Associate Director, Process/Facility Engineering

MSD

Remote

Quick summary

Work type
Remote
Location
Rahway, NJ
Salary
$142,400–$224,100 / yr
Posted
2 days ago
Closes
Jul 11, 2026
Nearby
99+ roles within 25 mi

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $189k
This role $183k
$132k most similar roles pay here $240k

This role pays less than 52% of similar roles. Most pay $148,500–$229,750 — the shaded band above. At the midpoint, this role pays about $183k versus about $189k for comparable roles.

Based on 239 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 25 open roles on FindRole.

Listed pay typically runs $142,400–$224,100 across 25 roles with salary data.

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View all roles at MSD

At a glance

TL;DR · Associate Director, Process/Facility Engineering

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The Associate Director – Process/Facility Engineering role at the Chemical Engineering Research & Development Department in Rahway, NJ involves leading technical and project management responsibilities for two potent development labs. This hands-on leadership position requires overseeing small teams to plan and execute shop floor operations, manage GMP processing, and drive strategic improvements. Key tasks include liaising with lab-based team members, executing batches, managing electronic batch records, and supporting compliance initiatives. The ideal candidate should have a background in chemical engineering or related fields, experience in small molecule drug substance development, and proficiency in preparing cGMP documents. Familiarity with potent compound processing, containment systems, and clean room operations is preferred. This role demands expertise in GMP regulations, electronic batch record systems, and process hazard analysis to ensure the quality and safety of clinical supplies while fostering a culture of innovation and collaboration.

Skills

GMP SOP cGMP Potent Compound processing Isolators Process utility systems Maintenance coordination Compliance investigations Change management Electronic batch record systems Clean room operations Equipment qualification US GMP regulations EU GMP regulations Safety compliance Process Hazard Analysis Level of Protection Analysis

What you'll do

  • Lead small teams in planning and executing shop floor operations for projects.
  • Manage operations specialists, including onboarding and technical growth oversight.
  • Oversee campaign planning and equipment utilization for GMP processing.
  • Review Process Descriptions and provide coaching to development teams.
  • Support process improvement initiatives and maintain consumables inventory.

What we're looking for

  • Bachelor’s degree in Chemical Engineering, Chemistry, Biology, Pharmaceutical Sciences or related field with 7+ years of relevant experience.
  • Experience in small molecule drug substance and biologics process development.
  • Ability to prepare Standard Operating Procedures (SOPs) and cGMP documents.
  • Technical mentorship and leadership skills for project teams and direct reports.
  • Hands-on execution and management of GMP processing and non-GMP development work.
  • Familiarity with US and EU GMP and Safety compliance regulations.

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