Jobs for Quality Intern

RN Safety & Quality Coordinator Women & Children Health - Relocate to Naples, FL

DEPARTMENT: 18383 - Safety & High ReliabilityLOCATION: 350 7th Street North, Naples, FL, 34102WORK TYPE: Full TimeWORK SCHEDULE: 8 Hour DayABOUT NCHNCH is an independent, locally governed non-profit delivering premier comprehensive care. Our healthcare system is comprised of two hospitals, an alliance of 700+ physicians, and medical facilities in dozens of locations throughout Southwest Florida that offer nationally recognized, quality health care.NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.Join our mission to help everyone live a longer, happier, healthier life. We are committed to care and believe there's always more at NCH - for you and every person we serve together. Visit nchjobs.org to learn more.JOB SUMMARYThe RN Safety & Quality Coordinator for Women & Child Health is a professionally trained RN responsible for leading performance improvement activities associated with the full spectrum of services within Maternal and Child Health including but not limited to data abstraction, collection and analytics for participation in performance improvement activities and reporting relevant to the Florida Perinatal Quality Collaborative, Florida Department of Health, and community partners, Perinatal Core Measures, Leapfrog Group reports and assigned physician contract services. The coordinator organizes performance improvement processes for Women and Child Health service with an emphasis on clinical guidelines, evidenced based practices and outcomes management to deliver on the organizational strategic goals. The coordinator guides the development, ongoing review, implementation, education and documentation of evidence-based best practice guidelines, care delivery and process improvement for Women and Child Health services. The coordinator supports the functions of Quality & Patient Safety with clinicians, providers, and IT staff to improve EMR documentation to support quality data reports, mandatory quality reporting and performance metrics. The coordinator supports educational training including SIMS training and drills related to Women & Child Health services. The coordinator supports high reliability methods for patient safety and a just culture.ESSENTIAL DUTIES AND RESPONSIBILITIES– Other duties may be assigned. · Coordinates the education and ongoing development of the WCH team on emerging developments through organizing learning sessions. · Coordinates teams and manages projects focused on achieving clinical performance improvement, strategic imperatives, goals, and objectives. · Acts as a liaison to various organization wide and medical staff departmental committees where WCH data is relevant. · Communicates with contracted abstracting services to ensure NCH internal data is managed, abstracted, and delivered in a timely and accurate fashion. · Follows all protocols for documentation and maintenance of databases. · Maintains compliance with all required reporting, assures deadlines are met impacting hospital reimbursement and public healthcare ratings agencies. · Identifies and facilitates solutions to quality issues, which arise from the data analysis. · Analyzes, summarizes, and provides written reports to WCP team, highlighting performance metrics and opportunities. · Provides the WCP team with timely performance feedback (reports) of identified evidence-based quality metrics that enhance patient care and safety. • Communicates with NCH IT to improve clinical progress reports for internal performance monitoring. · Organizes collaborative improvement meetings with the WCP team and other multidisciplinary stakeholders. Documents meeting minutes. • Identifies potential topics for research related to the programs. • Keeps up to date on all current literature, studies, and training and serves as the primary resource to share this information with relevant stakeholders. · Maintains a database of clinical protocols for reference and review on a recurring basis (at least annually) to assure quality outcomes. · Works with multidisciplinary teams’ system wide to ensure compliance and success with Emergency Room treatment with use of evidence-based practices and regulatory standards. EDUCATION, EXPERIENCE AND QUALIFICATIONS· Minimum of BSN from an accredited nursing program required. · Minimum of 3 years of nursing experience required; Labor and Delivery experience preferred. · Licensed as a Registered Nurse in the State of Florida (or obtained within 1 year of hire). · Basic Life Support (BLS) certification required from the American Red Cross or American Heart Association. · Experience with an electronic medical record preferred. · Quality data analysis, performance improvement and lean process experience preferred. Certification in Healthcare Quality (CPHQ) or IHI healthcare quality training within 2 years of hire. · Maintains open communication with the leadership at NCH Healthcare Systems regarding quality improvement, protocols, and public reporting/ratings agencies. · Utilizes improvement methodologies including lean six‐sigma and PDSA cycles for rapid‐cycle change. · Must have ability to use judgment and discretion in dealing with confidential information. · Hight to intermediate computer knowledge: Uses Microsoft applications and ability to learn and utilize various computer databases and E.M.R. navigation, reports, and dashboards.

Dynamic Environment

Quality Inspector

Modula Inc. Columbus, OH

Job Description Job Description Description: Who We Are: Modula is the leading US manufacturer of vertical lift modules (VLM) and automated storage and retrieval systems. Modula US has Manufacturing plants in Dayton, OH and Lewiston, ME, and remote locations throughout the US. Our corporate global headquarters is in Italy with many locations around the globe. Modula’s goal is to be an exceptional workplace admired for growing and developing talented employees and leaders, building innovative products through the development of a highly skilled and engaged workforce. Modula’s Values: We are culture and value driven; regardless of position and title we are all in all the time. Passion- Proud of our work/Modula, love what you do, positive energy, go the extra mile, engaging. Pursuit of Excellence- Continuous improvement, committed, attention to detail. Accountability- Lead by example, follow through, integrity, create trust with team & customers. Agility- Flexible & adaptable, embrace change, ability to multi-task, sense of urgency. Teamwork- Proactive & effective communication, respect, humility, curious, openminded, diversity. Basic Functions and Scope of Job: The Quality Inspector is responsible for maintaining quality standards, inspecting and documenting new part qualification, in-process production, finished product, and incoming parts and materials. Key Responsibilities: Approve in-process production by confirming specifications; conducting visual and measurement tests; communicating required adjustments to production supervisor and/or machine operators Inspect final products before shipment, including electrical testing Monitor in-process manufacturing operations to ensure adherence to quality techniques, practices and procedures Document inspection results by completing reports and logs; summarizing re-work and waste; inputting data into quality database Working with Engineering to qualify and verify new parts or assemblies Maintain safe and healthy work environment by following standards and procedures; complying with legal regulations Update job knowledge by participating in educational opportunities Ensure that the organization’s Quality Management System conforms to customer, internal, ISO 9001, and regulatory requirements Approve incoming materials by confirming specifications; conducting visual and measurement tests; rejecting and returning unacceptable materials Document Non-conformances, recommend actions and help work towards solutions Monitor, measure, and review internal Quality processes Responsible for accuracy and timely inspection/calibration of monitoring and measuring devices Maintain knowledge of standards, regulations/laws, issues, and news with respect to product (service) quality Perform other duties as assigned Please note: this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time, with or without notice. It is expected that this cross-functional role will perform other duties as assigned. Requirements: Qualifications and Skills: This role is pivotal in coordinating the company's quality inspection of our products. The individual in this position must have a high degree of integrity, resourcefulness, and professionalism in working with colleagues, clients, and vendors. Relationship building, internal customer service, and the ability to follow up in a timely manner are critical for success. The ideal candidate will have relative experience, excellent communication and time management skills, and manufacturing aptitude. To be successful in this role, a qualified applicant should possess the following attributes: Minimum education of a high school diploma or equivalent Minimum of one (1) year of related experience; combination of education and experience can be considered; electrical testing experience a plus Working knowledge of Microsoft Suite applications (Microsoft Word, Excel, and Outlook) Skilled with general inspection equipment (Calipers, depth gage, tape measure, etc.) Blueprint reading skills are a must Welding and metal fabrication experience is a plus Welding inspection experience is a plus ISO 9001:2015 experience preferred Ability to travel highly desired PHYSICAL QUALIFICATIONS Work Environment (Position / % of time per day or frequency): Walking / 20% Standing / 20% Sitting / 5% Computer, Electronic Use / 35% Twisting, turning, and squatting / 20% Pulling, Pushing / Up to 50 lbs. Lifting / Up to 50 lbs. Modula Inc. is an EEO (Equal Employment Opportunity) Employer. Our search and selection processes are based on identifying qualified candidates who are highly motivated to grow with our company. Employment decisions are based on the principles of equal employment opportunity. Recruitment, testing/assessment, selection, and promotion will be administered without regard to race, color, sexual orientation, physical or mental disability, religion, age, ancestry or national origin, whistleblower activity, previous assertion of a claim or right under worker’s compensation, marital status, genetic information, or any other characteristic protected by federal, state, or local law.

