Senior Technician, Sterile Operations - Shared Services

CamWebDir; Rahway (NJ); On-site; USD 68,000 - 107,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) retirement plan

Paid holidays

Job summary

CamWebDir in Rahway, NJ seeks a Senior Technician, Operations to support GMP clinical supply and sterile formulation in the FLEx Center. The role involves hands-on sterile processing, equipment assembly, and both open aseptic and closed formulation within Grade environments, ensuring traceable GMP documentation and adherence to procedures.

The position requires meticulous attention to detail, teamwork, and the ability to operate in a fast-paced manufacturing setting, with cross‑training

Qualifications

• High School Diploma or GED with ≥5 years pharma manufacturing experience.
• Associates degree with ≥3 years pharma manufacturing experience.
• Bachelors degree in engineering tech or related field.

Responsibilities

• Read and follow drawings to assemble sterile equipment.
• Operate cleaning and sterilization equipment (autoclaves, parts washers).
• Receive, inspect, and store sterile supplies in the cleanroom.
• Prepare and formulate sterile products in Grade A/C environments.
• Perform visual inspections of products and components for defects.
• Maintain meticulous GMP documentation and records.

Skills

GMP Documentation

Attention to Detail

Communication Skills

Teamwork

Troubleshooting

Schedule Management

Leadership

Cross-functional Collaboration

Education

High School Diploma/GED + 5 years pharma manufacturing

Associates Degree in Science/Engineering + 3 years pharma

Bachelors Degree in Engineering Technology

Tools

Microsoft Office

MODA

PAS‑X

SAP

HMI

Calibration/Maintenance DB"

Job description

CamWebDir in Rahway, NJ seeks a Senior Technician, Operations to support GMP clinical supply and sterile formulation in the FLEx Center. The role involves hands-on sterile processing, equipment assembly, and both open aseptic and closed formulation within Grade environments, ensuring traceable GMP documentation and adherence to procedures.

The position requires meticulous attention to detail, teamwork, and the ability to operate in a fast-paced manufacturing setting, with cross‑training