Senior Sterile Ops Technician – Shared Services

Merck; Rahway (NJ); On-site; USD 75,000 - 118,000; Full time

Job summary

Merck in Rahway, NJ, seeks a Sr. Technician, Operations for hands-on sterile processing in a Grade C environment. You will assemble equipment, perform aseptic formulation, sterilization, and visual inspection while maintaining GMP documentation.

The role requires collaboration across formulators, engineers, QA, and facilities to support clinical supply. You will work 2nd shift in a 100% on-site setting, with opportunities to cross-train in filling and related areas, contributing to continuous

Qualifications

• GMP pharmaceutical manufacturing experience is required.
• Strong written and verbal communication skills.
• Proficient with MS Office, HMI, PAS-X, SAP and related systems.
• Willingness to lift up to 50 lbs and work in a cleanroom.
• Ability to work independently and in a team, with OT flexibility.

Responsibilities

• Assemble sterile equipment per drawings for clinical development and manufacturing.
• Operate sterilization equipment and manage cleanroom processes.
• Receive, inspect, and store sterile supplies ensuring inventory accuracy.
• Prepare sterile products following batch records and GMP standards.
• Perform visual inspections and maintain detailed process records.
• Collaborate with formulators, engineers, and QA for compliance.

Skills

Aseptic Operations

Biological Sciences

Bioprocess Engineering

Cleanroom Operations

GMP

Laboratory Processes

Physical Abilities

Process Control

Process Improvements

Production Scheduling

Sterile Products

Education

High School Diploma/GED

Associates Degree in Science/Engineering

Bachelors Degree in Engineering Technology

Tools

Microsoft Office

HMI

PAS-X

SAP

Calibration Database

Job description

Merck in Rahway, NJ, seeks a Sr. Technician, Operations for hands-on sterile processing in a Grade C environment. You will assemble equipment, perform aseptic formulation, sterilization, and visual inspection while maintaining GMP documentation.

The role requires collaboration across formulators, engineers, QA, and facilities to support clinical supply. You will work 2nd shift in a 100% on-site setting, with opportunities to cross-train in filling and related areas, contributing to continuous