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Pharmaceutical Quality Control Manager Jobs in Silver Spring, MD

QC Manager

Germantown, MD ยท On-site

$95K - $120K/yr

Job Title: QC Manager Department: Quality Control - Analytical GENERAL DESCRIPTION: * QC Manger is ... Advanced experience with QC testing in pharmaceutical or biopharmaceutical laboratories

Quality Control Manager Location: Fort Belvoir, VA Employment Type: Full-Time | On-site The candidate will be performing all facets of safety and quality control management, submittal tracking, daily ...

Quality Control Manager This role leads the full quality control program for a major $127 million renovation project in Fairfax, VA, spanning demolition, restructuring, and new vertical construction ...

Quality Control Manager

Chantilly, VA ยท On-site

$100K - $120K/yr

Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years ... Manage and supervise QC laboratory personnel with varying levels of experience, assigning the work ...

The Quality Control Manager is responsible for developing, implementing, maintaining, and independently administering the contract's Quality Control Plan. The Quality Control Manager evaluates ...

The Quality Control Manager is responsible for developing, implementing, maintaining, and independently administering the contract's Quality Control Plan. The Quality Control Manager evaluates ...

The Quality Control Manager is responsible for developing, implementing, maintaining, and independently administering the contract's Quality Control Plan. The Quality Control Manager evaluates ...

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Pharmaceutical Quality Control Manager information

See Silver Spring, MD salary details

$31.5K

$84.1K

$133.9K

How much do pharmaceutical quality control manager jobs pay per year?

As of Aug 6, 2026, the average yearly pay for pharmaceutical quality control manager in Silver Spring, MD is $84,070.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $103,400.00 per year, depending on experience, location, and employer.

What does a pharmaceutical quality control manager do?

A Pharmaceutical Quality Control Manager oversees the testing and quality assurance processes involved in manufacturing pharmaceutical products. They ensure that all products meet regulatory standards and company specifications for safety, efficacy, and quality. This role includes supervising laboratory staff, developing and implementing quality control procedures, and maintaining compliance with government regulations such as Good Manufacturing Practices (GMP). They also analyze data, investigate quality issues, and work closely with other departments to resolve any problems. The ultimate goal is to ensure that patients receive safe and effective medications.

What is the difference between Pharmaceutical Quality Control Manager vs Pharmaceutical Quality Assurance Specialist?

AspectPharmaceutical Quality Control ManagerPharmaceutical Quality Assurance Specialist
CredentialsTypically requires a degree in pharmacy, chemistry, or related field; certifications like CQE or GMP training are commonSimilar credentials; often holds degrees in life sciences and certifications in GMP and QA practices
Work EnvironmentOversees laboratory testing, quality control labs, and production environmentsFocuses on developing, implementing, and auditing quality assurance systems across production
Employer & Industry UsageUsed in pharmaceutical manufacturing, biotech, and related industriesCommonly employed in pharmaceutical companies, ensuring compliance and process quality

While both roles require similar educational backgrounds and certifications, the Pharmaceutical Quality Control Manager primarily manages laboratory testing and quality control processes, whereas the Pharmaceutical Quality Assurance Specialist focuses on establishing and maintaining quality systems and compliance. Both are essential for ensuring product safety and efficacy in the pharmaceutical industry.

What are some common challenges faced by pharmaceutical quality control managers in ensuring compliance with regulatory standards?

Pharmaceutical Quality Control Managers often face the challenge of staying current with evolving regulatory requirements from agencies such as the FDA or EMA. They must ensure all laboratory processes, documentation, and product testing meet strict guidelines, which can be complicated by new technologies or changing manufacturing practices. Another challenge is managing cross-functional communication between production, R&D, and regulatory affairs to promptly address quality issues. Successfully navigating these challenges requires a keen eye for detail, strong leadership, and ongoing professional development.

What are the key skills and qualifications needed to thrive as a pharmaceutical quality control manager?

