Evening-Shift Non‑Sterile Process Engineer

MSD; Rahway (NJ); On-site; USD 87,000 - 137,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

Comprehensive benefits

Job summary

MSD is seeking a Non-Sterile Specialist, Engineering for Rahway, NJ on second shift. The role focuses on maintaining facilities, utilities and manufacturing equipment in compliance with GMP and safety, while applying Reliability Maintenance practices to support timely clinical and development batches.

Responsibilities include equipment validation, changes management, deviations investigations, and GMP documentation. Collaboration with QA, Facilities, OEMs and vendors is required.

Qualifications

• Bachelor’s degree in engineering; 2+ years in pharma manufacturing operations for OSD products preferred.
• Knowledge of cGMP, QA, safety policies and environmental procedures.
• Experience with CMMS and equipment maintenance processes.
• Strong troubleshooting: mechanical/electrical/automation.
• Ability to work across Quality and Facility domains and communicate clearly.

Responsibilities

• Maintain facility, utilities and equipment per GMP and safety requirements.
• Support equipment validation from commissioning to decommissioning.
• Manage changes, periodic reviews, deviations, NCs/CAPAs and GMP documentation.
• Coordinate installation and commissioning of new equipment and support regulatory interactions as SME.
• Assist in procurement, capital requests, and vendor coordination.

Skills

Adaptability

cGMP Guidelines

Electronic Batch Records

GMP Compliance

Process Optimization

SOP Writing

Education

Bachelor’s degree in engineering

Tools

SAP Plant Maintenance

eVal/Kneat

ProCal CCMS

CMMS

Job description

MSD is seeking a Non-Sterile Specialist, Engineering for Rahway, NJ on second shift. The role focuses on maintaining facilities, utilities and manufacturing equipment in compliance with GMP and safety, while applying Reliability Maintenance practices to support timely clinical and development batches.

Responsibilities include equipment validation, changes management, deviations investigations, and GMP documentation. Collaboration with QA, Facilities, OEMs and vendors is required.