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Biopharmaceutical Manufacturing Associate Jobs (NOW HIRING)

Manufacturing Associate Location: Novato, CA Type: Contract Compensation: $28.00 + shift ... Operate and support biopharmaceutical manufacturing processes including mammalian cell culture ...

Job Title: Manufacturing Associate Location: Novato, CA Type: Contract Compensation: $28.00 ... Operate and support biopharmaceutical manufacturing processes including mammalian cell culture ...

PA · Hybrid

GSK is a global biopharma company with a special purpose - to unite science, technology and talent ... The Production organization is comprised of manufacturing associates, supervisors, managers, and ...

PA · Hybrid

GSK is a global biopharma company with a special purpose - to unite science, technology and talent ... The Production organization is comprised of manufacturing associates, supervisors, managers, and ...

Manufacturing Associate Location: Novato, CA 94949 Type: Contract Compensation: $28.00 per hour ... Support biopharmaceutical manufacturing processes, including cell culture, filtration ...

Manufacturing Associate Location: Novato, CA 94949 Type: Contract Compensation: $28.00 per hour ... Support biopharmaceutical manufacturing processes, including cell culture, filtration ...

Manufacturing Associate Location: Novato, CA 94949 Type: Contract Compensation: $28.00 per hour ... Support biopharmaceutical manufacturing processes, including cell culture, filtration ...

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Biopharmaceutical Manufacturing Associate information

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How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Jun 29, 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, and why are they important?

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 June 2026, with employment types broken down into 66% Full Time, 32% Part Time, 1% Temporary, and 1% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $56,412 per year, or $27.1 per hour.
Manufacturing Associate

Manufacturing Associate

System One Holdings, LLC

Novato, CA • On-site

$28 - $32.20/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 9 days ago


Job description

Job Title: Manufacturing Associate
Location: Novato, CA
Type: Contract
Compensation: $28.00 + shift differential
Contractor Work Model: Onsite - onsite
Hours: Sunday- Tuesday, alternating Wednesdays from 6am-7pm
Overview
Leading biotechnology company looking for an experienced Manufacturing Associate. Ideal candidates should have a Bachelor's degree in science or engineering, or Associates degree in science or Biotech certificate with 2+ years of biotech manufacturing or regulated industry experience.
Responsibilities
  • Operate and support biopharmaceutical manufacturing processes including mammalian cell culture, filtration, chromatography, centrifugation, purification, and bulk drug formulation.
  • Monitor process performance and identify issues, escalating concerns and supporting resolution to maintain production continuity.
  • Execute manufacturing steps according to standard operating procedures and batch records in a cGMP-regulated environment.
  • Provide feedback on operational procedures and support updates to incorporate new technologies, standards, and best practices.
  • Write and review technical and process documentation as required.
  • Utilize quality systems to document and address deviations, CAPAs, change controls, and related compliance activities.
  • Support process optimization initiatives and departmental performance metrics.
  • Gain working knowledge of manufacturing automation and data systems such as LIMS, MES, and PI.
  • Participate in cross-functional projects and support implementation of business systems such as TrackWise and ERP platforms.

Requirements
  • Bachelor's degree in a science or engineering discipline or Associate's degree in a science-related field or biotech certificate with 2+ years of experience in biotech manufacturing or another regulated industry.
  • Experience working in cGMP-regulated manufacturing environments.
  • Understanding of biopharmaceutical manufacturing processes such as cell culture, filtration, chromatography, or protein purification.
  • Ability to write and review technical documentation and operational procedures.
  • Experience working with quality systems such as deviations, CAPAs, and change controls.

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.
Ref: #558-Scientific