Process Engineer

3 weeks ago


Rahway, New Jersey, United States GMP Engineering Inc. Full time

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. Our company is growing, and we are seeking a talented professional to join our cross-functional engineering team as a Jr. Process Engineer.

As a Jr. Process Engineer, you will be responsible for developing and delivering 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.

Key responsibilities include:

  • 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

Requirements:

  • 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.


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