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Global QA GMP/GDP Compliance Manager

Munich , Germany

Acino AG, based in Munich, is part of the Acino Group, a Swiss pharmaceutical company and a leader in advanced drug delivery technologies with its headquarters in Zurich.

Acino out-licenses its own products and manufactures third party products mainly for the European market. In its commercial operations, Acino has a clear focus on selected emerging markets in the Middle East, Africa, the CIS Region, and Latin America. We operate in some of the most dynamic countries of the world. We value courage, commitment, trust, and empathy and provide an environment that supports initiative and effort. We are proud to be action-oriented and open-minded, with a strong focus on quality and product availability, even in remote and hard to reach areas of the world.

We are constantly expanding our market position with a future-oriented international business strategy. Therefore, we are looking for a dedicated and motivated person to strengthen our team in Munich, Germany as

Global QA GMP/GDP Compliance  Manager

Major accountabilities include, but are not limited to:

  • Oversight of ACINO sites/offices from a GMP and GDP compliance perspective, support the implementation of Acino quality requirements at Acino manufacturing sites and local/regional offices
  • Initiate, revise, and review corporate Quality Management System documents according to the master plan, provide trainings to support the global implementation
  • Manage the global metrics and reporting program as well as the global quality issue escalation process
  • Manage the corporate Acino 3rd party qualification and audit process (coordination and follow up with Acino sites, maintenance of electronic database)
  • Manage the internal and external global lead auditor qualification and training process
  • Perform Quality GMP/GDP audits at ACINO affiliates and external Third parties
  • Establish and monitor the annual global audit, 3rd party Risk assessment and TQA plans
  • Lead improvements and global implementation of Quality Tools (Trackwise etc.)
  • Support quality improvement plans and QA Due Diligence 3rd party qualification activities
  • Lead cross-functional Projects
  • Support optimization of global business processes in cooperation with different functions and local sites
  • Support and assist the Global Head GMP/GDP Compliance

Your profile:

  • Master’s degree in pharmacy, chemistry, biology or another life science
  • Minimum 5 years of pharmaceutical industry experience either in quality, production or development, gained in an international environment
  • Project Management experience
  • relevant experience as lead Quality GMP/GDP auditor
  • Business English fluent

Your competencies:

  • Excellent knowledge of GxP requirements
  • High analytical and process-oriented mindset combined with the capability of understanding complex situations and processes
  • Good collaboration skills
  • Ability to communicate effectively and proactively with superiors and peers
  • Culture awareness and understanding the way of behavior in different cultures
  • Eagerness to learn and continuously improve

We offer a very attractive working environment within a highly motivated team with excellent working conditions. You can expect the following benefits:

  • A job in a crisis-proof pharmaceutical company
  • An international working environment in a constantly growing company
  • A quality and customer-oriented environment
  • A motivated, agile and service-oriented team
  • Interesting and highly diversified tasks that provide a broad basis for your future career in the pharmaceutical industry
  • Attractive salary and flexible working hours (possibility of home office)

This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If you are interested in this role we are looking forward to hearing from you.

Please apply via our HR system here.

Note that only direct applications via our HR system (follow the link above) will be considered.

Further Information

Our team is happy to respond to any questions about the role or Acino you may have:

We are looking forward to hearing from you.

Only direct applications are considered.

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