Downstream Manufacturing Associate

Job Description

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.