GMP Biopharma Manufacturing Associate
-
Manufacturing / Production
Pharmaceutical Manufacturing -
Quality Assurance - QA/QC
Job Description & How to Apply Below
Actalent is hiring for a Manufacturing Associate in Plainville, MA to support biopharmaceutical production operations in a GMP-regulated environment. You will work on batch documentation, quality systems, and cleanroom processes while gaining hands-on experience in biotechnology manufacturing.
The role emphasizes accuracy, collaboration, and adherence to GMP standards, with opportunities for hands-on training and career development within a growing biopharmaceutical organization.
Consider building your career as a GMP Biopharma Manufacturing Associate at ACTalent.
All applications are reviewed carefully by our team.
The position is based in Plainville, MA, United States.
This opportunity is part of our work in Engineering.
The advertised compensation is 37.000 - 39.000.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the GMP Biopharma Manufacturing Associate role in the description above.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
View / Apply for Jobs
Matching My Jurisdiction