Quality Professional - Deputy RP 50% (f/m/d)
Jona, CH
vor 4 Tg.

Teva Pharmaceuticals International GmbH

Teva Pharmaceuticals International GmbH ( TPIG ) is a subsidiary of Teva Europe based in Switzerland. The company trades mainly Global Specialty medicines & Branded Generics Products with many markets in EU and the US.

The company is also hosting the trading hub for our Latin American markets. The company is engaged in manufacturing and sales activities which are coordinated out from its headquarter in Jona.

Business Purpose

Teva Pharmaceuticals International GmbH is looking for a Quality Professional to execute the Quality Systems & Quality Compliance tasks related to Good Distribution Practice (GDP) and trading activities of Teva Pharmaceuticals International GmbH (TPIG), and to support the TPIG Responsible Person acting as deputy.

As QA point of contact for global and local operations teams you ensure integration of QA requirements in business operations efficiency.

Main Responsibilities

  • Execute the daily Quality tasks related to the trading business of TPIG, including :
  • Release of materials (APIs and Specialty drugs) for trade
  • Approval of suppliers and customers
  • Review of supply chain trade flows
  • Review & approval of documents for Change Control
  • Management of Deviations and CAPAs
  • Review of Quality Agreements
  • Management of training activities
  • Participation in GDP inspections and audits, as needed
  • Conducting and supporting self-inspections at regular intervals and ensuring that self- inspections are completed according to approved self-inspection program
  • Identification, communication and mitigation of Quality risks for TPIG
  • Perform gap assessments and review of local procedures
  • Provide information and support to Quality Councils and Management Review
  • Support decision making on Quality events linked to TPIG
  • Process QA information in TrackWise and other electronic systems
  • Support TPIG supply chain initiatives and projects with impact on Quality
  • Requirements

  • University Degree in Science
  • 3-5 years of experience in a Quality Assurance role in the Pharmaceutical industry with practical knowledge of Good Manufacturing Practice
  • Knowledge of Swissmedic requirements applicable to GDP
  • Good understanding of Supply Chain related topics as well as related risks and global regulatory implications
  • You are structured and organized
  • Being quality conscious you pay high attention to details being able to review & manage documentation (shipping documents, and related GDP documents / records etc.)
  • You are a communicative teamplayer
  • You are flexible, and open to changes
  • Fluent German and English (written & oral) is a must
  • Proactivity and independency round up your profile
  • Our Offer

  • We offer a demanding, and manifold job opportunity with a high degree of personal responsibility
  • We value and welcome motivated personalities with sound professional competence
  • We offer progressive employment conditions as well as a market competitive remuneration package
  • Reports To

    Senior Manager Quality

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    Human Resources

    Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

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