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Biopharmaceutical Manufacturing Associate Jobs (NOW HIRING)

TekWissen LLC

Manufacturing Associate

Portsmouth, NH · On-site

$20 - $26/hr

Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom ... Manufacturing Associate Location: Portsmouth, NH, 03801 Duration: 12 Months Job Type: Temporary ...

FUJIFILM Biotechnologies

By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing ... Associate 2 High School Diploma or GED with 2 years of related experience in Life Sciences ...

FUJIFILM Biotechnologies

By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing ... Associate 2 High School Diploma or GED with 2 years of related experience in Life Sciences ...

TekWissen LLC

Manufacturing Associate

Portsmouth, NH · On-site

$20 - $23/hr

Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom ... Biotechnologist Associate / Manufacturing Associate Location: Portsmouth, NH, 03801 Duration: 12 ...

Kinetic Personnel Group

Be Seen First

Biopharma Manufacturing Roles Degree Required

Irvine, CA · On-site

$20 - $26/hr

The Manufacturing Associate - Buffer Preparation supports cGMP manufacturing operations by ... biotech, biopharmaceutical, or CDMO environments * Hands-on experience with buffer and solution ...

TekWissen LLC

Manufacturing Associate

Houston, TX · On-site

$20 - $24/hr

Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom ... Manufacturing Associate / Environmental Monitoring (EM) Core Technician Location: Houston, TX, ...

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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 8, 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.
Manufacturing Associate - Biologics (Multiple Openings) - NIGHT SHIFT

Manufacturing Associate - Biologics (Multiple Openings) - NIGHT SHIFT

Fujifilm

Holly Springs, NC • On-site

Other

Posted 19 days ago

Fujifilm rating

8.3

Company rating: 8.3 out of 10

Based on 66 frontline employees who took The Breakroom Quiz

47th of 516 rated manufacturers

Job description

Position Overview
We have opportunities for Manufacturing Associates at several levels within our Drug Substance production teams who are willing and able to work on a NIGHT SHIFT (Approximately 6:00PM-6:00AM).
These roles will execute manufacturing processing steps and associated activities when operational. You will also participate in operational readiness projects and commissioning/qualification projects. Our brand-new facility will be 24/7 operational and our manufacturing teams work 12-hour shifts on a 2-2-3 calendar rotation.
*** Please note that this posting represents multiple openings within our manufacturing organization ***
Company Overview
FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.
We're looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we're proud to cultivate a culture that will fuel your purpose, energy, and drive-what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together!
Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity.
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: https://www.fujifilm.com/us/en/about/region/careers
Job Description
What You'll Do
During the project phase, you may:
  • Participate and support testing activities, such as: FAT, PQ etc.
  • Support and contribute in the preparation of the documentation package (i.e. Standard Operating Procedures and Work Instructions)
  • Contribute to the preparation for operational readiness related to Weigh and Dispense, bulk Drug Substance or Drug Product manufacturing
  • Possible assignments include, supporting projects related to procedure review and/or creation, development or transfer of manufacturing business processes, testing and commissioning support

Once we are operational, you may:
  • Lead, execute and document manufacturing processing steps and/or manufacturing support activities, process monitoring and control
  • Perform operations of functional area
  • Execute validation protocols according to cGMP Standard Operating Procedures (SOPs)
  • Own or establish processes and trainings to become a trainer for coworkers
  • Maintain compliance of GMP documents and ensure your own training level is compliant and maintained
  • Support and/or assist senior level associates or supervisor with scheduling daily activities for your functional area, as needed
  • This role requires shift work (weekend and potential for nights)
  • Perform other duties as assigned

Basic Requirements
  • Manufacturing Associate 2
  • High School Diploma or GED with 2 years of related experience in Life Sciences Manufacturing OR
  • Associate's Degree in Life Sciences with 0 years of related experience OR
  • Equivalent Military training/experience

  • Manufacturing Associate 3
  • High School Diploma or GED with 4 years of related experience in Life Sciences Manufacturing OR
  • Associate's Degree with 2 years of experience in Life Sciences Manufacturing OR
  • BA/BS in Life Sciences with 0 years of experience OR
  • Equivalent Military training/experience

  • Manufacturing Associate 4
  • High School Diploma or GED with 6 years of experience in Life Sciences Manufacturing OR
  • Associate degree with 4 years' experience in Life Sciences Manufacturing OR
  • BA/BS with 2 years of experience in Life Sciences Manufacturing OR
  • Equivalent Military training/experience

  • Manufacturing Associate 5
  • High School Diploma or GED with 8 years' experience in a Life Sciences Manufacturing environment OR
  • Associate Degree with 6 years' experience in a Life Sciences Manufacturing environment OR
  • BA/BS, preferably in Life Sciences/Engineering with 4 years of experience in Life Sciences Manufacturing OR
  • Equivalent Military Experience

WORKING CONDITIONS & PHYSICAL REQUIREMENTS
  • Be exposed to an environment that may necessitate respiratory protection.
  • Be exposed to noisy environments.
  • Have a normal range of vision
  • Climb ladders and stairs of various heights.
  • Experience prolonged sitting, standing, walking, bending, stooping and stretching throughout the shift, up to 12 hours.
  • Use hand-eye coordination and manual dexterity sufficient to operate a computer keyboard, telephone, calculator, and other office equipment is required.
  • May be required to lift up to 50 pounds on occasion.

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.
EEO Information
Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.
ADA Information
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).

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About Fujifilm

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With each Industry we enter, We’ve learned to Leverage and Adapt our knowledge, Expertise and rRsources to make the World a better place. When it comes to Innovating for a Healthier World and a more sustainable society, we’ll NEVER STOP. Fujifilm will contribute to the social challenges by creating new value in a wide range of business domains through innovation in Products, Services, and Technological Development. We launched our Healthcare Business with X-ray film in 1936. And now, We are developing our business in areas of prevention, diagnosis, and treatment as a Comprehensive Healthcare Company. We will never stop Innovating for a Healthier World.

Industry

Chemical manufacturing

Company size

10,000+ Employees

Headquarters location

Minato-ku, Tokyo, JP

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