Work Life Balance

Quality Manager

HEART OF OHIO FAMILY HEA LTH CENTERS Columbus, OH

Job Description Job Description Summary : The primary function of the Quality Program Manager is responsible for providing day to day management of the quality improvement program. Responsible for coordinating activities of quality department staff, suggesting process changes, measuring data, and completing QA activities to achieve organization goals for quality measures for programs like UDS, Accountable Care/Clinically Integrated Networks, Ohio Medicaid CPC, CPC Kids, CMC, and individual insurance plan contracts. Reports to : Director of Quality and Clinical Systems Supervises : Yes Dress Requirement : Business Casual Work Schedule : Monday through Friday during standard business hours Times are subject to change due to business necessity Exempt Essential Job Duties and Responsibilities Work with supervisor and members of clinical leadership to develop, implement, monitor, and measure plans to improve processes and quality outcomes. Work with supervisor, clinical leadership, data analytics team, and external data vendor Unity PHM to analyze data, clean data, and perform quality assurance activities. In collaboration with supervisor, Chief Medical Officer, and others, the position is responsible for carrying out system-wide quality programs. Assists with developing, planning, and implementing policies and procedures. Works closely with supervisors, clinical teams, and non-clinical teams for quality improvement efforts. Assists with designing processes for quality improvement purposes. Plays a key role in maximizing revenue from value-based care, pay-for-performance, and risk adjustment contracts. Ensure compliances with program requirements. Examples include individual insurance plan contracts, Accountable Care/Clinically Integrated Networks, Ohio Medicaid CPC, CPC Kids, and CMC programs. Focuses on better healthcare value and quality, including the improvement of clinical outcomes, patient experience, patient safety, costs, revenue, productivity, efficiency, employee and physician satisfaction, and process reliability. Leads or participates in meetings related to quality improvement. Coordinate, manage and report UDS measures and other data related to clinical quality. Manages performance improvement projects to assure milestones and key performance indicators are met within defined parameters. Documents the results of projects, and submits other documentation as requested. Develop and motivate department staff. Interview, monitor time and attendance, and manage performance of subordinates. Report on clinical quality measures internally and externally. Provide updates to internal and external stakeholders on progress in quality initiatives. Support data collection and reporting related to grants. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice. Qualifications Education: Bachelor’s degree in a related field required. Examples include nursing, healthcare administration, public health, or similar. Certifications such as CPHQ and Lean Six Sigma are beneficial, but not required. Experience: At least four years of experience in the healthcare field, quality, data analytics, and/or management strongly preferred. Master’s level education and appropriate background may substitute for some experience. Knowledge of clinical operations including the functions of the front and back-office utilization information systems is preferred. Previous experience working in an outpatient clinic is preferred. Knowledge/Abilities: Excellent communication skills, both written and verbal, are required. Strong organization and time management skills are required. Ability to work independently and demonstrate initiative is required. Proficiency with Microsoft Office is required. Displays cheerful demeanor and makes positive comments when on duty. Works cooperatively with other staff members. Displays sensitivity in a multi-cultural environment. General understanding of the medical billing process is preferred. Equipment Operated : Telephone Computer Printer Fax machine Copier Other office equipment as assigned Other office and medical equipment as assigned Facility Environment : Heart of Ohio Family Health operates in multiple locations, in Columbus, OH. All facilities have a medical office environment with front-desk reception area, separate patient examination rooms, nursing stations, pharmacy stock room, business offices, hallways and private toilet facilities. All facilities are ADA compliant. The patient examination rooms and office area is: kept at a normal working temperature sanitized daily maintains standard office environment furniture with adjustable chairs maintains standard office equipment; i.e., computer, copier, fax machine, etc. at a normal working height Physical Demands and Requirements : these may be modified to accurately perform the essential functions of the position: Mobility = ability to easily move without assistance Bending = occasional bending from the waist and knees Reaching = occasional reaching no higher than normal arm stretch Lifting/Carry = ability to lift and carry a normal stack of documents and/or files Pushing/Pulling = ability to push or pull a normal office environment Dexterity = ability to handle and/or grasp, use a keyboard, calculator, and other office equipment accurately and quickly Hearing = ability to accurately hear and react to the normal tone of a person’s voice Visual = ability to safely and accurately see and react to factors and objects in a normal setting Speaking = ability to pronounce words clearly to be understood by another individual

