Compliance Specialist
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 Noord-Brabant Netherlands.
- Participating in all activities associated with the company’s QMS
- Documenting of non-conformance reports – technical writing
- Ensure superfluous communication with stakeholders
- Experience in a pharmaceutical environment is an asset
- (theoretical) GDP and GMP compliance knowledge
- Some experience with CAPA’s, non-conformances and electronic QMS
- Excellent analytical skills and communicatively strong
- Fluent in English
The Company
They are a one of the biggest multinationals that market pharmaceutical and biotech products. They invest in research, development and marketing of innovative products that provide solutions for health issues.Role Description
You will be regulating the activities associated with the quality system for the department of Supply Chain. You will constantly be translating between company requirements and external factors and will be making sure all procedures are compliant and where necessary follow up. The appointment will initially be for one year.Responsibilities
- Responsible for timely completion of CAPA’s and non-conformances- Participating in all activities associated with the company’s QMS
- Documenting of non-conformance reports – technical writing
- Ensure superfluous communication with stakeholders
Requirements
- BSc. in Pharmacy of life-science related field- Experience in a pharmaceutical environment is an asset
- (theoretical) GDP and GMP compliance knowledge
- Some experience with CAPA’s, non-conformances and electronic QMS
- Excellent analytical skills and communicatively strong
- Fluent in English
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