The associate will lead the method qualification and handover to QC of new container closure integrity system (Mass extraction and high voltage leak detection) for testing incoming syringes and vials.The main duty of the position is to qualify analytical methods for a new technology of container closure integrity system (ME + HLVD) and handover the equipment to QC at the end of the project. The associate will be responsible for the design and execution of the qualification protocol for the various vial and syringes format, Writing the operating procedure for the equipment + all required associated document, Establishing a training program for the end users in QC.
- Stein AG
Global pharma company
Are you looking to work in a global growth company where you can make a real difference? Then you are right with us!
Degree in Sciences / engineering
As per industry
The candidate should have a minimum 2 years of experience in GMP environment with handspn experience in equipment qualification or method validation. The person should have worked in the area of QC. Expereince in the area of syringes & vials testing is preferred.
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If you are interested then kindly send your resume to: firstname.lastname@example.org