Quality Technician

Gojob Columbus, OH

Job Description Job Description The Product Quality Technician facilitates the inbound, proactive inspection of products by conducting functional and visual inspections as per test instructions, recording test results, segregating, and controlling the release of products into available inventory when products have been confirmed to have met the required specifications. Quality Technicians collaborate closely with key stakeholders across the company to assist in troubleshooting and resolving product quality issues. *Performs inbound product reviews, functional testing and visual inspection of new and existing products to ensure they meet our quality standards. Selects samples of finished goods from inventory to proactively audit the quality of the products being received from vendors and records the results. *Performs audits to follow up on customer reported issues, confirms if the inventory is exposed to the customer reported defect and communicates the findings to Product Management and Product Quality groups. *Records the inspection results and prepares reports summarizing the results of inbound/ in process inspections and communicates the findings to the Product Management, Product Quality and Supply Chain groups. Product Performance: Inspect, test, and verify the product meets functional and visual requirements. Product Information Availability: Verify the product content on the website is active. Product Information Quality: Check for information discrepancies on product labeling, packaging, and manuals Product Availability: Prioritize high priority products for inspection and release into inventory to support customer demand. Requirements: Education: High School diploma or GED equivalent. Experience: 2 to 5 years of experience in a Quality related role Experience in MS Office including Excel and Outlook Some familiarity and experience with computer hardware products Strong time management skills Have industry knowledge of quality processes, inspections, and test procedures. Strong attention to detail Company Description Gojob is the #1 Workforce-As-A-Service platform that leverages Tech and Data to make the labor market more fluid & accessible, and empower workers with dignity. Company Description Gojob is the #1 Workforce-As-A-Service platform that leverages Tech and Data to make the labor market more fluid & accessible, and empower workers with dignity.

Pharmacy Intern

Gifthealth Columbus, OH

Job Description Job Description Salary: Ranging from $17 to $20 Shift hours between: Monday-Friday 6am - 10pm and Saturday 8am - 2pm. Multiple shift times available. About Gifthealth Gifthealth is on a mission to bring an easier, more affordable pharmacy experience to patients and providers around the country. In less than a year, we have served thousands of patients and are expanding nationally at a rapid pace. Health is our most precious gift. And our team believes it should be a priority, not a privilege. We are Gifthealth. About the Pharmacy Team Our pharmacy team is the reason patients keep coming back to Gifthealth. Our pharmacy interns are an essential part of the team. As an intern, you will receive real world experience in a fast paced pharmacy atmosphere. You will have the ability to make an impact in many patients' lives outside of what you may have learned in the classroom. This role is more than just stocking shelves and collecting copays, it is building relationships internally and externally to create a wonderful pharmacy experience. How youll Help Us Improve Healthcare: Under the supervision of the pharmacist, assisting in the practice of pharmacy, in accordance with state, federal, and company policy Assisting pharmacists and other healthcare providers in delivering patient care and services that are within the state scope of practice for pharmacy interns including patient counseling and other health services (i.e. blood pressure, medication therapy management, etc.) Handling telephone calls that do not require personal attention of the pharmacist, including those to physicians Assisting and supporting the Pharmacy Department with inventory management activities, such as ordering, unpacking, checking and storing shipment of pharmaceuticals Maintaining knowledge of Gifthealth asset protection techniques, and filing claims for warehouse overages (merchandise received, but not billed), shortages (merchandise billed, but not received), order errors or damaged goods involving Rx drugs Using pharmacy systems to obtain patient and drug information and process prescriptions Modeling and delivering a distinctive and delightful customer experience under guidance of the pharmacy team Learning and championing the pharmacy policy, procedures and customer service necessary to perform as a future pharmacist Maintaining an active educational license, a complete clinical documentation file with hard copy documents (to be stored on site) and active CPR licensure documentation as required by participation in clinical services Compliance with all assigned training and participation in immunization, medication therapy management, health screening and all other current clinical programs A Few Things About You Enrollment in an accredited pharmacy school and a current, state-specific pharmacy intern license Immunization training certificate (as soon as available and applicable to professional standing in school) Flexible availability and capacity to assist as needs arise (Availability for at least one shift per week required) Timeliness and dependability to complete requirements and attend scheduled shifts Drive to stay current and competent in all pharmacy-related functions Excellent customer service skills, genuine empathy, and professional behavior and appearance Ambition, diligence and ability to commit to the team's goals Our Offer To Ensure You Choose Gifthealth Competitive compensation based on education level Ability to work closely with a team of healthcare experts that share in the passion of improving medication accessibility and affordability Competitive compensation ranging from $17-20 per hour based on experience and performance. 401k plan with employer match If you are a dedicated and compassionate individual looking to make a meaningful impact on our pharmacy team, we encourage you to apply! To apply, please submit your resume and a cover letter outlining your relevant experience and explaining why you are an ideal fit for this role. We eagerly await your application!

Dynamic Environment

Quality Manager 20742

General Employment Columbus, OH

Job Description Job Description Are you an experienced quality leader with a hands-on approach to problem-solving? Do you thrive in high-stakes environments where precision and continuous improvement are essential? GEE Group is seeking a Quality Manager for a premier Tier 1 automotive manufacturing client. This role is pivotal in fostering a zero-defect culture, ensuring product excellence, and driving collaboration between customers, suppliers, and internal teams. What You’ll Do: Champion quality initiatives and lead a team of engineers, coordinators, and technicians to uphold the highest standards. Act as the primary liaison for customer and supplier quality discussions, providing technical expertise and strategic guidance. Oversee new model launches, ensuring seamless integration of quality processes from suppliers to mass production. Implement and enhance quality control methods, including TS/ISO standards and SPC tools. Get hands-on—roll up your sleeves and lead problem-solving efforts directly on the plant floor. Manage departmental planning to align short- and long-term quality objectives with business goals. Travel domestically and internationally (~15%) to support quality operations. What We’re Looking For: Bachelor’s degree (Engineering preferred). Proven leadership experience in a manufacturing environment, ideally within Tier 1 automotive. Strong background in technical problem-solving, project management, and part maturation. Ability to interpret technical drawings and experience with 3D CAD software. Expertise in TS/ISO quality standards, mistake-proofing methodologies, and SPC tools. Proficiency in Microsoft Office Suite, with strong Excel and PowerPoint skills. Hands-on mentality—willingness to engage directly with production, suppliers, and customers. Flexibility to travel (~15%) as needed. Preferred Qualifications: Master’s Degree (MBA or technical field). Six Sigma Green or Black Belt certification. CATIA V5 experience. Strong documentation, leadership, and business planning abilities. If you're a results-driven quality professional looking for your next challenge, apply today!

