Sterile Operations Technician: GMP & Visual Inspection

Merck; New Jersey; On-site; USD 60,000 - 75,000; Full time

Job summary

Merck in Rahway, NJ seeks hands-on GMP pharmaceutical staff for sterile formulation, aseptic processing, and visual inspection in a Grade C environment. Roles involve assembling sterile equipment, operating sterilization systems, and managing sterile supplies with strict documentation.

Collaboration with formulators, engineers, QA, and facilities is essential to deliver timely clinical production. Ideal candidates have at least 2 years of GMP experience, proficiency with SAP and MS Office, and

Qualifications

• Minimum 2 years of GMP Pharmaceutical experience.
• Proficiency in computer systems including SAP, Microsoft Office, and calibration databases.
• Willingness to lift 50 lbs and perform gowning in cleanroom environments.
• Strong written and verbal communication skills.

Responsibilities

• Assemble sterile equipment per drawings for clinical development and manufacturing.
• Operate cleaning and sterilization equipment including autoclaves and parts washers.
• Receive, inspect, and store sterile supplies ensuring proper inventory levels.
• Prepare and formulate sterile products in Grade A isolator and Grade C environment.
• Perform visual inspections of products and components for defects and non-conformities.
• Maintain meticulous batch records and environmental condition documentation.
• Follow GMP SOPs and support deviations, investigations, and CAPA.
• Collaborate with formulators, engineers, QA, Safety, and Facilities to ensure timely delivery.

Skills

Written and verbal communication

GMP knowledge

Team collaboration

Attention to detail

Documentation

Education

High School Diploma/GED

Tools

SAP

Microsoft Office

Calibration/Maintenance Database

Equipment HMI

PAS-X (preferred)

Job description

Merck in Rahway, NJ seeks hands-on GMP pharmaceutical staff for sterile formulation, aseptic processing, and visual inspection in a Grade C environment. Roles involve assembling sterile equipment, operating sterilization systems, and managing sterile supplies with strict documentation.

Collaboration with formulators, engineers, QA, and facilities is essential to deliver timely clinical production. Ideal candidates have at least 2 years of GMP experience, proficiency with SAP and MS Office, and