Quality assurance project 6 tot 8 maanden
Location: NetherlandsSIRE 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-Holland Netherlands.
hey a world leader in healthcare. A company that delivers their part in a healthier world. In over 140 counties they help people and animals with medicals, vaccines etcetera in an innovative way. If you like to be challenged in your work, this is the company to work for.
ROLE DESCRIPTION
You will be responsible to ensure cGMP compliance for the quality systems. On the site you will make sure you get insight in the quality and compliance. It is your responsibility to develop, improve and maintain the Quality Systems including the QMS strategy. The end date of this project is not yet known, expected 6-8 months.
RESPONSIBILITIES
As an interim QA officer you will focus on coordinating and improving the quality policy. You have the ability to optimize the current work methods and take a leading role in this part.
- Lead internal and external audits
- Coordinate Health Authority inspections
- Promoting Lean behaviours and manage your team
- Coordinate, describe, document, research the processes
REQUIREMENTS
- BSc. or MSc.
- At least 5 years of QA experience within the pharmaceutical industry
- Experience within regulated environment
- Project management skills
- Fluent in English and Dutch
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.
