Sr. Specialist, Compliance/Engineering - Oral Solid Dosage (Onsite)

MSD

Remote

Quick summary

Work type
Remote
Location
Rahway, NJ
Salary
$117,000–$184,200 / yr
Posted
14 days ago

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $170k
This role $151k
$107k most similar roles pay here $210k

This role pays less than 68% of similar roles. Most pay $140,850–$200,096 — the shaded band above. At the midpoint, this role pays about $151k versus about $170k 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 17 open roles on FindRole.

Listed pay typically runs $117,000–$184,200 across 16 roles with salary data.

Most-posted roles

View all roles at MSD

At a glance

TL;DR · Sr. Specialist, Compliance/Engineering - Oral Solid Dosage (Onsite)

The Senior Engineer (2nd Shift) in the Research Labs at Company's Pharm Ops Engineering team supports non-sterile process equipment and utilities for oral solid dosage (OSD) product manufacturing across clinical, developmental, and commercial programs. This role involves providing independent engineering support during second-shift operations with minimal supervision, troubleshooting mechanical, electrical, and automation systems, and ensuring compliance with GMP requirements. Key responsibilities include developing shift-change notes, reviewing technical documentation to resolve issues, supporting deviation response and investigations, and maintaining GMP documentation. The ideal candidate has a Bachelor’s degree in engineering and at least 5 years of experience in pharmaceutical manufacturing operations, along with expertise in CMMS/CCMS platforms and validation tools like Kneat. Strong analytical skills, adaptability, and proficiency in quality engineering are essential for this role within the highly regulated environment of OSD product manufacturing.

What you'll do

  • Independently provide engineering support for OSD process equipment during second shift.
  • Develop and deliver shift-change notes to ensure continuity with the first shift team.
  • Diagnose and resolve technical issues by reviewing relevant documentation and collaborating with cross-functional teams.
  • Support routine manufacturing activities, deviation responses, and investigations using engineering principles and OSD knowledge.
  • Author and maintain GMP documentation for equipment qualification and compliance.

What we're looking for

  • Bachelor’s degree in engineering with 5+ years of experience in pharmaceutical manufacturing operations for OSD formats.
  • Demonstrated commissioning and qualification experience supporting GMP manufacturing equipment in regulated environments.
  • Hands-on familiarity with OSD process equipment, including granulation, milling, blending, drying, tablet compression, coating, and encapsulation.
  • Strong technical troubleshooting capability across mechanical, electrical, and automation systems.
  • Experience performing root cause analysis and supporting technical investigations in a manufacturing environment.
  • Proficient with CMMS/CCMS platforms and validation documentation tools like Kneat.

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