Jobs in Triangle

Human Resource Lead - Full Time - Outlet Store

Belk, Inc. & Belk eCommerce LLC Triangle, VA

The Human Resource Lead position is responsible for leading the execution of the human resources, scheduling and cash office functions. Responsibilities include associate recruitment, hiring, on-boarding, benefits, employee relations, training, performance, policy communication, and scheduling. The Human Resource Lead is a non-exempt role reporting to the Human Resource Manager or Store Manager. •Ensure that Associate on-boarding is executed proficiently, accurately and in a timely manner. Ensures I-9/E-Verify and background check compliance •Lead the performance appraisal process and maintains personnel files •Ensure benefit administration and communication occurs in a timely manner •Assists with employee relations by witnessing associate coaching and counseling; submit termination requests as directed by executives and administer exit interviews •Submit Workday changes and ensures data accuracy •Prepare, process and meet weekly payroll deadlines. Ensure payroll is accurate •Train all new associates and managers on the scheduling process and system navigation •Work with store executives to ensures a timely schedule is provided to associates (3 weeks in advance) •Partners with the Store Manager to ensure all requests for time off and availability changes in the system have been addressed •Partner with store executives to create a store schedule the meets store budget, base staffing, and weekend percent guidelines through minimal edits •Lead the Office-Deposit function that includes all aspects of monetary maintenance in the store including processing the deposit, maintaining store petty cash funds (registers and vault), and performing the sales audit function •Human Resource Lead will act as a key-holder with responsibility for leading the support staff as appropriate Minimum Education & Experience: •High School Diploma or GED equivalent required •2-3 years of experience in retail and/or HR •Ability to use computer keyboard, standard telephone and other related business equipment •Ability to lift files, open file cabinets, bend, stoop, reach, and stand as necessary •Must be able to maintain Confidentiality Physical Requirements: •Ability to stand/walk for long periods of time •Ability to work at a safe and steady pace

Dynamic Environment

Materials Management Coordinator

Biogen Triangle Township, NC

Job Description Job Description Job Description About This Role The Materials Management Coordinator plays a pivotal role in supporting cross-functional teams within the RTP Bio/Pharma environment, ensuring seamless coordination of inbound & outbound shipments, inventory management, and process improvements. This role collaborates with various departments, including Quality Sample Control, Biogen Logistics, Global Trade Management (GTM), and Materials Planning, to manage the shipment and storage of raw materials, drug substances, drug products, and cell banks. What You’ll Do Collaborates with RTP (both sites) cross-functional teams including but not limited to: Quality Sample Control, Biogen Logistics, Global Trade Management Team (GTM), Materials Planning, Carriers for the coordination of all outbound RTP sample control, raw material, Drug Substance, Drug Product, cellbank shipments, to include invoices, packing slips, etc. required for shipment Monitors Syncade, Manufacturing Execution System (MES) Demand & Gathering reports and creates move orders to ensure material availability Supports investigations from Materials Management processes Maintains current on all applicable department trainings, including DOT & IATA hazmat shipping Assists with Release / Close cycle counts – coordinating with Materials Management team on reconciliation Coordinate the ordering of materials and supplies based on demand and inventory levels Attends tech transfer meetings and reports out to Materials Management team requirements needed to support manufacturing Ensures departments work orders are closed on-time Additional job duties as assigned Qualifications Required Skills High School Diploma or equivalent plus minimum 4 years of experience working in materials management/logistics in a GMP or cGMP environment OR Associate's Degree plus minimum 3 years of experience working in materials management/logistics in a GMP or cGMP environment OR Bachelor's Degree plus minimum 2 years of experience working in materials management/logistics in a GMP or cGMP environment Strong knowledge of Microsoft Office Suite Strong organizational and communication skills Preferred Skills Experience using Oracle Executive Business Suite Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

