturing environment. May work in a cold, hot or wet environment. May work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection. Can work non-traditional work hours or work extended hours, including weekends and holidays. More about us: At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and the best patient support programs. Takeda is a patient-focused company to inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. GMSGQ ZR1 Takeda Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. For Location: USA - IL - Round Lake - Drug Delivery U.S. Base Salary Range: $108,500.00 - $170,500.00 The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained , certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based e mployee s may be eligible for s hort - t erm and/ or l ong- t erm incentive s . U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Locations USA - IL - Round

Sr Quality Assurance Specialist II - QA Ops - Global Pharmaceutical Leader (Hiring Immediately)

Takeda Pharmaceutical Round Lake, IL

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role: The QA Specialist II oversees daily activities within Quality Assurance Operations. You will work as part of aa team, providing quality leadership and ensuring product quality and compliance. Main responsibilities include Quality on the Shop Floor (QOTSF), Acceptable Quality Limit (AQL) inspections, incoming raw material release, documentation review (e.g., batch records and electronic batch records), and approvals for investigations and change controls. You will uphold Takeda’s Quality Culture elements of keeping it simple, taking pride in doing it right, ensuring a speak up culture and overseeing and demonstrating commitment to Quality. How you will contribute: Oversee and approve Standard Operating Procedures (SOPs) and other quality documentation relevant to the Quality department and all areas of the plant. Develop, delivers, and approves training materials related to Quality operations, ensuring agreement across all plant areas. Manage a QA Operations team, encouraging continuous development and ensuring the achievement of performance goals. Provide leadership and oversight to quality operations and other responsibilities and escalate. Manage investigations and CAPAs for the Quality department, providing oversight and approvals for compliance across all plant operations. Oversee and approve change controls within the Quality department, ensuring understanding of existing compliance requirements. Provide Quality approval for labeling artwork and packaging material specifications using artwork management software. Lead Quality project teams, presenting project plans, progress, and risks to plant management, and representing the organization to regulatory bodies. Approve documentation following cGMP guidelines, identifying opportunities for process improvements and ensuring compliance on the manufacturing floor. Review and approve raw materials following SOPs, releasing materials for manufacturing use, resolving issues related to materials release, and overseeing preprinted material accountability, material receipt, and JDE inventory management system issues. Be a subject matter expert (SME) during internal and external regulatory audits, presenting Quality operations to auditors. Collaborate with Manufacturing and Engineering teams through Quality on the Shop Floor (QOTSF) programs to lead sound, compliant Quality decisions. Conduct gap assessments and implement global processes to enhance Quality operations. Manage Final Container sampling processes and Quarantine and Reject processes for materials and finished products. Experience with visual inspection and AQL processes related to parenteral drugs. Knowledge of manufacturing processes related to aseptic filling, visual inspection, and packaging. Knowledge of FDA, EMA, CFDA, PDA Regulations, application of Good Data and Documentation Practices (GDDP) and application of current Good Manufacturing Practices (cGMP). What you bring to Takeda: Bachelor's degree in science, engineering, or other related technical field. 6 years of related work experience. Important Considerations At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. You may: You will be asked to not be allergic to Cephalosporin drugs. Ability to walk 1-3 miles and lift 10 lbs. during a workday is required. Indoor working conditions. May work around moving equipment and machinery. Some Clean Room and cool/hot storage conditions. May work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas. Will need to remove all make-up, jewelry, contact lenses, nail polish and artificial fingernails while in the manufacturing environment. May work in a cold, hot or wet environment. May work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection. Can work non-traditional work hours or work extended hours, including weekends and holidays. More about us: At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and the best patient support programs. Takeda is a patient-focused company to inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. GMSGQ ZR1 Takeda Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. For Location: USA - IL - Round Lake - Drug Delivery U.S. Base Salary Range: $108,500.00 - $170,500.00 The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained , certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based e mployee s may be eligible for s hort - t erm and/ or l ong- t erm incentive s . U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Locations USA - IL - Round

Best Match

Senior QA Operations Analyst II (Hiring Immediately)

