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An established industry player is seeking a dedicated professional to supervise and optimize production processes. This role involves coordinating production schedules, leading quality investigations, and ensuring compliance with safety and GMP regulations. You will contribute to enhancing operational efficiency and participate in exciting capital projects. Join a forward-thinking company committed to uniting science and technology to improve health outcomes globally, where your contributions will make a significant impact. This is a fantastic opportunity for growth in a supportive environment that values innovation and teamwork.
To supervise, execute, and monitor activities within the value stream to ensure reliable and optimal operation of processes, equipment, utilities, and facilities, aiming to achieve target production levels while complying with current Good Manufacturing Practice (cGMP), quality, safety, occupational hygiene, and environmental protection standards.
GSK is a global biopharma company committed to uniting science, technology, and talent to combat disease, impacting the health of billions and fostering a thriving workplace where people can grow, innovate, and feel valued. We focus on vaccines, medicines, and research in infectious diseases, HIV, respiratory/immunology, and oncology.
If you share our ambition to make a difference, join us at this exciting moment in our journey to get Ahead Together.
GSK does not accept referrals from employment agencies without prior written authorization. All agencies must contact GSK's HR department for approval before referring candidates. Unauthorized actions will be considered without GSK's consent, and GSK will not be liable for fees arising from such referrals.