What are the responsibilities and job description for the Process Engineer Specialist position at GMP Engineering Inc.?
GMP Engineering Inc. is a specialized engineering company with international exposure and subject matter expertise in the design, fabrication, and qualification of sterile, high-purity, and potent containment process equipment and plants. We offer a true creative engineering design work environment with a wide range of interesting projects in the bio-pharmaceutical, personal care, and food industry.
Job Summary:
You will be part of a cross-functional engineering team as a Junior Process Engineer. You will develop and deliver conceptual, preliminary, and detailed design packages through to CQV for GMP-compliant integrated process equipment and unit operations used in the manufacturing of pharmaceutical drug substances and products.
Main Responsibilities:
- Design Basis Development
- Process Alternatives Evaluations
- User Requirement Specifications (URS)
- Process Flow Diagrams (PFDs)
- Process Piping and Instrumentation Diagrams (P&IDs)
- Process Integration of Unit Operations
- Equipment Plot Plans and Layout Drawings
- Equipment Sizing and Specification
- Commissioning & Qualification Protocol Development and Execution
About Us:
We are growing our company size and capabilities through recruitment of talented professionals. Our primary work location will be at our New Jersey site. However, a significant aspect of the role will involve intermittent international travel, including extended periods spent at equipment vendors for Factory Acceptance Tests (FATs) and at client sites for Commissioning, Qualification, and Validation (CQV) activities.