Takeda Pharmaceutical Round Lake, IL

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role: The QA Specialist II oversees daily activities within Quality Assurance Operations. You will work as part of aa team, providing quality leadership and ensuring product quality and compliance. Main responsibilities include Quality on the Shop Floor (QOTSF), Acceptable Quality Limit (AQL) inspections, incoming raw material release, documentation review (e.g., batch records and electronic batch records), and approvals for investigations and change controls. You will uphold Takeda’s Quality Culture elements of keeping it simple, taking pride in doing it right, ensuring a speak up culture and overseeing and demonstrating commitment to Quality. How you will contribute: Oversee and approve Standard Operating Procedures (SOPs) and other quality documentation relevant to the Quality department and all areas of the plant. Develop, delivers, and approves training materials related to Quality operations, ensuring agreement across all plant areas. Manage a QA Operations team, encouraging continuous development and ensuring the achievement of performance goals. Provide leadership and oversight to quality operations and other responsibilities and escalate. Manage investigations and CAPAs for the Quality department, providing oversight and approvals for compliance across all plant operations. Oversee and approve change controls within the Quality department, ensuring understanding of existing compliance requirements. Provide Quality approval for labeling artwork and packaging material specifications using artwork management software. Lead Quality project teams, presenting project plans, progress, and risks to plant management, and representing the organization to regulatory bodies. Approve documentation following cGMP guidelines, identifying opportunities for process improvements and ensuring compliance on the manufacturing floor. Review and approve raw materials following SOPs, releasing materials for manufacturing use, resolving issues related to materials release, and overseeing preprinted material accountability, material receipt, and JDE inventory management system issues. Be a subject matter expert (SME) during internal and external regulatory audits, presenting Quality operations to auditors. Collaborate with Manufacturing and Engineering teams through Quality on the Shop Floor (QOTSF) programs to lead sound, compliant Quality decisions. Conduct gap assessments and implement global processes to enhance Quality operations. Manage Final Container sampling processes and Quarantine and Reject processes for materials and finished products. Experience with visual inspection and AQL processes related to parenteral drugs. Knowledge of manufacturing processes related to aseptic filling, visual inspection, and packaging. Knowledge of FDA, EMA, CFDA, PDA Regulations, application of Good Data and Documentation Practices (GDDP) and application of current Good Manufacturing Practices (cGMP). What you bring to Takeda: Bachelor's degree in science, engineering, or other related technical field. 6 years of related work experience. Important Considerations At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. You may: You will be asked to not be allergic to Cephalosporin drugs. Ability to walk 1-3 miles and lift 10 lbs. during a workday is required. Indoor working conditions. May work around moving equipment and machinery. Some Clean Room and cool/hot storage conditions. May work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas. Will need to remove all make-up, jewelry, contact lenses, nail polish and artificial fingernails while in the manufacturing environment. May work in a cold, hot or wet environment. May work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection. Can work non-traditional work hours or work extended hours, including weekends and holidays. More about us: At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and the best patient support programs. Takeda is a patient-focused company to inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. GMSGQ ZR1 Takeda Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. For Location: USA - IL - Round Lake - Drug Delivery U.S. Base Salary Range: $108,500.00 - $170,500.00 The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained , certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based e mployee s may be eligible for s hort - t erm and/ or l ong- t erm incentive s . U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Locations USA - IL - Round

Lead Quality Assurance Coordinator - Operational Excellence (Hiring Immediately)