High salary

Sr. Manager Raw Materials Planning

Biogen Triangle Township, NC

Job Description Job Description Job Description This is a full time, on site position with M-F business hours About This Role   The Sr Manager, Planning leads the material planning function for the RTP Bio DS Manufacturing Site for both clinical and commercial programs. This individual is responsible for planning /managing a large scale raw material inventory and ensuring three internal manufacturing facilities have adequate raw material on hand to support production. The Sr Manager leads a team that collaborates daily with Manufacturing, Warehouse, Scheduling, Quality, and Procurement to resolve raw material issues, scheduling conflicts, inventory levels, and delivery requirements. Develops raw material inventory forecast levels and monitors KPIs and material risk metrics to drive improvements against targets. Works closely with the Site Leadership Team to support the business requirements and minimize the risk of production stoppage due to raw material issues. What You’ll Do   Responsible for raw materials planning and inventory control activities, forecasted demand including LRP, safety stock levels by completing IO Model fine tuning and static SS assessments, expiry reporting Manage planning settings including PIM / EBS set up and sourcing / transfer rules. Responsible for troubleshooting system issues that impact material planning Complete Expired and Obsolete report quarterly and presents the information to the site leadership team. Drives mitigation strategies for E&O reduction Lead direct reports and works with cross functional teams to develop mitigations plans for materials with supply issues (material alerts) to maintain the production plan and corporate partner revenue globally Monitors KPIs and material risk metrics to drive improvements against targets Other duties as assigned Qualifications Required Skills   Bachelor’s degree (preferred in chemical/biochemical engineering or supply chain) plus minimum 7 years of experience working in a GMP quality environment within biotech/pharmaceutical industry OR High school diploma or equivalent plus minimum 10 years of relevant experience Experience with raw materials planning in a GMP manufacturing facility; Superuser/SME with enterprise applications (e.g. Infor, Oracle) and PLM Previous supervisory experience with demonstrated leadership skills and possess the ability to manage complexity and multiple priorities Exceptional written and oral communication skills Aptitude for recognizing opportunities for improvement in systems or processes and recommending solutions Ability to influence with authority, pro-actively builds healthy working relationships between their department and other groups Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Sr. Manufacturing Technician (Maintenance)

Biogen Triangle Township, NC

Job Description Job Description Job Description About This Role As a Sr Manufacturing Technician (Maintenance), you will manage the day-to-day activities within the Maintenance department. This position will work Day shift starting at 6 AM and workign 10 hour shifts. Schedule will rotate 1 week working Mon-Thur and the follwoing week Tue-Fri. What You'll Do Perform and ensure PM’s and CM’s are performed on Process and Utility Equipment Ensure maintenance activities are coordinated with operational activities Provide guidance for less senior mechanics in their day-to-day activities Help manage small projects and programs within the maintenance department Filli in for the Maintenance Supervisor as required and keep the Supervisor abreast of activities within the department Who You Are You are a problem solver and team player that is eager to learn new technical equipment and processes. This position will provide you the opportunity to collaborate with a broader engineering and maintenance group to support manufacturing and essentially to make a difference in patient lives. Qualifications This work requires occasionally climbing ladders, crawling into tight spaces, moving/lifting test equipment up to 50 lbs. as well as working in clean spaces where gowning is required. Ability to stand for up to 3 hours at a time is also required. High School Diploma or Equivalent plus 7+ years' experience in pharmaceutical or biotech manufacturing environment or related manufacturing environment. Preferred Skills Practical knowledge and application of GMP regulations. MS Word, MS Excel, MS Power Point and MS Project. Excellent oral and written communication skills. Ability to work when called in for issues, extended shifts, and weekends as needed Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Facilities Technician III - Nights

Biogen Triangle Township, NC

Job Description Job Description Job Description This position will work a 12-hour rotating shift with a 2,3,2,2,3 rotation, 7PM - 7AM As Facilities Technician III, you will operate and repair all plant utilities; including medium pressure boilers, chillers, cooling towers, air compressors, Reverse Osmosis, USP water systems, water softeners, WFI stills, clean steam generators, Sterility Isolator, parts washers, fire monitoring systems, sprinkler systems, Bio safety cabinets, process waste streams, electrical systems including lighting, nitrogen compressed gas delivery systems. Furthermore, you will provide troubleshooting expertise on problem utility equipment and serve as system expert for the utility systems under guidance of other Technicians when necessary. What You’ll Do Operate all utility systems that supply manufacturing. Train others as needed on operation and maintenance of utility systems and serve as system expert. Maintain utility systems and respond to critical alarms. Log readings on various plant equipment systems and investigate when alarms occur. Monitor utility systems through the BMS control systems. Conduct tours through the mechanical spaces to ensure no adverse events have occurred. Alarm response for all associated GMP areas and controlled spaces. Who You Are You are a problem solver and team player that is eager to learn new technical equipment and processes. This position will provide you the opportunity to collaborate with a broader engineering and maintenance group to support manufacturing and essentially to make a difference in patient lives. Qualifications This work requires occasionally climbing ladders, crawling into tight spaces, moving/lifting test equipment up to 50 lbs. as well as working in clean spaces where gowning is required. Ability to stand for up to 3 hours at a time is also required. High School Diploma or equivalent with 4+ years prior industry experience OR 2 years trade school plus experience OR commensurate military experience. Position requires knowledge and usage of hand and power tools to perform assignments. Preferred Skills: Excellent communication (written and verbal), organization and time management skills. Ability to interpret mechanical specification drawings and other technical data sheets. Basic computer skills. (Microsoft Office Suite). Proficient with lock-out tag-out safety procedures and energized system work practices. Able to follow written and oral instructions for complex tasks Ability to work rotating shifts, night shifts, extended shifts, and/or weekends Practical knowledge of GMP’s Prior experience as a utility operator in a complex pharmaceutical or biopharmaceutical manufacturing environment. Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Quick Apply

