Summary
Date Posted: Friday, April 29, 2022 , Base Salary: Not Disclosed

JOB DETAILS:
BRIEF JOB DESCRIPTION:
• Basic knowledge of pharma industry and GMP requirements
• Supporting all phases of capital projects from concept through to implementation and close-out. Support design, construction, commissioning and qualification, project schedule and cost.
• Help maintain a strong safety culture and performance in the implementation of capital projects.
• Help ensure successful delivery of projects which meet business needs. Deliver cost effective projects in line with our project management procedures and best practices.
• Developing and maintaining collaborative relationships with stakeholders
• Identify effective & innovative engineering design solutions which meet project client / end user requirements.
• Plan and support the delivery of projects which meet all regulatory requirements including safety, quality and environmental requirements.
• Ensure that equipment qualification activities are completed in line with site procedures, cGMP and best practices.
• Develop and improve new and existing standards within the engineering department improving the service offered to clients/end-users
• Generate and maintain project schedules to plan and track project activities over the life-cycle of the project.
• Develops project objectives after alignment with Management.
• Develops project specifications by studying plant design, customer requirements, and performance standards and preparing cost estimates
• Provides timely engineering solutions to problems associated with project assignments • Have solid knowledge about installation, startup, and commissioning
• Maintains project schedule by monitoring project progress ,coordinating activities and resolving problems
• Controls project plan by reviewing design, specifications, and plan and schedule changes and recommending actions and follow up the project Progress.
• Controls project costs by approving expenditures (administering contractor contracts)
• Prepares project status reports by collecting, analyzing, and summarizing information
• Maintains project records and documentation such as meeting minutes, specifications (URS, FRS, etc.), drawings (P&ID, schematics), change control.

QUALIFICATIONS & EXPERIENCE:
• Bachelor’s Degree in Engineering (Chemical/Mechanical preferred)
• 3 – 15 years related work experience
• Pharmaceutical experience preferred
• Instrumentation & Controls experience a plus
• GMP/cGMP knowledge a plus
• PMP certification is a plus

Work Hours: 8

Experience in Months: 36

Level of Education: Bachelor Degree

Job application procedure
Applications via Email to: careers@dawalifesciences.com

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