Takeda Pharmaceutical Round Lake, IL

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role: The QA Specialist II oversees daily activities within Quality Assurance Operations. You will work as part of aa team, providing quality leadership and ensuring product quality and compliance. Main responsibilities include Quality on the Shop Floor (QOTSF), Acceptable Quality Limit (AQL) inspections, incoming raw material release, documentation review (e.g., batch records and electronic batch records), and approvals for investigations and change controls. You will uphold Takeda’s Quality Culture elements of keeping it simple, taking pride in doing it right, ensuring a speak up culture and overseeing and demonstrating commitment to Quality. How you will contribute: Oversee and approve Standard Operating Procedures (SOPs) and other quality documentation relevant to the Quality department and all areas of the plant. Develop, delivers, and approves training materials related to Quality operations, ensuring agreement across all plant areas. Manage a QA Operations team, encouraging continuous development and ensuring the achievement of performance goals. Provide leadership and oversight to quality operations and other responsibilities and escalate. Manage investigations and CAPAs for the Quality department, providing oversight and approvals for compliance across all plant operations. Oversee and approve change controls within the Quality department, ensuring understanding of existing compliance requirements. Provide Quality approval for labeling artwork and packaging material specifications using artwork management software. Lead Quality project teams, presenting project plans, progress, and risks to plant management, and representing the organization to regulatory bodies. Approve documentation following cGMP guidelines, identifying opportunities for process improvements and ensuring compliance on the manufacturing floor. Review and approve raw materials following SOPs, releasing materials for manufacturing use, resolving issues related to materials release, and overseeing preprinted material accountability, material receipt, and JDE inventory management system issues. Be a subject matter expert (SME) during internal and external regulatory audits, presenting Quality operations to auditors. Collaborate with Manufacturing and Engineering teams through Quality on the Shop Floor (QOTSF) programs to lead sound, compliant Quality decisions. Conduct gap assessments and implement global processes to enhance Quality operations. Manage Final Container sampling processes and Quarantine and Reject processes for materials and finished products. Experience with visual inspection and AQL processes related to parenteral drugs. Knowledge of manufacturing processes related to aseptic filling, visual inspection, and packaging. Knowledge of FDA, EMA, CFDA, PDA Regulations, application of Good Data and Documentation Practices (GDDP) and application of current Good Manufacturing Practices (cGMP). What you bring to Takeda: Bachelor's degree in science, engineering, or other related technical field. 6 years of related work experience. Important Considerations At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. You may: You will be asked to not be allergic to Cephalosporin drugs. Ability to walk 1-3 miles and lift 10 lbs. during a workday is required. Indoor working conditions. May work around moving equipment and machinery. Some Clean Room and cool/hot storage conditions. May work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas. Will need to remove all make-up, jewelry, contact lenses, nail polish and artificial fingernails while in the manufacturing environment. May work in a cold, hot or wet environment. May work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection. Can work non-traditional work hours or work extended hours, including weekends and holidays. More about us: At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and the best patient support programs. Takeda is a patient-focused company to inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. GMSGQ ZR1 Takeda Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. For Location: USA - IL - Round Lake - Drug Delivery U.S. Base Salary Range: $108,500.00 - $170,500.00 The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained , certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based e mployee s may be eligible for s hort - t erm and/ or l ong- t erm incentive s . U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Locations USA - IL - Round

Software Developer - Web

Uline Round Lake, IL

Software Developer - Web Pay from $80,000 to $119,000 per year 2200 S. Lakeside Drive, Waukegan, IL 60085 Develop custom solutions and enjoy a great career at Uline. Bring your extensive skillset to a place ready to employ every facet of it. Collaborate on customer-facing and internal projects among a team of dedicated fellow developers. *Visa sponsorship available for this position. Better together! This position is on-site in Pleasant Prairie, WI or Waukegan, IL based on need, and we are looking for people who share our passion. Position Responsibilities Apply industry best practices and cutting-edge techniques to design, develop, test, deploy, support and maintain sophisticated web applications based on business requirements. Enhance and support our world-class e-commerce and mobile sites, along with sales, intranet and internal web applications. Collaborate closely with the development team to ensure process consistency and timely completion of deliverables. Conduct design and code reviews to help maintain code quality, performance and application responsiveness. Minimum Requirements Bachelor's degree in Computer Science, Information Technology or a related field. 2+ years of web development experience. Strong understanding of object-oriented design, web application architecture and relational database design. Proven experience in delivering web and e-commerce solutions using technologies like .NET, MVC, C# and JavaScript (jQuery or TypeScript). Proficiency in writing T-SQL queries and stored procedures. Experience in writing automated unit tests to ensure high-quality code. Familiarity with Java, Agile methodology, Angular, Dynatrace, Cassandra or ELK a plus. Benefits Complete medical, dental, vision and life insurance coverage and other wellness programs. 401(k) with 6% employer match. Multiple bonus programs. Paid holidays and generous paid time off. Tuition Assistance Program that covers professional continuing education. Employee Perks Café featuring affordable daily meal options from local restaurants. On-site fitness center and beautifully maintained walking paths. Best-in-class, clean, modern facilities. About Uline Uline, a family-owned company, is North America’s leading distributor of shipping, industrial, and packaging materials with over 9,000 employees across 13 locations. Uline is a drug-free workplace . EEO/AA Employer/Vet/Disabled #LI-MW2 #CORP (#IN-PPITDEV) Our employees make the difference and we are committed to offering exceptional benefits and perks! Explore Uline.jobs to learn more! #J-18808-Ljbffr

