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Head of Quality Management Systems

SIRE Life Sciences®

Switzerland, zagranica

SIRE Life Sciences®

Head of Quality Management Systems

Location: Switzerland

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Medical Devices organization, based in Switzerland.

My client is a global Medical Devices company. They are a well-known brand within the Medical Devices industry, focussed on excellent quality and research. Next to this, they are a company dedicated to their people with a stimulating environment. They are dedicated to the continuous improvement of their personnel, their products and their facilities.

ROLE DESCRIPTION

In this role, you will be responsible for the QMS for three production sites, in both Switzerland and Germany. Your office will however be based in Switzerland.

RESPONSIBILITIES

- Lead the QA team and be responsible for all processes (training, document control, validation, audits, NCRs, CAPA, supplier management)
- Establish and develop het quality organisation for the whole organisation
- Responsible for all non-conformities and CAPAs
- Cooperation with other departments (R&D, Regulatory, Manufacturing, Operations and others)
- Representing the organisation in the Program Management Office
- Coordinate the integration of the Quality Assurance and Regulatory Affairs for new plants (including strategy, tracking, consulting with all stakeholders)
- Report directly to the VP of Quality and Regulatory Affairs.

REQUIREMENTS

- Long-term work experience in the Pharmaceutical or Medical Devices sector
- Experience with Quality Management Systems
- Experience with database, data evaluation and making reports
- Knowlegde in Trackwise, Visual Basics, SAP, MS Office
- Extensive knowledge of ISO 13485 and 21 CFR 820 standards
- Fluent in English, fluent in German

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Michael Lynch.

Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
SIRE Life Sciences®

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