Director, Pharmaceutical Commercialization Technology

MSD

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
Rahway, NJ
Salary
$173,200–$272,600 / yr
Posted
6 days ago
Freshness
Confirmed live yesterday
Closes
Oct 3, 2026

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $249k
This role $223k
$158k most similar roles pay here $315k

This role pays less than 70% of similar roles. Most pay $217,450–$280,500 — the shaded band above. At the midpoint, this role pays about $223k versus about $249k for comparable roles.

Based on 240 similar postings.

Employer

About MSD

MSD (Merck Sharp & Dohme) is the international name for Merck & Co., a major U.S.-based pharmaceutical company.

MSD currently has 35 open roles on FindRole.

Listed pay typically runs $117,000–$184,200 across 35 roles with salary data.

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View all roles at MSD

At a glance

TL;DR · Director, Pharmaceutical Commercialization Technology

As the Director, Pharmaceutical Commercialization Technology, you will lead a high-performing department of engineers and scientists within the Manufacturing Division. You will oversee the development of robust processes for small-molecule, solid-dosage drugs, bridging the gap between discovery and commercial launch. Your daily responsibilities include executing program strategies, managing control strategy development, overseeing experimental designs across scales, and performing data analysis to ensure reliable supply. You will manage core functions including clinical supply stewardship, safety teams, digital strategy, and capital projects while fostering a culture of continuous improvement. The role requires expertise in oral drug product formulation, process characterization, manufacturing scale-up, and technology transfer. Essential skills include Good Manufacturing Practices (GMP), regulatory submission authoring, and cross-functional leadership. You will navigate the complexities of pharmaceutical commercialization to ensure life-saving medicines reach patients through stable global supply chains.

What you'll do

  • Lead a department of 10 to 20 engineers and scientists to develop robust processes for small-molecule drugs.
  • Develop product portfolio strategies including control strategy development, experimental designs, and data analysis.
  • Drive operational excellence by translating high-level priorities into actionable steps and holding teams accountable.
  • Identify system gaps and lead continuous improvement initiatives across the organization.
  • Build and manage cross-functional partnerships with technical, quality, and manufacturing networks.
  • Mentor and develop a diverse workforce using a comprehensive employee development toolkit.
  • Oversee core functions including clinical supply stewardship, safety teams, digital strategy, and capital projects.
  • Manage programmatic strategies involving regulatory filings, site selection, technology transfer, and financial forecasting.

What we're looking for

  • Bachelor of Science with experience, Master of Science with , or Ph.D. with required.
  • Must possess deep technical expertise in oral drug product formulation and process development.
  • Proven track record in small molecule commercial process development, scale-up, and technology transfer to supply.
  • Experience in end-to-end drug product development from commercialization through to supply.
  • Experience authoring regulatory submissions and responding to regulatory questions.
  • Demonstrated ability in leading cross-functional teams and managing organizational change.
  • Excellent interpersonal, communication, and collaboration skills are required.
  • Proficiency in situational effectiveness and structuring communications for executive levels (preferred); Rahway, NJ location (preferred).

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