CAREGIVER in ROUND LAKE BEACH IMMEDIATE START

Assisting Hands - Deerfield Round Lake Beach, IL

Have you ever thought about a job where you just need to be someone’s friend? Are you: C aring and compassionate? A ctive? R esponsible and reliable? E mpathetic? G racious? I ntelligent? V ery honest? E asy-going? R eady to help? Do you have a school diploma and are you at least 18 years old? Do you want to become a FAMILY TEAM MEMBER , willing to make this world better, to be a shoulder for somebody who really needs it? WHY JOINING ASSISTING HANDS DEERFIELD? Believe us, with us you will have a nice, kind & understanding FAMILY MEMBER & FRIEND instead of a boss. And, for sure, there are other things we are offering YOU: A ccess to your online profile with your schedule; S hifts available: day time shifts, night time shifts, overnights, week days, weekends; S taff helping you and available for you 24/7; I mmediate start; S upportive Team; T raining and continuing education opportunities; I ndependence; N ice bonus program; G rowth opportunities; Hours over 40 and hours on holidays are paid time and a half; A flac Health Insurance benefits; N o waiting 2 weeks for your pay, WE PAY WEEKLY; D irect deposit; S ign on bonuses. Just give us a chance, you will not regret it! Turn your passion for helping people into a brilliant career. If you don’t know anything about this job and don’t have any experience, no worries, we will teach you! Just send me your resume to [email protected] . Or just call me at 847-558-2228 to set up an interview. Or call me just to talk. Or text me at 847-558-2228. Or fax me, same number. Sorry, reference and background check required for all employees. #J-18808-Ljbffr

CAREGIVER in ROUND LAKE BEACH IMMEDIATE START

Assisting Hands Home Care Round Lake Beach, IL

Have you ever thought about a job where you just need to be someone’s friend? Are you: C aring and compassionate? A ctive? R esponsible and reliable? E mpathetic? G racious? I ntelligent? V ery honest? E asy-going? R eady to help? Do you have a school diploma and you are at least 18 years old? Do you want to become a FAMILY TEAM MEMBER , willing to make this world better, to be a shoulder for somebody who really needs it? Overall, you are a precious candidate, aren’t you? WHY JOINING ASSISTING HANDS DEERFIELD? Believe us, with us you will have a nice, kind & understanding FAMILY MEMBER & FRIEND instead of a boss. And, for sure, there are other things we are offering YOU: A ccess to your online profile with your schedule; S hifts available: day time shifts, night time shifts, overnights, weekdays, weekends; S taff helping you and available for you 24/7; I mmediate start; S upportive Team; T raining and continuing education opportunities; I ndependence; N ice bonus program; G rowth opportunities; Hours over 40 and hours on holidays are paid time and a half; A flac Health Insurance benefits; N o waiting 2 weeks for your pay, WE PAY WEEKLY; D irect deposit; S ign on bonuses. Just give us a chance, you will not regret it! Turn your passion for helping people into a brilliant career. If you don’t know anything about this job and don’t have any experience, no worries, we will teach you! Just send me your resume to [email protected] . Or just call me at 847-558-2228 to set up an interview. Or call me just to talk. Or text me at 847-558-2228. Or fax me, same number. Sorry, reference and background check required for all employees. #J-18808-Ljbffr

