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Biopharmaceutical Manufacturing Associate Jobs in Reston, VA

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 21-25

Biopharmaceutical Manufacturing Associate information

See Reston, VA salary details

$19

$28

$41

How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for biopharmaceutical manufacturing associate in Reston, VA is $28.22, according to ZipRecruiter salary data. Most workers in this role earn between $23.99 and $33.03 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.
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What cities near Reston, VA are hiring for Biopharmaceutical Manufacturing Associate jobs? Cities near Reston, VA with the most Biopharmaceutical Manufacturing Associate job openings:
Infographic showing various Biopharmaceutical Manufacturing Associate job openings in Reston, VA as of August 2026, with employment types broken down into 1% As Needed, 67% Full Time, 29% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $58,688 per year, or $28.2 per hour.

$25 - $32/hr

Full-time

Life, PTO

Re-posted 6 days ago


Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 54 frontline employees who took The Breakroom Quiz

60th of 86 rated pharmaceutical


Job description

Process Maintenance Technician

Position Summary

  • Work Schedule: Monday to Friday 10pm-6:30am

  • 100% on-site in Manassas, VA

Our Manassas, Virginia site is a part of the Consumer Health division and provides expanded capabilities in soft chews and lozenges. With extensive development and manufacturing expertise and a wide range of flavors, ingredients, and colors available, we can work with complex formulations to help create engaging new products consumers will love.

The Process Maintenance Technician is responsible for performing emergency and routine maintenance on all manufacturing equipment, including equipment changeovers, and assisting production personnel as necessary to minimize downtime. The Process Maintenance Technician is responsible for the installation and repair of electrical, mechanical, hydraulic, and pneumatic systems and ensuring that equipment is maintained in top working condition through troubleshooting, repair, and preventative maintenance.

The Role

  • Perform basic PMs, mechanical maintenance, repairs across the site, and assist small scale process improvement projects.

  • Build the foundation for machines, grind, and file machinery parts.

  • Construct and install equipment such as shafting, conveyors and tram rails.

  • Transfer equipment to the applicable site for maintenance to avoid contamination or safety hazards.

  • Help maintain good housekeeping in mechanical and facility areas.

  • Maintains cleanliness and upkeep of repair shop, maintenance office, and storage areas including all equipment, tools, supplies, and materials.

  • Observe and follow Good Manufacturing Practices (GMP), Standard Operating Procedures (SOP), Food Safety Plan (HACCP) and Food Quality Plan (FQP.)

  • Other duties as assigned.

The Candidate

  • Associate degree with 2+ years of relevant experienceor High School Diploma and 5+ years of relevant experience or technical/vocational training required.

  • Background in industrial maintenance or skilled trades in the food industry is preferred.

  • Ability to troubleshoot various types of equipment.

  • Looking for combination of hands-on experience with current machinery or similar.

  • Technicians should be able to run conduit and wire electrical control panels according to NEC guidelines.

  • Ability to program Allen Bradley PLC's and HMI's.

  • Pipefitting, plumbing, welding, and fabrication are preferred.

  • Ability to read and understand electrical schematics, mechanical drawings, and vendor documentation.

  • The employee must regularly lift and /or move up to 50 pounds, frequently lift and/or move up to 100 pounds and occasionally lift and/or move up to 1000 pounds.

  • While performing the duties of this Job, the employee is regularly required to walk and stand; frequently talk or hear; use hands to finger, handle, or feel and reach with hands and arms, and stoop, kneel, crouch, crawl, climb or balance. The employee is occasionally required to sit, taste or smell.

Why You Should Join Catalent

  • Several Employee Resource Groups focusing on D&I

  • Potential for career growth within an expanding team

  • Diverse, inclusive culture

  • 152 hours of PTO + 8 Paid Holidays

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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