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Biopharmaceutical Manufacturing Associate Jobs in Edison, NJ

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$18

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$40

How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for biopharmaceutical manufacturing associate in Edison, NJ is $27.49, according to ZipRecruiter salary data. Most workers in this role earn between $23.41 and $32.16 per hour, depending on experience, location, and employer.

What is a biopharmaceutical manufacturing associate?

As a biopharmaceutical manufacturing associate, your primary responsibilities are to prepare equipment and materials for the production of biopharmaceutical products. Your duties include moving the product, supplies, and inventory to support the manufacturing process and operating devices like autoclaves and washers. You monitor the production and operations, make adjustments to increase efficiency, and ensure that you are meeting all safety regulations. You work with downstream and upstream processes to control quality. You are also in charge of preparing reports and reviewing GMP documents to ensure compliance with laws and industry regulations.

What does a biopharmaceutical manufacturing associate do?

A Biopharmaceutical Manufacturing Associate is responsible for producing biopharmaceutical products such as vaccines, antibodies, or therapeutic proteins under strict regulatory guidelines. Their tasks typically include preparing equipment, monitoring production processes, maintaining sterile environments, and ensuring that all procedures adhere to Good Manufacturing Practices (GMP). They may also be involved in quality control, documentation, and troubleshooting equipment issues. This role is crucial for ensuring the safety, efficacy, and quality of biopharmaceutical products.

What are the key skills and qualifications needed to thrive as a biopharmaceutical manufacturing associate?

To thrive as a Biopharmaceutical Manufacturing Associate, you need a solid background in life sciences or engineering, with knowledge of GMP (Good Manufacturing Practices) and often a relevant bachelor’s degree or associate’s certification. Familiarity with bioprocessing equipment, automation systems like SCADA, and quality control tools is essential. Attention to detail, teamwork, and strong communication skills are crucial soft skills for this role. These competencies ensure the safe, accurate, and compliant production of high-quality biopharmaceutical products.

What are some common challenges faced by biopharmaceutical manufacturing associates, and how can they be addressed?

Biopharmaceutical Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP) and troubleshooting equipment malfunctions under tight production schedules. To address these challenges, associates are trained extensively on standard operating procedures and cross-functional communication to quickly resolve issues. Teamwork and attention to detail are essential, as the role frequently involves collaborating with quality assurance, engineering, and process development teams to ensure product safety and compliance. Continuous learning and proactive problem-solving are key to success in this dynamic environment.

What is the difference between Biopharmaceutical Manufacturing Associate vs Quality Control Technician?

AspectBiopharmaceutical Manufacturing AssociateQuality Control Technician
Primary RoleSupports production processes, prepares materials, and ensures manufacturing runs smoothlyPerforms testing and inspection of products to ensure quality standards
Required SkillsKnowledge of GMP, aseptic techniques, and manufacturing proceduresLaboratory skills, attention to detail, knowledge of testing methods
Work EnvironmentCleanrooms, manufacturing floors, production facilitiesLaboratories, testing labs, quality control areas
CertificationsGMP training, sometimes cGMP certificationLab safety, GMP, and quality assurance training

The Biopharmaceutical Manufacturing Associate focuses on supporting the production process in manufacturing environments, while the Quality Control Technician specializes in testing and verifying product quality. Both roles require GMP knowledge and work in regulated settings, but their daily tasks and skill sets differ significantly.

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What cities near Edison, NJ are hiring for Biopharmaceutical Manufacturing Associate jobs?

Cities near Edison, NJ with the most Biopharmaceutical Manufacturing Associate job openings:

Biopharmaceutical Manufacturing Associate jobs near you
Infographic showing various Biopharmaceutical Manufacturing Associate job openings in Edison, NJ as of August 2026, with employment types broken down into 88% Full Time, 6% Part Time, and 6% Contract. Highlights an 89% In-person, and 11% Hybrid job distribution, with an average salary of $57,182 per year, or $27.5 per hour.

Downstream Manufacturing Associate

Global Life Science Hub

Piscataway, NJ • On-site

Other

This job post has expired 1 day ago. Applications are no longer accepted.

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.

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