QA System Manager - temporary 6 months

  • Contract type Temporary Assignment - 6 months
  • Place
  • Reference 201825-120-3
  • Assignment start date asap
  • Sector Chemistry & Life Sciences
  • Publication date 17.11.2020
  • Apply

For our client, a renowned pharmaceutical company located in Aesch (BL), we are looking for a

QA System Manager - temporary 6 months

Your assignment

This position is responsible for managing and coordinating the quality compliance activities at each manufacturing area. This position will be part of the Quality System Team. The role is to assist the Head of Quality with assuring timely investigations, resolution of issues and implementation of corrective measures by using scientific principles, root cause analysis and compliance minded corrective and preventative actions related to manufacturing.

- Maintains awareness of current GMP and ISO-trends and manufacture processes and supports continuous improvement
- Maintain key Quality system elements: Deviation, Change control, CAPA, OOS
- Prepare SOPs and investigation documents as well as tracking- and trending-analysis and KPIs relevant to business process
- Resolve production discrepancies and customer complaints as related to product release, which must take into account all manufacturing processes, quality testing and customer requirements
- Provide support for regulatory agency inspections / customer audits / internal audits
- Provide support for the supplier qualification process management
- Maintain facility good quality standard
- Recommends changes in established processes to quality
- Report and take any necessary action to prevent quality problems from occurring
- Provide support to QA department for special projects
- Stay current with key regulatory and certifying agency guidelines and regulations
- Provide support to the regulatory team (Pharma and IVD)

Your profile

- Minimum MSc in Biotechnology, Biology, Microbiology, Chemistry, Pharmacy or Food science related fields
- Min of 3+ years' experience with proven track record in a GMP or ISO production site
- Product classification; Definition of applicable standards; Conformity assessment procedures
- Fluent in English & German
- Ability to multitask
- Self-driven, results oriented, able to work independently
- Excellent communication / presentation skills
- Excellent record keeping / documentation skills
- Excellent Organization skills
- Detail oriented


This multifaceted project provides the opportunity to apply and increase your expert knowledge in an renowned pharmaceutical company. Also the possibility of contract extension is given. To apply for this vacancy, please click the button "apply" and upload your complete application documents (CV, job references and proof of qualification) with your notice period and salary expectations. We are looking forward receiving your application today!

About Manpower
Manpower Switzerland offers its customers more than 55 years of experience in the recruitment, selection and placement of permanent and temporary staff, as well as in HR solutions. Its network of 50 branches active in all linguistic regions, 20,000 temporary staff, 1,500 permanent placements and over 5,000 clients – including small, medium and large companies – in all sectors of industry make Manpower one of Switzerland’s leading providers of workforce management solutions.
Our 3 promises
“We are passionate about what we do. This passion is a motivating and driving force, ensuring excellent placement opportunities for you.”
“We care about the people we work with. Including you. That’s why our collaborations are based on trust.”
“We take on our responsibilities. For you, that means security and exciting prospects.”

I'd like to apply

Your Manpower consultant
Veronika Walz

Life Sciences Competence Center
Picassoplatz 4
4052 Basle

T: +41 58 307 2441

Speculative application

Haven't found what you're looking for? Send us a speculative application, and we will get in touch as soon as we hear of an opportunity for you!

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