Technical Integrator (Drug Product)
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 Pharmaceutical organization, based in Zuid-Holland Netherlands.
ROLE DESCRIPTION
You will be working on the department which is responsible for formulation development, fill/finish process development as well technical oversight of drug product manufacturing at contract manufacturing organizations. In addition, the department conducts in-use stability (pharmacy manual) studies including verification of blinding procedures.
RESPONSIBILITIES
- Lead subteams for several projects, ensuring timely completion of the project deliverables in the functional area (including supply of pre-clinical and clinical drug product batches)
- Represent your team in a multidisciplinary environment.
- Signal resource or technical issues and ensure alignment within the department and with the rest of the organization
- Contribute to the design of drug product development strategies with the functional groups
- Review and edit as responsible person within related sections in regulatory submissions.
REQUIREMENTS
- PhD or MSc in pharmacy, engineering, chemistry or related discipline with a minimum 8 years of experience with drug product development in the biopharmaceutical industry.
- Experience with projects in Phase 1-3 and beyond, as well as hands-on experience with formulation development, fill/finish processes and/or GMP manufacturing are strong advantages.
- Experience with vaccines is preferred
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Rowin van der Zwaan.
