Senior Process Utilities Engineer – Pharma/Biotech

TAI

New Castle (DE)

On-site

USD 125,000 - 175,000

Full time

14 days+

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Benefits offered by this job

Overtime pay
Profit Sharing Bonus
PTO and Holidays
Health benefits

Job summary

TAI, a leading engineering and integration firm, seeks a Senior Process (Utilities) Engineer/SME in New Castle, DE. You will design essential process utility systems for pharma/biotech operations, develop technical specs, and coordinate multidisciplinary design efforts from concept through implementation.

You will lead studies, validate designs, and prepare cost estimates, while ensuring compliance with client standards and regulatory requirements.

Qualifications

  • Bachelor's degree in Mechanical or Chemical Engineering.
  • Professional Engineer licensure preferred.
  • Minimum of eight (8) years of process design engineering experience.
  • Minimum of eight (8) years of experience preparing and reviewing PFDs, P&IDs, equipment and piping specifications.
  • Minimum of three (3) years of experience supporting Pharma/Biotech/Life Science projects.

Responsibilities

  • Prepare Project Technical Requirements Specification for all systems; specify performance requirements and client standards.
  • Research applicable industry standards; prepare engineering studies and design analyses.
  • Develop engineering specifications and project cost estimates.
  • Review work of design team; monitor progress and alert managers to scope changes.
  • Coordinate project document completion and CAD design deliverables.
  • Interpret codes; work with officials and design professionals as needed.

Skills

Process design
Client-facing
Leadership
PFD/P&ID knowledge

Education

Bachelor's degree in Mechanical or Chemical Engineering

Tools

AutoCAD
Microsoft Office

Job description

TAI, a leading engineering and integration firm, seeks a Senior Process (Utilities) Engineer/SME in New Castle, DE. You will design essential process utility systems for pharma/biotech operations, develop technical specs, and coordinate multidisciplinary design efforts from concept through implementation.

You will lead studies, validate designs, and prepare cost estimates, while ensuring compliance with client standards and regulatory requirements.

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