Senior Associate QA (3 shifts)

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 Pharmaceutical organization, based in Noord-Brabant Netherlands.

They are an international company located in Breda.

ROLE DESCRIPTION

Act as a first point of contact in case of production queries (quality related) during packaging and labeling operations. Work together with production and maintenance team to resolve the quality related problems.

RESPONSIBILITIES

- Coach production and maintenance staff to improve on quality and to limit number of errors;
- Review and approve class I Non Conformances;
- Review and approve batch records;
- Complete batch release preparation prior to Qualified person disposition;
- Perform finished product checks during production runs.

REQUIREMENTS

- MBO or Bachelor’s degree in Life Sciences or related field or the equivalent combination of education and/or experience;
- Typically 3 (Bachelor) or 5 (MBO) years of related Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry, with experience in batch record review and investigations;
- Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and/ or Good Clinical Practice (GCP) knowledge with the ability to interpret and apply in mainly routine cases;
- Manufacturing and/or Quality analytical processes and operations;
- Fluent in English language.

OTHER

3 Shifts:
- Early: 0630-1500
- Late: 1430-2300
- Night: 2230-0700

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