GMP Manufacturing Associate II, Bioprocessing
Overview
You will own bioprocessing operations for clinical and commercial production of transformative medicines, working in a GMP environment in Norwood, MA. You will partner with Quality Assurance, Quality Control, Logistics, and Process Development to ensure quality and compliance. This 6-month contract role offers a supportive, team-oriented culture focused on continuous learning and high standards.
What You'll Do5
- 1Operate bioprocessing equipment per SOPs to produce clinical and commercial batches.
- 2Monitor process operations to maintain compliance with GMP specifications and document results.
- 3Partner with Quality Assurance to support product disposition and investigate deviations.
- 4Identify and implement process improvements to increase efficiency and reduce risk.
- 5Maintain a clean, safe, organized work area following safety and environmental guidelines.
Requirements6
- 13+ years of GMP manufacturing experience in bioprocessing.
- 2Hands-on experience with bioreactors, centrifugation, chromatography, and filtration.
- 3Strong understanding of SOPs, cGMP regulations, and documentation practices.
- 4Ability to lift 50 lbs and stand for extended periods.
- 5Excellent communication skills and ability to collaborate across teams.
- 6Bachelor's degree in biology, chemistry, or related field preferred.
Salary Insight
$71 - $81k per year
Location
Required Skills
Similar open positions
Explore active roles that match your skills and interests.
RoslinCT US
VerifiedCell Processing Associate I Boston
Join RoslinCT as a Cell Processing Associate I to lead manufacturing processes for cell therapies. This role drives production in an ISO V and VII cleanroom environment. You will collaborate across teams to ensure compliance and deliver high-quality clinical materials.
Bionova Scientific LLC
VerifiedSenior Manufacturing Associate, Upstream Bioprocessing
You will own complex upstream unit operations in a GMP cell culture environment, driving bioreactor runs from seed train to harvest at Bionova Scientific. You will serve as a subject matter expert and trainer for junior staff, leading troubleshooting and continuous improvement on the floor. Your work supports a rapidly growing CDMO backed by Asahi Kasei Group, where your technical judgment shapes batch execution and client outcomes. This role stands out because you will have minimal oversight, direct involvement in CAPA and investigations, and a voice in technology selection.

System One
VerifiedManufacturing Associate, Biopharmaceutical Manufacturing
Own biopharmaceutical manufacturing operations at a Novato site, applying mammalian cell culture and purification techniques to produce bulk drug substance. Collaborate with a cross-functional team in a cGMP environment to support process optimization and technology transfer. This contract role offers $28.00/hr plus shift differential, with a Sunday-Tuesday schedule and alternating Wednesdays, providing a unique work-life balance.
Just - Evotec Biologics, Inc.
VerifiedManufacturing Associate II Downstream Purification | Just Evotec
As a Manufacturing Associate II in Downstream Purification, you will execute cGMP biotherapeutics production at commercial scale, owning single-use bioreactor operations, chromatography, and product filtration on a Day shift (Sun-Wed, 7am-6pm). You'll operate MES systems, initiate non-conformances, and support new product introductions. This site-based role in Redmond, WA demands precision and curiosity, offering direct impact on worldwide biotherapeutic access.
Actalent
VerifiedManufacturing Technician, GMP Reagent Production
You will execute wet lab activities for reagent production and process transfer, supporting next-generation sequencing products at scale. You will report to the manufacturing lead and collaborate with process development, manufacturing, and quality teams. This role offers hands-on experience in a regulated biotech environment, directly contributing to molecular diagnostics innovation.
Asahi Kasei
VerifiedSenior Manufacturing Associate, Upstream Cell Culture
You will own upstream unit operations for a rapidly growing CDMO in Fremont, CA, executing complex runs with single-use and stainless-steel bioreactors to support client timelines. As a GMP SME, you will train junior staff, lead troubleshooting, and drive continuous improvement on the floor. You will report to the Manufacturing Supervisor and coordinate with cross-functional teams to ensure production schedules. This role offers direct impact on process development and quality systems in a dynamic, science-driven environment.