Chicago, IL, USA
11 months ago
We are currently working with a very large pharmaceutical client based in Chicago, listed as one of the top 50 employers in the world by Forbes magazine. This particular company are in the middle of an exceedingly exciting growth phase and are investing $2.5 billion in this particular site alone.
Your main responsibilities as a validation engineer would include testing systems used to develop or manufacture products in a cGMP environment, planning and leading validation strategies for small to medium scale projects, collecting and evaluating validation test data and investigation into any discrepancies.
Education and Experience:
- Minimum 3+ years validation experience (EQ, UQ, FQ, PQ)
- Training experience
- Experience working closely with other departments
- Bringing programs and SOPs up to current industry standards.
- English language skills
Press the apply now button to get in touch with one of our Life Sciences specialists!