MSW Clinical Intern

Cook Counseling and Consulting Inc. Columbus, OH

Job Description Job Description Salary: 2000 per semester Job Title: MSW Student Intern - Psychotherapy and Group Facilitation Location: Gahanna, Ohio Practice Setting: Mid-sized Group Private Practice Position Type: In-Person Internship Duration: Duration is determined by the course requirements for your MSW program. These requirements vary by university, program, and academic standing. About Us: We are a dynamic mid-sized group private practice located in Gahanna, Ohio, committed to providing quality mental health services to our community. As part of our commitment to social responsibility, we offer pro bono programming for military sexual trauma survivors, providing specialized support to those in need. Internship Overview: We are seeking a motivated MSW student intern to join our team and contribute to our mission of supporting individuals affected by military sexual trauma (MST). The internship will focus on providing psychotherapy to clients in our new MST pro bono program, clients who experience a variety of mental health symptoms, as well as observing and facilitating group therapy and peer support groups. The intern will work closely with the clinical director to build a strong foundation of clinical skills in a supportive and collaborative environment. Key Responsibilities: 1. Psychotherapy: Provide individual psychotherapy to clients enrolled in our pro bono programming for military sexual trauma, providing psychotherapy for clients with various mental health concerns, utilizing evidence-based therapeutic approaches. Observation of psychotherapy with children, teens, adults, couples, families and groups. 2. Group Therapy and Peer Support: Observe and facilitate group therapy and peer support groups under the guidance of the clinical director. Contribute to the development and implementation of group programming. 3. Collaboration: Work closely with the clinical director and other team members to ensure cohesive and client-centered care. Participate in case consultations and team meetings. 4. Clinical Skill Development: Engage in ongoing training and supervision to enhance clinical skills. Receive constructive feedback to support professional growth. 5. Compliance: Adhere to ethical guidelines and standards, including maintaining client confidentiality. Ensure compliance with all academic requirements outlined by the university. Qualifications: 1. Currently enrolled in an MSW degree program. 2. Ability to pass a background check. 3. Obtain a Social Work Trainee (SWT) license. 4. Commitment to completing all academic requirements outlined by the university. Skills and Attributes: 1. Empathy and sensitivity to the needs of trauma survivors and those with various mental health concerns. 2. Strong interpersonal and communication skills. 3. Ability to work collaboratively in a team-oriented environment. 4. Eagerness to learn and apply evidence-based therapeutic approaches. Benefits: 1. Supervision and mentorship from experienced licensed professionals. 2. Exposure to diverse clinical experiences in a group private practice setting. 3. Opportunities for professional development and training. 4. Contribution to a meaningful and socially responsible mission. Application Process: To apply, please submit your resume, a cover letter outlining your interest and relevant experience, and contact information for two professional references. Interviews will be scheduled for qualified candidates. This internship will need to be approved by your university's field education program if we are not already an approved organization. Deadline for Application: We are seeking interns who are prepared to start in the spring 2024 semester. Join us in making a positive impact on the lives of military sexual trauma survivors. This internship offers a unique opportunity to gain valuable clinical experience while contributing to a cause that matters. We look forward to welcoming a dedicated and passionate MSW student intern to our team. Job Type: Contract Salary: $12.00 - $18.00 per hour Benefits: Continuing education credits Flexible schedule Professional development assistance Tuition reimbursement Healthcare setting: Clinic Outpatient Medical specialties: Addiction Medicine Psychiatry Patient demographics: Adolescents Adults Children Older adults Schedule: Choose your own hours Day shift Evening shift Work Location: In person

Intern Project Assistant

OCP Contractors Columbus, OH

Job Description Job Description Project Assistant Intern Location: Columbus, OH 43215 Full Job Description: About Us: In today’s market, OCP is an industry leader in GPS layout, framing, installation of load-bearing mid-rise structures, prefabrication, and Building Information Modeling tools. Innovation is at the core of OCP’s culture, and continually drives the company forward. Through processes designed with safety and innovation in mind, OCP consistently maximizes efficiency and quality in work, for a successful project delivered on-time and on budget. With access to a strong, highly trained skilled trades workforce in 3 key markets of Ohio, OCP is able to deliver projects consistently on-time and with superior craftsmanship. OCP has maintained a reputation for excellence showcased within the robust, high-profile portfolio of work throughout the Ohio area. The imprint of OCP’s superior work over the years can be seen within the skyline of every major Ohio city. Job Summary: OCP has an opportunity beginning Spring 2025 for a Project Assistant Intern at our Columbus office. This is an excellent opportunity for a college student pursuing a degree to work in the construction field. This internship will include experience in a variety of experiences in the construction Project Management related areas such as: RFI process, project schedules, developing internal and external relationships, lean construction, and submittal processes. Duties/Responsibilities: Support the Project Managers, Superintendent and Foreman in the construction process throughout all phases of the life cycle of a project Update and communicate 6 week look ahead Monitor, maintain and communicate project schedules Contribute to submittal process Contribute to RFI process Contribute to the buyout of the subcontractors, vendors and suppliers Develop professional relationships with OCP build team Develop professional relationships with appropriate customer contacts Propose ideas for improvements and identify wastes in-line with lean construction methods Attend job meetings as needed Other duties as assigned Required Qualifications: In pursuit of degree in Construction Science or Construction Management Basic understanding of construction industry is helpful Attention to detail Ability to work independently Ability to communicate effectively, both orally and in writing Posses strong problem solving and time management skills Strong desire to learn Qualified applicants should forward their resumes to [email protected] to be considered for this position.

Quick Apply

Quality Control - Hiring Immediately

swipejobs LLC Columbus, OH

Job Description Job Description Apply Today, Work Today Weekly Pay Job Description: We are Hiring Immediately for a Quality Control position in an exciting warehouse facility! Job involves inspecting and approving materials by confirming specifications, conducting visual and measurement tests, and rejecting and returning unacceptable materials. Job Requirements: Ask about our Employee Rewards Program May be required to lift up to 25lbs May be required to perform repetitive motions Must have reliable transportation Must be able to work in a team environment Additional Information: Ask about our Employee Rewards Program Benefits include medical insurance, dental insurance, vision insurance and life insurance Some positions may not require background check or drug test Full-time, Part-time $ 15.0/hr Shifts Available: 1st Shift 2nd Shift 3rd Shift For this or other positions in your area. LI23 LIBF24

