Supervisor, pds sterile manufacturing

This job is with Thermo Fisher Scientific, an inclusive employer and a member of my Gwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.Work Schedule Standard (Mon-Fri)Environmental Conditions Adherence 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 DescriptionAtThermo 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 aPDS Sterile Manufacturing Supervisorto 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 c GMP 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 c GMP, 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+ yearsof experience in pharmaceutical or biotechnology manufacturing,2+ yearsof supervisory or leadership experience in a GMP-regulated environmentPreferred QualificationsStrong knowledge ofc GMP regulationsandFDA requirementsExperience withaseptic processingandcleanroom operationsFamiliarity withenvironmental monitoringand aseptic techniquesExperience withbatch record reviewand manufacturing documentationKnowledge ofLean, 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