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Assistant Project Manager (cGMP - Pharmaceutical) JD816656

JD816656

DPS Engineering is looking for a Project Manager to work with a BioPharma client in the Boston, MA area. This individual will provide Project Management and support to Capital Projects in the areas of Facility/Utility/Process Equipment Design, Procurement, Construction, Installation Commissioning and Qualification/Validation.

Category:
Project Manager
Location:
Massachusetts
Years of Experience Req.:
3+
Date Posted:
15/02/2019
Days Remaining:
13
Employment Type:
Full-time
Education Level Req.:
Bachelors

Assistant Project Manager (cGMP - Pharmaceutical)                         JD816656

Boston, MA area

 

DPS Engineering is looking for a Project Manager to work with a BioPharma client in the Boston, MA area. This individual will provide Project Management and support to Capital Projects in the areas of Facility/Utility/Process Equipment Design, Procurement, Construction, Installation Commissioning and Qualification/Validation.

 

Responsibilities:

  • Lead and manage aspects of assigned projects that support improvements around biologics operations.
  • Ability to lead cross-functional teams and execute projects in an active biologics/pharmaceutical environment.
  • Must be able to assist in directing the planning, design, and implementation of capital projects.
  • Manage project costs, schedule and scope as it relates to quality and stakeholder requirements.
  • Balance project risk and uncertainty through risk management and mitigation plans.
  • Lead communication of project status updates with senior leadership.

 

Qualifications and Education: 

  • Bachelor’s degree in Chemical, Mechanical or other related Engineering or relevant field.
  • 2+ years’ minimum experience in process/project engineering or related roles.
  • Project Management experience with ability to execute projects on time and on budget.
  • Experience working in a cGMP biotech environment, regulatory, engineering and construction techniques.
  • Familiar understanding of Quality Systems including change control, deviation management, and commissioning/qualification standards.
  • Experience facilitating meetings and establishing safe practices in a cGMP environment.
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