Upstream Biomanufacturing Associate (12‑Hr Shifts)

Biogen

Milwaukee (WI)

On-site

USD 33,000 - 44,000

Full time

8 days ago

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Benefits offered by this job

Medical, Dental, Vision, & Life ins.
Fitness & Wellness programs
Paid vacation and holidays
401(k) with company match
Tuition reimbursement

Job summary

Biogen is seeking Manufacturing Associates for our Research Triangle Park (RTP) facility to support Upstream Cell Culture operations. You will work on bioreactors, perform inoculations, and help maintain cell culture processes in a clean, cGMP environment.

Roles require flexibility for 12-hour shifts on a 2-2-3 calendar with days (6:00 AM – 6:00 PM ET) and potential Nights. Strong documentation, SOP adherence, and cross-functional collaboration are essential.

Qualifications

  • Bachelor’s degree in STEM or equivalent with 0+ years for II or 0+ years for III; flexibility on credentials.
  • Knowledge of cGMP, SOPs, and good documentation practices.
  • Experience in a GxP environment or biopharma manufacturing is preferred.

Responsibilities

  • Prepare bioreactors using CIP/SIP recipes in DeltaV.
  • Perform filtration, centrifugation, and harvest operations.
  • Calibrate pH and DO probes and inoculate bioreactors across scales.
  • Support cell growth with media feeds and process additions.
  • Document activities in compliance with cGMP and SOPs.

Skills

SOP adherence
Documentation/Data integrity
Shift work experience
Aseptic technique
Cross-functional collaboration

Education

Bachelor’s degree in STEM
BioWorks Certificate / associate degree
High School Diploma + relevant experience

Tools

DeltaV
Syncade

Job description

Biogen is seeking Manufacturing Associates for our Research Triangle Park (RTP) facility to support Upstream Cell Culture operations. You will work on bioreactors, perform inoculations, and help maintain cell culture processes in a clean, cGMP environment.

Roles require flexibility for 12-hour shifts on a 2-2-3 calendar with days (6:00 AM – 6:00 PM ET) and potential Nights. Strong documentation, SOP adherence, and cross-functional collaboration are essential.

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