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Manager, Quality Control

Job in Germantown, Montgomery County, Maryland, 20875, USA
Listing for: Precigen
Full Time position
Listed on 2026-09-18
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Data Analyst
Salary/Wage Range or Industry Benchmark: 105000 - 140000 USD Yearly USD 105000.00 140000.00 YEAR
Job Description & How to Apply Below

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Manager, Quality Control

Full-time Regular Management - MNG Germantown, MD, US

7 days ago Requisition

Salary Range: $ To $ Annually

Job Title:Manager, Quality Control

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 , Assay Control and Critical Reagents
  • Review equipment IOQ’s and Re-Qualifications
  • 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.
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