Manufacturing Associate
1010 Celgene - Summit (Corp)Role Overview
1010 Celgene - Summit (Corp) is hiring a entry-level Manufacturing Associate. This is a full-time role in Summit. posted 2 days ago. Full responsibilities, required qualifications, and the apply link are listed in the description below.
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Job Description
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. Position Summary Our Associates play a crucial role in supporting routine Cell Therapy manufacturing operations. We are looking for innovative, intellectually curious individuals with a general understanding of Good Manufacturing Practices (GMPs). Successful candidates must be goal-oriented and flexible, with the ability to work effectively on a team while demonstrating safety, quality, and GMP compliance at all times. Duties & Responsibilities Execute Cell Therapy Manufacturing operations in compliance with Source Governing Documents (SOPs, Work Instructions, Batch Records, Forms) Prioritize safety; report safety events within 24 hours and immediately escalate compliance issues Complete all documentation contemporaneously and in accordance with GMP requirements, including ALCOA+ Execute the daily unit operations schedule across multiple shifts, including people, product, and material flow Perform aseptic processing and maintain cleanroom environmental conditions as required Complete training assignments on time and verify training completion prior to performing any GxP tasks Author and/or follow Manufacturing operating procedures in compliance with cGMP requirements Execute transactions in all electronic systems and adhere to business continuity processes Qualifications Education: U.S.: Associate's or Bachelor's degree in a related field preferred; minimum high school diploma or equivalent required Netherlands: MBO, level 3 or 4 in a science-related field or equivalent Experience & Skills: 0–1 years of cGMP cell therapy manufacturing, bioprocessing, or relevant experience Basic understanding of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing preferred Proficiency in common computer tools (word processing, spreadsheets, web-based applications) Meticulous attention to detail and strong personal accountability Excellent interpersonal skills; collaborative, attentive, and approachable Ability to maintain professional relationships with management and co-workers Working Conditions Must be able to stand/walk for extended periods Must be able to work in a cleanroom environment performing aseptic processing in ISO 5 biosafety cabinets, with required PPE (safety shoes, glasses, aprons, face shields, PAPR, lab coats, full body gowns, hairnets, gloves, and hearing protection) Must be able to lift/carry up to 30 lbs / 15 kg and push/pull up to 50 lbs / 25 kg multiple times per day Must be able to work in a BSL2 / ML1 environment handling human blood components and areas with vapor phase liquid nitrogen exposure Must be available to work assigned shifts including Days, Evenings, Nights, Weekends, and/or Holidays This job description describes the general nature of the role. Additional duties may be assigned as needed by management. If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Compensation Overview: Summit West - NJ - US: $27.83 - $33.72per hour The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include: Health Coverage: Medical, pharmacy, dental, and vision care. Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. Work-life benefits include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. *Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1603347 : Manufacturing Associate Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.
Frequently Asked Questions
How do I apply for the Manufacturing Associate position at 1010 Celgene - Summit (Corp)?
Use the Apply button above to submit your application directly to 1010 Celgene - Summit (Corp). Most applications take less than 5 minutes if your resume and contact details are ready, and you'll be routed to the employer's official application system to finish.
Where is the Manufacturing Associate position at 1010 Celgene - Summit (Corp) located?
This position is based in Summit. 1010 Celgene - Summit (Corp) has not indicated remote or hybrid options for this role, so candidates should plan for on-site work.
What does a Manufacturing Associate at 1010 Celgene - Summit (Corp) earn?
1010 Celgene - Summit (Corp) has not disclosed a salary range in this posting. Many employers share specifics later in the interview process; you can also ask during a recruiter screen if compensation transparency is important to you.
When was the Manufacturing Associate role at 1010 Celgene - Summit (Corp) posted?
This role was posted on June 12, 2026 (2 days ago). It's still listed as actively hiring; we re-confirm openings against the source system multiple times per day and remove closed roles.
Is the Manufacturing Associate role at 1010 Celgene - Summit (Corp) entry-level?
Yes. This is an entry-level position. Strong candidates typically have 0-2 years of relevant work experience, internships, or significant project work. Read the full description for any specific qualification requirements 1010 Celgene - Summit (Corp) has listed.
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