Quality Engineer I

Forge Biologics Columbus, OH

Job Description Job Description About Forge Forge, a member of Ajinomoto Bio-Pharma Services, is a gene therapy development engine, focused on enabling access to life changing gene therapies and helping bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in gene therapy manufacturing and therapeutics development to the table, helping to champion teams that are navigating the long road from the lab bench to the bedside. Our goal is simple but vital to patients living with disease, and we take it seriously. With a patient-first approach, we are forging new models for working together to better accelerate these transformative medicines to reach those who need them the most.  About the Role We are currently seeking a Quality Engineer I to join the Forge Biologics team. The Quality Engineer will work as part of a cross functional team providing quality oversight, review and approval of engineering, validation, and quality system deliverables to ensure that products and processes meet the appropriate regulatory agency requirements, internal company standards and current industry best practices. This includes but may not be limited to commissioning and qualification of GMP equipment and facilities, validation of computerized systems, and process performance qualification. The individual chosen for this position will work in close partnership with all operational departments and/or external parties to support GMP manufacturing of drug products. The focus of this role is to employ site approaches to ensure Forge provides and maintains a state-of-the-art gene therapy facility for pre-clinical and commercial viral vector and plasmid products. What You'll Do Review and Approval of Calibration and Preventive maintenance events within a Computerized Maintenance Management System (CMMS). Review and approval of validation documents across validation disciplines developed by functional validation teams, ensuring the documentation meets regulatory requirements and quality standards (Commissioning & Qualification, Computer System Validation, Process Performance Qualification, etc.) Initiate/Update Risk Assessments on systems and processes. Perform risk analysis and failure prevention analysis. Support early-stage process validation activities including Tech Transfer and Quality by Design, as necessary. Provide analytics and statistical process control support to quality and operations. Provide support to quality investigations, CAPA's, Continuous improvement and change controls by providing technical and validation insight and impact assessments. Assist with resolving issues arising from internal quality assessments/audits, future regulatory inspections, and aid in driving closure of inspection issues by preparing appropriate responses and corrective action resolutions. Support internal/external audits from a quality engineering and validation perspective. Employ Good Document Practices (GDP) when recording data, maintaining archives, and drafting and reviewing documents. Demonstrate technical expertise to define approaches and execution of system validation activities in accordance with cGMP, cGxP, CFR 21 Parts 11, 210, 211, ICH Q7, Q8, Q9 and applicable regulations, good engineering practice and industry standard procedures. What You'll Bring Bachelor's Degree in Engineering, Science or equivalent technical background Experience working in a GMP Environment with Quality Management Systems Working knowledge of cGMPs, ISPE Guidelines, Data Integrity, 21 CFR Part 11 and Annex 11 Regulations, and Industry Good Practices for Installation, Operational, and Performance Qualifications, along with Standard Operating Procedures. Must have strong attention to detail, be organized and proactive. Strong verbal and written communication skills. Ability to meet deadlines and use critical thinking skills to problem-solve effectively. Preferred Previous experience with Commissioning, Qualification, & Validation (CQV) processes Previous Biologics or Gene Therapy experience Contract Manufacturing experience This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned. Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Life at Forge We are a team of diverse, driven and passionate people working together to trailblaze a new model for how we make medicines to treat patients with genetic diseases. Our team members use their creativity and talent to invent new solutions, meet new demands, and offer the most effective services in the industry. Forge's core values lay the foundation for H.O.P.E. It provides us a common purpose that we all understand, work towards and live by.  H ARDWORKING - We work hard and smart, making a persistent and determined effort toward success. Working hard, with focus and desire is the key. O PEN - We strive to be approachable, actively listen and encourage others to contribute and speak up. We positively offer and receive constructive feedback. P URPOSE DRIVEN - We are passionate about working towards and delivering on our mission to manufacture gene therapies. E NGAGED - We are fully absorbed by and enthusiastic about our work and take positive action to further Forge's vision, mission and goals. We've Got You Covered We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly Un FORGE ttable. Health, Dental, and Vision insurance that starts on your first day at Forge, with 90% of premiums covered for team members as well as dependents Flexible PTO (plus 14 paid company holidays) Annual bonus for all full-time employees 401(K) company match Fully-stocked kitchen with free food/drinks 12 weeks of paid parental leave - additional discount programs include childcare support & dependent care Employee Assistance Program Wellness benefits (financial planning services, mental health counseling, employer paid disability) Professional & Personal development resources - LinkedIn Learning, a dedicate training staff in-house, mentoring opportunities & access to leadership development coaches

Software Quality Engineer

Jumpmind, Inc. Columbus, OH

Job Description Job Description Job Description The Software Quality Engineer will be focused on all phases of the software development process and must have strong experience and skills in a variety of capabilities, including engineering and technology, verbal and written communication, problem-solving, reasoning and logic, and practical skills. Requirements Core Responsibilities ● Drive the overall quality discipline. ● Develop standards and procedures to determine product quality and release readiness. ● Identify and report on key KPIs for product quality. ● Drive innovation and streamline the overall testing processes. ● Drive the tooling, technologies, and testing processes. ● Perform and document risk analysis. ● Maintain an effective test case bank by documenting and maintaining test cases, and by developing and maintaining automated tests. ● Establish and maintain the automated testing framework. ● Create robust test plans. ● Perform manual and automated testing, tracking and reporting on test progress and results. ● Review user interfaces for consistency and functionality. Qualifications ● Bachelor’s degree in Computer Science (CS), Information Technology (IT), or a related field, OR completion of an IT bootcamp focused on Java development. ● Strong programming skills, particularly in Java. ● Experience with automated testing frameworks and tools. ● Solid understanding of software quality assurance methodologies, tools, and processes. ● Proven ability to write clear, concise, and efficient code. ● Familiarity with Agile development methodologies. ● Excellent problem-solving, analytical, and reasoning skills. ● Strong verbal and written communication abilities. ● Ability to work collaboratively in a team environment.

Quality Supervisor

Altium Packaging LLC Columbus, OH

Location Address: 1917 Joyce Avenue, Columbus, Ohio 43219 Work Shift: Salary Exempt (United States of America) The quality control supervisory is responsible for leading a quality team to drive best practices in quality control, and to quickly and effectively address any quality issues that arise in production. Essential Function - Roles/Responsibilities Work with the quality team in order to correct any quality issues that may arise as well as train and develop your team to better handle quality issues. Present quality cases or arguments to the Plant Manager in an effective way. Follow through logical processes for the resolution of quality issues. Maintain contact with customers on a weekly basis for follow up and proactive quality solutions. Serve as a point of contact for customer complaints, create an action plan to solve the complaint, and see through to a solution. Provide support to the production team. Monitor and participate in the plant's safety program. Monitor and review quality forms and paperwork for accuracy. Qualifications: Required: 2 years experience in quality control. Proficient computer skills. Communicate effectively in both written and oral formats. Be able to train and perform follow-up with the quality team. Developed leadership skills. Be able to work independently. Be willing to ask for help when necessary. Preferred: Experience with GMP's HACCP program experience Familiar with regulatory auditing Experience with calibration schedules Experience with quality hold processes 2 or 4 year degree Altium Packaging, Our Culture Differentiates Us! We incorporate our Guiding Principles into all aspects and at all levels of the organization and use them as a framework for decision-making. We believe our Guiding Principles foster a culture of excellence that benefits both employees and customers. Our Guiding Principles Act with Integrity & in Compliance Drive Value Creation Be Disciplined Entrepreneurs Focus on the Customer Act with Humility Treat others with Dignity and Respect Seeking Fulfillment in your Work We Believe in Rewarding our Most Important Resource - Our People! We show our commitment to Total Rewards by providing a competitive, comprehensive benefits package. In addition to medical, dental and vision plans, company holidays and vacation days, tuition reimbursement, learning and training opportunities, bonus potential, and a 401(k) plan with company contributions, Altium Packaging locations offer rewards and recognition programs and opportunities to make a difference in the community. EEO Statement We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state or local protected class. Take your career to the next level at Altium Packaging!

