Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.Discover Impactful Work:You will join a newly-established mRNA GMP manufacturing facility in Monza and will take part to the site overall conformance by advising on licensing strategies applicable to the innovative mRNA suite while partnering with the Qualified Person and realizing regulatory compliance activities per domestic & foreign requirements while interacting with relevant health authorities.You will be instrumental in supporting the mRNA business entity's growth by being the Regulatory and Compliance point of contact for new projects while liaising with Customer's technical/regulatory counterparts, promoting our services offering and facilitating regulatory related activities.A day in the Life:Regulatory Knowledge & ExpertiseAdvance knowledge on Italian laws and regulatory environment by leaning into specialized industry trade association working groups, digest and disseminate information, assist in impact assessment and implementation.Stay abreast on ATMPs/mRNA regulatory ecosystem in major jurisdictions (EU, USA, ICH) by monitoring relevant pharmaceutical legislation and guidance and leveraging from internal community of practices.Regulatory complianceFrom a site perspective:Lead the strategy definition for the establishment license extension to meet Customer needs, frame and submit corresponding facility data packages to regulatory agencies (primarily AIFA)Provide regulatory assessment and guidance on new product introductionResponsible for the issuance, maintenance and archiving of all domestic and foreign authorizations (AIFA manufacturing/import license & GMP certificate, FDA e-establishment registration, JP accreditation, etc.)Supervise the life-cycling of Site/Drug Master Files and ensure relevant submissionsSupport regulatory inspections and related preparedness activitiesEstablish and maintain relevant processes/SOPs and systems/databaseCollaborate in change management related to site regulatory compliance dutiesFrom a product perspective:Responsible for the setting and maintenance of Customer's product registration information (CMC data base)Accountable for the translation of product registration information into production and quality control master documents through key materials review ( drug substance/bulk drug substance specifications, batch records …)Collaborate to components compliance and evolving regulations by partnering with Quality Control ( TSE, elemental impurities, nitrosamines ...)Participate to change control process by defining regulatory requirements ( process, batch size, starting material supplier change ...)Set-up and optimize necessary regulatory systems and SOP in relation to these activitiesEnsure adequate archiving of relevant documentsProject Regulatory LiaisonBe the site regulatory liaison face to the Customer, follow-up on project regulatory submission plan (primarily clinical)Draft quotations, deliver regulatory services parcels in relation to the site and supporting a Customer application ( SMF, DMF, foreign accreditation, facility registration questionnaire …) and track invoicesPromote CMC regulatory services as part of our integrated offering concept by connecting and mutualizing capacities through Global Regulatory ATX SMERegulatory reportingResponsible for ensuring adherence to key deliverables' regional plan fostering into Global Regulatory Affairs reportingKeys to Success:EducationBachelor degree in Life Sciences ( Pharmacy, Chemistry, Microbiology ...)ExperienceMinimum 7 years working in a regulatory role with biopharmaceutical industry (ideally with exposure to ATMPs)Knowledge, Skills, AbilitiesWell-versed on site licensing requirements for clinical and commercial bulk manufacturing according to AIFA, EMA and FDA primarily as well as having an understanding of the respective proceduresGeneral knowledge of phase-appropriate biologics CMC regulatory requirements for clinical and commercial bulk manufacturing in a GMP environmentAdaptable to a dynamic work environmentAgile in interacting with management & leadership as well as Customers and other external partnersCustomer-centric attitude with strong business acumentAbility to work with cross-functional teams as well as in a matrixed environmentAbility to prioritize workload to meet timelinesEffective verbal and written communication skillsRigorous and attention-to-detail skills, especially in the completion and review of regulatory documentationsAbility to advise on regulatory solutions and influence partnersSound skills in typically office electronic platforms and IT solutionsPhysical Requirements / Work EnvironmentAdhere to OHS policies and procedures and ensure safe and healthy workplace environment.Thermo Fisher Scientific is an Equal Opportunity Employer. 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.Join us!