Intern, Analytical Development

Biogen Triangle Township, NC

Job Description Job Description Job Description This application is for a 12-week internship role from June - August 2025. Resume review begins in January 2025. Here in Analytical Development - Structure elucidation (AD-SE) team, we support the development of small molecule and oligonucleotide therapeutics by developing innovative analytical technologies and establishing control strategies. We are seeking a highly creative and self-motivated candidate to join us as an intern student in 2025. This role will develop and optimize analytical methods on the UPLC-High Resolution MS system in the lab in RTP, NC campus. This role will also support oligonucleotide stability study using the mass spectrometry-based methods. This position requires adequate knowledge in analytical techniques such as LC and LC/MS. Position Description Design, execute and document experiments; analyze, interpret and present data/results; write technical reports; establish SOPs, etc. Develop and optimize analytical methods on the UPLC-High Resolution MS system. Test and analyze stability samples using mass spectrometry-based methods. Characterize degradation pathway of oligonucleotide. Attend relevant meetings and seminars to learn the development of therapeutic oligonucleotide. Qualifications Laboratory experience is required, and knowledge of oligonucleotide chemistry and characterization is highly desired Hands-on experience in chemical analysis by mass spectrometry and/or LC-MS To participate in the Biogen Internship Program, students must meet the following eligibility criteria: Legal authorization to work in the U.S. At least 18 years of age prior to the scheduled start date Be currently enrolled in an accredited community college, college or university Education Students pursuing MS or PhD in analytical chemistry are preferred. Candidates in chemistry, chemical engineering, pharmaceutical science are also considered. Location This role is on-site in Research Triangle Park, NC. Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Sr. Reliability Engineer I (Maintenance Reliability)

Biogen Triangle Township, NC

Job Description Job Description Company Description Job Description About This Role The Sr. Reliability Engineer I applies Reliability Engineering methodologies to optimize design requirements and performance of critical assets across the site. Originates and develops analysis methods for determining reliability of components, equipment and processes. Acquires data and analyzes the data. Prepares and communicates information to define reliability problems, recommend improvements and avoid failures. In addition, this Sr. Role partners with responsible engineers, maintenance, operations, quality, project engineers and other stakeholders to establish and execute reliability strategies throughout the Asset Life-Cycle. Champions and applies reliability tools such as Failure Mode and Effect Criticality Analysis, Reliability Modeling and Prediction, Reliability Growth, Maintainability, Availability and Root Cause Failure Analysis. What You'll Do Perform detailed analyses of site manufacturing and utilities process equipment to establish and implement reliability strategies (RCM) which minimizes failures or the impact of failures in the most cost-effective manner. Lead or Support asset criticality assessments and the development of FMEA and FMECA to support the reliability strategy. Work with Planner/ Schedulers and Parts-room Attendants to ensure that Job Plans and Spares strategies are consistent with the Reliability strategies to mitigate risk. Identify opportunities to enhance equipment reliability and performance. Lead or assist in Root Cause Analyses and failure investigations in support of deviations or safety events as necessary. Lead or support the implementation of projects to optimize performance and reliability of equipment across the sites, by collaborating with cross-functional teams to ensure successful project implementation. Consult with project teams and Responsible Engineers to establish reliability targets, maintainability and total cost of ownership and employ the appropriate reliability tools early in the life cycle of new equipment and to establish measurable performance criteria to achieve reliability targets. Utilize Maintenance and Reliability KPI’s for continuous Improvement. Work across multiple site functions to ensure the reliability and maintainability of new and modified installations Collaborate with other sites and Global functions to establish corporate standards and best practices in Reliability Engineering. Qualifications B.S. in Engineering and 4-6 years of manufacturing experience. Experience leading Root Cause Failure Analyses, Criticality Assessments, FMEA’s Experience with reliability modeling, reliability growth analysis and allocation. Competency MS Word, MS Excel, MS Power Point and MS Project, Mini-Tab, JMP or other Statistical analysis platforms Excellent oral and written communication skills. Assignments are moderately complex in nature where ability to recognize deviation from accepted practice is required. Judgment is required in resolving problems & making routine recommendations. Preferred Qualifications Experience in pharmaceutical or biotech manufacturing. Practical knowledge and application of GMP and EMEA regulations. Certified Reliability Engineer or Certified Maintenance and Reliability Professional. Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Sr. Engineer I - Clinical Label and Pack

