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Biopharmaceutical Manufacturing Associate Jobs in Reston, VA

Fladger Associates

Senior Scientist

Gaithersburg, MD · On-site

$98K - $135K/yr

Knowledge of protein biochemistry and degradation mechanisms, biopharmaceutical manufacturing processes, combination drug products, and/or biophysical analytical methods is required. * Hands-on ...

Guidehouse

Bioassay Researcher

Silver Spring, MD · On-site

$85K - $141K/yr

Understanding of biopharmaceutical manufacturing, process development, biotechnology research and regulatory operations. * Knowledge of insulin and GLP-1 receptor signaling pathways or related ...

Guidehouse

Bioassay Researcher

Silver Spring, MD

$85K - $141K/yr

Understanding of biopharmaceutical manufacturing, process development, biotechnology research and regulatory operations. * Knowledge of insulin and GLP-1 receptor signaling pathways or related ...

ADVI Health

Senior Data Scientist-RWE

Washington, DC · On-site

$126K - $158K/yr

Our global client roster includes biopharma manufacturers, MedTech, precision medicine diagnostics ... • Mentor Associates on basic methods and quality standards. Core Competencies Technical ...

Catalent, Inc.

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 ...

Diedre Moire Corp.

Calibration Technician

Annandale, VA · On-site

$90K - $140K/yr

Calibration Tech Metrologist - Biopharma Laboratory - Annandale, VA Metrology Metrologist Field ... Associate Degree Minimum Experience Requirements: 2-5 years Job City Location: Annandale Job State ...

Catalent, Inc.

Maintenance Manager

Manassas, VA · On-site

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 ...

All JobsBiopharmaceutical Manufacturing Associate JobsBiopharmaceutical Manufacturing Associate Jobs in Reston, VA

Biopharmaceutical Manufacturing Associate information

See Reston, VA salary details

$19

$28

$41

How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Jul 16, 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, 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 Reston, VA as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% 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.

Senior Scientist

Fladger Associates

Gaithersburg, MD • On-site

$98K - $135K/yr

Contractor

Posted 5 days ago

Job description

Gaithersburg, MD
Contract Duration: 12-36 months
Rate: Negotiable

Responsibilities:

  • Excellent employment opportunity for a Senior Scientist in the Gaithersburg, MD area.
  • The Late-Stage Formulation Sciences Group is responsible for development of intended commercial formulations to advance the late-stage biologics portfolio, and the life cycle management of commercialized products.
  • The group plays an integral part in the design and development of patient centric drug products.
  • This is a Scientific position, and the incumbent will be responsible for late-stage formulation development of biologic products.
  • Will be involved in the design and execution of formulation risk assessments and characterization studies, and development formulation control strategies for Drug Substance and Drug Product.
  • Ensure robustness of intended commercial formulations, suitability for intended use of container closure/packaging systems, and in-use compatibility with clinical administration components.
  • Expected to exercise technical discretion and scientific rigor in experimental protocol design, data analysis, and results interpretation.
  • Other responsibilities include authoring of marketing applications and provision of support to regulatory responses to approval.
  • Develop new strategies and approaches to advance late-stage formulation development and deliver scientific and operational objectives.

Experience:

  • BS, MS, or PhD in Chemistry, Biochemistry, Pharmaceutical Sciences, Engineering, applied Sciences
  • Knowledge of protein biochemistry and degradation mechanisms, biopharmaceutical manufacturing processes, combination drug products, and/or biophysical analytical methods is required.
  • Hands-on experience with high-performance size exclusion chromatography (HPSEC), particle characterization and sizing (e.g., light obscuration), and aggregate characterization methods are strongly preferred.
  • Experience with formulation and biopharmaceutical development, characterization, control strategy, quality risk management, and/or CMC regulatory guidance and filings is preferred.
  • Skills leading, planning, and executing complex projects on tight timelines are important.