Quality Compliance Lead: GMP/GDP & Regulatory

Teva Pharmaceuticals

Basel

Vor Ort

CHF 140.000 - 190.000

Vollzeit

14 Tage+
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Benefits dieser Stelle

Competitive compensation
Dynamic environment
Career growth
High-performing team

Zusammenfassung

Teva Pharmaceuticals is seeking a Quality Manager/QP to oversee quality compliance and regulatory activities for TPIG in Switzerland. You will drive the Teva Quality Management System across the business unit and act as the primary contact for health authorities.

Strong leadership, English fluency and cross-functional collaboration are essential. The role requires GMP/GDP expertise, experience with supplier qualifications, and the ability to coordinate recalls and quality improvements across

Qualifikationen

  • Master’s Degree required in pharmaceutical sciences or related field.
  • Minimum of 2 years’ experience as a Quality Manager / QP / RP in pharma.
  • GMP/GDP knowledge and regulatory experience for Switzerland.

Aufgaben

  • Roll out Teva Quality Management System at the business unit level.
  • Ensure GMP/GDP compliance and promote quality culture.
  • Lead GMP and GDP training at a local level.
  • Manage supplier approvals, quality agreements and third-party service providers.
  • Coordinate recalls and quality incidents with cross-functional teams.

Kenntnisse

Fluent English
Leadership
Stakeholder collaboration
MS Office

Ausbildung

Master’s Degree in Pharmaceutical Sciences, Business, Healthcare or equivalent

Tools

MS Office

Jobbeschreibung

Teva Pharmaceuticals is seeking a Quality Manager/QP to oversee quality compliance and regulatory activities for TPIG in Switzerland. You will drive the Teva Quality Management System across the business unit and act as the primary contact for health authorities.

Strong leadership, English fluency and cross-functional collaboration are essential. The role requires GMP/GDP expertise, experience with supplier qualifications, and the ability to coordinate recalls and quality improvements across

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