Optical Sales Associate Meijer Optical #22100, Round Lake Beach, IL

U.S .Vision Round Lake Beach, IL

Our heritage in eye care spans more than 100 years. In 1885, opticians William Wall and Charles Ochs opened their first eyeglass store and manufacturing facility in Philadelphia, PA. Their reputation for fine eyewear and superior eye care grew, and Wall & Ochs was soon synonymous with exceptional quality and great value. In the early 1970’s, Wall & Ochs became U.S. Vision in response to a growing reputation for quality and the customer base that came with it. Today, we have more than 350 locations located in JCPenney, Meijer, Boscov’s and AAFES. What you’ll do: The successful Optical Sales Associate delivers excellence to provide a professional and positive experience for all patients, customers, colleagues, and business partners and works with the Optical Sales Manager in the: Commitment to deliver excellence in customer service and satisfaction Driving of sales and controlling expenses Accountability to achieve personal and store goals Execution of effective operational and procedural processes Engaging with patients and customers to fulfill prescriptive eyewear needs What we need: Optical / Retail skills preferred Sales ability to C onnect with customers, U ncover their needs, R ecommend items based on their needs and E ducate the customer on their purchases as outlined in our CURE selling model Polished and professional communication and customer-centric service skills Able to use POS and computer systems Capable of working with and servicing and interacting with diverse people Self-motivation, action-oriented, and a creative problem solver open to feedback and learning Reliability and punctuality in attendance Flexibility for scheduling, and able to work weekends, select holidays, as well as special sales events Ability to meet the physical needs of the job and multi-task in a busy work environment US Vision is an Equal Opportunity Employer. We value diversity and an inclusive, accessible workplace. We are committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at US Vision are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, sexual orientation, gender identity and/or expression, past or present military service, or any other status protected by the laws or regulations in the locations where we operate. US Vision is a Drug-Free work environment. We participate in the E-Verify program. Benefits: Health Care Plan (Medical, Dental & Vision) Retirement Plan (401k, IRA) Life Insurance (Basic, Voluntary & AD&D) Paid Time Off (Vacation, Sick & Public Holidays) #J-18808-Ljbffr

