Lead Upstream Biotech Manufacturing Associate
Listed on 2026-10-12
-
Manufacturing / Production
Pharmaceutical Manufacturing, Validation Engineer, Quality Engineering
Planet Pharma is seeking an Upstream Manufacturing Associate III (Lead) to provide technical leadership and coordinate upstream manufacturing activities in a cGMP environment. The role leads batch execution, troubleshooting, and cross-functional collaboration across QA, QC, MSAT, and supply chain.
The candidate will oversee cell culture activities, harvest and filtration, process monitoring, and continuous improvement initiatives to drive operational excellence.
The Lead Upstream Biotech Manufacturing Associate role at Planet Pharma is now open for applications in Pennington, NJ, United States.
The position is based in Pennington, NJ, United States.
This opportunity is part of our work in Engineering.
The advertised compensation is 33.000 - 52.000.
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 Lead Upstream Biotech Manufacturing Associate role in the description above.
(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).