1

Biomanufacturing Associate Jobs in Gaithersburg, MD

Be Seen First

The Biomanufacturing Associate II plays an integral role within CRL's gene therapy manufacturing function by applying biological, bioprocess, manufacturing, mechanical, application, system, and ...

Responsibilities Support full biomanufacturing process with buffer prep, column packing ... or Associate's degree in a related discipline with no experience. Experience with aseptic ...

Responsibilities Support full biomanufacturing process with buffer prep, column packing ... or Associate's degree in a related discipline with no experience. Experience with aseptic ...

IBBR researchers seek to advance therapeutic development, biomanufacturing, and state-of-the-art ... The Post-Doctoral Associate will work on developing advanced multifunctional polymers for cutting ...

IBBR researchers seek to advance therapeutic development, biomanufacturing, and state-of-the-art measurement technologies, to support accelerated delivery of safe and effective medicines to the ...

Biomanufacturing Associate information

See Gaithersburg, MD salary details

$29.2K

$152.6K

$335.5K

How much do biomanufacturing associate jobs pay per year?

As of Aug 21, 2026, the average yearly pay for biomanufacturing associate in Gaithersburg, MD is $152,569.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,400.00 and $229,600.00 per year, depending on experience, location, and employer.

What is a biomanufacturing associate?

A Biomanufacturing Associate is a professional who assists in the production of biopharmaceutical products, such as vaccines and therapeutic proteins, using biological systems like living cells. They are responsible for operating equipment, monitoring processes, following strict safety and quality protocols, and documenting production activities. Biomanufacturing Associates play a vital role in ensuring that products are made efficiently and meet regulatory standards in highly controlled environments.

What are the key skills and qualifications needed to thrive as a biomanufacturing associate?

To thrive as a Biomanufacturing Associate, you need a solid understanding of biotechnology, aseptic techniques, and good manufacturing practices (GMP), often supported by a degree in biology, chemistry, or related fields. Familiarity with bioprocessing equipment, batch record documentation, and quality control systems is typically required. Attention to detail, teamwork, and strong problem-solving skills help individuals excel in this role. These competencies ensure safe, consistent, and high-quality production of biopharmaceutical products in regulated environments.

What are some common challenges faced by biomanufacturing associates, and how can they be addressed?

Biomanufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), handling complex bioprocess equipment, and meeting tight production deadlines. These challenges can be managed by staying organized, following detailed protocols, and actively participating in ongoing training. Collaborating closely with team members and supervisors also helps ensure that any deviations or equipment issues are quickly identified and resolved, maintaining product quality and safety standards.

What is the difference between Biomanufacturing Associate vs Quality Control Technician?

AspectBiomanufacturing AssociateQuality Control Technician
Required CredentialsAssociate degree in biology, chemistry, or related fieldAssociate degree or certification in quality control or laboratory techniques
Work EnvironmentManufacturing floor, production areasLaboratories, testing facilities
Employer & Industry UsageBiotech, pharmaceutical manufacturingPharmaceutical, biotech, and medical device companies

Biomanufacturing Associates focus on the production process, operating equipment, and ensuring manufacturing runs smoothly. Quality Control Technicians primarily perform testing and inspections to ensure product quality. While both roles require technical skills and work in related environments, their core responsibilities differ, with manufacturing associates involved in production and QC technicians in quality assurance.

What are popular job titles related to Biomanufacturing Associate jobs in Gaithersburg, MD?

For Biomanufacturing Associate jobs in Gaithersburg, MD, the most frequently searched job titles are:

What job categories do people searching Biomanufacturing Associate jobs in Gaithersburg, MD look for?

The top searched job categories for Biomanufacturing Associate jobs in Gaithersburg, MD are:

What cities near Gaithersburg, MD are hiring for Biomanufacturing Associate jobs?

Cities near Gaithersburg, MD with the most Biomanufacturing Associate job openings:

Infographic showing various Biomanufacturing Associate job openings in Gaithersburg, MD as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 25% Part Time, 1% Temporary, and 2% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $152,569 per year, or $73.4 per hour.

Biomanufacturing Associate

Azaaki Solutions

Rockville, MD • On-site

$31.50/hr

Contractor

Posted 9 days ago

Be Seen First

After you apply to this job, you can share why you’re interested to jump to the top of the candidate list.


Job description

Title: BMA Upstream

BMA I Pay Rate $25.50

BMA II Pay Rate $28.50
Location: Rockville MD 20850

Duration: 4+Months

Description:

Initial shift schedule (core hours) is 8:00 am - 4:30 pm w/ 30 min unpaid lunch Monday through Friday
OT and weekend work may become required
there is a possibility of extension or conversion at end of 6 months

Position Summary:

The Biomanufacturing Associate II plays an integral role within CRL’s gene therapy manufacturing function by applying biological, bioprocess, manufacturing, mechanical, application, system, and technology principles, processes, procedures, inputs, and outputs, for designated production processes and handovers within a regulated environment to ensure the timely production and release of quality products, based on client specifications.

Key Responsibilities and Duties:

  • Apply and adhere to SOPs, cGMP, GLP, Quality, and Safety requirements.
  • Effectively execute a range of tasks, in line with SOPs, in the following area:
    • Upstream Activities (e.g., solutions, media aliquot, and buffer preparation and autoclave materials for cell culture, staging of raw materials, seed train, bioreactor set up, fermentation monitoring and/or harvest).
  • Follow instructions when performing planned manufacturing activities, in alignment with the batch record.
  • Prepare, edit, and complete quality documents. Well-versed in applying GDP.
  • Ensure data integrity - accurately document and review work prior to submission.
  • Document, record, investigate, and report observed process variances/deviations, in real time.
  • Follow instructions when operating equipment. Prepare, clean, and maintain equipment/tools.

Title: BMA Downstream

Location: Rockville MD 20850

Duration: 4+Months

Pay Rate $31.50/hr.

Qualifications:

  • HS Diploma/equivalent and 6 years of related experience, A.S. with 5 years, or a B.S. in biology/life sciences, bioengineering, or related discipline with 3 years of related experience.
  • Prior cell/gene therapy experience in a highly technical role, covering a wide range of tasks, within a cGMP/biotech manufacturing environment or related industry/role.
  • Informal coaching or project management experience is desirable.
  • Qualified as a LEAN trainer or willing to become qualified.

 Pay Rate $23.5/hr.

Initial shift schedule (core hours) is 8:00 am - 4:30 pm w/ 30 min unpaid lunch Monday through Friday
OT and weekend work may become required
there is a possibility of extension or conversion at end of 6 months

Preferred Qualifications for the role

? High School Diploma or Associate Degree with 0-2 years of experience in Downstream biologic production processes in a GMP environment in a Life Sciences Company; or

? Bachelor of Science in science or Engineering and 0-1 years of experience in Downstream biologic production processes in a GMP environment in a Life Sciences Company

? Basic knowledge and understanding of purification processes

? Ability to obtain sufficient hands-on experience with chromatography systems (AKTA systems at different scales) and approaches (Affinity, IEX, MMC), TFF modalities, and single use mixing systems

? Ability to learn to operate manual and semi-automated equipment in support of routine production with supervision? Experience in the preparation of buffers