QA manager / potential QP

Bedrijfsnaam: -
Plaatsingsdatum: 13/09/2018
Standplaats: -

Functieomschrijving

SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Pharmaceutical organisation, based in Noord-Holland Netherlands.The CompanyIt’s an unique organization, nowhere else in the world is medical, pharmaceutical and scientific knowledge combined into one innovative company. It’s a dynamic organization combining medical, pharmaceutical and diagnostic knowledge into one company.

Role DescriptionAre you good at working together across the boundaries of your own department and easily build and maintain contacts? Are you able to contribute to the next level of our quality systems required for the preparation and release of laboratory reagents? Are you a natural leader with conviction that can properly utilize the years of experience present at the QA / QC department? Then this is the job for you! It’s a position for at 6 months with possibility to extend.

ResponsibilitiesYou will responsible for managing the QA / QC department as well as taking account and monitoring quality systems and actively contributing to improvements and process optimization / process validations. Next to that you will be responsible for the following:
- Compiling, modifying and / or evaluating the necessary documentation (SOPs)
- Evaluating whether procedures comply with applicable laws and regulations in collaboration with other disciplines and departments
- You are a Qualified Person under the EU CE-IVD Legislation, and be responsible for the regulatory compliance of the organization, documentation, declaration of conformity, performance evaluations and vigilance

Requirements- Msc degree biotechnology or pharmaceutical industry
- Minimum 5 year international experience in manager QA/QC
- Experience with QMS is a plus
- Experience with implementing quality improvements
- Experience with product registrations

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.

 

Aanbod/arbeidsvoorwaarden
-

Samenvatting

Plaatsingsdatum :
13/09/2018
Referentienummer :
95389
Standplaats :
-
Adres :
-
Postcode :
9723 HK
Opleidingsniveau :
WO
Uren :
Nader te bepalen
Dienstverband :
Vast
Werkervaring :
3 - 5 jaar
Contactgegevens :
bekijk