Manufacturing Cell Processing Supervisor

Manufacturing Cell Processing SupervisorLocation: Winston-Salem, NCSchedule: Monday-Friday 8am-5pmSalary Range: $100,000-$110,000/year plus bonus potentialPosition Overview:The Manufacturing Cell Processing Supervisor is responsible for leading day-to-day operations on the manufacturing floor, ensuring that all production activities are conducted safely, compliantly, and efficiently in a regulated, aseptic environment. This role supervises personnel, supports GMP documentation, coordinates with cross-functional teams, and contributes to continuous process improvements.Key Responsibilities:Supervision & Team Leadership:Provide direct supervision and task assignments to manufacturing staff, maintaining active presence during critical processing steps.Mentor, coach, and train team members to build technical and professional competencies.Conduct regular one-on-one meetings, performance evaluations, and career development discussions.Support hiring, onboarding, training compliance, and performance management of the team.Maintain individual training plans and ensure team readiness through up-to-date training records.Production Oversight:Ensure all documentation is complete and accurate at the end of each shift.Manage daily production schedules and team assignments.Support technology transfer from development into manufacturing.Monitor and adjust production workflows to meet operational goals.Coordinate raw material inventory with supply chain to meet production demand.Perform aseptic manufacturing in controlled environments following cGMP standards.Execute ERP system transactions, including material requests, production tracking, and BOM updates.Communicate issues and observations across departments to ensure resolution.Quality, Safety & Compliance:Review and approve GMP documentation such as batch records, deviations, change controls, and logbooks.Enforce safety protocols and maintain a safe working environment for all personnel.Ensure strict compliance with FDA, EMA, and internal regulatory standards.Maintain audit readiness and represent manufacturing during audits and cross-functional meetings.Lead deviation investigations and support authoring of SOPs and technical documentation.Drive inspection readiness and support timely release of batches through accurate documentation review.Operational Excellence:Lead shift transitions, assign daily duties, attend meetings, and communicate production updates.Support process improvements and continuous improvement projects.Troubleshoot operational issues and lead resolution efforts in collaboration with other departments.Adapt plans to meet changing priorities and resource needs.Collaborate with senior management and demonstrate clear, concise communication.Qualifications:Minimum 4 years’ experience in manufacturing (6+ years without a degree); prior supervisory experience required.AAS or BS degree preferred.Strong knowledge of GMP and regulatory requirements (FDA, EMA), including biologics and cell/gene therapy operations.Skilled in aseptic techniques, environmental controls, cleanroom operations, and technical writing.Proficiency in ERP systems and document control software.Excellent organizational, time management, and problem-solving skills.Experience with statistical methods, auditing techniques, and deviation management.Ability to work cross-functionally and adapt in a fast-paced, regulated environment.Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. #J-18808-Ljbffr