What are the responsibilities and job description for the Process Engineer position at GMP Engineering Inc.?
We are a specialized engineering company with international exposure and subject mater 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.
POSITION:
You shall be part of a cross-functional engineering team in the role of Jr. Process Engineer. You shall 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.
SUMMARY:
Working under the guidance of a senior engineer you shall be responsible for:
- 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
SKILLS:
- Strong interpersonal skills and the ability to work in a team environment.
- Ability to manage and coordinate cross-functional project teams.
- Ability to prioritize multiple tasks.
- Self-directed, resourceful, and able to work independently with minimal oversight.
- Excellent written and verbal communication skills.
- Ability to work effectively in a fast-paced multi-tasking environment.
EDUCATION:
Bachelor’s degree in engineering with 3 years of experience within the pharmaceutical/ biopharmaceutical industry preferable.
LOCATION:
The primary work location will be in our New Jersey office. However, a significant aspect of the role may involve intermittent international travel, including extended periods spent at equipment vendors for Factory Acceptance Tests (FATs) and at the client's site for Commissioning, Qualification, and Validation (CQV) activities.