Commissioning Qualification Validation Engineer

Our client in Visp is seeking a Commissioning Qualification Validation (CQV) Engineer to join their team on a temporary contract to support their CAPEX project, minimum 6 months (very likely to extend or transition into permanent role)

This role involves a diverse array of tasks centered around validating equipment and facilities, ensuring compliance with cGMP standards. As a CQV Engineer, you will oversee the installation of equipment, develop validation protocols, execute validation procedures, and meticulously document results.

Key Responsibilities:

• Coordinate equipment installation and validate facilities and utilities.
• Develop and execute IQ/OQ/PQ protocols in accordance with cGMP requirements.
• Generate validation documentation including URS, DQ, FMEA, Risk Assessments, FAT, SAT, and various protocols.
• Write comprehensive reports detailing validation activities.
• Identify opportunities to improve validation processes and implement efficiencies.
• Participate in Quality Systems activities such as Document Management, Change Control, Non-Conformities, and CAPA’s.
• Support the Engineering team in preparing validation, requalification, and maintenance programs.

Requirements:

• Bachelor’s Degree in a Science or Technical field.
• 3-6 years of experience in an advanced level within the Pharma industry.
• Proficient in technical writing with a keen attention to detail.

***Please only apply if you are eligible to work in Switzerland and the EU***

***Please forward your application should you meet the requirements above – applications which do not meet these requirements will not be considered***

headcount AG