Get more replies from employers
Send a job-specific resume in minutes.
GMP Engineering Inc. is seeking a Jr. Process Engineer to join a cross-functional team focused on designing, fabricating, and qualifying sterile, high-purity containment equipment for pharma applications.
You will develop conceptual through CQV design packages for GMP-compliant processes. Under supervision, you will craft Design Basis, URS, PFDs, P&IDs, layouts, and equipment sizing, and support commissioning/qualification activities.
We are 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 are growing our company size and capabilities through recruitment of talented professionals. 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.
You will be part of a cross-functional engineering team in the role of Jr. 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.
Working under the guidance of a senior engineer you will be responsible for:
The primary work location will be in our New Jersey site. However, a significant aspect of the role will involve intermittent international travel, including extended periods (up to 30%) spent at equipment vendors for Factory Acceptance Tests (FATs) and at the client\'s site for Commissioning, Qualification, and Validation (CQV) activities.