Biogen Triangle Township, NC

Job Description Job Description Job Description About This Role As a Sr. Engineer I at our Research Triangle Park (RTP) facility, you will be essential to our Labeling and Packaging operations for bottles, vials, blisters, and syringes, playing a key role in delivering life-changing therapies to patients. This position offers a unique chance to engage in both the startup and ongoing operations phases, providing a well-rounded experience in pharmaceutical engineering. The Sr. Engineer I designs, specifies, installs, commissions and validates new process equipment, provides engineering technical support and troubleshooting for assigned process and facility equipment. The incumbent would support technology transfer of new processes into the facility, provide project engineering support as required for new equipment installations and modifications to existing equipment and have the ability to manage medium to large engineering projects with little direction. In addition, they would develop validation protocols, oversee validation testing and final report approvals. This role will work with and provide some direction to contractors and participate in and lead multi-function teams to implement change and improvements on existing processes. What You’ll Do Responsible for supporting manufacturing operations by troubleshooting process equipment system issues and identifying improvements. Update preventative maintenance job plans, equipment standards, drawings and specifications as necessary. Provide engineering technical support and troubleshooting for plant utilities and facilities systems. Participate in multi-functional teams to implement changes and improve on existing processes Provide responsible engineering and validation support for process and utility systems. Specifically design and develop validation protocols, provide expertise to associated equipment and automation design / modifications, support FAT (Factory Acceptance Testing), equipment startup, & commissioning efforts, as required. Identify and lead process equipment related projects, including technology transfers, capital projects, and modifications. Provide input & guidance to Tech Transfer and area efforts, provide technical evaluations of process equipment including validation requirements for change controls and associated action plans. Provide support with presenting discussion topics during health authority (e.g. – FDA) and partner inspections with regards to engineering and validation practices and policies. Who You Are You are an experienced equipment engineer who likes to troubleshoot and investigate improvements to increase site operations and passionate about learning new technologies and working in a cross-functional environment. You are accountable for achieving milestones in equipment projects and are passionate about making a difference and have a strong desire to contribute to a mission-driven organization. You thrive in a fast-paced environment and are eager to learn and grow. Your adaptability and attention to detail make you a valuable team player in the complex field of biomanufacturing. Qualifications Bachelor's degree in engineering. Minimum of 4 years of experience in process equipment engineering, preferably in a biologics pharmaceutical environment. Experience with pharmaceutical process equipment or production facility operations required. Practical knowledge and application of GMP regulations and guidelines (ISPE, USP, PIC/S, Annex, ICH, etc.). Competency in DeltaV, MS Word, MS Excel, MS Power Point and MS Project. Excellent organization, time management, oral and written communication skills. Ability to work on-site and on-call, extended coverage support and weekends as needed. Strong communication skills (both verbal and written) and ability to work as part of a team. Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Manufacturing Associate III

Biogen Triangle Township, NC

Job Description Job Description Job Description Job Description This position will work 12-hour DAY SHIFTS (approx. 6:00am - 6:00pm) on a 2-2-3 rotation About This Role Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. This position will be in our Parenteral Filling operations, and our teams operate across the following units: Component Preparation Compounding What You’ll Do Execute daily manufacturing activities, to include operating process equipment and executing validation protocols according to cGMP Standard Operating Procedures (SOPs) Document and record all cGMP data & information (including deviations) for processing steps and equipment activities. Create and revise key documentation like batch records, SLRs, and equipment logbooks Help maintain a clean and safe work environment, always focusing on audit readiness of process areas Be a team player and leader; always showing up to contribute your energy and focus Assist in investigations of procedural deviations Adhere to aseptic gowning and operating procedures Actively participate and lead in training and development initiatives, both for personal growth and for that of your team members Who You Are You are someone developing a deep passion for doing work that furthers a mission to save lives. You have a high degree of demonstrated learning agility, are energetic, and love a fast-paced work environment where everything you do is incredibly impactful. Biomanufacturing is complex, so you have the mental flexibility to be adaptable to whatever comes your way. Qualifications Qualifications Required Bachelor’s Degree (STEM preferred) plus at least 6 months of directly transferrable experience OR BioWork Certificate or Associate’s Degree plus at least 1 year of directly transferrable experience OR High School Diploma (or equivalent) plus at least 1.5 years of directly transferrable experience Capable of working twelve (12) hour shifts in a predetermined schedule rotation Ability to lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds Strong desire to learn and grow quickly - demonstrated experience employing learning agility Adaptable to changing needs and demands, comfortable navigating a dynamic environment Strong communication skills (both verbal and written) and ability to work as a part of a team Additional Information Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States. Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Manufacturing Associate IV - Clinical Label and Pack

