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SIRE Life Sciences®

Quality Assurance Manager GMP & GDP


SIRE Life Sciences®

Quality Assurance Manager GMP & GDP

Location: Netherlands

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 Noord-Brabant Netherlands.

Our client is specialized in manufacturing and distribution of Pharmaceuticals.

ROLE DESCRIPTION

Leading the site QA team

- Responsible for release and distribution quality
- Responsible for improving the quality standards
- Responsible for translating GDP, GMP and other requirements to existing processes

RESPONSIBILITIES

- Batch release
- Team management
- Training of staff according to GxP
- Maintain and Improve QMS

REQUIREMENTS

- Master / W.O. level or similar experience
- Knowledge of GMP and GDP
- Fluent in English and Dutch
- Excellent communication skills
- 5+ years’ experience in industry | 2+ years’ experience in Quality role
- Auditing experience advantageous
- QP Qualifications (advantageous)

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

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SIRE Life Sciences®

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 Noord-Brabant Netherlands.

Our client is specialized in manufacturing and distribution of Pharmaceuticals.

ROLE DESCRIPTION

Leading the site QA team

- Responsible for release and distribution quality
- Responsible for improving the quality standards
- Responsible for translating GDP, GMP and other requirements to existing processes

RESPONSIBILITIES

- Batch release
- Team management
- Training of staff according to GxP
- Maintain and Improve QMS

REQUIREMENTS

- Master / W.O. level or similar experience
- Knowledge of GMP and GDP
- Fluent in English and Dutch
- Excellent communication skills
- 5+ years’ experience in industry | 2+ years’ experience in Quality role
- Auditing experience advantageous
- QP Qualifications (advantageous)

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

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 / Production Audit
New

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