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CMC Biologics Quality Control Director, Physichemical Testing

Teva Pharmaceuticals
Full-time
Remote friendly (West Chester, PA)
United States
Operations

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Role Summary

CMC Biologics Quality Control Director, Physichemical Testing. Lead and oversee the Physiochemical Testing group within a GxP-compliant QC laboratory, directing strategy, method development/transfer/validation, and regulatory readiness for in-process, release, stability, raw materials, and contract lab testing in support of preclinical, clinical, and commercial activities.

Responsibilities

  • Overseeing QC laboratory operations by managing a team of professionals and junior managers who execute physiochemical CGMP testing.
  • Establishing and maintaining strategies for method and/or process implementation, continuous improvement initiatives, and method transfer and validation processes.
  • Developing strategies and approaches for special studies, as applicable.
  • Ensuring compliance with applicable ICH, GxP and safety regulations as an individual contributor as well as an educator and manager of junior staff.
  • Supporting general GxP and data integrity compliance in both routine and non-routine work activities for both internal and external contract lab testing, including data review/approval and staff training.
  • Providing oversight and/or support of QC lab investigations, audits, inspections, and communications with regulatory agencies and health authorities.
  • Providing support for staff who identify, write, revise, manage and implement standard operating procedures, work instructions, standard practices, protocols, and reports.
  • Engaging, coaching, motivating and empowering staff to ensure their skills match their roles and to continually develop, thereby improving productivity and efficiency of the department operations.
  • Participating in capital equipment procurement, workforce planning, and other critical business processes.

Qualifications

  • Education: Minimum: BS/MS in a relevant discipline; Preferred: PhD in Biochemistry or Analytical Chemistry.
  • Experience: 10-15+ years (BS/MS/PhD) in the (Bio)pharmaceutical industry with deep technical knowledge in physiochemical testing applications and one or more areas of drug development.
  • Leadership: Proven ability to create and maintain a productive multidisciplinary team; lead matrixed and cross-functional teams; administer and coordinate physiochemical testing activities; resolve issues to meet project goals; foster an innovative/creative culture.
  • Specialized Knowledge: LIMS, TrackWise or VEEVA Quality Management Systems, Documentum-based systems.
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