Quality Engineering Intern Summer 2025

PACCAR Inc Columbus, MS

Quality Engineering Intern Summer 2025 Date: Jan 13, 2025 Location: Columbus, MS, US, 39701 Company: PACCAR Company Information PACCAR is a Fortune 500 company established in 1905. PACCAR Inc is recognized as a global leader in the commercial vehicle, financial, and customer service fields with internationally recognized brands such as Kenworth, Peterbilt, and DAF trucks. PACCAR ENGINE COMPANY PACCAR Engine Company's $400 million engine manufacturing and technology facility is located in Columbus, Mississippi. The engines produced at the Mississippi plant are PACCAR Engine Company's most fuel-efficient and highest-technology diesel engines. Requisition Summary Quality Co-Op/Intern Job Functions / Responsibilities Work closely with machining and assembly department personnel and provide engineering support with timely responses to problems being worked. Identify root cause for problems that occur during the engine manufacturing process and work with appropriate organizational departments and/or suppliers to implement permanent corrective actions. Assist with machining or assembly department corrective actions related to daily PQI and internal campaign issues. Complete and analyze data and identify trends and facilitate improvement actions. Interact with team members to implement solutions. Maintain a problem-solving database which tracks problem resolution. Utilize effective communication and problem-solving skills to foster an effective team environment which continually strives for improvements in safety, quality, productivity, and efficiency. Develop and implement quality-engineered systems for new processes/products and transfer products. Provide assessments and advice on the robustness of Quality System implementation. Develop SPC and Training plans in support of new product launches. MAIN JOB RESPONSIBILITIES: Working in a Quality Engineering role with other functional groups, provide support of new process/product and transfer products. Provide QA Engineer(s) direction, analysis, and recommendations to assure effective quality control and associated risk management plans. Write, review and/or approve process and product validation protocols and reports, equipment qualifications, engineering change orders. Provide technical leadership for Failure Mode and Effects Analysis (FMEA) and Control Plans for both Process and Design FMEAs. Support Complaint investigations as appropriate. Own the FMEA process. Assure proper use of statistical tools to analyze data, make acceptance decisions, and improve process capability (DOE, SPC) throughout the organization. Ensure that development activities follow control requirements and the product is properly transferred to manufacturing. Assure all control plans meet necessary requirements to ensure effective product acceptance including appropriate inspection requirements, equipment and gauge requirements, and sampling plans. Initiate and investigate Corrective and Preventative Actions (CAPA) as appropriate. Assure process audit program established and implemented. Lead Continuous improvement activities and support Lean environment and re-work/scrap reduction. Assist in development, review and approval of process and equipment validation. Qualifications & Skills The candidate we seek will be currently enrolled in an Engineering Program and have completed their Sophomore year of College. Excellent technical, verbal, written, and presentation skills. Proven problem-solving skills are required. Ability to work in a self-directed environment is preferred. Must be flexible to work portions of day and evening shifts. Be able to stand for prolonged periods of time. Preference will be given to the candidate who can work 40 hours/week. MS Office, specifically Excel spreadsheets. A 3.0 GPA or higher is preferable. Additional PACCAR Website Information PACCAR is an Equal Opportunity Employer/Protected Veteran/Disability. #J-18808-Ljbffr

Intern

EMCOR Group Inc. Columbus, OH

Shambaugh & Son, L.P. 5870 Carbonmill Dr South Bend, IN 46628, USA Shambaugh & Son L.P., a wholly-owned indirect subsidiary of EMCOR Group, Inc., is a customer-driven, single-source, self-performing construction/engineering firm. We specialize in the Design-Build method of construction resulting in fast-track delivery of project improvements to our customers. We are one of the largest specialty contractors in the U.S. and the only one with all eight M.E.P (Mechanical, Electrical, Process, Automation, Refrigeration, HVAC, Plumbing, and Fire Protection) design and installation capabilities in-house. We perform more than $1 billion of construction projects per year with over 3,000 employees throughout 50 states from our home office in Fort Wayne, Indiana. Our success has been driven by our ability to attract and retain dedicated, knowledgeable and seasoned professionals to become part of the Shambaugh team, as we continue to build on our 90+ year Shambaugh success story. At Shambaugh, we recognize people as our most important resource and it is our mission to produce the industry’s highest level of quality services and productivity on every project in order to develop repeat customers, maximize return on investment, and provide professional growth opportunities for people in the organization. Job Summary: An intern will have a variety of assignments to ensure a well-rounded experience. The goal of any internship is for the individual to learn and explore areas of interest. Essential Duties and Responsibilities: Learn the responsibilities of your desired profession Fulfill administrative duties around the office Run errands for the staff Incorporate academic knowledge into hands-on work Work with AutoCAD or REVIT Work closely with senior professionals Complete required safety training Qualifications: Attending an academic program (High School or University) Proficient computer skills, including Microsoft Office Suite (Word, PowerPoint, and Excel) Must be 18 years of age Excellent written and verbal communication skills Self-directed and able to work without supervision Energetic and eager to tackle new projects and ideas Willingness to learn new skills #J-18808-Ljbffr

