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At GSK, we unite science, technology, and talent to get ahead of disease together. Our goal is to improve the lives of billions across the world. By bringing together outstanding people in an inclusive environment, we can make an impact on a global scale. As a Production Manager (First Line Leader) at GSK, you’ll play a key role in ensuring the safe, efficient, and high-quality production of our products. You’ll collaborate with cross-functional teams, drive process improvements, and foster a culture of safety and continuous learning. We’re looking for someone who is passionate about leadership, thrives in a team-oriented environment, and is committed to delivering excellence every day.
Job Responsibility:
Schedule and execute site equipment, facilities and utilities in a qualified state
Develop strategies to meet requirements for the site master validation plan
Plan, organize and prioritize staffing as to manage to the site Master Validation Plan for equipment, facilities and utilities
Develop and execute documentation and protocols required to support all changes to do the installation of new equipment and manufacturing processes as well as any changes resulting from factory maintenance activities or interventions
Participate on the site Validation Governance Board in collaboration with other board members and stakeholders and set site wide strategies
Make fully informed decisions and provide compliance and technical solutions
Provide managerial oversight to the assigned team of Engineers to fully develop work potential, prepare for promotional opportunity and provide a sense of job satisfaction
Maintain a sold understanding of current FDA, Current Good Manufacturing Practices (cGMP), corporate guidelines, and industry best practices for this field and implement these standards daily
Responsible for on time compliance records of project engineering department
Manage department budget and support departmental, plant, and corporate goals
Manage vendors and consultants to ensure that contracts contain appropriate technical specifications are delivered as required
Provide technical expertise during regulatory audits
Participate in site Operational Excellence initiatives and author, review, revise, or approve Standard Operating Procedures (SOP’s) as required
Provide technical support for utility systems including purified water systems, compressed air systems, chilled water systems and steam systems
Requirements:
Associate degree in a science or engineering related discipline or 10+ years plus experience in an equivalent lead role such as Production or Maintenance Lead, etc.
3+ years of experience of pharmaceutical processes, systems, equipment and applicable government regulations
2+ years of leadership experience in a manufacturing environment.
Nice to have:
Bachelor’s degree in mechanical or chemical engineering
Excellent knowledge of cGMPs
Strong written and oral communication skills
Proficient in equipment troubleshooting
Good management skills
Technical expertise in P&ID nomenclature, instrumentation and electrical wiring diagrams
Proficient in SAP (work orders, history, maintenance plans)
Good knowledge of cGMPs, and experience in an FDA regulated environment
Excellent written and oral communication skills
Experience working in a highly regulated Good Manufacturing Practices (GMP) environment
Experience leading facility equipment programs and leading maintenance teams
Leadership experience in coaching and collaborative working