Part-Time Sales Associate - Famous Footwear

Famous Footwear Round Lake Beach, IL

270 E Rollins Rd, Round Lake Beach, IL 60073, USA Job Description If you're looking for that next step in your career, make it famous! To us, famous isn’t about standing out in the crowd. It’s about feeling good where you stand right now. Famous Footwear is your place for athletic, fashion and casual shoes for the whole family from hundreds of name brands. As a Famous Footwear Sales Associate , you are passionate about providing the best shoe store experience for every customer. You do this by creating a welcoming environment and in-store culture where customers say, “I’ll take it” and are loyal to your store, our brands, and our company. You are a team player, celebrating individual and team successes. You are committed to staying informed about trends and sharing that knowledge with customers, ultimately building engaging customer experiences. Most importantly, you LOVE shoes and regardless of your style, you help every person who enters the store experience a little bit of that Famous Feeling. What You’ll be Doing Ace Retail Operations: You’ll ensure daily store tasks (pricing, shipment processing, fulfillment and inventory) are dialed in, keeping the store running like a tightly laced sneaker. Utilizing our company standards as a framework for success, you’ll deliver on our goal of keeping the store clean, organized, and all our famous styles easily shoppable. Be a Famous Culture Influencer: Champion our Famous culture with pride by embodying the behaviors that power our Customer Connection. You’ll provide stellar customer engagement, leaving customers wowed with consistently top-notch experiences powered by your attentiveness and determination to deliver them the styles and brands they crave. Elevate to Your Goal-Crushing Era: You’ll bring your best to each day; take accountability for your effort and its impact on Famous Footwear’s overall performance. You’ll review store performance and drive sales with purpose and urgency to achieve goals. Every shoe sale counts! As a ‘goal-getter’, you deliver clear, concise and timely communications to the entire store team and employ active listening to ensure understanding among teammates. Act with Integrity: Your high standards will keep you sticking to company policies and procedures. Always acting with integrity, you’ll be open to and seek feedback to improve your skillset and further your professional development! Bring the Positive Vibes: Embrace diversity and inclusivity as our team superpower, upholding a work environment where every associate feels included and respected. Maintain a positive and proactive mindset, even in the face of challenges, you’re the type of person to uplift and support others. To help others be their best, you’ll help your teammates be their best selves by assisting with training and development when needed. Be a Shoe-off: You are shoe-obsessed (no judgment.) When a customer enters the store, you’re a shoe sleuth on the hunt for the perfect styles to suit their needs. It brightens your day to make shoe recommendations and ensure our customers leave the store with the perfect fit…and that Famous Feeling. Essential Functions: Other responsibilities may be performed as needed to ensure the needs of the business are met. Overtime hours may be required to meet business needs. Our Shoe Discounts: No matter your style, we’ve got your perfect fit covered with a 30% Associate Discount across Caleres’s retail stores – Famous Footwear, Naturalizer, Sam Edelman, and Allen Edmonds. Relaxed Dress Code & Small Team Environment: You will be a valued member in a supportive and hands-on setting. Our relaxed dress code policy lets you showcase your authentic self while you work. Daily Access to Pay: Love an early pay day? Get paid as you earn (without the fees) with Dayforce Wallet. Ease of Transferring Locations: We have over 850 store locations you can easily transfer within. Career Development and Learning Opportunities: We provide education assistance of up to $7500 per year for full-time associates and provide opportunities for associates who want to grow their careers at our corporate offices. Employee Assistance Programs: Receive 24/7 access to a comprehensive suite of individual support options, including emotional support, work-life solutions, legal guidance, financial resources and more, via online & phone. Benefit Offerings: PTO, Health, and Retirement for eligible full-time associates. To learn more details about our Total Rewards program, visit www.yourcaleres.com . Preferred Qualifications & Education High School Diploma/GED Able to build constructive and effective relationships within store Demonstrates an ability to communicate positively with store associates at all levels Must exercise independent judgment and discretion partnering with Store Sales Manager as needed Strong working knowledge of general retail practices and procedures Ability to work effectively within a team Ability to work a flexible schedule to meet the needs of the business, including holidays, nights, weekends and extended hours Physical Requirements and/or Environment Ability to regularly lift up to 40 lbs. from floor level to above shoulder height utilizing appropriate equipment and safety techniques; Ability to meet demands of frequent walking, standing, stooping, kneeling, climbing, pushing, pulling, and repetitive lifting; Ability to be mobile on the sales floor for extended periods of time. Famous Footwear is part of Caleres Inc., a diverse portfolio of 15 global footwear brands including Sam Edelman, Naturalizer, Vionic, Dr. Scholl's, Allen Edmonds, and many more. Caleres' legacy includes more than 140-years of craftsmanship, a passion for fit and business savvy, with a mission to continue to inspire people to feel great…feet first. Caleres is an Equal Opportunity Employer by choice. We believe our company should be as diverse as the consumers we serve. We seek and engage talented individuals from all backgrounds, ethnicities, genders, lifestyles, and belief systems. Caleres and Famous Footwear are invested in our Associates. We regularly review our pay matrices and update appropriately based on need. Starting pay is determined by several factors, including relevant skills, qualifications, and experience. The actual pay rate will equal or exceed the required minimum wage applicable to the job location. Please visit yourcaleres.com to review all associated benefits. 270 E Rollins Rd, Round Lake Beach, IL 60073, USA #J-18808-Ljbffr

