Position Details
About this role
This role involves supporting routine operations in a sterile drug product manufacturing facility, troubleshooting equipment, and ensuring compliance with regulatory standards.
Key Responsibilities
- Troubleshoot production equipment
- Establish new processes
- Support continuous improvement projects
- Collaborate with cross-functional teams
- Ensure regulatory compliance
Technical Overview
The position requires expertise in sterile equipment, automation systems like PLC, DCS, MES, and aseptic processing within a GMP environment.
Ideal Candidate
The ideal candidate is a mid-level engineering professional with at least 5 years of experience in sterile processing and pharmaceutical manufacturing. They possess strong technical expertise in equipment like autoclaves, lyophilizers, and automation systems, with a focus on quality and compliance.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Lack of experience with sterile equipment, No familiarity with GMP or GXP, Less than 5 years relevant experience, Inability to work on-site in Rahway, NJ
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