Quality Control & Quality Assurance Technician

Esi Electrical Contractors, Inc. Columbus, OH

Quality Control & Quality Assurance Technician Job Category: Skilled Trades, Technicians & Operators Requisition Number: QUALI002443 Posted: January 2, 2025 Employment Type: Full-Time Work Location: On-site Location CYPRES 255 Rathmell Rd Columbus, OH 43207, USA Job Responsibilities Responsible for understanding, upholding, and promoting the Everus 4EVER Strategy: Employees | Value | Execution | Relationships. Plan, direct and supervise company quality control functions and activities as established by corporate dictate. Prepare, obtain approval, issue, and implement company quality control (assurance) program manual in compliance with owner contract and company requirements. Perform activities such as audits, preparation of company standards, notification to management of quality problems, etc. Provide administrative and technical direction to all quality control personnel, including personnel administration, resolution of technical problems, development/approval of in-house training, etc. Act as liaison with owner, regulatory agencies, subcontractors and/or internal departments on quality-related matters. Ensure company standards are outlined and effectively implemented. Insure adequate corrective measures are implemented in cases of non-compliance. Perform other duties as assigned. Minimum Education and Work Experience Requirements Four-year engineering degree plus a minimum of 8 years quality control/assurance experience or equivalent. Required Key Skills and Competencies A thorough knowledge of regulatory agency quality control/assurance activities. Experience in construction activities. Proven ability to supervise personnel. Excellent organizational, leadership, communication, and analytical skills. Strong attention to detail, and the ability to prioritize and complete projects on schedule. Advanced knowledge and skills in the use of various Microsoft Office applications including Word, Excel, and PowerPoint. Application Deadline 1/31/2025 Company Overview ESI Electrical Contractors is a proud partner in the growth and development of cities and communities across Ohio. We are always looking for motivated, hard-working people to join our team. Build Ohio while you build your career with us! Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities #J-18808-Ljbffr

Quality Control & Quality Assurance Technician

Esi Electrical Contractors, Inc. Columbus, OH

Quality Control & Quality Assurance Technician Job Category : Skilled Trades, Technicians & Operators Requisition Number : QUALI002443 Apply now Posted: January 2, 2025 Full-Time On-site Locations Columbus, OH 43207, USA Description Responsible for understanding, upholding, and promoting the Everus 4EVER Strategy. Employees | Value | Execution | Relationships Plan, direct and supervise company quality control functions and activities as established by corporate dictate. Prepare, obtain approval, issue, and implement company quality control (assurance) program manual in compliance with owner contract and company requirements. Perform activities such as audits, preparation of company standards, notification to management of quality problems, etc. Provide administrative and technical direction to all quality control personnel – includes personnel administration, resolution of technical problems, development/approval of in-house training, etc. Act as liaison with owner, regulatory agencies, subcontractors and/or internal departments on quality related matters. Ensure company standards are outlined and effectively implemented. Ensure adequate corrective measures are implemented in cases of non-compliance. Perform other duties as assigned. Minimum Education and/or Work Experience Requirements Four-year engineering degree plus a minimum of 8 years quality control/assurance experience or equivalent. Required Key Skills and Competencies A thorough knowledge of regulatory agency quality control/assurance activities Experience in construction activities Proven ability to supervise personnel Excellent organizational, leadership, communication, and analytical skills are essential Requires strong attention to detail, and the ability to prioritize and complete projects on schedule Advanced knowledge and skills in the use of various Microsoft Office applications including Word, Excel, and PowerPoint Application Deadline - 1/31/2025 Build Your Career with ESI ESI Electrical Contractors is a proud partner in the growth and development of cities and communities across Ohio. We are always looking for motivated, hard-working people to join our team. Build Ohio while you build your career with us! Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities #J-18808-Ljbffr

Intern - Columbus

EMCOR Group Inc. Columbus, OH

S.A. Comunale has been a local industry leader for end-to-end mechanical, fire protection, and HVAC services for nearly 100 years. We offer our clients significant financial strength, unmatched bonding capability, an award-winning safety program, and large-scale purchasing power. With 12 locations and over 950 employees, including 600 skilled tradesmen throughout Ohio, Pennsylvania, New Jersey, Maryland, and West Virginia, S.A. Comunale can work in virtually every market sector and facility type. Job Title: Intern A Project Manager Intern will be assigned a mentor(s) to observe their functions and processes. They will assist the Project Manager mentor in overseeing all aspects of the project using planning, monitoring, and controlling processes. A Project Manager Trainee will assist with the coordination and completion of multiple projects and to this end will aid in a variety of tasks including setting deadlines, assigning responsibilities, monitoring and summarizing progress of the project, and familiarizing themselves with required project reports and paperwork. Responsibilities: Accurately define project requirements Assist with creating job schedules Coordinate the delivery of tools and fabrication Identify and manage the personnel assigned to each project and track their labor efficiency Attend job progress meetings and initiate change orders and contract progress billings with the Project Manager Learn how to estimate remaining 'cost-to-complete' for monthly WIP reporting Manage the day-to-day operations of assigned projects so that they are completed on time and on budget in correlation with the Project Manager Work with clients to brainstorm creative solutions to their problems and ensure their needs are met through our customized solutions Ensure projects follow established guidelines that ensure they are completed as efficiently as possible Communicate with team members regarding project needs Ability to work in a fast-paced dynamic environment Read and analyze job cost reports Respond timely to inquiries from management Assist with collections as required Qualifications: To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education / Work Experience: Recent graduate or currently enrolled full-time at an accredited university, pursuing a Bachelor's degree in Construction Management, or other similar degree is required. Knowledge of sprinkler systems/plumbing and previous construction internship/experience is a plus. Must have a basic understanding of key project management principles and construction processes required. Computer Skills: Significant experience with Microsoft Office (i.e., Word, Excel, PowerPoint) applications. We offer our employees a competitive salary and comprehensive benefits package and are always looking for individuals with the talent and skills required to contribute to our continued growth and success. Equal Opportunity Employer/Veterans/Disabled. #J-18808-Ljbffr

Quality Assurance

Computech Corporation Columbus, OH

Computech Corporation provides IT and consulting services to various customers across the globe. We are a Minority Certified Company with over 15 years of industry experience. Our global delivery model and proven track record enable companies to realize improved business efficiency and increased profitability. Job Description Description: QAS3 to help IT design, pilot, and implement the software quality assurance review process. Will help development teams test software quality for production deployment. This position will function as a highly skilled Quality Assurance Specialist with specific responsibilities that include: Proactively engage in the end-to-end software testing cycle as it pertains to the project. Work closely with and follow direction from QA Manager. Contribute to the establishment of and meet quality goals and objectives for the project. Contribute to all aspects of quality assurance for the project including establishing relevant metrics, applying industry best practices, and developing new tools and processes to ensure quality goals are met. With input from QA Manager and team, develop and execute test cases, scripts, plans, and procedures (manual and automated). Work with the ODPS project team to test updates, patches, and repairs to the application software components in the development, test, and QA environments. Develop software changes for promotion to production following best practice and standards as defined by the ODPS ITO. Take corrective action, subject to the ODPS Management approval, to resolve all issues and problems encountered with testing to ensure the applications perform as required. Design, execute, and maintain automated test scripts. Additional Information Requirements: 7 Years in testing IT products and applications. 5 Years automation experience using MS Visual Studio Coded UI, Team Foundation Server, and Microsoft Test Manager. 5 Years Development/scripting skills in C#. 5 Years in End to End Test Automation experience. 5 Years demonstrated experience in converting existing manual test cases to automation scripts. 5 Years conducting test case reviews to ensure scenarios accurately capture business functionality. Contributes to continuous process improvements to increase the efficiency of QA and development. Excellent communication skills both written and oral. Needs to show at least 1 year Quality Assurance experience in a technical capacity with a large organization such as ODPS. The experience must encompass the writing of test strategies, test scenarios, test plans, and test scripts. Must have at least 1 year experience working on Agile/Scrum IT projects. Must have experience working with Microsoft Test Manager on at least one project. #J-18808-Ljbffr

