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Contract Project Engineer

3 months ago

Glendale, United States EPM Scientific Full time

EPM are currently partnering with a global Pharmaceutical company who are looking for Contract Project Engineer to help with an uplift in work. This role is based in Glendale, CA - onsite 5 days a week. W2 ONLY.


Essential Duties and Responsibilities


  • Execute and assist in the management of customer corporate CAPEX and site-specific OPEX projects, ensuring adherence to project timelines, budgets, and quality standards.
  • Work closely with internal and external stakeholders, including clients, project teams, and vendors, to understand project requirements and expectations.
  • Proactively identify and mitigate project risks and issues, implementing corrective actions as needed.
  • Develop and execute change control documents to manage alterations effectively, ensuring alignment with project objectives.
  • Develop design specifications, including User Requirement Specifications (URS), Functional Specifications (FS), and Design Specifications (DS) to guide project development.
  • Conduct Factory Acceptance Tests (FATs) and Site Acceptance Tests (SATs) to validate the functionality and compliance of systems and equipment.
  • Develop and execute thorough commissioning test protocols to ensure the successful integration and functionality of systems.
  • Review and comprehend various construction drawings, including Process Flow Diagrams (PFDs), Piping and Instrumentation Diagrams (P&IDs), and architectural, mechanical, and electrical drawings.
  • Draft Standard Operating Procedures (SOPs) pertaining to the operation, maintenance, and calibration of equipment, utilities, and facilities.
  • Collaborate in supporting Failure Modes and Effects Analysis (FMEAs) on equipment and utility systems, contributing to risk assessment and mitigation strategies.


Qualifications

  • BS in Engineering, Science or equivalent technical degree.
  • Minimum of 2 years of experience in project engineering within the pharmaceutical and/or medical device industry.
  • Proven track record of successfully managing projects of medium to high complexity.
  • Strong project management skills, including the ability to create and execute detailed project plans.
  • Solid understanding of GMP regulations and industry standards.
  • Experience in executing validation protocols and generating thorough documentation.
  • Strong analytical and problem-solving skills with attention to detail.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and collaboratively in a dynamic team environment.


Scope

  • Start Date: ASAP
  • 40 hours per week
  • 6 month contract with option to extend
  • Glendale, CA - has to be 5 days a week Onsite
  • W2 ONLY
  • Rate up to $45ph