Validation Engineer - DPS Group Global : Job Details

Validation Engineer

DPS Group Global

Job Location : Swiftwater,PA, USA

Posted on : 2025-01-03T15:18:15Z

Job Description :

Immediate Need: CQV Engineer

Location: Swiftwater, PA

Start Date: January 13th, 2025

Duration: >3 years (seeking full time employment with salary and benefits)

We are urgently seeking a skilled CQV (Commissioning, Qualification, and Validation) Engineer to join a critical technology transfer project in Swiftwater, PA. This role is ideal for someone with expertise in pharmaceutical manufacturing and a passion for navigating complex challenges in a fast-paced environment.

About the Project:

This project involves transferring a vaccine process to an existing manufacturing and laboratory facility, accommodating both small- and large-scale production. While the project includes some retrofit aspects, it's focused on integrating new product operations within an existing infrastructure.

Phases: Combined feasibility and conceptual phases currently underway, with the design phase slated for early next year.

Challenges: Extreme scheduling pressures and tight deadlines require a dynamic problem-solver who thrives under pressure.

Key Responsibilities:

  • Execute CQV activities for equipment and processes, ensuring adherence to regulatory standards and project timelines.
  • Support the technology transfer of vaccine processes into an existing facility.
  • Develop and execute IQ, OQ, and PQ protocols for small- and large-scale manufacturing and lab operations.
  • Collaborate with cross-functional teams to address technical challenges and scheduling constraints.
  • Provide detailed documentation and reporting to support regulatory compliance.

Qualifications:

  • Bachelor's degree in engineering, Life Sciences, or a related field.
  • Strong experience in CQV, particularly in technology transfer projects within the pharmaceutical or biotech industries.
  • Familiarity with retrofitting existing facilities and integrating new product operations.
  • Proven ability to manage scheduling pressures and tight deadlines in a high-stakes environment.
  • Solid understanding of GMP, FDA regulations, and vaccine manufacturing processes.

What We Offer:

  • The opportunity to contribute to a high-impact vaccine technology transfer project.
  • A fast-paced, collaborative environment where innovation and problem-solving are key.
  • Competitive compensation and a chance to work on the cutting edge of pharmaceutical engineering.

Apply Now! This is an urgent hire for an immediate start. If you're up for the challenge, send me a message for more details!

Apply Now!

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