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Merck

Makes medicines, vaccines and animal treatments

Director – Operations

Manufacturing & Production OperationsConfirmed live in the last 24 hours
Full-timeElkton, VA, USA

About the Job

Requirements

  • A bachelor's degree is required; Chemistry, Chemical Engineering, Pharmaceutical Sciences, Engineering, or a related scientific or technical discipline is preferred.
  • At least 10 years of relevant experience in pharmaceutical or other regulated manufacturing environments.
  • Leadership experience in Manufacturing, Technical Operations, Quality Operations, Engineering, and/or Production Planning.
  • Experience leading teams with direct and indirect reports.
  • Strong knowledge of current Good Manufacturing Practice (cGMP), quality systems, regulatory readiness, and safety and environmental practices.
  • Demonstrated experience with operational planning, project leadership, or site ramp-up/start-up activities.
  • Proven ability to lead in complex environments and manage multiple priorities across functions.
  • Strong business acumen and experience with financial stewardship and resource planning.
  • Experience applying Lean Six Sigma, continuous improvement, and structured problem-solving tools.
  • Master’s degree in Science, Engineering, Business, or a related discipline is preferred.
  • Experience in small molecule active pharmaceutical ingredient (API) manufacturing or commercial pharmaceutical operations is preferred.
  • Prior experience supporting a manufacturing site start-up, transformation, or ramp-up is preferred.
  • Experience developing future-state operating models, organizational structures, or operational governance systems is preferred.
  • Lean Six Sigma certification or deep practical application of Lean tools is preferred.
  • Experience in a highly matrixed global manufacturing environment is preferred.
  • Demonstrated success in talent development, employee engagement, and succession planning is preferred.
  • Experience with capacity planning, capital planning, supply planning, and sales and operations planning (S&OP) is preferred.
  • Familiarity with inspection readiness, deviation management, and broader quality systems in a regulated environment is preferred.

Responsibilities

  • Serve as a member of the Site Leadership Team and help align Integrated Process Team (IPT) priorities with site and company strategy.
  • Provide direction to establish tactical and strategic plans that support active pharmaceutical ingredient (API) ramp-up and long-term operational success.
  • Partner across the site and with above-site teams to ensure strong coordination, decision-making, and execution.
  • Represent the IPT and the site as needed with internal stakeholders and external partners.
  • Lead the development of the future-state operating model for API operations at Elkton, Virginia.
  • Support site start-up, ramp-up, and operational readiness activities through project leadership and cross-functional coordination.
  • Help define organizational structure, organizational culture, operating rhythms, governance, and capability needs for the evolving site.
  • Ensure readiness plans, risk assessments, and implementation plans are developed and executed effectively.
  • Ensure safe, compliant, reliable, and right-first-time API operations in support of production and supply objectives.
  • Lead operational reviews and daily management routines to maintain visibility into performance, issues, and priorities.
  • Drive structured problem solving and use performance metrics to identify trends, action plans, and opportunities for improvement.
  • Support production planning, resource deployment, and issue resolution to meet site objectives.
  • Promote lean thinking and continuous improvement to improve flow, throughput, right-first-time performance, and operational stability.
  • Support and/or own budget planning and financial stewardship for the IPT, including operating and capital spend.
  • Partner with site leadership to identify opportunities for productivity, efficiency, and cost improvement.
  • Ensure resources are allocated effectively to support current and future business needs.
  • Promote a strong quality culture and support a state of permanent inspection readiness.
  • Ensure cGMP compliance and effective management of deviations, investigations, and corrective actions.
  • Partner with Quality, EHS, Engineering, Technical, and Supply Chain teams to support site priorities and maintain strong compliance standards.
  • Ensure appropriate training, documentation, and change management practices are in place to support safe and compliant operations.
  • Champion a strong safety culture and support risk management activities across the IPT.
  • Lead, coach, and develop a team of leaders and contributors to build a high-performing organization.
  • Foster a culture of accountability, collaboration, empowerment, and continuous learning.
  • Support talent development, succession planning, and ongoing skill-building within the IPT.
  • Communicate clearly and regularly to align the team around priorities, expectations, and performance.

About the Company

Merck

Makes medicines, vaccines and animal treatments

Merck develops prescription medicines, vaccines and veterinary treatments for patients, health systems and animal owners worldwide. Its vaccine portfolio includes Gardasil 9, which helps prevent cancers and other diseases caused by several types of human papillomavirus. The company takes potential treatments through laboratory research and clinical trials, then manufactures and sells approved products to drug distributors, hospitals, physicians and governments. Its animal health division sells medicines and vaccines to veterinarians, farmers and pet owners, while selected drug partnerships also earn shared profits or royalties. Founded in 1891, Merck is headquartered in Rahway, New Jersey.

Company size
10,001+
Company stage
IPO
Headquarters
Rahway, NJ
Founded
1891

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