To thrive as a Pharmaceutical Quality Control Manager, you need a strong background in pharmaceutical sciences, chemistry, or a related field, often supported by a relevant degree and experience in quality assurance. Familiarity with analytical instruments (e.g., HPLC, GC), quality management systems, and regulatory standards like GMP or FDA guidelines is typically required. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and ensuring compliance. These skills ensure product safety, regulatory adherence, and efficient team operations in a highly regulated industry.

Is pharmaceutical quality control management a good career?

Pharmaceutical quality control management is a stable and important career in the healthcare industry, focusing on ensuring product safety, efficacy, and compliance with regulations. It typically requires knowledge of Good Manufacturing Practices (GMP), laboratory skills, and certifications such as a degree in pharmacy, chemistry, or related fields. The role offers opportunities for advancement and job stability due to the ongoing demand for quality assurance in pharmaceuticals.
What job categories do people searching Pharmaceutical Quality Control Manager jobs in Silver Spring, MD look for? The top searched job categories for Pharmaceutical Quality Control Manager jobs in Silver Spring, MD are:
What cities near Silver Spring, MD are hiring for Pharmaceutical Quality Control Manager jobs? Cities near Silver Spring, MD with the most Pharmaceutical Quality Control Manager job openings:
Infographic showing various Pharmaceutical Quality Control Manager job openings in Silver Spring, MD as of June 2026, with employment types broken down into 83% Full Time, 16% Part Time, and 1% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $84,070 per year, or $40.4 per hour.

QC Manager

Precigen, Inc

Germantown, MD โ€ข On-site

$95K - $120K/yr

Full-time

Re-posted 22 days ago


Job description

Job Title: QC Manager

Department: Quality Control - Analytical

GENERAL DESCRIPTION:

  • QC Manger is responsible for overseeing a team of QC Analysts and is also responsible for maintaining the QC Laboratory in a state of cGMP compliance.

    DUTIES AND RESPONSIBILITIES:
  • Training, coaching, and development of QC staff
  • Develop, revise, and review SOPs, qualification/validation protocols and reports.
  • Write deviations, CAPA’s and own change controls.
  • Review/Provide guidance for deviations/CAPA’s generated by QC Analysts
  • Responsible for reviewing invalid assays and lead invalid assay investigations
  • Participating in OOS investigations
  • Responsible for ensuring all analytical data generated by QC lab to be initiated on time and completed within established TAT’s.
  • Perform review of QC documentation (equipment logbooks, sol’n prep record, cell line records, TRF’s, etc)
  • Ensure test results are entered into the appropriate reports
  • Track/Trend Ref. Std, Assay Control and Critical Reagents
  • Track equipment cleaning/PM/Calibration schedules
  • Review equipment IOQ’s and Re-Qualifications
  • QC Process/Procedure continuous improvements
  • Perform other duties as needed

EDUCATION AND EXPERIENCE:

  • BS degree in the Biological Sciences, Bioengineering, or Chemistry.
  • 7+ years of experience performing QC activities in the pharmaceutical and biotech industry under GMP guidelines, with demonstrated expertise in multiple disciplines and assays.
  • 2+ years of supervisory experience.
  • Advanced experience with QC testing in pharmaceutical or biopharmaceutical laboratories
  • Familiarity with analytical testing procedures: qPCR, HPLC, ELISA, Cell-based Assays, etc.


DESIRED KEY COMPETENCIES:

  • Demonstrated ability to manage a team and work independently on projects, and review project data and provide summary analysis reports based upon the data
  • Ability to provide support for regulatory and client audits, as well as interact with clients.
  • Ability to effectively negotiate and build collaboration amongst individuals.
  • Ability to be self-motivated, proactive, accountable, and flexible
  • Demonstrate the ability to develop, coach and mentor key employees.
  • Excellent interpersonal, verbal, and written communication skills are essential in this collaborative work environment.
  • High attention to detail, highly organized, and excellent documentation skills
  • Strong scientific, analytical, and problem-solving skills as well as sound judgment, to identify problems and leads efforts to resolve them
  • Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based on upon changing priorities.