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IPS-Integrated Project Services, LLC

Integrated design, engineering, construction management

CQV Engineer 2

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeSomerset County, NJ, USA

About the Job

Requirements

  • A Bachelor of Science in Engineering is required.
  • At least 2 years of relevant experience is required.
  • Experience in pharmaceutical, biotech, medical device design, construction, commissioning, validation, or quality assurance is required.
  • Must be able to stand, sit, and walk for prolonged periods, and stoop, kneel, crouch, and crawl as required.
  • Must be able to lift and move objects weighing up to 50 pounds and climb ladders as necessary.
  • Must be able to work in indoor and outdoor environments, including varying working conditions.
  • Must be able to adhere to strict cleanroom gowning protocols.
  • Must have access to reliable transportation.
  • This is a safety-sensitive position involving field work at client sites in construction, process, packaging, manufacturing, research, or other non-administrative areas.

Responsibilities

  • Perform cGMP compliance-based services, including commissioning, qualification, validation, and consulting, as defined in project agreements with IPS clients.
  • Follow IPS and client standards and requirements, industry practices for commissioning, qualification, and validation services, and regulatory requirements.
  • Perform standalone commissioning services for non-FDA-regulated clients as needed.
  • Write commissioning, qualification, and validation documents using established standards and templates, including commissioning forms, protocols and summary reports, standard operating procedures, impact assessments, specifications, and factory and site acceptance tests.
  • Perform field and site activities, including attending and witnessing factory and site acceptance tests as an IPS client representative.
  • Execute commissioning forms and witness vendor start-up and testing.
  • Execute commissioning, qualification, and validation protocols.
  • Walk down and verify system drawings, including P&IDs and as-built drawings.
  • Compile data and prepare reports for completed commissioning, qualification, and validation activities, including ETOPs and protocol data packages.
  • Assist with deviation investigations and resolve problems and issues encountered during field execution.
  • Work with the Project Delivery department or Construction Management for start-up and vendor testing; witness and troubleshoot as required.
  • Perform commissioning, qualification, and validation of equipment and systems, including computer system validation and automation, in support of pharmaceutical, biotech, and medical device industries.
  • Read, understand, and use IPS best practices and standard operating procedures for compliance services.
  • Perform work to meet IPS budget requirements and quality standards.
  • Provide consistent, complete, and timely feedback and reports to IPS project leaders, project managers, or management about project status and issues, as requested.
  • Travel up to 100% or as required by the assigned project; the role may be assigned to a client site for an extended period, and overnight travel or staying in the client's city may be required depending on the assignment.
  • Conduct interviews either in person or virtually; video is required.

Desired Qualifications

  • Experience writing and executing PFC, FC, IQ, OQ, and PQ forms or protocols for GMP utilities, equipment, systems, and software.
  • General exposure and experience in a GMP or validation discipline, with knowledge and understanding of pharmaceutical design, build, commission, and validate processes and their relationship to regulatory requirements and cGMP regulations in the EU and U.S. FDA.

About the Company

IPS-Integrated Project Services, LLC

Integrated design, engineering, construction management

IPS provides design, engineering, and construction management for complex facilities, especially in the pharmaceutical and biotech industries. Its products work by integrating these services into one team from the project’s start, coordinating planning, detailed design, procurement, and construction management to align with a client's business goals and move a project from concept to operational facility. The company differentiates itself through integrated delivery across disciplines and a global footprint (five continents), supported by growth through strategic acquisitions and Berkshire Hathaway backing, which adds financial strength and scale. IPS’s goal is to help life-science clients bring critical facilities online efficiently, with predictable cost, schedule, and quality, by delivering coordinated design, engineering, and construction management under one umbrella.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Philadelphia, PA
Founded
1989

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