Quality Compliance Sr Manager

:Support and facilitate the implementation of the Pharmaceutical Quality System, ensuring compliance with cGMP regulations and Corporate StandardsProactively assess site cGMP inspection readiness, identify potential gaps, and collaborate with relevant functions to develop action plansLead the preparation, management, and follow-up of Regulatory Authorities and Clients inspectionsLead all aspects of the execution of internal and external auditing programsProvide guidance and coordination to ensure production processes and cleaning and equipment validation meet cGMP and Corporate StandardsDevelop a culture of collaboration and partnership with site functionsDrive people and organization development, leading performance and development of team membersRequirements:MsC or higher diploma in chemistry, biotech, or pharmaceutical fieldsMinimum of 10 years of experience in Pharma Operations, with a focus on QA leadershipExperience in Quality Units of a pharmaceutical company, demonstrating a strong compliance backgroundKnowledge of Sterility Assurance is crucialExperience in people management and developmentFluent in English and ItalianExcellent leadership abilities, including the capacity to lead change, adopt a forward-thinking approach, and cultivate a collaborative team environment.Excellent listening, negotiation, and communication skillsPragmatic and demonstrates a focus on achieving desired outcomesThermo Fisher Scientific Inc. is an Equal Opportunity Employer.
We value diversity and inclusion in our workforce, and all qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age, or disability status.Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.Join us!