Stellent IT hiring Process Engineer (Validation) in Spencer, Indiana, United States | LinkedIn (2024)

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Stellent IT hiring Process Engineer (Validation) in Spencer, Indiana, United States | LinkedIn (2)

Process Engineer (Validation)

Stellent IT Spencer, IN

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Stellent IT Spencer, IN

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Job Title: Process Engineer IILocation: Spencer, IN (Onsite at 780 Brookside Drive Spencer, IN 47460)

Job Description: Our client, a Global Medical Device Manufacturer, is seeking a Process Engineer II to join their team in Spencer, IN. The engineer will be working on a new product accessory for a valve replacement device.

Job Purpose: Develop products, materials, processes, or equipment for projects of moderate complexity. Compile, analyze, and report operational, test, and research data to establish performance standards for newly designed or modified products, processes, and materials.

Key ResponsibilitiesParticipate in and contribute to project teams, including product design and development, test of materials, preparation of specifications, process capability studies, research investigations (animal and clinical studies), report preparation, and process/test documentation. Design and coordinate standard engineering tests and experiments. Design, procure, and fabricate tooling and fixtures. Troubleshoot new products/process problems related to design, material, or process. Summarize, analyze, and draw conclusions from test results. Prepare standard reports/documentation to communicate results to the technical community. Invent/create concepts and designs for new products/processes and submit idea disclosures. Demonstrate PDP/TPD system knowledge through the delivery of high-quality deliverables.

Quality Systems Duties And Responsibilities

  • Build Quality into all aspects of work by maintaining compliance with all quality requirements.

Preferred Qualifications

  • BS degree in engineering; preferably ME, Biomed, Polymer Science, Chem Engr. with science background
  • 2-4 years of experience
  • Must have medical device experience.
  • Must have process validation experience.
  • Must either have SolidWorks, or similar.
  • Must have Minitab experience.
  • Windchill experience - preferred
  • Thermoplastic experience - highly preferred
  • Understanding of GD&T Geometric Dimensioning and Tolerancing

General Comments

  • Onsite position with flexible day hours (8:00 am - 4:30 pm).

Effective 5/7/24 to Suppliers: Manager needs 2-4 years of industry experience post-graduation with at least 1 year in the medical device industry. Candidates must be proficient with creating IQ OQ PQ protocols.

Experience Requirements

  • At least 1-year post-graduation experience working in a medical device company.
  • Proficient with creating IQ OQ PQ protocols.
  • Process characterization and validation experience.
  • Independent worker with problem-solving abilities

Best RegardsPiyushTechnical RecruiterStellent ITEmail: piyush@stellentit.comCall- +1 609 546-9245

Gtalk: piyush@stellentit.com

  • Seniority level

    Mid-Senior level

  • Employment type

    Full-time

  • Job function

    Management and Manufacturing

  • Industries

    Staffing and Recruiting

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