Freelance QA Manager
Location: BelgiumSIRE 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 and Medical Devices organization, based in Antwerpen Belgium.
Small Medical Devices company in Antwerp.
ROLE DESCRIPTION
- Sterilisatie (validiaties) + bi compatibiliteit verder uitwerken in SOP (gamma + EtO)
- Voor 3 producten: nieuwe grondstof voorstellen welke niet door de testen komen, + verdere implementatie en overdracht naar productie
- clinical evaluation opstellen volgens MEDDEV 2.7-1 voor nieuw model catheter (ivm visibility)
- 2x verouderde TF bijwerken (oa risico analyse, biocomp, clinical evaluation etc)
- Evaluatie + update bestaande clinical evaluations naar MEDDEV 2.7-1 rev 4
- Marketing en kwaliteit/+productinfo op punt zetten. Info in catalogus pagina’s moet bewezen worden in TF
- Input aanleveren voor lopende R&D dossier
- Analyse + rapport met onderbouwing temperatuur range voor houdbaarheid producten tussen 0-30C
RESPONSIBILITIES
See above
REQUIREMENTS
- Direct available
- Fulltime
- 3 months
- Senior person
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Tim Thuijs.
