Consultant QA Manager
Location: NetherlandsSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Pharmaceutical organisation, based in Zuid-Holland Netherlands.
It is a GMP environment. You will train your team in GMP guidelines. Furthermore you will take a overview of a team of 5 QA specialists.
- Follow regulatory guidelines
- QMS management
- Internal and External audits
- Handling of deviations and CAPA’s in the systems
- Develop training materials
- Lead QA projects
- Coordinate, describe, document, research the processes
- Knowledge of Quality Management principles and GMP
- Experience with audits
- Leading skills
The Company
A multinational Pharmaceutical company.Role Description
As an consultant QA manager you will manage the Quality Management Systems in line with regulatory. CAPA’s need to be performed and you will audit internal and external for suppliers.It is a GMP environment. You will train your team in GMP guidelines. Furthermore you will take a overview of a team of 5 QA specialists.
Responsibilities
Besides lead, coach and develop the QA specialists, you will be building the strategy and goals of the QA department.- Follow regulatory guidelines
- QMS management
- Internal and External audits
- Handling of deviations and CAPA’s in the systems
- Develop training materials
- Lead QA projects
- Coordinate, describe, document, research the processes
Requirements
- MSc. or BSc in related field- Knowledge of Quality Management principles and GMP
- Experience with audits
- Leading skills
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