Interim QA Manager
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 Biotechnology organization, based in Noord-Brabant Netherlands.
They 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 for the coordination and planning of the stability work processes and you are responsible for the QA team. In projects you will be the contact person for Stability and you will take over some QP tasks when the QP is not available. You will coordinate and watch over the regular QA tasks. 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. Think in an innovative way to lead (international) projects in the Stability area.
- Lead internal audits and represent the company at external visits
- Handling of deviations and CAPA’s in the systems
- Maintain EHS/ GMP and be problem solving for abnormalities
- Coordinate, describe, document, research the processes
- You will take over the QA manager role at absence
REQUIREMENTS
- BSc.
- At least 5 years of QA experience within the pharmaceutical industry
- Management skills
- Audits & self-inspection
- Knowledge of Stability processes and technical knowledge of QA systems and backgrounds
- 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 Amber Moet.
