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) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)Job DescriptionAt 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.Position SummaryWe 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.Key ResponsibilitiesSupervise and coordinate daily sterile manufacturing operationsEnsure compliance with cGMP, FDA, and company quality standardsMonitor production performance and maintain adherence to schedulesReview batch records and ensure accurate documentationLead, coach, and develop manufacturing team membersSupport investigations, deviations, and corrective actionsPromote a strong culture of safety, quality, and continuous improvementCollaborate cross-functionally with Quality, Engineering, and other departmentsIdentify and implement process and operational improvementsEducationBachelor’s degree in Science, Engineering, Chemistry, Economics, Business or a related STEM field (preferred)Experience3+ years of experience in pharmaceutical or biotechnology manufacturing,2+ years of supervisory or leadership experience in a GMP-regulated environmentPreferred QualificationsStrong knowledge of cGMP regulations and FDA requirementsExperience with aseptic processing and cleanroom operationsFamiliarity with environmental monitoring and aseptic techniquesExperience with batch record review and manufacturing documentationKnowledge of Lean, Six Sigma, or other continuous improvement methodologiesStrong project management and organizational skillsAbility to manage multiple priorities in a fast-paced environmentExperience driving operational excellence and quality improvementsProficiency with Microsoft Office and manufacturing systemsExcellent written and verbal communication skillsStrong interpersonal skills and ability to work cross-functionally