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Project Engineer (cGMP - Pharmaceutical) JD817615

JD817615

DPS Engineering is looking for a proven Project Engineer to work with a BioPharma client in the Boston, MA area. Ideal candidates should have a strong understanding of GMPs and experience providing Project Engineering support in highly regulated or pharmaceutical/biotech facilities.

Category:
Project Engineer
Location:
Massachusetts
Years of Experience Req.:
3+
Date Posted:
15/02/2019
Days Remaining:
12
Employment Type:
Full-time
Education Level Req.:
Bachelors

Project Engineer (cGMP - Pharmaceutical)            JD817615

Boston, MA area

 

Summary:

 

DPS Engineering is looking for a proven Project Engineer to work with a BioPharma client in the Boston, MA area. Ideal candidates should have a strong understanding of GMPs and experience providing Project Engineering support in highly regulated or pharmaceutical/biotech facilities.

 

Responsibilities:

  • Provide engineering and technical support related to operation, maintenance, design, installation, start-up/commissioning, testing and qualification of product and infrastructure equipment and systems.
  • Must be able to author URSs and other engineering lifecycle documents as required.
  • Will be expected to manage a portfolio of projects together as there are multiple scopes to be managed.
  • Support the design and qualification of improvements, changes or upgrades to the equipment and start-up and validation documents.
  • Identify and schedule project events around manufacturing operations.
  • Identify materials required to support project execution work.
  • Communicate project requirements to vendors to obtain proposals for equipment and piping changes.
  • Provide project design and cost estimates.

 

Education and Experience:

  • Bachelor’s degree in Mechanical or Chemical Engineering.
  • Minimum 3+ years’ experience providing Project Engineering support.
  • Candidate must be able to work across functional areas such as operations, maintenance, quality and validation.
  • Proficiency in the arena of process, utility and/or building engineering in cGMP environment within a biopharma facility.
  • Working knowledge of documents such as P&IDs, URS, FRS, and qualification documents.
  • Effective verbal and written communication skills.
  • Excellent interpersonal, teamwork, and leadership skills required.
  • Participates in determining objectives of assignment and plans, schedules and arranges own activities in accomplishing milestone achievements.
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