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Biopharmaceutical Manufacturing Associate Jobs (NOW HIRING)

Fujifilm

Manufacturing Associate 5

Holly Springs, NC · On-site

By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing ... Associate's Degree * BA/BS Degree, preferably in Life Sciences or Engineering * Proficient ...

FUJIFILM Biotechnologies

By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing ... and/or assist senior level associates or supervisor with scheduling daily activities on ...

FUJIFILM Biotechnologies

By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing ... and/or assist senior level associates or supervisor with scheduling daily activities on ...

Fujifilm

Manufacturing Associate 2

Holly Springs, NC · On-site

By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing ... Associate's Degree + 2 years direct experience in cGMP manufacturing environment OR * Bachelor ...

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How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Jun 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, 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.
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Biopharmaceutical Manufacturing Associate jobs near you
Infographic showing various Biopharmaceutical Manufacturing Associate job openings in the United States as of May 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $56,412 per year, or $27.1 per hour.
MCS Manufacturing Associate, Biopharma (JP9784)

MCS Manufacturing Associate, Biopharma (JP9784)

3 Key Consulting

Thousand Oaks, CA

Other

Posted 2 days ago

Job description

Job Title: MCS Manufacturing Associate, Biopharma (JP9784)
Location:Thousand Oaks, CA. 91320
Employment Type: Contract
Business Unit:Cell Culture
Duration:Initial 3 months with likely extensions
Posting Date:3/29/2022
Notes:Onsite
3 Key Consulting is hiring aMCSManufacturing Associatefor a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
The Associate of Manufacturing will work in a dynamic production environment at the client's Thousand Oaks Site supporting development, clinical, and launch activities. Under general supervision, employee will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs).
Responsibilities include:
  • Hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipment
  • Preparing buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs)
  • Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance
  • Performing and monitoring critical processes with the ability to perform basic troubleshooting
  • Performing in-process sampling of equipment and operating analytical equipment
  • Performing washroom activities: clean small and large scale equipment used in production activities
  • Maintaining an organized and clean workspace
  • Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work
  • Initiating quality reports
  • Drafting and revising documents (SOPs, MPs)
  • Identifying, recommending, and implementing improvements related to routine functions
  • Assisting in the review of documentation for assigned functions (equipment logs, batch records)
  • Performing activities that include periods of rigorous, repetitive work
  • Working around high-pressure systems and occasionally work around heavy equipment
  • Available to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs) as dictated by the production schedule
Basic Qualifications:
Bachelor's degree OR
Associate's degree and 4 years of Manufacturing /Operations experience OR
High school diploma / GED and 6 years of Manufacturing /Operations experience
Able to work in teams to complete operational tasks
Able to take direction well, follow documents and policies at all times
Able to take initiative
Creates positive work environment through interactions with team members
Able to regularly lift up to 35lbs, push and pull objects that require up to 50lbs of force, and work on your feet for long durations
Able to perform the list of physical movements that may be necessary to perform daily functions on the production floor: bending, reaching above the head, climbing, kneeling, squatting, stooping, walking upstairs, and standing on portable stairs or ladders up to 6 feet off of the ground.
Preferred Qualifications:
Bachelor's Degree in Biology and/or Life Sciences
Mechanically inclined
Why is the Position Open?
Supplement additional workload on team.
Top Must Have Skills:
1) Mechanical and technical ability
2) Must be able to work all shifts
3) Must be able to understand GMP and compliance
4) Must take initiative
Day to Day Responsibilities:
Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves to support the manufacture of drug substance using SOP's.
Employee Value Proposition:
Extension is highly likely - unique knowledge and experience
Red Flags:
Not local in distance to Amgen
No degree
If they are looking for research position, this is not it.
They need mechanical experience or show aptitude
Unable to work all shifts and be flexible (evenings, weekends, etc)
Interview process:
Phone and Webex.
We invite qualified candidates to sendyour resume torecruiting@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this position, please feel free to look at the other positions on our websitewww.3keyconsulting.com/careers. You are welcome to also sharethis opportunity withanyone you think might be interested in applying for this role.

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