QC Manager

Precigen, Inc.

$90K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • BS degree in Biological Sciences, Bioengineering, or Chemistry.
  • 7+ years of QC experience in pharmaceuticals/biotech under GMP guidelines.
  • 2+ years of supervisory experience.
  • Advanced knowledge of QC testing in labs.
  • Familiarity with analytical methods: qPCR, HPLC, ELISA, Cell-based Assays.

Responsibilities

  • Oversee and develop a team of QC Analysts.
  • Develop, revise, and review SOPs and validation protocols.
  • Write deviations and CAPA documents, managing change controls.
  • Guide deviations and CAPA submissions from QC Analysts.
  • Lead investigations into invalid assays and participate in OOS cases.
  • Ensure timely completion of analytical data within established TATs.
  • Review QC documentation including logbooks and assay records.

Benefits

  • Support for professional development and training programs.
  • Opportunities for involvement in regulatory and client audits.
  • Collaborative work environment fostering team relationships.
  • Flexible work culture in a fast-paced environment.
Full 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.

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