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Project Manager

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GSK

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Location:
United States , Zebulon, North Carolina

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Category:
Manufacturing

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Contract Type:
Not provided

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Salary:

Not provided
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Job Description:

You will support the delivery of capital projects within the SE Capital Project Team involving large / high complexity facilities and/or production equipment or systems, ensuring that all outcomes meet the defined project objectives for cost, schedule, quality, and safety, while delivering the intended business benefits

Job Responsibility:

  • Plan and manage the site's most complex CapEx projects, leveraging extensive experience in successfully implementing equipment and facility changes within a GMP environment, and adherence to the GSK Project Management Framework (PMF)
  • Effectively resolving issues that have a potential to hinder the progress of project completion
  • Provide leadership and expertise on the PMF, ensuring the site's compliance with relevant standards and enhancing site capability through targeted training and coaching, while supporting gap closure as needed
  • Provide leadership and coaching to project engineers within the team, or other functional groups helping to develop project management capabilities
  • Provide leadership to the assigned functional areas working closely with area directors and personnel to develop robust multi-year investment plans as required by the GSK Facility Investment Process
  • Support area capital delivery versus budget and review/support area investments and performance against PMF compliance
  • Plan and develop a robust technical project scope or solution, manage and drive project team accountability, oversee project costs and schedules, mitigate risks, and monitor / control the project according to the GSK PMF
  • Ensure projects are delivered within the approved budget, on schedule, and to the defined scope while maintaining high standards of safety and quality
  • Anticipate risks to achieving critical milestones and establish effective contingency plans to maximize success against objectives
  • Coordinate and meticulously plan and control all elements of the project schedule, ensuring timely and effective project delivery
  • Provide continuous improvement (CI) and process confirmation around controls being in-place and in-use
  • Ensure that project design and delivery comply with all relevant EHS, engineering, and quality procedures/standards, leveraging the expertise of SMEs to confirm compliance throughout the project lifecycle
  • Develop a comprehensive construction plan with appropriate permits and risk assessments, ensuring safe execution and performing routine safety and quality confirmations with other experts
  • Serve as a clear example of best practice to other engineers in terms of safety
  • Ensure clear and effective communication across all organizational levels, covering all aspects of projects and the strategy for the assigned functional area
  • Interface and partner with the wider GSK engineering community, Centers of Excellence and other sites to contribute, share and leverage best practice project management as appropriate
  • Promote the following behaviors: display exemplary leadership, strategic vision, effective communication, proactive problem-solving, and a strong commitment to fostering teamwork and continuous improvement

Requirements:

  • Bachelor’s degree in engineering, science, project management, business or a related field
  • 15+ years’ experience delivering capital or operational projects in manufacturing or regulated environments
  • Technical experience with both GMP production Equipment and Facility/Utility systems
  • Experience with cGMP’s and FDA requirements
  • Experience working across multi-disciplinary teams and external partners
  • Knowledge of Pharmaceutical operational processes preferred
  • Experience with project tools and Microsoft Office
  • Experience with ERP or scheduling tools is desirable
  • Operational Excellence/GPS experience

Nice to have:

  • Master's degree in an Engineering discipline
  • Project management certification such as PMP or equivalent
  • Experience in pharmaceutical, biotech, or other regulated manufacturing environments
  • Experience with commissioning, qualification or operational handover activities
  • Hands-on use of cost forecasting, change control and risk register management
  • Experience leading matrixed teams and influencing senior stakeholders
  • Comfortable using digital tools for planning, reporting and collaboration
  • Understanding of drug development process
  • Strong communicator with experience working across multi-disciplinary teams and external partners
  • Demonstrate analytical reasoning and technical aptitude
  • Demonstrated commitment to safety, quality and ethical decision making
  • The ability to plan effectively to deliver sustainable complex CapEx projects
  • Ability to work fully independently
  • Excellent interpersonal skills, including the ability to work across the organization and interact/influence/negotiate effectively at all levels of management and peers
  • Ability to work well under pressure with tight timelines
  • Excellent consultative, listening, communications and analytical skills
  • Must be flexible, adaptable and a team player
  • Negotiation and conflict resolutions skills and ability to motivate highly skilled and trained individuals
  • High energy level, pro-active self-starter
  • Excellent written and oral communication skills
  • Professional Project Management certification preferred
  • GPS Level / Problem Solvent certifications desirable
What we offer:
  • Competitive base salary
  • Annual bonus based on company performance
  • Flexible working options available for most roles
  • Learning and career development
  • Access to healthcare & wellbeing programmes
  • Employee recognition programmes

Additional Information:

Job Posted:
February 17, 2026

Employment Type:
Fulltime
Work Type:
Hybrid work
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