Job Description

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QA Manager (QA Compliance) 100% (m/f/d)

Liesberg, Switzerland

Acino is a Swiss pharmaceutical company, leader in advanced drug delivery technologies. We have a clear focus on selected emerging markets in the Middle East, Africa, the CIS Region, and Latin America, and 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 Liesberg BL as

QA Manager, QA Compliance 100 % (m/w/d)

Major Accountabilities:

  • Create, review and approval of SOP to support continuous improvement of internal requirements to ensure GMP compliance
  • Process, track and ensure timely completion of changes with and without regulatory impact
  • Train employees in change control procedure
  • Process, track and ensure timely completion of deviations and associated corrective and preventive actions
  • Prepare, review and approval of annual product quality review
  • Compilation and analysis of batch specific data from SAP, LIMS, TrackWise®, PAS-X and contract database
  • Lead and participate in Health Authority inspections and customer audits, including processing related CAPAs
  • Planning and performing internal audits
  • Review and approval of documents from the areas of process transfer/validation, equipment, infrastructure qualification and technical changes
  • Review and approval of documents from the area of cleaning validation and environmental monitoring
  • Review and approval of analytical methods and validation
  • Implementation of quality improvement projects
  • Compiling and reporting corporate and customer-specific KPI

Your profile:

  • Education in pharmacy, natural sciences or equivalent
  • Sufficient experience with pharmaceutical technology or experience in the pharmaceutical industry
  • Several years of experience in the GMP regulated environment, preferably with processes involved in manufacturing, Quality (QA and QC), validation
  • Good communication skills and team-oriented personality with great initiative and a strong skills in coordinating cross-department teams and negotiation
  • Skilled in quality risk management
  • Reliable and careful work methods with a clear view of priorities
  • Well organized and quality oriented
  • Very good knowledge of English and German (oral and written)

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
  • 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 this sounds exciting, we would love to hear more about 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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