COMMISSIONNING, QUALIFICATION

For our Techfirm Industrial Services team, we would like to integrate a CQV Engineer ready to join us in Switzerland to take up new challenges together

As a CQV Engineer, you will provide the necessary expertise and assistance to further improve and maintain the quality standards for their operations and products.

• You are in charge of the commissioning and qualification of production equipment.
• You will write protocols and perform acceptance tests at the supplier and at the customer site (FAT/SAT).
• You will be responsible for the Installation, Operational and Performance Qualification (IQ, OQ, PQ) and write the reports.
• In collaboration with the Validation Department, you will work on various process validation projects (e.g. cleaning, sterility, freeze-drying).
• You will draft Validation Plans (VMP) up to Validation reports.

• Minimum Bachelor's degree in Life Sciences or Engineering.
• Minimum of 3 years of work experience in commissioning / qualification / validation (DQ, IQ, OQ, Commissioning) activities in the pharmaceutical/biotech industry.
• Experience with DeltaV (Emerson), COMOS/KNEAT platforms would be a real plus.
• Fluent English language written and verbal communication skills; any further language is a plus.
• cGMP knowledge and knowledge of regulatory requirements.

If you are interested in joining us, please send your CV to comeonboard@techfirm.ch.

Please note, that we can only consider Swiss or EU/EFTA nationals or applicants with a valid residence or work permit for Switzerland.

Mid-Senior level

Full-time

Quality Assurance

Human Resources