What are the responsibilities and job description for the Downstream Manufacturing Associate position at Global Life Science Hub?
DOWNSTREAM MANUFACTURING ASSOCIATE Piscataway, NJ - Full-Time, Permanent
We are seeking a Downstream Manufacturing Associate to join a well-established biologics manufacturer in Piscataway, NJ. This is a full-time permanent position - not a contract role.
You will be executing cGMP downstream purification processes at scale, working across engineering, clinical, and commercial batches in a regulated manufacturing environment. Hands-on, production floor work with real responsibility from day one.
What you'll be doing:
- Executing downstream purification processes at 50L to 1000L scale in a cGMP environment
- Operating and maintaining AKTA purification skids, TFF systems, and chromatography equipment
- Column packing, process troubleshooting, and data analysis
- Initiating and completing batch records, deviations, and investigations in line with GMP requirements
- Supporting environmental health and safety compliance on the manufacturing floor
What you need:
- 1-2 years hands-on experience in downstream cGMP manufacturing within biopharma or a CDMO
- Experience with AKTA or equivalent purification systems and TFF
- Mammalian cell culture or biologics manufacturing background
- Comfortable with GMP documentation - batch records, protocols, investigations
- BS or MS in biochemistry, biotech, chemical or biological sciences
Multiple levels available - MFG I, II, and III - so we are open to candidates across the experience spectrum.
If this sounds like your next move, apply directly or reach out to discuss.
Salary : $32 - $38