A Biotech company are looking for a Senior Process Validation Specialist to join them on an initial 6 month contract basis. Based at their site in Visp, with some remote working available.
Key duties & responsibilities:
Developing strategy for process specific validations, following protocols and SOP's
Risk Assessments
Working closely with the Quality Assurance team to ensure all validation documents comply with the relevant standards
Assessing any change requests related to the validation department
Preparation/ownership of CPV plans, reports and PQRs
Assist during process characterization
Point of contact for process validation
Supporting with audits
To discuss further, please send an updated CV to [email protected].