QA Manager Sterile Manufacturing
Location: GermanySIRE 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 Bayern Germany.
Global pharmaceutical company specialized in generic drugs, biologic and consumer health products.
With over 50 years of outstanding track record contributing to the pharmaceutical industry.
The company has proven to be able to bring products into the market faster, ensuring clinical, high production and distribution standards.
ROLE DESCRIPTION
The QA Sterile Development Manager will be located in the Munich site and will report to teh Quality Director.
In this role he/ she will manage a team of 8 people integrated by 4 QA officers and 4 Quality operators.
In this position the QA Manager will ensure the daily operations of the QA activities on the shop floor team.
Develop a good relationship with the release team.
Main contact person for manufacturing operations, analytical development, laboratory and packaging.
Investigation of deviations, CAPAs, OOS, complaints...
Participation in internal/ external audits
We are looking for a problem solver and a good manager who can bring unity to the team.
RESPONSIBILITIES
- Team management and coordination
- Coordination of the daily quality work in the manufacturing floor
- Supervision and investigation of CAPAs, OOS and deviations
- Development and implementation of new SOPs to bring efficiency
- Participation in internal/ external audits
REQUIREMENTS
- Scientific background (Bachelor/ Master) in pharmacy, biology, chemistry, biochemistry ...
- 5-10 years of experience in aseptic manufacturing
- Strong knowledge of GMP (in production)
- Proven track record as team manager
- Proficient German and English skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Patricia Oses Equiza.
