Qualification and Validation Engineer

On behalf of our client in the Life Science industry, Harvey Nash is looking for a Validation Engineer for a 6 month project in Ticino

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 Swiss 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. I'm looking forward to receiving your application.