QA and QP / Bio- Pharma / Temporary / nearby Breda

Bedrijfsnaam: -
Plaatsingsdatum: 22/04/2019
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 Pharmaceutical and Biotechnology organisation, based in Noord-Brabant Netherlands.The CompanyOur client is a professional Pharmaceutical organisation, based in Noord-Brabant Netherlands. This international company is leading in the field of human medicines in the biotechnology industry. The department in Breda has a challenging and interesting position for a QP/QA specialist.

Role DescriptionIn this role you act as a Qualified person, you are responsible for releasing finished drug product lots while ensuring compliance with the requirements of the marketing authorization and good manufacturing practices. As a Specialist Plant QA, you provide guidance and direction to Production, Maintenance & Engineering and Quality staff regarding compliance with quality standards and procedures.

ResponsibilitiesAs QA/QP Specialist you are responsible for:

- You partner daily with production and engineering staff to support, enable and improve the production process
- You partner with production staff in performing risk analysis and the establishment of quality limits and requirements
- You own, review and approve production and plant QA related documents (e.g. SOPs, Forms, Training)
- You review and approve deviations and CAPA, initiate and own as needed.
- You perform impact assessment as part of change controls impacting production or QA processes
- You review and approve production equipment maintenance work orders
- You review and approve test protocols before use in production
- You perform GMP compliance checks in production
- You participate in internal audits and lead as appropriate
- Participate in regulatory inspections and partner audits
- You assist in development and delivery of GMP training for QA and production staff
- You lead and participate in Plant QA related projects/global QA initiatives as needed
- You lead and assist in various investigations as needed
- You assist in validation activities as needed including review and approval of validation documents

RequirementsWhat do you need to be successful in this role?

- Master’s in science in Pharmacy or equivalent
- Knowledgeable, skilled and eligible to fulfill the requirements of EU directive 2001/83/EC article 49 (Qualified Person).
- Thorough knowledge of the processes involved in clinical and commercial manufacturing (GMP), warehousing, supply chain, equipment engineering principles and validation.
- Acquired practical experience in Good Manufacturing Practice (GMP) ideally in a Secondary Packaging manufacturing setting
- Fluent in English

Other informationThe job is temporary with the duration of 52 weeks. Interesting? Apply!

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Diana Prieto Reyes.




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