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Biotech Manufacturing Associate Jobs in Linden, NJ

System One

Manufacturing Associate Level II

Edison, NJ · On-site

$20/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Job Title: Manufacturing Associate Level II Location: Edison, NJ Type: Contract To Hire ... Bachelor's degree in biotechnology, Biochemistry, Chemical Engineering, or a related field with 3+ ...

Legend Biotech US

Operations Associate

Raritan, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Legend Biotech is seeking an Operations Associate (2nd Shift) as part of the Technical Operations team based in Raritan, NJ. Role Overview This position is responsible for performing manufacturing ...

Legend Biotech US

Operations Associate

Raritan, NJ

Legend Biotech is seeking an Operations Associate (2nd Shift) as part of the Technical Operations team based in Raritan, NJ. Role Overview This position is responsible for performing manufacturing ...

TOFFLON USA LLC

Be Seen First

Field Service Engineer

Springfield, NJ · Remote

$80K - $100K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Qualifications * Bachelor's degree or Associate degree in Mechanical Engineering, Electrical ... Pharmaceutical Packaging * Pharmaceutical or Biotech Manufacturing Equipment * Strong ...

TOFFLON USA LLC

Be Seen First

Field Service Engineer

Springfield, NJ · Remote

$80K - $100K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Qualifications * Bachelor's degree or Associate degree in Mechanical Engineering, Electrical ... Pharmaceutical Packaging * Pharmaceutical or Biotech Manufacturing Equipment * Strong ...

TCWGlobal

Process Equiptment Engineer

Bridgewater, NJ · On-site

$40 - $60/hr

The ideal candidate has GMP manufacturing, process support, MSAT, biotech/pharma production, or ... MSAT Associate * Bioprocess Technician * GMP Production Support Technician * Equipment Support ...

TCWGlobal

Process Equiptment Engineer

Bridgewater, NJ

$40 - $50/hr

The ideal candidate has GMP manufacturing, process support, MSAT, biotech/pharma production, or ... MSAT Associate * Bioprocess Technician * GMP Production Support Technician * Equipment Support ...

TCWGlobal

GMP Production Support Engineer

Bridgewater, NJ · On-site

$40 - $50/hr

The ideal candidate has GMP manufacturing, process support, MSAT, biotech/pharma production, or ... MSAT Associate * Bioprocess Technician * GMP Production Support Technician * Equipment Support ...

Cellares

Cell Therapy Manufacturing Specialist

Bridgewater, NJ · On-site

$20 - $45/hr

  • Medical

  • Dental

  • Vision

  • Retirement

Train and mentor new manufacturing associates on procedures, aseptic techniques, equipment and ... biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy * Must know ...

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All JobsBiotech Manufacturing Associate JobsBiotech Manufacturing Associate Jobs in Linden, NJ

Biotech Manufacturing Associate information

See Linden, NJ salary details

$12

$21

$34

How much do biotech manufacturing associate jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for biotech manufacturing associate in Linden, NJ is $21.53, according to ZipRecruiter salary data. Most workers in this role earn between $16.88 and $24.09 per hour, depending on experience, location, and employer.

What is a biotech manufacturing associate?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

What does a biotech manufacturing associate do?

A biotech manufacturing associate is responsible for producing biological products in a laboratory or manufacturing setting, following strict safety and quality protocols. They operate equipment, prepare materials, monitor processes, and document production activities to ensure compliance with regulatory standards. Strong attention to detail and knowledge of GMP (Good Manufacturing Practice) are essential for this role.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

What are some common challenges faced by biotech manufacturing associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

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

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.
What job categories do people searching Biotech Manufacturing Associate jobs in Linden, NJ look for? The top searched job categories for Biotech Manufacturing Associate jobs in Linden, NJ are:
What cities near Linden, NJ are hiring for Biotech Manufacturing Associate jobs? Cities near Linden, NJ with the most Biotech Manufacturing Associate job openings:
Biotech Manufacturing Associate jobs near you
Infographic showing various Biotech Manufacturing Associate job openings in Linden, NJ as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 29% Part Time, 2% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $44,781 per year, or $21.5 per hour.

Manufacturing Associate Level II

System One

Edison, NJ • On-site

$20/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 26 days ago

Job description

Job Title: Manufacturing Associate Level II Location: Edison, NJ Type: Contract To Hire Compensation: $20.00 Work Model: Onsite Responsibilities

  • Prepare and maintain buffers and media required for downstream processes.
  • Ensure accurate formulation and timely availability of all solutions.
  • Maintain detailed records of preparation and usage.
  • Operate and maintain chromatography systems for protein purification.
  • Monitor process parameters and ensure consistent product quality.
  • Troubleshoot and resolve any issues that arise during chromatography runs.
  • Perform TFF operations for concentration and diafiltration of biopharmaceutical products.
  • Optimize TFF parameters to achieve desired product specifications.
  • Document all TFF activities and results.
  • Conduct viral filtration to ensure the safety and purity of biopharmaceutical products.
  • Validate and monitor viral filtration processes.
  • Maintain compliance with regulatory standards for viral safety.
  • Perform aseptic processing in a clean room environment.
  • Adhere to strict aseptic techniques to prevent contamination.
  • Ensure compliance with Good Manufacturing Practices (GMP).
  • Maintain a clean and organized work environment.
  • Follow all clean room protocols and procedures.
  • Participate in regular clean room maintenance and cleaning activities.
  • Maintain accurate and detailed records of all manufacturing activities.
  • Ensure compliance with GMP and regulatory requirements.
  • Participate in audits and inspections as needed.
  • Other duties as assigned.

Requirements

  • Ability to follow instructions and procedures.
  • Excellent problem-solving and analytical skills.
  • Effective communication, leadership and teamwork abilities.
  • Strong knowledge and experience working in a biopharmaceutical cGMP- regulated environment.
  • Must have GMP Manufacturing experience in Pharmaceuticals, Medical Devices, Biologics, Cleanroom environments, or Chemical Processing.
  • Bachelor’s degree in biotechnology, Biochemistry, Chemical Engineering, or a related field with 3+ years of relevant experience.
  • H.S diploma with 4+ years of experience will be considered in lieu of Bachelor’s Degree.
  • Technical training or certifications are a plus.
  • Must be comfortable working in cleanroom and sterile environments, with ability to follow strict protocols.
  • Strong interest in a cross-functional manufacturing role with growth opportunity.
  • Must have flexibility with supporting hours outside of 8am-5pm when needed.
  • Open to a Temp-to-Hire opportunity for long-term employment (Others have converted recently).
  • This position requires the ability to stand for extended periods, bend, and lift objects weighing up to 50 pounds.
  • Candidates must be physically capable of performing these tasks safely and effectively.
  • Requires availability to work flexible shifts including overtime, evenings, weekends and holidays, as operational needs require.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#M- #LI- Ref: #550-Joule Headquarters