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Process Development Engineer

Job in Erie, Erie County, Pennsylvania, 16501, USA
Listing for: ClinLab Solutions Group
Full Time position
Listed on 2026-11-01
Job specializations:
  • Engineering
    Process Engineer, Quality Engineering, Manufacturing Engineer, Chemical Engineering
Salary/Wage Range or Industry Benchmark: 110000 - 170000 USD Yearly USD 110000.00 170000.00 YEAR
Job Description & How to Apply Below

Job Title: Senior Process Development Engineer

Summary:

The Senior Process Development Engineer will drive the development, validation, and improvement of manufacturing processes for advanced product lines. This role is integral to all stages of product development, from research and design to production, ensuring robust and efficient processes that meet high-quality standards. The position requires technical expertise, leadership, and a proactive approach to process innovation and problem-solving.

Responsibilities:

  • Lead process validation activities, including authoring and executing IQ/OQ/PQ protocols and reports, and establishing validation acceptance criteria.
  • Conduct and document process risk analyses, implement statistical sampling plans, and develop testing strategies to ensure product specifications are met.
  • Establish and maintain stable, capable manufacturing processes aligned with quality and production goals.
  • Apply process development best practices and continuously seek opportunities for process improvement and innovation.
  • Develop and refine novel manufacturing techniques as product designs evolve, ensuring adaptability and scalability.
  • Support daily manufacturing operations through process engineering initiatives and continuous improvement projects.
  • Evaluate process changes, material interactions, and conduct process trials with thorough documentation and protocol adherence.
  • Collaborate with cross-functional teams, including Quality and R&D, to drive process development and ensure compliance with safety and regulatory standards.

Qualifications:

  • Experience working under ISO
    9001 and/or ISO
    13485 manufacturing standards.
  • Medical device manufacturing experience required.
  • Demonstrated leadership of engineering and technical teams in a manufacturing environment.
  • Strong understanding of roll-to-roll manufacturing processes.
  • Expertise in process validation/verification, FMEA, and DOE methodologies.
  • Proficiency in conducting experiments and analyzing results using statistical analysis software.
  • In-depth knowledge of polymer materials.
  • Advanced degree in Polymer Science, Chemistry, Chemical Engineering, or a related technical discipline preferred.
  • Versatile, self-motivated, and able to manage multiple project aspects simultaneously.
  • Detail-oriented with strong documentation and reporting skills.
  • Proficient in Microsoft Office applications, including Word, PowerPoint, and Excel.
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