API Operations Director: Ramp-Up & Excellence

Merck

Elkton (VA)

On-site

USD 173,000 - 273,000

Full time

9 days ago
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Benefits offered by this job

Annual bonus
Long-term incentive
Medical/dental/vision benefits
401(k) plan

Job summary

Merck is seeking a Director, IPT Leader for API at Elkton, VA to shape the future operating model and drive site readiness for a growing small molecule facility. You will lead strategic planning, cross-functional coordination, and a high-performing IPT to ensure safety, quality, and on-time delivery.

The role requires 10+ years in regulated manufacturing with strong cGMP knowledge, Lean Six Sigma, and financial stewardship.

Qualifications

  • Bachelor’s degree or higher in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Engineering, or related discipline.
  • Demonstrated experience in pharmaceutical or regulated manufacturing environments.
  • 10+ years of relevant experience with leadership experience across Manufacturing/Engineering/Quality/Operations.
  • Strong knowledge of cGMP, quality systems, regulatory readiness and safety practices.

Responsibilities

  • Lead Site Leadership Team to align IPT priorities with site and company strategy.
  • Develop future-state operating model for API operations at Elkton, VA.
  • Oversee site ramp-up, startup readiness, and cross-functional coordination.
  • Drive safe, compliant, reliable API operations and delivery performance.
  • Champion lean thinking and continuous improvement for flow and right-first-time performance.
  • Manage budget planning, financial stewardship, and resource allocation.

Skills

Adaptability
API Manufacturing
Biopharma Industry
Lean Six Sigma
Project Leadership
Regulatory Compliance
Data Analysis
Decision Making
Financial Budgeting
Manufacturing Planning

Education

Bachelor’s degree in relevant field

Tools

Lean Six Sigma Certification

Job description

Merck is seeking a Director, IPT Leader for API at Elkton, VA to shape the future operating model and drive site readiness for a growing small molecule facility. You will lead strategic planning, cross-functional coordination, and a high-performing IPT to ensure safety, quality, and on-time delivery.

The role requires 10+ years in regulated manufacturing with strong cGMP knowledge, Lean Six Sigma, and financial stewardship.

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