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Quality Control Manager in Advanced Therapy Medicinal Product

ModenaPosted Yesterday
Full-timeonsite

Job Description

Position Summary:

We are seeking an experienced Quality Control (QC) Manager – ATMP to lead QC laboratory operations supporting GMP manufacturing of advanced therapy medicinal products. This role is critical in ensuring timely and compliant release of patient-specific therapies and maintaining the highest standards of quality and regulatory compliance.

Key Responsibilities:

  • Manage day-to-day QC lab operations, including raw materials, in-process, and final product testing

  • Lead analytical method qualification, validation, and transfer

  • Oversee analytical methods including flow cytometry, qPCR/ddPCR, and cell-based assays

  • Ensure timely execution and review of testing to support batch release

  • Manage external contract workers, ensuring outsourced QC testing operations are performed as required and within the planned timeframe

  • Author, review and approve technical reports and QC documentation

  • QC data collection and analysis

  • Ensure GMP compliance, including handling deviations, OOS/OOT, CAPAs, and change control

  • Lead and develop QC team members

  • Oversee laboratory equipment qualification and environmental monitoring

  • Support regulatory inspections and filings

  • Provide support to perform internal audits

  • Represent QC team at technical meetings presenting and discussing results

  • Promote and maintain a high level of GMP awareness and compliance

Qualifications and experience:

  • Degree in Biology, Biotechnology, Pharmacy, or related field; PhD preferred

  • 5+ years of QC experience in ATMP (cell therapy and gene therapy preferred)

  • Relevant previous experience as QC manager

Required Skills & Abilities:

  • Solid expertise in cytofluorimetry (data acquisition and analysis)

  • Strong expertise in biochemistry, microbiological, molecular biology and cell culture methods

  • Ability to analyze data, summarize results, and identify solutions

  • Excellent knowledge of current GxP guideline and ATMP regulations

  • Strong leadership and communication skills

  • Positive, team player and problem-solving attitude

  • Accurate, with excellent prioritization and organization skills

  • Commitment to the assigned deadlines and ability to deliver them tightly

  • Good knowledge of Microsoft Office applications

  • English intermediate level is required (written and spoken)

  • Good verbal, written, and interpersonal communication skills

  • Ability to work independently, maintaining a team-focused attitude

  • Open-minded and problem-solving attitude.

FR : Dans le cadre de sa politique Diversité, Evotec étudie, à compétences égales, toutes les candidatures dont celles des personnes en situation de handicap.

ENG : In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities.

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Quality Control Manager in Advanced Therapy Medicinal Product at Evotec | Renata