Research Associate III - Chemical Characterization,

Baxter International Inc. Round Lake, IL

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives— where your purpose accelerates our mission. Your Role at Baxter This is where your work saves lives. We currently have an opening for a versatile Analytical Chemist who can play the role of analytical lead, direct and execute lab experiments, and facilitate Operational Excellence in the Medication Delivery R&D chemistry lab in Round Lake, Illinois. What you'll be doing: Act as a study contributor, such as aiding in the design and execution of extractables and leachables, method development, validation, and transfer studies. Conduct impurities studies (routine and non-routine) by performing chemical analysis utilizing LC, GC, and/or ICP with various detections including MS and associated wet chemistry and sample preparation techniques. Collaborate with other functions such as project management, regulatory, extractables, toxicology, biocompatibility, manufacturing and quality in project teams. Participate in investigations that correspond to atypical or out-of-specification/out-of-trend results. Leverage critical thinking skills to drive the investigation to conclusions based on sound scientific principles. Create, update, and maintain equipment and analytical procedures. Maintain knowledge of and demonstrate adherence to relevant Quality System Regulations and other regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities. This applies to governmental and international industry requirements, procedures, regulations, and standards e.g., related to method validation (USP, ICH). Have an in-depth knowledge and understanding of cGxP and related regulations and guidance. Leverage operational excellence in the execution of laboratory activities. Evaluate analytical results, identify trends, exceptions, and interpretation of results relative to product requirements, definitions and/or project goals. Competent in interpreting analytical data and presenting in a form that is suitable for a wide-ranging audience. Communicate clearly with management, peers, cross-functional teammates, and non-technical audiences by openly sharing project status and hurdles and seeking input from other team members. What you'll bring: Bachelor’s degree in a scientific discipline (such as Analytical or Organic chemistry) with at least 5+ years, MS with at least 3+ years, or PhD with at least 0 + years of experience in relevant discipline. Required knowledge and demonstrated experience of analytical chemistry with relevant laboratory skills (hands-on experience with wet chemical techniques and instrumental analysis including LC/MS/UV, GC/MS/FID, and ICP-MS). Experienced with analytical method development, validation, and transfer. Possesses a good understanding of ICH, USP guidelines and cGxP practice. Experience with MassHunter, Sciex Analyst, Empower, E-noval and/or other analytical instruments software systems. Ability to learn quickly and to solve problems in a timely manner using critical thinking and analytical chemistry skills. Designs experiments and draws meaningful conclusions from lab data in addition to critically review peers’ work. Demonstrates quality and detail-oriented work. Provides and accepts critical feedback from others in a constructive manner. Adapts to changes and has an Agile mindset. Works in a team environment and demonstrates an inclusive attitude. Embraces diversity and inclusion, values differences. Willingness to work across multiple time zones. Possess strong time management and project management skills. Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time. #J-18808-Ljbffr

Library Assistant I- Adult Services

Alsip-Merrionette Park Public Library District Round Lake, IL

The Round Lake Area Public Library is seeking a candidate who will provide excellent customer service, support, and programming to our diverse community. The ideal candidate is a tech-savvy problem-solver with strong decision-making skills, the ability to work independently, and a focus on helping patrons navigate resources and services. REQUIRED EDUCATION AND EXPERIENCE: High school diploma or GED. One to three years previous work experience in a public service environment required; public library experience preferred. A Bachelor’s degree, LTA certificate or comparable education is preferred. DUTIES AND RESPONSIBILITIES: Provide outstanding customer service in person, on the telephone, and via e-mail and other forms of electronic communication. Assist and instruct patrons of all ages on the use and access of library resources including but not limited to: online catalog, Hoopla, Overdrive/Libby, computers, copiers, printers, Book Scan Station, faxing, program registration, and Microsoft office products. Assist patrons with basic internet skills such as filling out forms, uploading documents, downloading documents, printing from email, attaching documents to email, composing email, and searching. Perform collection development responsibilities in multiple assigned areas including selection, utilization analysis and weeding tasks. Research, schedule, plan, organize, develop program ideas, develop materials, coordinate program logistics as appropriate and present programs for target populations. Provide reference and reader’s advisory services to adults and teens. Create and maintain in-library displays of materials. Keep the Adult Services area tidy by picking up debris, maintaining orderly arrangement of chairs and tables, and returning materials to carts. Assist and instruct patrons in use and troubleshooting of the variety of equipment found in the Library’s makerspace. Attend and participate in staff, department, and other job-related meetings and continuing education events as needed. Prepare monthly reports. Carry out opening and/or closing procedures for the department. May be designated Person – In – Charge in the absence of Director. Other duties as assigned. KNOWLEDGE, SKILLS, ABILITIES: Ability to speak, read, and write in English required. Ability to speak, read, and write in Spanish preferred. Excellent oral and written communication skills. Good knowledge of adult and teen literature including current authors, classic titles, and trends. Deal calmly and effectively with a wide range of individuals, in some instances under stressful or emergency conditions. Knowledge of and ability to utilize the Dewey Decimal System. Strong skills in problem solving and decision-making. Take direction and accurately follow instructions to work independently. Handle multiple activities or interruptions at once. Ability to schedule work efficiently and set priorities. Ability to work a flexible schedule. Work positively and effectively as a team member. PHYSICAL REQUIREMENTS/WORKING CONDITIONS: While performing the duties of this job, the Library Assistant is regularly required to stand; walk; run; sit; use hands to handle, or feel; reach with hands and arms; push; pull; carry; climb; stoop; bend; stretch; kneel; talk; and hear. The Library Assistant is required to remain in a standing position for extended periods of time. The Library Assistant must occasionally lift and/or move up to 50 pounds. The Library Assistant will assist patrons of all ages in a very busy environment. Specific vision abilities required by this job include close vision, color vision, and ability to adjust focus. Ability to withstand weather extremes. Work is performed inside a typical interior/office work environment. Work may be performed off site. Work may be performed in front of a computer. Work may be performed in inclement weather. Demonstrate good eye-hand coordination. Bending, stooping, and ability to reach library materials from high and low shelves. Ability to move a two-sided book cart loaded with up to 300 lbs. of books and other library materials. BENEFITS Paid time off: 42 hours annually. How to Apply Assistant Director and Head of Adult Services, Round Lake Area Public Library, Lake County. Hours 12-19 hours per week. #J-18808-Ljbffr

