Position: Director

Job type: Full-time

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Job content

7087 Mylan Pharma GmbH

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

Viatris empowers people worldwide to live healthier at every stage of life.

We Do So Via

Access – Providing high quality trusted medicines regardless of geography or circumstance;

Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and

Partnership – Leveraging our collective expertise to connect people to products and services.

Every day, we rise to the challenge to make a difference. In this Role you will act as FvP of our entities in Switzerland and perform the direct technical supervision of the company, ensuring the correct handling of medicinal products and fulfilling the obligations according to HMG and AMBV. You sign for the quality of the medicinal products produced, in particular also taking into account the requirements of marketing authorization and EU GMP / GDP-Guideline.

Furthermore, Your Key Responsibilities Include
  • Leading the Quality team of 8 employees
  • Supervise the pharmaceutical business of our Entities in Switzerland and ensure the correct handling of the medicinal products
  • Ensure that only medicinal products are released onto the market that meet the specifications in force and are produced in accordance with Good Manufacturing Practice (GMP)
  • Ensure that medicinal products are stored and distributed in accordance with the rules of Good Distribution Practice (GDP)
  • As a FvP you decide independently from the management about the approval or non-release of a batch (including returns), including the subsequent blocking of already released batches up to the possible recall of the drug
  • ensure that the requirements stipulated in the Swiss “Arzneimittel-Bewilligungsverordnung (AMBV)” and the Therapeutic Products Act (TPA; Heilmittelgesetz (HMG)) are met
  • The FvP is named on the establishment licence of Swissmedic and for narcotic drugs for our entities
  • ensure that the requirements of all relevant national and international guidelines and internal policies/SOPs are met
The Minimum Qualifications For This Role Are
  • University degree in pharmacy or equivalent degree (e.g chemistry or natural sciences as stipulated in AMBV Chapter 2, Section 1, Article 5 and AMBV Chapter 2, Section 2, Article 10.
  • Adequate and sound experience in the pharmaceutical industry and/or manufacturing sites
  • Experience in personnel management in a pharmaceutical environment
  • Several years of experience and expertise in quality assurance
  • Will to succeed, clear goal orientation and the ability to implement objectives together with the team
  • Independent, structured and solution-oriented approach to work and clear focus on corporate objectives
  • Fluent in German and English (French and/or Italian are a plus)
A t Viatris, we offer competitive salar ies , benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer.
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Deadline: 10-05-2024

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