Biogen Triangle Township, NC

Job Description Job Description Job Description About This Role As a Manufacturing Associate at our Research Triangle Park (RTP) facility, you will be essential to our Labeling and Packaging operations for bottles, vials, blisters, and syringes, playing a key role in delivering life-changing therapies to patients. This position offers a unique opportunity to engage in both the startup and ongoing operations phases, providing a well-rounded experience in pharmaceutical manufacturing. You will have the opportunity to develop and refine your skills in pharmaceutical labeling and packaging, gaining hands-on experience during our dynamic startup phase which include the creation and refinement of Standard Operating Procedures (SOPs), batch records, logbooks, etc. What You’ll Do Assist in the preparation and eon of equipment validation and calibration activities. Operate and maintain packaging and labeling equipment, ensuring compliance with GMP (Good Manufacturing Practices) and SOPs. Maintain accurate documentation of production activities, including batch records and logbooks. Collaborate with cross-functional teams to troubleshoot and resolve production issues. Adhere to gowning and operating procedures. Ensure the cleanliness and organization of the work area, adhering to safety protocols and procedures. Who You Are You are passionate about making a difference and have a strong desire to contribute to a mission-driven organization. You thrive in a fast-paced environment and are eager to learn and grow. Your adaptability and attention to detail make you a valuable team player in the complex field of biomanufacturing. Qualifications Bachelor’s Degree (STEM preferred) + at least 2 years of transferrable experience OR BioWork Certificate or Associate’s Degree + at least 2.5 years of transferrable experience OR High School Diploma (or equivalent) plus at least 3 years of directly transferrable experience Technical writing experience Strong attention to detail and ability to follow strict procedures. Ability to learn and work in a fast-paced, deadline-driven environment. Ability to lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Adaptable to changing needs and demands, comfortable navigating a dynamic environment. Strong communication skills (both verbal and written) and ability to work as part of a team. Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Intern, Environmental Health and Safety

Biogen Triangle Township, NC

Job Description Job Description Job Description This application is for a 12-week internship role from June - August 2025. Resume review begins in January 2025. The RTP Bio Environmental Health and Safety (EHS) team serves the site EHS needs which includes adherence to environmental and safety compliance and risk management. The team works closely with manufacturing, facilities, engineering, laboratories and other groups to help the organization ensure the safety of all employees and ensure environmental regulations are adhered to. To do this, EHS participates in many activities and tasks which includes inspections, investigations, root cause analysis, risk assessments, report generation, training and other key compliance activities. Position Description This role with help the organization ensure compliance with EHS regulatory requirements and adherence to Biogen EHS Management System: Help the EHS department with communication materials. Support inspections related to programs, (ladder safety, laboratory safety, etc. Develop EHS Spotlight communications. Conduct safety audits and inspections. Complete chemical inventory in laboratories and manufacturing Data analytics of myEHS EHS Management system. Under the direction of site personnel – assist with EHS event investigations. Liaison with the EHS department on special continuous improvement projects Help with site Sustainability initiatives Qualifications Be familiar with Microsoft Office suite, such as PowerPoint, Word, Outlook Demonstrate verbal and written communication skills Organized, can work on multiple tasks at a time, self-motivated To participate in the Biogen Internship Program, students must meet the following eligibility criteria: Legal authorization to work in the U.S. At least 18 years of age prior to the scheduled start date Be currently enrolled in an accredited college or university, with a graduation date no earlier than August 2025. Education Interest or undergraduate majors in Environmental Health Science, Industrial Hygiene, Safety Management or related Life Sciences degree. Location This role is on-site in Research Triangle Park, NC. Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Work Life Balance

Co-op, Quality Assurance

Biogen Triangle Township, NC

Job Description Job Description Job Description This application is for a 6-month student role from July - December 2025. Resume review begins in January 2025. Position Description The RTP Bio Quality Assurance Co-Op is responsible for contributing to key tactical and operational activities within Quality Assurance at the Biogen Research Triangle Park (RTP) facility on an 8:00am-4:30pm M-F shift. The RTP Bio Quality Assurance Co-Op’s responsibilities include, but are not limited to: Work Order Management, Standard Work Planning and Metric reporting. Projects include: Work with QA Operations personnel to define the content, sequence, and timing for various quality standard work activities in order to measure and continuously improve work activities. Activities will give insight into the quality operations activities of a biopharmaceutical operation. Support streamlining/ reduction of the work order processes and improve completion timelines. Identify key work order activities and drivers and identification of barriers/ hindrances to timely completion. Work with quality engineering and site engineering departments to define continuous improvement opportunities. Prepare and analyze metrics to ensure Quality departmental goals are attained. Support the Quality Assurance team with assessment of Quality metric data for continuous improvement opportunities. Escalate to Quality Management any departures from departmental goals. Other projects as needed. Qualifications Ability to lead and deliver results in an interactive matrixed environment Strong written and oral communication skills, relationship building, and leadership skills Experience with general office software applications (MS Word, Excel, PowerPoint, etc.) To participate in the Biogen Internship Program, students must meet the following eligibility criteria: Legal authorization to work in the U.S. At least 18 years of age prior to the scheduled start date Be currently enrolled in an accredited community college, college or university Education Actively completing a bachelor’s degree (preferably in a science field) and have completed at least their first year of undergraduate degree. This is not available to anyone that has already completed their undergraduate degree. Location This role is on-site in Research Triangle Park, NC Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Sr. Associate III, Quality Assurance (Quality Engineering)