Dynamic Environment

Little Caesars - Crew Member - 1727

Careers at Little Caesars Round Lake Beach, IL

Come join our family and become a Pizza GENIUS! Title: Little Caesars Pizza – Crew Member Join the Little Caesars Pizza!Pizza! Family Do you like pizza? Do you like having fun? If so, we would love for you to join our family! Be A Pizza Genius: Provide excellent customer service Prep, cook, and serve food Achieve high customer satisfaction Work in a fast-paced, team-oriented environment Maintain clean work environment Other responsibilities as assigned Why We Are ExtraMostBestest: Free pizza every week Fun atmosphere Wear jeans every day (company provided shirt and hat) Flexible schedules On-site training Advancement opportunities State-of-the-art technology, systems, and equipment Now Hiring ALL shifts/hours! Full and part-time! Start With A Slice And Leave With The Whole Pie: Hard-working crew members can quickly work toward becoming an Assistant Manager, Store Manager, and beyond! Many of our most successful executives and franchisees have started their careers in the stores learning our operations! Who We Are: Little Caesars is built on a strong foundation of family, fun, and pizza! For more than 60 years, Little Caesars has been family-owned and operated. We believe in a fun and welcoming environment where everyone works hard and plays hard. We hit our goals and take time to recognize and celebrate individual and team success. Our purpose is to be heroes to our customers by making their lives easier, and our success as a big-town name is because of our focus on small-town values. Compensation: Salary: $15.00 This position is not benefit eligible. At Little Caesars, we value our employees’ time on and off the clock. So, whether you like working mornings, afternoons, nights, or weekends, you’ll still have time for your family, friends, and/or school. With the right attitude and a passion for pizza, the opportunities are endless at Little Caesars! All items listed above are illustrative and not comprehensive. They are not contractual in nature and are subject to change at the discretion of Little Caesars Enterprises Inc. Little Caesar Enterprises, Inc. is an Equal Employment Opportunity employer. All qualified applicants will receive consideration for employment without regard to that individual’s race, color, religion or creed, national origin or ancestry, sex (including pregnancy), sexual orientation, gender identity, age, physical or mental disability, veteran status, genetic information, ethnicity, citizenship, or any other characteristic protected by law. The Company will strive to provide reasonable accommodations to permit qualified applicants who have a need for an accommodation to participate in the hiring process (e.g., accommodations for a job interview) if so requested. This company participates in E-Verify. PRIVACY POLICY #J-18808-Ljbffr

Jobs in Round Lake