Manufacturing Associate

# Manufacturing Associate
1010 Celgene
- Summit (Corp)
Full Time junior Summit, New Jersey, USPosted 2 days ago##

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.## Resume Keywords to Include Make sure these keywords appear in your resume to improve ATS scoring

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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:  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,…