QA Manager CMO
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 an International Pharma company with suppliers all over the world.
ROLE DESCRIPTION
- Responsible for maintaining compliance at our CMO's
- Contact point for Contract Manufacturers
RESPONSIBILITIES
- Ensure that products at CMO are compliant with GMP
- Evaluate CMO's and their performance
- Escalate cGMP/Regulatory compliance problems
- Asses supplier quality and KPI's
- Risk management
- Complaint monitoring
- Ensure that right people are involved of changes, deviations, audit findings and complaints
- Approve QA Agreements
REQUIREMENTS
- Degree in Chemistry, Pharmacy, Biology, Microbiology or related
- 5+ years experience in Quality
- Knowledge of cGMP
- Speaking fluent English
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.
Opis stanowiska
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 an International Pharma company with suppliers all over the world.
ROLE DESCRIPTION
- Responsible for maintaining compliance at our CMO's
- Contact point for Contract Manufacturers
RESPONSIBILITIES
- Ensure that products at CMO are compliant with GMP
- Evaluate CMO's and their performance
- Escalate cGMP/Regulatory compliance problems
- Asses supplier quality and KPI's
- Risk management
- Complaint monitoring
- Ensure that right people are involved of changes, deviations, audit findings and complaints
- Approve QA Agreements
REQUIREMENTS
- Degree in Chemistry, Pharmacy, Biology, Microbiology or related
- 5+ years experience in Quality
- Knowledge of cGMP
- Speaking fluent English
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.
Dodatkowe informacje
- Ostatnia aktualizacja
- Wymiar etatu
- Pełny etat
- Rodzaj umowy
- Własna działalność
- Liczba wakatów
- 1
- Min. doświadczenie
- 2 lata
- Min. wykształcenie
- Wyższe licencjackie
- Branża / kategoria
- Praca Kontrola jakości / Audyt produkcji