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SIRE Life Sciences®

Quality Assurance Manager

Switzerland, zagranica Pełny etat

SIRE Life Sciences®

Quality Assurance Manager

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 Biotechnology and Pharmaceutical organization, based in Basel-Stadt Switzerland.

Our client is a manufacturer of API's in central Switzerland.

ROLE DESCRIPTION

Responsible for Quality Assurance Tasks at our clients operating facility.

RESPONSIBILITIES

Ensuring and maintaining compliance as well as supporting valid cGMP- guidelines
Editing Quality Assurance tasks such as batch review and release, deviations and OOS handling
Assisting in internal and external audits
Assessing and approving of cGMP-relevant documents

REQUIREMENTS

University degree (MSC/PhD ) in chemistry, biochemistry, pharmacology or biology
Excellent knowledge in the field cGMP biopharmaceutical substances
At least 5 years of experience in the pharmaceutical industry (preferably manufacturing site)
Team-orientated, flexible and open personality
Good communicator with a self-employed and target oriented approach
Fluent language skills (w/s) 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 admin admin.

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SIRE Life Sciences®

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 Basel-Stadt Switzerland.

Our client is a manufacturer of API's in central Switzerland.

ROLE DESCRIPTION

Responsible for Quality Assurance Tasks at our clients operating facility.

RESPONSIBILITIES

Ensuring and maintaining compliance as well as supporting valid cGMP- guidelines
Editing Quality Assurance tasks such as batch review and release, deviations and OOS handling
Assisting in internal and external audits
Assessing and approving of cGMP-relevant documents

REQUIREMENTS

University degree (MSC/PhD ) in chemistry, biochemistry, pharmacology or biology
Excellent knowledge in the field cGMP biopharmaceutical substances
At least 5 years of experience in the pharmaceutical industry (preferably manufacturing site)
Team-orientated, flexible and open personality
Good communicator with a self-employed and target oriented approach
Fluent language skills (w/s) 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 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