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Biopharmaceutical Manufacturing Associate Jobs in Virginia

Maintenance Mechanic

Manassas, VA · On-site

$25 - $32/hr

With extensive development and manufacturing expertise and a wide range of flavors, ingredients ... Associate degree with 2+ years of relevant experience or High School Diploma and 5+ years of ...

Maintenance Mechanic

Manassas, VA · On-site

$25 - $32/hr

With extensive development and manufacturing expertise and a wide range of flavors, ingredients ... Associate degree with 2+ years of relevant experienceor High School Diploma and 5+ years of ...

Associate degree or 5-10 years of related experience and/or training * Strong analytical, problem ... biopharma and consumer health companies of all sizes to advance new medicines from early ...

Showing results 41-46

Biopharmaceutical Manufacturing Associate information

See Virginia salary details

$18

$26

$39

How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for biopharmaceutical manufacturing associate in Virginia is $26.89, according to ZipRecruiter salary data. Most workers in this role earn between $22.88 and $31.44 per hour, depending on experience, location, and employer.

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 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 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 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 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 popular job titles related to Biopharmaceutical Manufacturing Associate jobs in Virginia?

For Biopharmaceutical Manufacturing Associate jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Biopharmaceutical Manufacturing Associate jobs in Virginia look for?

The top searched job categories for Biopharmaceutical Manufacturing Associate jobs in Virginia are:

What cities in Virginia are hiring for Biopharmaceutical Manufacturing Associate jobs?

Cities in Virginia with the most Biopharmaceutical Manufacturing Associate job openings:

Infographic showing various Biopharmaceutical Manufacturing Associate job openings in Virginia as of August 2026, with employment types broken down into 100% Full Time. Highlights an 83% In-person, and 17% Hybrid job distribution, with an average salary of $55,928 per year, or $26.9 per hour.

Quality Assurance Specialist I

Catalent Pharma Solutions

Manassas, VA • On-site

Full-time

Medical, Dental, Vision, PTO

Posted 7 days ago


Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

63rd of 86 rated pharmaceutical


Job description

About Site

The ~70,000squarefoot Manassas facility operates within Catalent's Consumer Health portfolio, supporting programs from early development through commercial manufacturing and packaging. It is designed for dietary supplement and foodsafety cGMP operations, making it distinct from Catalent's traditional pharmaceutical and biologics manufacturing sites.

Position Summary

We have an opportunity for a Quality Assurance Specialist I to join our team. In this role, you will audit products and processes during production and packaging to ensure compliance with quality standards. You will communicate deviations, assist with special projects, and maintain adherence to SQF, Food Safety Plan (HACCP), and Food Quality Plan (FQP) standards. This position also serves as alternate cover for QA Specialist II.

Shift: 10pm-6:30am Monday to Friday
Location: Manassas, VA
100% Onsite

The Role

  • Conduct detailed quality audits of production lines to ensure products meet established standards

  • Verify equipment such as metal detectors, x-ray machines, and scales

  • Audit operator paperwork for compliance with quality requirements

  • Report deviations to the QA Supervisor with complete details

  • Identify and report housekeeping issues requiring attention

  • Document non-compliance areas and ensure corrective actions are implemented

  • Collaborate with Production and Packaging Managers, Supervisors, and associates on daily issues

  • Enter and track result data using computer systems

  • Comply with SQF, Food Safety Plan (HACCP), and Food Quality Plan (FQP) standards

  • Ensure compliance with FDA and cGMP standards for Quality Control, including ongoing training

  • Maintain Dietary Supplement's Identity, Purity, Strength, and Quality

  • Serve as alternate cover for QA Specialist II

  • Participate in all required training to perform job responsibilities

  • Perform other duties as assigned

The Candidate

Minimum Requirements

  • Ability to communicate effectively in English, both verbally and in writing

  • High School Diploma

  • Ability to communicate with all line-level positions and management

  • Strong attention to detail

  • Self-starter with ability to work independently with minimal supervision

  • Ability to assert effectively when needed

  • Strong interpersonal skills to build cross-functional and multinational relationships

  • Strong analytical skills

  • Ability to read and follow Standard Operating Procedures and Test Methods

  • Knowledge of Good Manufacturing Practices (GMP) and Quality systems

  • Must be able to lift and/or move up to 50 pounds

  • Frequent standing, walking, reaching, stooping, kneeling, crouching, or crawling; occasional sitting, climbing, balancing, tasting, or smelling

  • Approximately 85% of the role involves walking and standing

Preferred Skills & Background

  • Knowledge of spoken Spanish is a plus

  • Bachelor of Science in Food Science or related major is preferred

Why You Should Join Catalent

  • Positive and fast-paced working environment focused on continuous improvement and innovation

  • Competitive Paid Time Off plus 8 paid holidays

  • Medical, dental, and vision benefits effective on day one

  • Tuition Reimbursement to support your educational goals

  • Engaging site activities such as potlucks, cookouts, and monthly birthday recognitions

  • Employee Resource Groups promoting diversity and inclusion

  • Environmentally friendly initiatives and community engagement programs

  • Defined career path with annual performance reviews and growth opportunities

  • WellHub program for physical and mental wellness

  • Perkspot discounts from over 900 merchants across various categories

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


What Catalent employees say

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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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