Associate Engineer - Commissioning, Qualification, Validation (CQV)

MSD

Confirmed live today High trust
Closes in 3 days

Quick summary

Work type
On-site
Location
Rahway, NJ
Salary
$71,900–$113,200 / yr
Posted
5 days ago
Freshness
Confirmed live today
Closes
Sep 17, 2026 (soon)

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $154k
This role $93k
$57k most similar roles pay here $209k

This role pays less than 98% of similar roles. Most pay $130,268–$177,900 — the shaded band above. At the midpoint, this role pays about $93k versus about $154k 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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View all roles at MSD

At a glance

TL;DR · Associate Engineer - Commissioning, Qualification, Validation (CQV)

The Associate Engineer - Commissioning, Qualification, Validation (CQV) provides engineering, commissioning, qualification, validation, and quality engineering support for the Rahway FLEx center. This role focuses on maintaining equipment, facilities, utilities, and computer systems to ensure compliance with cGMP and safety standards for non-sterile Oral Solid Dosage and Inhalation products. Daily responsibilities include troubleshooting mechanical, electrical, and automation issues; developing and executing CQV documentation such as validation protocols and master plans; and supporting capital projects. The role requires proficiency in Good Documentation Practices, root cause analysis, and risk assessments like FMEAs. Key technical skills include experience with CMMS, CCMS, and paperless electronic validation systems. Candidates should be familiar with pharmaceutical processing equipment, including tablet compression and spray drying, while utilizing tools for reliability maintenance to support manufacturing operations across various development and scale-up programs.

What does a Engineer earn?

Median $185000 from 256 postings across 54 companies.

See salary data

What you'll do

  • Provide engineering and quality support for facilities, utilities, and equipment to ensure compliance with GMP standards.
  • Troubleshoot mechanical, electrical, and automation issues while driving operational improvements.
  • Develop, author, execute, and maintain commissioning, qualification, and validation (CQV) documentation and protocols.
  • Perform decommissioning and periodic review activities for critical systems and manufacturing equipment.
  • Support the installation of new capital projects and facility improvements.
  • Maintain accurate GMP engineering drawings and equipment database tracking records.
  • Lead root cause analysis, CAPA development, and risk assessments like FMEA and PHA.
  • Support internal and external audits by providing timely responses to regulatory observations.

What we're looking for

  • Bachelor’s degree in Mechanical or Chemical Engineering.
  • Minimum 1 years of related pharmaceutical experience or relevant internship experience.
  • Experience with cGMP, Good Documentation Practices (GDocP), and pharmaceutical manufacturing plant operations.
  • Knowledge of commissioning, qualification, and validation (CQV) processes including periodic review.
  • Troubleshooting skills in mechanical, electrical, and automation systems.
  • Ability to support capital projects and perform equipment maintenance for utility systems.
  • Experience with CMMS (ProCal), CCMS (SAP), or other paperless electronic validation systems (preferred).
  • Experience with pharmaceutical processing equipment, Lean/Six Sigma, and risk assessment tools like FMEA and PHA (preferred).

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