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Merck

Makes medicines, vaccines and animal treatments

Operations Specialist - Project Management

Project ManagementPosted on Nov 9
Full-timeDurham, NC, USA

About the Job

Requirements

  • A bachelor's degree in Engineering, Science, Business, Project Management, or a related field is required.
  • A minimum of two years of relevant experience in manufacturing, operations, quality, engineering, project management, or a related regulated environment is required.
  • Demonstrated written and verbal communication skills are required, including the ability to create clear technical or business documentation.
  • The role requires the ability to work independently, manage competing priorities, and escalate issues with clear recommendations.
  • The role requires project coordination, organization, facilitation, and action tracking; basic schedule, risk, and dependency management; attention to detail and commitment to data integrity; and the ability to collaborate across functions, ask questions, and escalate concerns appropriately.
  • Adaptability, learning agility, and a continuous-improvement mindset are required.

Responsibilities

  • Support Pre-Approval Inspection and filing-readiness plans by tracking deliverables, owners, due dates, dependencies, and open actions.
  • Update readiness trackers and dashboards so milestones, risks, gaps, and recovery actions are visible and current.
  • Coordinate meetings, prepare materials, document decisions, and follow up with owners on assigned actions.
  • Help organize inspection evidence, procedures, training records, and filing-related documents for review by subject matter experts.
  • Raise schedule, documentation, or compliance concerns promptly to the project manager or workstream lead.
  • Maintain project and portfolio records, including project status, priorities, milestones, risks, resource needs, and dependencies.
  • Support project intake and portfolio review activities by gathering information and preparing standard summaries.
  • Prepare status reports and dashboards using approved templates and data sources.
  • Assist project leads with charters, action logs, risk registers, and project closeout documentation.
  • Promote accurate, timely updates across project tools and reporting routines.
  • Coordinate Change Review Board logistics, including agenda preparation, intake tracking, meeting materials, minutes, and action follow-up.
  • Gather required information from cross-functional partners to support assessment of proposed changes.
  • Document decisions, conditions, owners, and due dates clearly and accurately.
  • Track changes and open actions through implementation and closure; escalate overdue or blocked items.
  • Support updates to Change Review Board templates, metrics, and standard work.
  • Author and coordinate incident and deviation records in partnership with Operations, Quality, Engineering, Technical Operations, and other subject matter experts.
  • Build clear, fact-based event narratives and support problem definition, impact assessment, root-cause analysis, corrective and preventive actions, and on-time record progression.
  • Facilitate investigation working sessions, track information requests and approvals, and maintain visibility to investigation milestones and potential delays.
  • Apply technical writing practices to ensure records are concise, accurate, traceable, and aligned with applicable procedures and current Good Manufacturing Practice expectations.
  • Develop and maintain integrated project schedules that include activities, logic, dependencies, milestones, critical paths, constraints, and resource assumptions.
  • Partner with workstream leads to update progress, evaluate schedule impacts, identify recovery options, and communicate forecast changes.
  • Produce routine schedule and milestone reporting for project teams and governance forums, emphasizing exceptions and decisions required.
  • Support continuous-improvement initiatives that strengthen planning, governance, cycle time, right-first-time performance, and execution reliability.
  • Participate in site tier processes, gemba walks, readiness reviews, and other operational routines as assigned.
  • Provide periodic off-shift or weekend support as required by business needs, inspection-readiness activities, incident response, or project milestones.
  • Travel up to 10% based on business needs.

Desired Qualifications

  • Experience working in pharmaceutical, biologics, vaccine, medical device, or other regulated manufacturing environments.
  • Familiarity with inspection readiness, regulatory filings, change control, deviations, investigations, or corrective and preventive actions.
  • Experience with Microsoft Project or similar planning and tracking tools.
  • Basic knowledge of current Good Manufacturing Practice, root-cause analysis, Failure Mode and Effects Analysis, Lean, or Six Sigma methodologies.
  • Lean Six Sigma certification or comparable project management or continuous-improvement training.

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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