ppSupervisor, PDS Sterile Manufacturing /p /brpAzienda : Thermo Fisher Scientific Inc. Tipo Lavoro : Tempo pieno Italy /p /brpbWork Schedule /b /p /brpStandard (Mon-Fri) /p /brpbEnvironmental Conditions /b /p /brpAdherence 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) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) /p /brpbJob Description /b /p /brpAt Thermo Fisher Scientific, you’ll do meaningful work that makes a positive impact on a global scale. Join our team and help bring our Mission to life every day—enabling our customers to make the world healthier, cleaner, and safer. We empower our employees with the resources and opportunities to achieve their career goals while developing innovative solutions to some of the world’s toughest challenges, from protecting the environment to ensuring food safety and supporting the search for cancer treatments. /p /brh3Position Summary /h3 /brpWe are seeking a PDS Sterile Manufacturing Supervisor to join our manufacturing operations team. In this role, you will lead and support production teams involved in sterile pharmaceutical manufacturing, ensuring operational excellence, product quality, and full compliance with cGMP standards and FDA regulations. This position combines strong technical expertise with people leadership. You will coordinate production activities, oversee manufacturing processes, and drive continuous improvement initiatives while fostering a culture of safety, quality, and accountability.

/p /brh3Key Responsibilities /h3 /brul /brliSupervise and coordinate daily sterile manufacturing operations /li /brliEnsure compliance with cGMP, FDA, and company quality standards /li /brliMonitor production performance and maintain adherence to schedules /li /brliReview batch records and ensure accurate documentation /li /brliLead, coach, and develop manufacturing team members /li /brliSupport investigations, deviations, and corrective actions /li /brliPromote a strong culture of safety, quality, and continuous improvement /li /brliCollaborate cross-functionally with Quality, Engineering, and other departments /li /brliIdentify and implement process and operational improvements /li /br /ul /brh3Education /h3 /brul /brliBachelor’s degree in Science, Engineering, Chemistry, Economics, Business or a related STEM field (preferred) /li /br /ul /brh3Experience /h3 /brul /brli3+ years of experience in pharmaceutical or biotechnology manufacturing, /li /brli2+ years of supervisory or leadership experience in a GMP-regulated environment /li /br /ul /brh3Preferred Qualifications /h3 /brul /brliStrong knowledge of cGMP regulations and FDA requirements /li /brliExperience with aseptic processing and cleanroom operations /li /brliFamiliarity with environmental monitoring and aseptic techniques /li /brliExperience with batch record review and manufacturing documentation /li /brliKnowledge of Lean, Six Sigma, or other continuous improvement methodologies /li /brliStrong project management and organizational skills /li /brliAbility to manage multiple priorities in a fast-paced environment /li /brliExperience driving operational excellence and quality improvements /li /brliProficiency with Microsoft Office and manufacturing systems /li /brliExcellent written and verbal communication skills /li /brliStrong interpersonal skills and ability to work cross-functionally /li /br /ul /p #J-18808-Ljbffr

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