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Biotech Manufacturing Associate Jobs in Newark, NJ

System One

Manufacturing Associate Level II

Edison, NJ · On-site

$20/hr

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+ ...

System One

Production Operator

Orangeburg, NY · On-site

$21 - $23/hr

Support manufacturing operations involving medical devices, diagnostics, pharmaceutical, or biotech ... Manufacturing Associate * Machine Operator * Medical Device Manufacturing * Diagnostics ...

System One

Production Operator

Orangeburg, NY · On-site

$21 - $23/hr

Support manufacturing operations involving medical devices, diagnostics, pharmaceutical, or biotech ... Manufacturing Associate * Machine Operator * Medical Device Manufacturing * Diagnostics ...

System One

Production Operator

Orangeburg, NY · On-site

$21 - $23/hr

Support manufacturing operations involving medical devices, diagnostics, pharmaceutical, or biotech ... Manufacturing Associate * Machine Operator * Medical Device Manufacturing * Diagnostics ...

System One

Production Operator

Orangeburg, NY · On-site

$21 - $23/hr

Support manufacturing operations involving medical devices, diagnostics, pharmaceutical, or biotech ... Manufacturing Associate * Machine Operator * Medical Device Manufacturing * Diagnostics ...

System One

Production Operator

Orangeburg, NY · On-site

$21 - $23/hr

Support manufacturing operations involving medical devices, diagnostics, pharmaceutical, or biotech ... Manufacturing Associate * Machine Operator * Medical Device Manufacturing * Diagnostics ...

System One

Production Operator

Orangeburg, NY · On-site

$21 - $23/hr

... Manufacturing Associates to support the production of innovative medical device and diagnostic ... Support manufacturing operations involving medical devices, diagnostics, pharmaceutical, or biotech ...

System One

Production Operator

Orangeburg, NY · On-site

$21 - $23/hr

... Manufacturing Associates to support the production of innovative medical device and diagnostic ... Support manufacturing operations involving medical devices, diagnostics, pharmaceutical, or biotech ...

TOFFLON USA LLC

Be Seen First

Field Service Engineer

Springfield, NJ · Remote

$80K - $100K/yr

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

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

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

Biotech Manufacturing Associate information

See Newark, NJ salary details

$12

$21

$34

How much do biotech manufacturing associate jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for biotech manufacturing associate in Newark, NJ is $21.79, according to ZipRecruiter salary data. Most workers in this role earn between $17.12 and $24.38 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 are popular job titles related to Biotech Manufacturing Associate jobs in Newark, NJ? For Biotech Manufacturing Associate jobs in Newark, NJ, the most frequently searched job titles are:
What job categories do people searching Biotech Manufacturing Associate jobs in Newark, NJ look for? The top searched job categories for Biotech Manufacturing Associate jobs in Newark, NJ are:
What cities near Newark, NJ are hiring for Biotech Manufacturing Associate jobs? Cities near Newark, NJ with the most Biotech Manufacturing Associate job openings:
Biotech Manufacturing Associate jobs near you
Infographic showing various Biotech Manufacturing Associate job openings in Newark, NJ as of August 2026, with employment types broken down into 1% As Needed, 65% Full Time, 31% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $45,323 per year, or $21.8 per hour.

Manufacturing Associate II

Lynkx Staffing LLC

Saddle Brook, NJ

Full-time

Re-posted 6 days ago

Job description

Manufacturing Associate II Allendale, NJ Lynkx Staffing specializes in placing Biotechnology, Pharmaceutical, Medical Devices, IT & Human Resources professionals in New Jersey. Under the supervision of the Associate Manager, the Manufacturing Associate II processes, cultures, cryopreserves and otherwise manipulates cell products using aseptic techniques, according to written Standard Operating procedures, in accordance to facility GLP, GTP and GMP practices. Facility and personnel specific responsibilities will be regulated by company's policies or client procedures being performed at each Cellular Production Facility. The ideal candidate must have a collaborative and inquisitive nature, must possess excellent organizational and verbal and written communication skills and be flexible in their working hours.
  • Performs any and all required processing and manipulation required to produce and assess safe and efficacious products
  • Proficiently functions within an ISO Class 7 and 6 clean room environments, ensuring personal and product safety
  • Consistently produce a high level of documentation accuracy and clarity
  • Performs cryopreservation of products using DMSO base solutions and controlled-rate freezers
  • Proficiently operate and maintain equipment according to designed procedures. Assigned responsibilities could include but is not limited to COBE 2991 cell washer, Clinimacs cell separator, Elultra cell separator, controlled- rate freezers, temperature monitoring systems, alarm systems, biological safety cabinets, CO2 incubators, liquid nitrogen freezers, microscopes, pipets, wave bioreactors, refrigerators, ultra- cold freezers, water baths, tube sealers, dry shippers, centrifuges, sterile connection devices
  • Manipulate products according to established standard operating procedures and batch records such as enrichments, depletions, cell expansions, or volume reductions to achieve predetermined endpoints
  • Participating in clinical trial support and studies, may include but not limited to sample preparation, sample shipping, media and reagent preparation.
  • Thawing and/or washing cryopreserved hematopoietic cell products either at the Clinical Site or in the facility as specified by standard operating procedures
  • Performing facility and equipment duties such as periodic maintenance, preventive maintenance, for applicable methods and equipment, reporting facility and equipment problems to Assistance Manager, trouble-shooting facility and equipment problems as specified in standard operating procedures
  • Notifying Management of any deviation that may occur during processing or during equipment maintenance.
  • Applies knowledge of processing principles and techniques to make good judgement and appropriate decisions
  • Performs investigations for deviations and complete deviations and CAPA’s (Corrective and Preventive Actions) in a timely manner
  • Supports technology transfers into GMP manufacturing operations
  • Participate in the on-call program
REQUIREMENTS
  • BA/BS or Associate's Degree in a biologics or related field preferred
  • 2-4 + years of applicable experience in a clinical laboratory, hematology, blood banking, immunology or cGMP manufacturing
  • Current Medical Technologist license or equivalent is a plus
  • Aseptic/cell processing and clean room experience preferred
  • Demonstrates tact and courtesy in dealing with others
  • Strong work ethic, methodical approach to new challenges
  • GLP and GMP experience a plus
  • Must be able to work independently and with minimal supervision
  • Able to work in fast paced environment at times under pressure and with tight deadlines
  • Excellent organizational skills and attention to detail
  • Good verbal and written communication skills
  • Strong team-oriented interpersonal skills are essential
  • Ability to think strategically and tactically (detail-oriented)
  • Strong collaborative and influencing skills and ability to work well in a cross-functional, matrixed environment
  • Analytical and problem-solving skills
  • Strong written and oral communication skills
  • Ability to multi-task team is essential
  • Flexible and able to adapt to company growth and evolving responsibilities
  • Ability to work a flexible schedule that may include nights, weekends and/or holidays
  • Training Required; GMP, Gowning training/qualification, Aseptic process qualification (personal media fill)
  • Must have the ability to work in a team-oriented environment and with clients
  • Must be able to work during the weekend, holidays and as required by the company
Working EnvironmentMay be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluidsMust utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogenMust have the ability to work in the cleanroom environment for extended period of timeMust have the ability to work with specialized equipmentMust be able to handle the standard/moderate noise of the manufacturing facility Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.