QA Manager QP
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 Nordrhein-Westfalen Germany.
Our client is a middle-sized Pharma companies.
ROLE DESCRIPTION
- Review,and approve batch documentation and deviations
- Support shipment, quarantine and rejection procedures for materials at the site.
RESPONSIBILITIES
- Liaise with external contractors and personnel regarding release
- Prepare CAPA's related to release of finished product.
- Handle complaints, deviations, CAPA’s and change controls,
- Support recall
- Prepare review and approval of SOPs.
- Review or approval of other technical documents i.e. batch documentation, specifications, material specifications, qualification documentation, validation documentation, technical agreements.
REQUIREMENTS
- Pharmacist degree
- Fluency in German & English
- Several years of experience in QA under GMP / cGMP
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact admin admin.
Job Description
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 Nordrhein-Westfalen Germany.
Our client is a middle-sized Pharma companies.
ROLE DESCRIPTION
- Review,and approve batch documentation and deviations
- Support shipment, quarantine and rejection procedures for materials at the site.
RESPONSIBILITIES
- Liaise with external contractors and personnel regarding release
- Prepare CAPA's related to release of finished product.
- Handle complaints, deviations, CAPA’s and change controls,
- Support recall
- Prepare review and approval of SOPs.
- Review or approval of other technical documents i.e. batch documentation, specifications, material specifications, qualification documentation, validation documentation, technical agreements.
REQUIREMENTS
- Pharmacist degree
- Fluency in German & English
- Several years of experience in QA under GMP / cGMP
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact admin admin.
Additional Information
- Last updated
- Employment type
- Full time
- Contract type
- Self employed
- Number of vacancies
- 1
- Min. experience
- Two years
- Min. education
- Bachelor
- Industry / category
- Jobs in Quality Control