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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 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 ...

Lead Maintenance Mechanic

Rockville, MD · On-site

$27 - $35.75/hr

Minimum of 4 years of experience within a GMP biopharmaceutical or pharmaceutical manufacturing ... Associate degree in mechanical, electrical, industrial maintenance, engineering technology ...

Lead Maintenance Mechanic

Rockville, MD · On-site

$27 - $35.75/hr

Minimum of 4 years of experience within a GMP biopharmaceutical or pharmaceutical manufacturing ... Associate degree in mechanical, electrical, industrial maintenance, engineering technology ...

Lead Maintenance Mechanic

Rockville, MD · On-site

$27 - $35.75/hr

Minimum of 4 years of experience within a GMP biopharmaceutical or pharmaceutical manufacturing ... Associate degree in mechanical, electrical, industrial maintenance, engineering technology ...

Lead Maintenance Mechanic

Rockville, MD · On-site

$27 - $35.75/hr

Minimum of 4 years of experience within a GMP biopharmaceutical or pharmaceutical manufacturing ... Associate degree in mechanical, electrical, industrial maintenance, engineering technology ...

Lead Maintenance Mechanic

Rockville, MD · On-site

$27 - $35.75/hr

Minimum of 4 years of experience within a GMP biopharmaceutical or pharmaceutical manufacturing ... Associate degree in mechanical, electrical, industrial maintenance, engineering technology ...

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 21-38

Biopharmaceutical Manufacturing Associate information

See Reston, VA salary details

$19

$28

$41

How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Sep 1, 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 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 job categories do people searching Biopharmaceutical Manufacturing Associate jobs in Reston, VA look for?

The top searched job categories for Biopharmaceutical Manufacturing Associate jobs in Reston, VA are:

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.

Associate Director, Projects & Strategy, Analytical Sciences & Technology (AS&T)

BioNTech SE

Gaithersburg, MD • On-site

$146K - $234K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago


Job description

Gaithersburg, US   |   full time   |   Job ID: 11533 

About the Role:


As Associate Director, AS&T Projects & Strategy, you will play a key role in advancing our late-stage protein pipeline for Monoclonal Antibodies (mAbs) and Antibody-Drug Conjugates (ADCs) within the Analytical Sciences & Technology (AS&T) organization. In this position, you will serve as the main point of contact and oversee the coordination of all analytical activities across both internal teams and external analytical partners. In addition, you will represent the analytical network within the cross-functional late-stage CMC team, helping drive development programs forward toward commercialization.

 

Your Contribution:

   Represent the analytical function within cross-functional project teams and act as the primary interface for the CMC team and other key stakeholders.
   Coordinate analytical deliverables across internal analytical functions and external partners, ensuring alignment with the overall analytical development strategy.
   Shape and align the analytical control strategy in close collaboration with functions such as Regulatory Affairs, CMC, and Quality, ensuring compliance with regulatory expectations and health authority requirements.
   Provide leadership and oversight for analytical activities, ensuring transparent communication of progress, timelines, risks, and challenges to relevant stakeholders.
   Maintain end-to-end ownership of the analytical components of the CMC Module 3 dossier, including document preparation, review, and lifecycle maintenance.

 

A Good Match:


   An advanced degree in Biology, Chemistry, Pharmacy, Biotechnology, or a related scientific discipline, combined with over 10 years of experience in a regulated pharmaceutical environment.
   Broad experience within analytical functions, such as AS&T, Quality Control, or Analytical Development, with a focus on monoclonal antibodies (mAbs), multi-specific antibodies, and/or antibody-drug conjugates (ADCs).
   Strong track record in late-stage analytical development and commercial support for antibody-based products, ideally including experience with ADCs.
   Demonstrated leadership capabilities and solid experience in managing analytical projects.
   Deep understanding of relevant US and EU regulatory frameworks, including EMA and FDA requirements, CMC analytical development documentation, Good Manufacturing Practice (GMP), as well as compendial standards such as USP and Ph. Eur.
   Strong organizational skills, with the ability to analyze complex topics, break them down into manageable elements, and define timelines and dependencies accordingly.
   Proven ability to work effectively in intercultural, cross-functional, and global team environments.
   Excellent communication and stakeholder management skills.
   Highly motivated, adaptable, and comfortable working in a dynamic, fast-paced, and evolving environment.
   Experience supporting pre-approval activities, such as Pre-licensing Inspection (PLI) readiness, BLA preparation, and product launch activities, is considered an advantage.

Your benefits and remuneration:

Expected Pay Range: $146,300/year to $234,100/year + benefits, annual bonus & equity (bonus and equity is variable and dependent on company and individual performance). Compensation for the role will depend on several factors, including responsibilities of the job, education, experience, knowledge, skills, and abilities.

BioNTech US is committed to employee wellbeing and offers best-in-class benefits & HR programs to support an inclusive & diverse workforce. Salaried/Position-Targeted Hourly Employees working 30+ hours per week are eligible for our comprehensive benefits package. Benefits include but are not limited to:

  • Medical, Dental and Vision Insurance
  • Life, AD&D, Critical Illness Insurance
  • Pre-tax HSA & FSA, DCRA Spending Accounts
  • Employee Assistance & Concierge Program (EAP) available 24/7
  • Parental and Childbirth Leave & Family Planning Assistance
  • Sitterstream: Virtual Tutoring & Childcare Membership
  • Paid Time Off: Vacation, Sick, Bereavement, Holidays (including Floating) & Year-End U.S. Shutdown.
  • 401(K) Plan with Company Match
  • Tuition Reimbursement & Student Loan Assistance Programs
  • Wellbeing Incentive Platforms & Incentives
  • Professional Development Programs
  • Commuting Allowance and subsidized parking
  • Discounted Home, Auto & Pet Insurance

...and more! More details to be shared.
 

Located in the BioHealth Capital Region near Washington DC and ranked among the top biopharma hubs in the country, Gaithersburg, Maryland offers a unique and diverse cluster across industry, government, and academia for top talent and scientific innovation. As a pivotal player within the life sciences community, Gaithersburg is distinguished by its robust infrastructure and strategic location near the nation's capital. The city's strategic significance is amplified by its state-of-the-art manufacturing facilities that cater to the rigorous demands of the life sciences industry; Gaithersburg's manufacturing sector is defined by advanced technologies and complies with the most stringent regulatory standards, ensuring the production of high-quality pharmaceuticals, biologics, and medical devices. In the coming years, Gaithersburg will continue to be a vital contributor to the future of medical science and technology.

Apply now - We look forward to your application!

Apply for our Gaithersburg, US location and simply send us your documents using our online form.

By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider 'HireRight'. You will be informed accordingly by your BioNTech-Recruiter.