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You will provide quality oversight on the manufacturing floor to help ensure safe, compliant and timely supply. You will work with production, engineering, laboratory and quality colleagues to detect and resolve quality issues in real time. We value clear communication, practical problem solving and a commitment to high standards. This role offers hands-on learning, visible impact, and strong potential to grow your career while helping GSK unite science, technology and talent to get ahead of disease together.
Job Responsibility:
Perform in-process checks during manufacturing, filling and packaging to ensure procedures and specifications are followed
Perform review of batch documents for manufacturing, filling and packaging and laboratory
Assist in review and compilation of batch documentation to support timely and compliant product release
Support investigations into deviations, incidents and customer complaints and help implement corrective and preventive actions
Maintain oversight of retained samples, batch records and traceability in line with site policies
Coach production teams on good manufacturing practice and promote continuous improvement
Participate in internal audits, validations and quality risk assessments as required
Ensure that products are manufactured and released in accordance with GSK QMS, Local Regulatory and EHS requirements
Ensure the management of facilities/equipment condition assessments for GMP/GDP processes, facilities, and equipment to confirm that activities that may have a product quality impact
Requirements:
Bachelor’s or Master’s in any discipline with relevant experience
Minimum of 2 – 3 years’ experience in pharmaceutical manufacturing, production operations or quality assurance
Practical knowledge of Good Manufacturing Practice (GMP) and quality systems
Strong attention to detail and analytical skills
Good communication and teamwork skills in English
This role is on-site at a manufacturing facility in Pakistan and may require shift work
Knowledge in investigations, root cause analysis and CAPA implementation
Familiarity with quality management systems, data integrity and batch review and release processes
Exposure to internal audits, validation activities or regulatory inspections
Training in Lean, Six Sigma or continuous improvement methods
Prior experience coaching production teams or leading operational quality activities