Philogen S.p.A. is looking for a “ GMP Sterility Assurance Specialist/Expert ” who will report to the GMP Quality Assurance Manager and contribute to the definition, implementation, and verification of Contamination Control strategies, ensuring compliance with
Position Description We are now seeking a CQV Engineer to join our growing operations in Italy. The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and
Responsibilities Develop the documentation to support Commissioning, Qualifications, and Validation. Responsible for protocol writing and execution, field verification, and development of summary reports at client sites. Support documentation for the Commissioning, Qualification, and Validation of pharmaceutical
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Office, Some degree of PPE (Personal Protective Equipment)