QP / QA Specialist clinical products
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-Brabant Netherlands.
An international company who develops, produces and distribute medicinal products.
ROLE DESCRIPTION
You will be responsible for overall QA activities related to the clinical products like receiving, releasing and distributing. You will work close together with the QP for example releasing new products and approve artwork. It is your ambition to become the QP as well.
RESPONSIBILITIES
- All communication for QA activities for new introductions for clinical products
- Change control, reviewing, approval
- Product disposition handling
- Make quality policies and procedures compliance by directing and giving guidance to quality, clinical supply chain management, production and warehouse/distribution
- QA contact in acting for Non- conformances and CAPA’s
- Internal and external audits
- Writing reviewing and approving of procedures
- Lead and participate in projects and improvement efforts
- Take initiative by participating in global quality initiatives and implement the activities on the site
REQUIREMENTS
- MSc. Pharmacy or you have a license as a QP with a Bio-engineering/ Bio-medical Sciences or Life Sciences background
- At least 2-3 years working experience within the pharmaceutical industry and GMP environment and preferably GCP experience
- Ambition to become a QP, preferred that you are already a QP
- Fluent in English and preferably Dutch speaking
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.
