Beschreibung
On behalf of our client in the Life Science industry, Harvey Nash is looking for a Validation Engineer for a 6 month projects in various locations: Ticino, Visp area and Solothurn
The role
Support for the validation activities Ensuring that all compliance issues and requirements are addressed Create Validation Master Plans, Protocols, Summary Reports and other documentation associated with validations Facilitates successful team behaviour within Quality Systems and across functional areas Manages relationships externally and internally cross-functional and cross-departmental support, fostering overall effectiveness implement innovation and continuous improvement within the Validation process Requirements
Preferably experience in 21 CFR 820, 21 CFR 11 and European regulations associated with the medical device industry High understanding of GMP, Compliance, Validation Practices including the system development life cycle and Regulatory expectations Working experience of validation computer systems for use in a FDA regulated environment 2 years experience in medical devices/regulated environment BSc/MSc in scientific/engineering related field or equivalent Fluent English and German required, additional languages are an asset Are you available immediately, have experience working within a Life Science company?
Please send your complete CV (Word documents preferred)
For further details feel free to call me. Im looking forward to receiving your application.
