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The Production Supervisor will apply GSK Values and Expectations when managing and supporting daily tasks with a positive, team-oriented approach. Off-shift hours, including nights, may be required.
Job Responsibility:
Supervises Manufacturing Associates in operating cell culture equipment, preparing media and buffers, running chromatographic and filtration processes, and handling administrative duties
Oversees production, technology transfers (for NPI facility), and ensures training and ongoing development of staff
Leads or assists in investigations and resolutions alongside quality assurance and cross-functional teams
Acts as a departmental leader for process optimization, production scheduling, continuous improvement, and collaboration
Perform production activities alongside Manufacturing Associates and manage absences and timesheets as needed
Carry out responsibilities in compliance with Data Integrity principles, site SOPs, GSK EHS standards, and relevant legal requirements
Oversee and review documentation to confirm that the preparation of bulk biopharmaceutical intermediates meets cGMP, GSK, and other regulatory agency standards
Attend daily meetings, or assign a delegate, to discuss and adjust the production schedule as necessary
Support the implementation of new products and processes into the facility, including equipment and area changeovers
Maintain competency with current and emerging digital platforms (SAP, EBR, DeltaV, RTMS, etc.)
Develop expertise in their designated area by participating in area tours, supporting inspections, addressing technical issues, and managing deliverables
Assign work to Manufacturing Associates to meet production schedules, use resources efficiently, and achieve product delivery targets
Document Manufacturing Associate development and performance management activities
Collaborate with cross-functional teams to support safe and high-quality results
Adhere to Leader Standard Work to maintain consistent visibility within the manufacturing area
Requirements:
BS/BA or Associates Degree with 5 or more years of directly related experience
5+ years of direct experience within the pharmaceutical or biotechnology sector OR 2+ years of supervisory experience in a manufacturing environment
Experience in production areas such as cell culture, buffer preparation, media preparation, or purification
Nice to have:
Proven skill in resolving complex technical issues
Experience in using control systems for operating processes in modern large-scale biopharmaceutical plants
Verbal and written communication skills with an emphasis on teamwork and quality orientation
Ability to work effectively in a team environment and to lead and motivate individuals from diverse backgrounds
Proven commitment to quality and compliance
Strong leadership, interpersonal, and relationship-building abilities with a focus on teamwork
Effective communicator across shifts, departments, and functions, aligned with GSK Values
Thorough knowledge of production systems and their application