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Gmp Manufacturing Manager Jobs (NOW HIRING)

Precigen, Inc

GMP Manufacturing Associate

Germantown, MD · On-site

$70K - $85K/yr

GMP Gene Manufacturing Associate I/II will require a professional who thrives in a dynamic team ... Ability to manage multiple and varied tasks and prioritize workload * Prior Tangential Flow ...

Haemonetics Software Solutions

$68K - $116K/yr

... Job Summary The GMP Manufacturing Supervisor is responsible for leading and managing shift ... Leadership & People Management Conduct performance reviews, coaching, and corrective actions as ...

Haemonetics

Supervisor, GMP Manufacturing

Clinton, PA · On-site

$68K - $116K/yr

The GMP Manufacturing Supervisor is responsible for leading and managing shift operations to ensure safe, compliant, and efficient manufacturing of medical devices. This role drives production ...

ProMed Molded Products, Inc.

The GMP Manufacturing Lead supports ProMed's mission and values by applying and reinforcing the ... Coordinate with Planning, Quality, and Materials Management to sequence batches and resolve ...

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Gmp Manufacturing Manager information

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$30.5K

$97.6K

$153.5K

How much do gmp manufacturing manager jobs pay per year?

As of Sep 11, 2026, the average yearly pay for gmp manufacturing manager in the United States is $97,556.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,000.00 and $120,500.00 per year, depending on experience, location, and employer.

What is the difference between Gmp Manufacturing Manager vs Quality Assurance Manager?

AspectGmp Manufacturing ManagerQuality Assurance Manager
Primary FocusOversees manufacturing processes to ensure GMP compliance and product quality during productionEnsures products meet quality standards through audits, testing, and process improvements
CertificationsGMP training, manufacturing certificationsQuality management certifications (e.g., CQE, ISO auditor)
Work EnvironmentManufacturing facilities, production linesQuality labs, audit settings, office environments
Industry UsagePharmaceutical, biotech, and supplement manufacturingPharmaceutical, biotech, and medical device industries

While both roles ensure compliance and product quality, the Gmp Manufacturing Manager focuses on managing manufacturing operations, whereas the Quality Assurance Manager emphasizes quality control and audits. Both positions are essential in GMP environments and often collaborate closely to ensure product integrity.

What cities are hiring for Gmp Manufacturing Manager jobs?

Cities with the most Gmp Manufacturing Manager job openings:

What are the most commonly searched types of Gmp Manufacturing jobs?

The most popular types of Gmp Manufacturing jobs are:

What are popular job titles related to Gmp Manufacturing Manager jobs?

For Gmp Manufacturing Manager jobs, the most frequently searched job titles are:

Infographic showing various Gmp Manufacturing Manager job openings in the United States as of September 2026, with employment types broken down into 86% Full Time, 13% Part Time, and 1% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $97,556 per year, or $46.9 per hour.

GMP Manufacturing Associate

Germantown, MD • On-site

Precigen, Inc
Biotechnology Research and Development • 51 - 200 employees
Learn more about Precigen, Incexternal

$70K - $85K/yr

Full-time

Posted 6 days ago

Job description

GENERAL DESCRIPTION:

GMP Gene Manufacturing Associate I/II will require a professional who thrives in a dynamic team environment, brings meticulous attention to detail in the quality of their work and is proactive in implementing improvements. This position will perform a broad range of tasks in the cGMP manufacturing of clinical and commercial adenovector products. Prior experience in GMP manufacturing and operation of GMP process equipment are required.

DUTIES AND RESPONSIBILITIES: 

  • Perform manufacturing for clinical and commercial materials in GMP setting, including, but not limited to:
  • Assembling raw materials
  • Execute Master Batch Records (MBR) under current Good Manufacturing Practices (cGMPs.)
  • Following and assisting in the development of specific standard operating procedures (SOP), MBRs, deviations and summary reports for manufacturing
  • Support initiation and closure of deviations
  • Support routine cleaning and changeover procedures for clean room suites and equipment
  • Participating in and facilitating technology transfer
  • Work in a team based, cross-functional environment to complete production tasks.
  • Adhere to all safety and regulatory requirements while performing job functions.
  • This position requires occasional weekend and shift work.
  • Other duties as assigned.

EDUCATION AND EXPERIENCE:

  • Bachelor's degree or master degree in biology, biomedical science or life science
  • Minimum of one to three (1 – 3 for Associate 1, 3+ for Associate 2) years in a GMP environment required
  • Aseptic technique experience is required.
  • Knowledge in principles and practices of current Good Manufacturing Practices (cGMPs)
  • Prior cell culture and/or purification experience in a GMP facility is preferred.

DESIRED KEY COMPETENCIES:

  • Comfortable in a fast-paced company environment and able to adjust workload based upon changing priorities.
  • Self-motivated and willing to accept temporary responsibilities outside of initial job description and perform other responsibilities to support the needs of the department, as assigned.
  • Positive interpersonal skills.
  • Outstanding knowledge, and ability to apply scientific principles utilized to solve operational, as well as routine production tasks
  • Ability to troubleshoot unit operations.
  • Self-organizer, meticulous hands-on habits, keen attention to detail.
  • Ability to manage multiple and varied tasks and prioritize workload
  • Prior Tangential Flow Filtration (TFF) experience is preferred.

EOE MFDV