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Biopharmaceutical Manufacturing Associate Jobs (NOW HIRING)

Understand process theory and equipment operation, supporting biopharmaceutical manufacturing ... Associates degree in science or biotech certificate with 2+ years of experience in a biotech ...

Understand process theory and equipment operation, supporting biopharmaceutical manufacturing ... Associates degree in science or biotech certificate with 2+ years of experience in a biotech ...

Manufacturing Associate Location: Novato CA 94949 Type: Contract Compensation: $28.00/hr + shift ... Apply process knowledge of biopharmaceutical manufacturing, including mammalian cell culture, depth ...

Understand process theory and equipment operation, supporting biopharmaceutical manufacturing ... Associates degree in science or biotech certificate with 2+ years of experience in a biotech ...

Manufacturing Associate

Novato, CA · On-site

$28 - $32.20/hr

Manufacturing Associate Location: Novato CA 94949 Type: Contract Compensation: $28.00/hr + shift ... Apply process knowledge of biopharmaceutical manufacturing, including mammalian cell culture, depth ...

Manufacturing Associate Location: Novato CA 94949 Type: Contract Compensation: $28.00/hr + shift ... Apply process knowledge of biopharmaceutical manufacturing, including mammalian cell culture, depth ...

Manufacturing Associate Location: Novato CA 94949 Type: Contract Compensation: $28.00/hr + shift ... Apply process knowledge of biopharmaceutical manufacturing, including mammalian cell culture, depth ...

Manufacturing Associate Location: Novato CA 94949 Type: Contract Compensation: $28.00/hr + shift ... Apply process knowledge of biopharmaceutical manufacturing, including mammalian cell culture, depth ...

Understand process theory and equipment operation, supporting biopharmaceutical manufacturing ... Associates degree in science or biotech certificate with 2+ years of experience in a biotech ...

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Manufacturing Formulation Associate (Entry Level) A leading Contract Development and Manufacturing ... biopharmaceutical products. Committed to delivering high-quality manufacturing services while ...

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Biopharmaceutical Manufacturing Associate information

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$18

$27

$40

How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for biopharmaceutical manufacturing associate in the United States is $27.12, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $31.73 per hour, depending on experience, location, and employer.

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.

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 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 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 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 cities are hiring for Biopharmaceutical Manufacturing Associate jobs? Cities with the most Biopharmaceutical Manufacturing Associate job openings:
What are the most commonly searched types of Biopharmaceutical Manufacturing jobs? The most popular types of Biopharmaceutical Manufacturing jobs are:
What states have the most Biopharmaceutical Manufacturing Associate jobs? States with the most job openings for Biopharmaceutical Manufacturing Associate jobs include:
Infographic showing various Biopharmaceutical Manufacturing Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 28% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $56,412 per year, or $27.1 per hour.

Manufacturing Associate (Pharmaceuticals Entry Level)

RD Partners

Novato, CA • On-site

$28 - $32.20/hr

Contractor

Medical, Dental, Vision, Retirement

Posted 18 days ago


Job description

Position: Manufacturing Associate

Duration: 12-month contract

Location: Novato, California
Schedule: Alternating Saturdays, Sunday–Tuesday, 6:00 PM – 7:00 AM


Compensation:

  • 1st Shift: $28.00/hr
  • 2nd Shift: $30.80/hr (10% differential)
  • 3rd Shift: $32.20/hr (15% differential)
  • Eligible for shift differential pay and overtime pay


About the Role

We are seeking a motivated Manufacturing Associate to join a leading biopharmaceutical organization focused on advancing life‐changing therapeutics. This role is ideal for someone who enjoys hands‐on work in a fast‐paced, regulated environment and is eager to develop strong technical expertise in large‐scale biologics manufacturing.


Key Responsibilities

Process Operations & Technical Skills

  • Learn and execute core biopharmaceutical manufacturing processes, including:
    mammalian cell culture, depth filtration, tangential flow filtration (TFF), column chromatography, centrifugation, protein purification, and bulk drug substance formulation.
  • Develop strong process knowledge, understanding equipment operation and process theory.
  • Support continuous improvement and process optimization initiatives.
  • Identify and escalate processing issues and participate in implementing solutions.
  • Gain experience with automation and digital systems such as LIMS, MES, PI, and other manufacturing software.

Documentation & Compliance

  • Draft, review, and suggest improvements to process‐related documents and SOPs.
  • Assist with integrating new technologies, procedures, and standards.
  • Ensure all work adheres to cGMP requirements and utilize quality systems, including Deviations, CAPAs, and Change Requests.

Cross‐Functional Collaboration

  • Participate in departmental projects and contribute to achieving operational outcomes.
  • Learn and support additional business systems (e.g., TrackWise, ERP).
  • Assist with tracking and trending operational metrics.


Qualifications

  • Bachelor’s degree in a science or engineering discipline or Associate degree/Biotech certificate + 2+ years of experience in biotech manufacturing or another regulated industry.
  • Strong verbal and written communication skills.
  • Ability to work collaboratively, resolve conflict constructively, and support team‐based environments.
  • Demonstrated initiative, problem‐solving ability, and continuous improvement mindset.


Work Environment & Physical Requirements

  • Role involves strenuous, repetitive tasks and frequent bending, reaching, kneeling, climbing stairs/ladders, and performing equipment connections.
  • Must be able to lift/push/pull 25 lbs regularly.
  • Work may involve loud equipment and requires use of personal protective equipment (PPE).
  • This position requires night shift work, alternating weekends, and flexibility for off‐hours as needed.

Company Description

R&D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire & outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL.

The cornerstone of our success: a knowledgeable and experienced recruiting team.

Our life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.