Quality Manager

Group Management Services, Inc. Columbus, OH

Quality Manager Columbus, OH About Us: As seen on Spectrum TV and highlighted in the Columbus Dispatch , Connect Housing Blocks is revolutionizing affordable housing in Central Ohio. We're not just building homes, we're building communities. Our innovative modular construction techniques allow us to deliver high-quality, stackable apartments that are transforming neighborhoods across the region. With the ability to produce up to 1,500 housing units annually, we're making headlines and making a real difference in our community. Overview: Are you a detail-oriented leader with a passion for quality control and continuous improvement? Connect Housing Blocks is looking for a Quality Manager to oversee and enhance our quality management processes. You’ll play a key role in ensuring that our products meet the highest standards while leading initiatives to boost efficiency and customer satisfaction. If you’re ready to elevate our quality standards and drive continuous improvement, we want to hear from you! What You'll Do: Quality Leadership: Lead quality audits and inspections to ensure adherence to internal and external quality standards. Data-Driven Improvements: Analyze quality data and implement corrective actions to resolve issues and prevent recurrence. Collaboration: Work closely with Production Managers to establish consistent quality control processes. Training: Oversee the training of production staff in quality standards and procedures to ensure compliance. Documentation: Manage the documentation of quality procedures, ensuring all information is accurate and easily accessible. Continuous Improvement: Lead initiatives aimed at reducing waste, improving efficiency, and enhancing product quality. Process Enhancement: Promote a culture of process improvement to boost productivity and ensure product reliability. Qualifications: Education: Bachelor’s degree in quality management, Engineering, or a related field preferred. Experience: 3+ years of experience in a quality management role within a manufacturing environment. Skills: In-depth knowledge of quality management systems (ISO, Six Sigma) and methodologies. Communication: Strong verbal and written communication skills in English. Competencies: Attention to Detail: Maintain high standards by identifying and correcting errors in processes and products. Problem-Solving: Solve complex problems with effective solutions, driving continuous improvements. Process Improvement: Seek opportunities to enhance product quality and operational efficiency. Time Management: Efficiently manage time to meet project deadlines and support the team's productivity. Professionalism: Maintain composure under pressure and approach tasks with tact and focus. Physical Demands: This role requires the ability to work in both office and manufacturing environments, with frequent standing, walking, and lifting of up to 25 pounds. Work Environment: The work environment includes exposure to moving mechanical parts and varying climate conditions. The noise level is typically moderate, and the use of personal protective equipment (PPE) may be required. Apply Today: Don’t miss out on this opportunity to lead a team dedicated to excellence in quality management. Apply now to join Connect Housing Blocks as our next Quality Manager—let's build something great together! #J-18808-Ljbffr

High salary

Quality Supervisor

Jobot Columbus, OH

4 days ago Be among the first 25 applicants This range is provided by Jobot. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $65,000.00/yr - $75,000.00/yr Want to learn more about this role and Jobot? Click our Jobot logo and follow our LinkedIn page! Job Details Full-time 1st shift opportunity with a growing manufacturer in Columbus! This Jobot Job is hosted by Dan Asher. Are you a fit? Easy Apply now by clicking the "Easy Apply" button and sending us your resume. A Bit About Us Our client is a privately owned plastics packaging company in growth mode! Join an industry leader in food packaging solutions at their plant in Columbus, OH (newly renovated with a $10 million investment)! Day shift! Why join us? Comprehensive medical/dental/vision benefits 401k with company match at 4% Vacation/Sick Time Growth Opportunities Yearly raises Duties and Responsibilities Ensure compliance to food safety requirements Follow Good Manufacturing Practices (GMP) Adhere to safety rules and procedures Supervise the quality inspectors in their role of in-process inspection of finished goods and rollstock Lead quality inspectors to perform 1st piece inspection on all production startups, and ensure they perform timely in-process inspections throughout the production of finished goods, rollstock, equipment according to the sampling plan Perform 1st article inspection of new and revised tools Remain current on past and present complaints and provide guidance to quality inspectors regarding these nonconformances and their corrective actions. Ensure quality inspectors are monitoring extrusion lines according to the requirement in the Quality Inspector job description. Ensure the quality inspectors collect and maintain samples of nonconformances to facilitate accept, rework, or reject disposition decisions Provide the disposition decisions on the nonconforming product and rollstock When nonconforming product is placed on hold, follow up to make sure inspectors have logged the hold on the hold log, form NF-004; completed the hold form, NF-013 and attached hold signs to all pallets/gaylords/rolls placed on hold. Communicate with shipping and receiving daily regarding product on hold, and its status; and in turn request that the shipping and receiving team provide their priority level for any potential shipments(s) of these items Control inspector behavior in production and storage areas concerning food-safety programs, company policies, and other employee requirements. Ensure quality laboratories are well kept, cleaned regularly and do not contain prohibited items Oversee any repack/rework activities and ensure it is fully documented in terms of quantity of product salvaged and lost Manage return receipts by quarantining, counting, inspecting returns according to the RMA Receiving Checklist, form NF-036. Presenting the RMA Receiving Checklist, form NF-036 to the Quality Supervisor / Samples coordinator for disposition and issuance of credit Also provide the Quality Supervisor / Samples coordinator any other relevant information about the return, including issues with quantity, condition, etc. Qualifications High School diploma or GED Possess 3-5 years’ relevant experience in quality for plastic extrusion Familiarity with using computers and measuring equipment, such as micrometers, calipers, etc. Strong math skills Knowledge of quality systems, SPC and food safety standards, as well as analytical and problem-solving skills are preferred Interested in hearing more? Easy Apply now by clicking the "Easy Apply" button. #J-18808-Ljbffr