Biogen Triangle Township, NC

Job Description Job Description Job Description The schedule for this position is M-F Business hours (full time, on-site) About This Role The Sr. Associate III of Quality Engineering is responsible for understanding quality systems and maintaining oversight of GMP activities while supporting Automation, Engineering, Facilities, Manufacturing, and Quality Assurance/Quality Control stakeholders at the Biogen Research Triangle Park (RTP) Pharma facility. They should be proficient in their understanding of the quality systems and apply that knowledge in coaching and continuous improvement cross functionally and globally. Additionally, the Sr. Associate III will ensure oversight and completion of all departmental milestones associated with clinical and commercial product manufacture. What You’ll Do Assist in the development and implementation of Global Quality Systems, leading site and global initiatives, provide oversight with respect to the proper administration and adherence to all Biogen policies and procedures as well as regulatory licenses and regulations, and interfacing with key Engineering, Manufacturing, and Quality customers Review of GMP raw data for compliance, review and approval of GMP documentation (including CAPAs, change controls, drawings, exceptions, procedures, records, shutdown documentation, validation protocols, work orders, etc.), and identify gaps in existing quality systems and propose solutions to site management Support oversight of quality systems and GMP activities, as well as site performance monitoring systems – such as Quality Council, Site Management Review, Site Governance Boards (e.g., CAPA Review Board, Change Control Review Board, Deviation Review Board) Proactive identification and resolution of both technical and compliance issues/gaps. Develop and implement aspects of various Quality Systems/System Improvements Support site capital projects by providing GMP guidance, risk management input, and quality oversight during shutdown planning, release, and other major equipment/facility improvements May support internal and external inspections, assess and approve discrepancies from site, corporate, and regulatory guidance. In addition, support the manager for activities related to training of employees, as well as compliance with training policies Additional duties as assigned Qualifications Required Skills Bachelor’s Degree in engineering or related life sciences field Minimum 7-10 years of experience working in Quality in a biotech/pharmaceutical GMP environment Expertise with Change Control, Exceptions Management, and Record Issuance Thorough knowledge of current global Regulatory Quality requirements Knowledge of industry practices in Engineering, Quality Control, Quality Systems, and Validation Regulatory Agency inspection experience Robust knowledge of labeling/packaging operations and validation Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Intern, Quality Control (VTR)

Biogen Triangle Township, NC

Job Description Job Description Job Description This application is for a 12-week internship role from June - August 2025. Resume review begins in January 2025. The Validation, Transfer, and Registration (VTR) group within Quality Control (QC) manages analytical strategies for Biogen’s QC methods in commercial and late clinical products. We transfer analytical methods into the QC Chemistry lab and external labs, manage changes or issues with these methods during their routine use, and provide related information in regulatory registrations. We ensure that Biogen can control the quality of our medicines, so that they will have the expected safety and efficacy profile for patients. Position Description To advance the robustness of analytical methods used for QC at Biogen, this internship is focusing on new techniques for separation and quantification of oligonucleotide (oligo) therapeutics and their impurities. These techniques will be easier to implement in labs worldwide, less prone to error or subjectivity, and greener in the reagents used. Day to day responsibilities include Preparation of liquid chromatography (LC) mobile phases and oligo samples Setting up LC instruments (UPLC/HPLC) Data acquisition, data analysis Modification of instrumental conditions to produce the desired separation effect Discussion with Biogen staff on project direction HPLC/UPLC conditions in published works will be used to inform the initial conditions and parameters to optimize Main deliverable: report, poster, and/or presentation on optimized HPLC/UPLC conditions for a given molecule Example projects may include: Developing and optimizing a HPLC/UPLC method for purity analysis of oligos Trying out different mobile phases, columns, and parameters to improve the separation of impurities Analysis by mass spectrometry (MS) to determine identity of impurities Qualifications Strong interest in/experience with one or more of the following analytical chemistry techniques: HPLC, UPLC, mass spectrometry (MS) Familiarity with oligo biochemistry Interest in understanding pharmaceutical quality control in support of manufacturing To participate in the Biogen Internship Program, students must meet the following eligibility criteria: Legal authorization to work in the U.S. At least 18 years of age prior to the scheduled start date Be currently enrolled in an accredited community college, college or university, with a graduation date no earlier than August 2025. Education Preferred: Graduate students in pharmaceutics, chemistry, biochemistry, chemical engineering, or similar fields Will Consider: Rising 4th-year undergraduate students in pharmaceutics, chemistry, biochemistry, chemical engineering, or similar fields Location This role is on-site in Research Triangle Park, NC Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Co-op, Quality Control, Raw Materials

