Senior Quality Assurance Manager 100 % (m/f/d) and Deputy RP
Basel, CH
vor 2 Tg.

Mepha Schweiz AG

Mepha Schweiz AG, headquartered in Basle, is one of the leading pharmaceutical companies in Switzerland and since 2011 part of the Teva Group, the world's number one in the generics market.

Mepha Schweiz AG includes Teva Pharma AG and Mepha Pharma AG, the leader in the Swiss generics market. The company employs a total of 159 people and offers a broad product portfolio that currently covers 18 medical indication areas.

The sales companies Mepha Pharma AG and Teva Pharma AG together market around 300 branded and non-branded generics, over-the-counter medicines, dietary supplements and original preparations in the fields of central nervous system, respiratory diseases, oncology and infectiology.

The medicines are sold via pharmacies, self-dispensing physicians, drugstores and hospitals.

Business Purpose

Mepha Schweiz Ltd is currently looking for a Senior Quality Assurance Manager to support the Commercial Quality team. In this role you will perform the release of products of Mepha’s portfolio to the Swiss market, the management of quality incidents, new product launches, complaints, deviations, and change control procedures.

You will ensure GMP&GDP compliance by improving and maintaining the processes and documents of the quality management system, and contribute to audits and inspections.

You will act as Deputy of the Responsible Person and represent the QA team in cross functional projects.

Your tasks

  • Perform Swiss market releases in delegation of the RP, including deviation and change control management
  • Act as Deputy RP
  • Lead the management of quality incidents, complaints and recalls
  • Manage major product launches
  • Review PQRs
  • Manage Quality Technical Agreements
  • Create and maintain Standard Operating Procedures and Working Instructions, and contribute to the continuous improvement of processes and to trainings
  • Contribute to authority inspection readiness, support local authorities’ inspections, and perform internal audits
  • Represent the QA in internal cross functional working groups and in Teva’s European Commercial Quality organization
  • Collaborate with local functions, e.g. Regulatory Affairs, Pharmacovigilance, Supply Chain, Customer Services as well as internal and external suppliers
  • Your profile

  • You have a Master s Degree in Pharmacy, Medicines, Biology or an equivalent combination of education
  • You have minimum of 7 years of working experience in a pharmaceutical company; including a minimum of 5 years in a QA / QC function, ideally including Swiss market release
  • Knowledge of quality assurance and process organization within the pharmaceutical industry
  • Knowledge of GMP / GDP guidelines of the European and Swiss pharmaceutical legislation
  • Proficient computer skills in current software including MS Office
  • Excellent English and German language skills
  • You are a communicative teamplayer
  • Being quality conscious you pay attention to details, and work exactly
  • You are flexible, and open to changes
  • Proactivity and independency round up your profile
  • Our offer

  • We offer a demanding, and manifold job opportunity with a high degree of personal responsibility
  • A professional, and pleasant environment awaits you at the market-leading company in the field of generics
  • We value and welcome motivated personalities with sound professional competence
  • We offer progressive employment conditions
  • Reports To

    Head Commercial Quality Unit

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    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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