Director Principal Scientist, Biologics Drug Substance Commercialization

MSD

Confirmed live 2 days ago High trust
Closes in 5 days Remote

Quick summary

Work type
Remote
Location
West Point, PA
Salary
$173,200–$272,600 / yr
Posted
9 days ago
Freshness
Confirmed live 2 days ago
Closes
Sep 16, 2026 (soon)

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $221k
This role $223k
$156k most similar roles pay here $285k

This role pays less than 52% of similar roles. Most pay $177,250–$264,000 — the shaded band above. At the midpoint, this role pays about $223k versus about $221k 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 15 open roles on FindRole.

Listed pay typically runs $117,000–$184,200 across 15 roles with salary data.

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At a glance

TL;DR · Director Principal Scientist, Biologics Drug Substance Commercialization

Director/Principal Scientist, Biologics Drug Substance Commercialization joins the Manufacturing Division’s Biologics Drug Substance Commercialization team to lead late-stage and commercial biologics programs. This senior leadership role focuses on upstream cell culture, where the individual will oversee a team of scientists to drive process development, characterization, and validation activities essential for licensure and manufacturing. The candidate will manage technology transfers to internal and external sites, author regulatory documentation, and oversee scale-up efforts for complex modalities like multi-specific antibody therapeutics. Key technical requirements include expertise in cell culture process development, cGMPs, and analytical methods, alongside skills in lean leadership and operational excellence. The role solves critical manufacturing challenges by ensuring robust process characterization and seamless transition from clinical stages to commercial supply while fostering innovation within the upstream drug substance production environment.

What you'll do

  • Lead upstream drug substance teams to support late-stage clinical and commercial biologics programs.
  • Provide technical leadership for laboratory and manufacturing scale studies including process characterization and validation.
  • Manage technology transfer activities to internal and external manufacturing sites, including scale-up and readiness.
  • Author and review technical and regulatory documentation for submissions such as BLA sections.
  • Drive division-wide initiatives regarding manufacturing strategy, capability needs, and platform evolution.
  • Lead, coach, and mentor a team of upstream scientists to foster professional growth and scientific rigor.
  • Oversee resource planning, staffing strategies, and the development of a talent pipeline for future leaders.

What we're looking for

  • Must hold a BS, MS, or PhD in Chemical Engineering, Biological Engineering, Biochemical Engineering, or a related discipline.
  • Requires 16+ years of experience for a BS, 12+ years for an MS, or 8+ years for a PhD.
  • Must possess deep technical expertise in cell culture process development and biologics commercialization.
  • Must have proven experience supporting late-stage development and/or commercial manufacturing of biologics.
  • Must demonstrate the ability to lead, coach, and mentor a team of scientists.
  • Preferred experience includes hands-on work with technology transfer, scale-up, and validation of biologics processes.
  • Preferred experience includes working with multi-specific antibody therapeutics and complex antibody formats.
  • Preferred experience includes authoring regulatory submission content and knowledge of cGMPs and U.S./EU regulatory expectations.

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