Biogen Triangle Township, NC

Job Description Job Description Job Description This application is for a 6-month student role from July - December 2025. Resume review begins in January 2025. The Quality Control Raw Materials (QCRM) team is responsible for ensuring that all materials needed within manufacturing are inspected, sampled, tested, and released in order to meet manufacturing timelines. This team works closely with Materials Management and Planning to meet these commitments. As a co-op within this team, you can expect to learn how materials are introduced into the facility and how the quality control team ensures that these materials meet all quality standards before being released for use within the facility. Position Description As a co-op, you are responsible for engaging with team members and learning how the quality of raw materials used within manufacturing is ensured. Once trained, you will learn how to do performance checks of equipment such as balances and pH meters; you will help perform these checks daily as needed. You will also be trained on basic identification and compendial testing. Role Description: Train on basic laboratory techniques and procedures as assigned Train on identification testing as well as compendial testing for materials Learn how to use myCims, LIMS, and Oracle enterprise systems Complete assigned trainings and tasks Participate in team meetings Example projects may include: Support QC with the reduced testing initiative to reduce frequency of testing every raw material/component with procedural updates, spec revisions, etc. Support Retain Improvements including Retain Cage organization Learn basic identification techniques and compendial testing. Qualifications Conscientious self-starter with good attention to detail Ability to multi-task and balance multiple projects Strong communication skills Demonstrates flexibility and willingness to learn To participate in the Biogen Internship Program, students must meet the following eligibility criteria: Legal authorization to work in the U.S. At least 18 years of age prior to the scheduled start date Be currently enrolled in an accredited community college, college or university, with a graduation date no earlier than December 2025. Education Seeking rising sophomores, juniors and seniors, pursuing a degree in a scientific field. Location This role is on-site in Research Triangle Park, NC. Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Sr. Manager, Manufacturing - Parenteral Filling

Biogen Triangle Township, NC

Job Description Job Description Job Description About This Role Biogen is seeking an experienced manufacturing leader who is responsible for establishing and maintaining accountability and ownership of Parenteral Filling operations. Fostering a collaborative working environment throughout the manufacturing area, the Sr. Manager will ensure the successful execution of Biogen’s short and long-term manufacturing objectives. What You’ll Do Provide overall leadership and management of multiple direct and indirect reports (supervisors and manufacturing associates) for a drug product filling facility, operating across multiple shifts. Ensure successful delivery of short and long term manufacturing schedule through proactive scheduling and planning of activities. Address employee development opportunities and challenges through active coaching. Determine staffing needs and organizational structures required to efficiently meet production plans. Actively participate in hiring the best and work to develop an exceptional workforce. Drive major projects and programs for Biogen to completion, within schedule and budget. Evaluate, develop and implement continuous improvements and best practices for the area, including efficiency, capacity, and quality improvements. Actively participate and contribute to technology transfers, product launches, and implementation of process changes, typically working on cross-functional teams. Support cGMP compliance activities, acting as an area SME to review and approve cGMP documentation including SOPs, Batch Product Records, Change Controls, Investigations, etc. Develop and track area Key Performance Indicators (KPI), including identification of lead and lag metrics. Help drive overall area performance in delivery of area KPIs. Work to establish and maintain a safety focused culture. Proactively identify and remediate near-miss safety hazards. Who You Are You are a collaborative leader with technical experience in cGMP operations. You enjoy problem solving, continuous improvement and team development. Qualifications Required Skills Bachelor’s Degree (BA/BS) from a four-year college or university. (Engineering or Life Sciences preferred) 10+ years of direct experience in cGMP operations with a minimum of 5 years of people leadership experience within cGMP operations. Experiencing leading shop floor cGMP manufacturing teams (particularly in Parenteral Filling) is highly preferred. Demonstrated successful experience in leading operations in cGMP environment with a focus on team development, while building a collaborative, team-focused culture Comprehensive understanding of relevant cGMP requirements. Exceptional communication skills through all levels of an organization. Demonstrated ability to effectively operate within the sphere of control and sphere of influence. Ability to act independently, guided by broad area objectives. Ability to analyze complex problems and find common ground outcomes Availability to address urgent issues outside of typical work hours (i.e. weekends, holidays and non-scheduled work-days) Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

