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Quality Control Stability Manager Jobs in Reston, VA

Granules

Quality Control Manager

Chantilly, VA · On-site

Supervise the testing of bulk release, finished product and stability testing * Manage and supervise QC laboratory personnel with varying levels of experience, assigning the work schedule and ensure ...

Precigen, Inc

QC Manager

Germantown, MD · On-site

$95K - $120K/yr

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 ...

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$84.6K

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

As of May 30, 2026, the average yearly pay for quality control stability manager in Reston, VA is $84,605.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,900.00 and $104,000.00 per year, depending on experience, location, and employer.
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Quality Control Stability Manager jobs near you
Infographic showing various Quality Control Stability Manager job openings in Reston, VA as of May 2026, with employment types broken down into 4% As Needed, 31% Full Time, 61% Part Time, and 4% Contract. Highlights an 93% Physical, and 7% Remote job distribution, with an average salary of $84,605 per year, or $40.7 per hour.

Quality Control Manager

Granules Pharmaceuticals

Chantilly, VA • On-site

Full-time

Posted 10 days ago

Job description

Supervise the work of laboratory personnel engaged in performing routine finished product testing & stability testing, including planning laboratory work, evaluating work performed and handling procedural and technical laboratory problems. Execute according to high standards of quality at the lab through managing and continuously improving the effectiveness of laboratory quality processes and systems
Job Duties & Responsibilities
  • Supervise the testing of bulk release, finished product and stability testing
  • Manage and supervise QC laboratory personnel with varying levels of experience, assigning the work schedule and ensure assigned tasks are performed.
  • Review of test results for accuracy and proper documentation.
  • Review of specifications and STMs for in process and finished products.
  • Write OOS investigations, including finding root cause and corrective/preventive actions.
  • Supervise lab processes, including timely management of investigations, CAPA implementation to ensure sustainable compliance
  • Review of SOPs, lab related investigations, stability failure notifications, COAs, and compilation of stability related data. Responsible for timely release of in-process, finished product release COA's
  • Monitor and report the trends in bulk, finished products, and stability samples to QC/QA Management
  • Review of IQ, OQ, and PQ for new instruments, protocols/reports
  • Responsible for coordinating with other departments like warehouse, QA, Maintenance, purchase department, R&D in day to day activity for better operational requirements and to follow the cGMP requirements.
  • Responsible for the coordination of sample management, not limited to in-process, finished product and stability samples.
  • Monitor Quality Control, Safety and cGMP practices to assure compliance with internal and external regulations.
  • Perform other related duties as assigned to meet departmental and Company objectives.

Management Responsibility
  • Manage group of scientists.

Reports to
  • Associate Director / Director

Requirements
Knowledge & Skills
  • Ability to maintain integrity and honesty at all times
  • Ability to communicate and lead with transparency
  • Accountable for performance and results of department
  • Ability to assume additional responsibilities on own initiative.

Experience & Education
  • Requires minimum BA/BS in Biochemistry, Chemistry or related field with 10-15 years' experience in the biotech or pharmaceutical industry. Management experience in Quality Control required MS/MA.

Physical Requirements/Working Environment
  • Regular Laboratory environment with lab coats, safety glasses, 4-6hrs/day of standing while performing chemical test and able to stand for 4-6hrs/day.

Travel
  • No Travel requirement.

Disclaimer
The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.

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