QA specialist (1 year contract, can be extend)

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


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 Biotechnology organisation, based in Noord-Brabant Netherlands.The CompanyThis company is one of the largest pharmaceutical and biotechnological organization. They are committed to serve patients. They dedicate their days to turning the tide on serious, life-interrupting illnesses and pushing the boundaries of science to transform medicine.

Role DescriptionDo you want to work at a company with a clear mission to serve their patients? is your passion to maintain and improve the quality of the medicines? Then this is the job for you!

ResponsibilitiesYou will be responsible to provide daily oversight, guidance and support to Production staff in regards to compliance with Quality Policies and Procedures. You will need to handle CAPA’s mainly as initiator or QA-contact. Leading and assisting in various investigations as needed is also one of your responsibility. next to that you will be responsible for the following:
- Perform GMP compliance checks in production
- Own, review and approve SOP’s
- Handle change control records mainly as assessor or as QA contact
- Partner with Production staff in performing risk analysis and the establishment of quality limits and requirements.
- Assist in development and delivery of GMP training activities for QA and production staff.

Requirements- EU Pharmacist degree
- At least 3 years of related professional experience in dealing with Non Conformances and Change Control records
- Good problem solving skills
- Knowledge of GMP and GDP
- Experience in (bio)pharmaceutical production environment, in particular packaging and labeling

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.




Plaatsingsdatum :
Referentienummer :
Standplaats :
Adres :
Postcode :
9723 HK
Opleidingsniveau :
Uren :
Nader te bepalen
Dienstverband :
Werkervaring :
3 - 5 jaar
Contactgegevens :