Technician Process development
Location: NetherlandsSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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!
THE COMPANY
Our client is a professional Biotechnology and Pharmaceutical organization, based in Zuid-Holland Netherlands.
The company is a multinational with various R&D and production sites where (bio)pharmaceuticals are developed, produced and distributed.
ROLE DESCRIPTION
The technician has a rather hands-on role and will report to the senior technician and support him/her in the development, set up and improvement of the experiments within your department. The key tasks and responsibilities you will focus on are the development, qualification and validation of assays, performs tests for USP/DSP, characterization, stability, robustness and for release.
RESPONSIBILITIES
- execution of experiments and tests under the supervision of scientist(s) in accordance with predetermined protocols and workflows
- accurately document experiments and results according to procedures
- evaluation of results together with the scientist(s)
- writing (parts of) studyplans, SOPs and protocols
- implement new techniques and assays and stay up-to-date with novel technologies in the field
REQUIREMENTS
- Bachelor (HLO) or Master level or equivalent
- at least 1+ years experience in the industry working with USP and/or USP
- prior working experience in a strictly cGMP regulated environment in life sciences/pilot plant
- excellent knowledge of English (both oral and written) and Dutch preferably
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Alexander Wielemaker.