High salary

Manufacturing Associate I - Apprentice

Biogen Triangle Township, NC

Job Description Job Description Job Description Manufacturing Associate I – Apprenticeship Program About This Role An Apprenticeship at Biogen is a pathway to a long-term career in the biopharmaceutical industry. The 12-month program is a role directly within our operations combined with enrollment with a registered partner Community College to continue furthering your education. Throughout the program, you will be supported by customized on-the-job training and mentorship from trusted and experienced members of your team. We are hiring multiple Apprentices across a number of departments at our sites in Research Triangle Park. Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in producing & delivering our therapies to the patients who need them. MAs set up, operate, and maintain processing equipment by following established Standard Operating Procedures (SOPs) within a controlled environment, always following current Good Manufacturing Practices (cGMP). This position requires a schedule of a 10-hour shift Monday through Thursday weekly What You’ll Do Attend and actively participate in classroom & on-the-job training as well as direct shadowing of current team members to assist in the execution of daily manufacturing activities, including validation protocols Document and record all cGMP data & information (including deviations) for processing steps and equipment activities. Create and revise key documentation like batch records, SLRs, and equipment logbooks Help maintain a clean and safe work environment, always focusing on audit readiness of process areas Be a team player; always showing up to contribute your energy and focus Who You Are You are someone developing a deep passion for doing work that furthers a mission to save lives. You have a high degree of demonstrated learning agility, are energetic, and love a fast-paced work environment where everything you do is incredibly impactful. Biomanufacturing is complex, so you have the mental flexibility to be adaptable to whatever comes your way. Qualifications Required Skills Must be at least 18 years or age and hold a High School Diploma (or equivalent) Apprenticeship Program – Must have completed (or be in the process of completing) a NC BioWork Certificate Program (Pre-Apprenticeship) from a registered Community College AND be willing & able to complete additional coursework while working for Biogen as per NC BioNetwork Apprenticeship program requirements. Strong desire to learn and grow quickly - demonstrated experience employing learning agility Adaptable to changing needs and demands, comfortable navigating a dynamic environment Strong communication skills (both verbal and written) and ability to work as a part of a team Ability to lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Manufacturing Associate III

Biogen Triangle Township, NC

Co-op, Biotech Manufacturing

Biogen Triangle Township, NC

Job Description Job Description Job Description This application is for a 6-month student role from July - December 2025. Resume review begins in January 2025. The BIO Manufacturing team consists of Upstream, Purification, and Solutions Preparation and are focused on making safe and efficacious products for patients. Position Description We are seeking a motivated co-op student to join our Biotech Manufacturing team. The successful candidate will collaborate with cross-functional teams to create process maps for various tasks and develop innovative ways of working for day-to-day operations. The co-op student will also participate in data collection and analysis, support process improvements, and contribute to achieving production goals. Ideal candidates should be pursuing a degree in Biotechnology, Biochemistry, or a related field, possess strong analytical skills, and demonstrate a commitment to safety and quality in a fast-paced environment. This co-op opportunity offers experience in the biotech industry and the chance to contribute to impactful projects. Example projects may include: Create Process Flow Diagrams for varying processes (examples are: Work Orders, Kanban) Creating new ways of working and/or tools for day-to-day operations (examples are: team shift exchange, KPI metric development, etc) Qualifications Include the knowledge, skills, and abilities you may be seeking. Processing mapping skills Understanding of Operational Excellence Proficient in MS office programs & Technical Writing Self-Starter with good communication skills and willingness to learn new skills. To participate in the Biogen Internship Program, students must meet the following eligibility criteria: Legal authorization to work in the U.S. At least 18 years of age prior to the scheduled start date Be currently enrolled in an accredited community college, college or university Education Pursuing a Bachelor Degree (preferably in a discipline like Industrial Engineering with a focus on process mapping and operational excellence Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Engineer III, Manufacturing

Biogen Triangle Township, NC

Job Description Job Description Job Description About This Role The Engineer III Manufacturing designs, specifies and installs new equipment and provides engineering technical support and troubleshooting for assigned process equipment and area assets. Develops validation protocols, oversees validation testing and drafts final reports. Provides project engineering as required for new processing equipment installations and modifications to existing equipment. What You'll Do Support Manufacturing operations by troubleshooting issues and identifying equipment system improvements. Update standards, drawings and specifications as necessary. Identify and lead equipment related projects, including technology transfers, capital projects, and modifications. Complete project management tracking of deliverables for metrics & reporting. Provide input & guidance to Tech Transfer and project / area efforts, provide technical evaluations of validation requirements for core change controls & associated action plans. Author sections of Validation-related reports & project plans, approve Trackwise-generated workflows (deviations, global change controls) for equipment / automation-related changes, review automation protocols, & attend related meetings. Coordinate Equipment/Cleaning Validation Protocols (development, training, management, tracking) - includes time spent on production floor. Specifically design & develop validation protocols, provide expertise to associated equipment & automation design / modifications, support FAT (Factory Acceptance Testing), equipment startup, & commissioning efforts, as required. Who You Are You are accountable for achieving milestones in equipment projects, involving frequent internal and external communication. As a representative of the Manufacturing Engineering organization, your role carries the weight of potential delays and extra resource allocation if errors occur in your decisions or recommendations. Your commitment lies in delivering accurate and timely results, ensuring efficient processes to prevent setbacks. Qualifications Bachelor's degree in engineering. Practical knowledge and application of GMP and EMA regulations. 2-4 years of experience in manufacturing, preferably in a pharmaceutical or biotech environment. Competency in Process Controls and Distributed Controls Systems, MS Word, MS Excel, MS Power Point and MS Project. Excellent oral and written communication skills. Ability to work rotating shifts, extended shifts (including weekends) and on call as needed. Experience with either Fill Finish, Isolator (Bausch and Stroebel) and Lyophilizer technologies preferred. Additional Information Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.