Senior Specialist, Engineering

MSD

Confirmed live today High trust

Quick summary

Work type
On-site
Location
Rahway, NJ
Salary
$117,000–$184,200 / yr
Posted
5 days ago
Freshness
Confirmed live today
Closes
Sep 23, 2026

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $164k
This role $151k
$107k most similar roles pay here $214k

This role pays less than 58% of similar roles. Most pay $124,700–$203,300 — the shaded band above. At the midpoint, this role pays about $151k versus about $164k 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 24 open roles on FindRole.

Listed pay typically runs $117,000–$184,200 across 24 roles with salary data.

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At a glance

TL;DR · Senior Specialist, Engineering

Sr. Specialist, Engineering (Onsite) serves as a key member of the FLEx Sterile expansion project team within the Formulation, Laboratory, and Experimentation center. This role focuses on operational readiness for a new aseptic drug product filling facility, where the individual will lead workstreams involving equipment and facility design, system commissioning, and qualification. Day-to-day responsibilities include operating state-of-the-art formulation, filling, and lyophilization equipment, performing aseptic manipulations in Grade A barrier systems, and developing SOPs, batch records, and training curricula. The candidate must possess expertise in sterile drug manufacturing, GxP documentation, and risk assessments. Required technical skills include proficiency with robotics, automated systems, and data tools such as MS Access, Excel, Minitab, Power BI, and R Shiny. This role addresses the critical challenge of scaling production capacity for a diverse clinical pipeline including small molecules, biologics, vaccines, and antibody-drug conjugates.

What you'll do

  • Lead operational readiness workstreams including equipment design, system commissioning, and qualification for the facility expansion project.
  • Operate state-of-the-art aseptic drug product formulation, filling, and lyophilization equipment during the manufacturing cycle.
  • Perform manual and automated operations, general maintenance, and troubleshooting of complex machinery and robotics.
  • Develop and maintain SOPs, work instructions, batch records, and training curricula to ensure compliant go-live readiness.
  • Lead the planning and execution of digital tools for production process insights and predictive analytics.
  • Conduct dry runs, simulations, and readiness assessments to prepare personnel and processes for GMP manufacturing.
  • Identify and resolve compliance, environmental, safety, and process deviations while notifying appropriate personnel.

What we're looking for

  • Bachelor's degree in Engineering, Science, Operations Management, or equivalent with at least 5 years of relevant experience.
  • Master's degree with a minimum of 3 years of relevant experience.
  • Experience in sterile drug product manufacturing, aseptic technique, and GMP/clinical supply operations.
  • Ability to operate, set up, adjust, and troubleshoot complex equipment including robotics and automated systems.
  • Proficiency in preparing GxP documents, SOPs, and supporting investigations, change management, and Commissioning/Qualification/Validation.
  • Proficiency with data analysis tools such as MS Access, Excel, Minitab, Power BI, and R Shiny.
  • Experience in new GMP facility startup and knowledge of Lean principles.
  • Automation, Continuous Improvement, and Process Engineering (preferred).

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