Interim Quality Manager

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 Biotechnology and Pharmaceutical organization, based in Hessen Germany.

Our client is a constantly growing company which operates in the life sciences industries and is currently trying to replace the position as Quality Manager for six months (with a possible extension of another six months) due to a maternity leave.

ROLE DESCRIPTION

As an Interim Quality Manager you will be responsible for the temporary leadership of the quality assurance department, including the oversight of eight employees. Your daily work activities will contain controlling and guaranteeing flawless processes for the production of in-vitro diagnostics, with a special focus on qualification and validation of rooms and equipment. Further you will have responsibilities for project management and hygiene management.

RESPONSIBILITIES

- Temporary leadership of QA department
- Responsibility for eight employees
- Controlling and guaranteeing flawless IVD production processes
- Qualification and validation of rooms and equipment
- Hygiene management
- Project management

REQUIREMENTS

- Successful apprenticeship (CTA, BTA etc.) or a scientific university degree
- Experience in quality assurance (preferably in a GMP-regulated environment)
- Knowledge in ISO 13485 and 14791
- Fluency in German and English

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