Sr. Technician Transfer and Validation / Region Amsterdam / Pharma / QC and GMP

Bedrijfsnaam: -
Plaatsingsdatum: 21/02/2019
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-Holland Netherlands.The CompanyOur world needs ideas!

Our client is one of the world’s most research-intensive chemical companies, we have been developing leading solutions for numerous sectors - from construction to photovoltaics and cosmetics to rubber - for over 100 years. We have a global presence with production sites on three continents and 13,800 employees from 70 nations.

Are you looking for a dynamic, globally active technology company - yet at the same time, you appreciate a value-oriented, trusting company?

Then this is the right job for you!

Role DescriptionAt our Amsterdam-based center our client focuses on the GMP-compliant microbial based production of recombinant proteins, vaccines and live microbials as drug substance and drug product. Our client is currently looking to recruit a Senior Technician Transfer and Validation (f/m/d) for the Quality Control department. attention because it is only getting better.

ResponsibilitiesAs Sr. Technician you will be responsible for the following activities:
- Primary QC contact for external clients and partners
- Execution of multiple projects from preparation till completion
- Managing QC project deliverable within timelines
- Writing of method validation documentation (protocols/reports)

Sounds great doesn't it ?

RequirementsTheir is only one question left..Do you have what it takes?

Our client is searching for a candidate with the following aspects:
- University degree in medical biology, biochemistry, chemistry or biotechnology with minimal 3 years of work experience in biotechnology or pharmaceutical environment
- Extensive knowledge and experience about method validation, method qualification and method verification
- Well established oral and written communication capabilities in Dutch and English
- Maintain overview on diverse activities in multiple projects

Other informationOur client offers you exciting work as part of a team of experts who treat each other as equals. All over the world.

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 :