QA Manager / Pharma / Noord-Holland / GMP / Temporary role

Bedrijfsnaam: -
Plaatsingsdatum: 10/03/2019
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 organisation, based in Noord-Holland Netherlands.The CompanyThis client is a global pharmaceutical organization which is specialized in the research and the production of generics, OTC and API's. The focus of this company is to improve and reassure the quality of medications for the purpose of the patients. For a period of 6 months this company needs a Quality Assurance Manager to support and improve their quality team.

Role DescriptionAs the Quality Assurance Manager you will be responsible for maintaining the high quality standards at external manufacturing sites, which have to meet the GMP standards. You will be responsible for the compliance of the SOP and regulatory. Within this function you will be the POC for various team members and responsible for their results. You will be the designated person to make sure that the performance of the team live up to the standards and regulations and make adjustments where necessary.

Responsibilities- Managing and coaching of the manufacturing site
- Setting up and monitoring of the KPI's
- Ensuring the quality of audits and batch reviews
- Managing the quality of the end products according to the GMP standards
- Managing the manufacturing activities according the SOP
- Conducting risks assessments and managing complications
- Responsible for the product acquisitions
- Review of quality documents

Requirements- A Life Sciences BSc.
- At least 7 years of experience within the pharmaceutical industry, preferably in the QA
- At least 4 years of experience as a manager or team leader
- Knowledge of the current GMP standards
- Capable of risk assessment and compliance management
- Fluent English communication
- Assertive and result-oriented institution

Other informationIf you meet the above requirements and are motivated to work in a dedicated team with a challenging function, please let us know!

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




Plaatsingsdatum :
Referentienummer :
Standplaats :
Adres :
Postcode :
9723 HK
Opleidingsniveau :
Uren :
Nader te bepalen
Dienstverband :
Werkervaring :
5 - 10 jaar
Contactgegevens :