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Engineering Specialist

QRC Group, LLC
Posted 25 days ago, valid for 6 days
Location

Cidra, PR, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • The job is for a Validation Specialist with expertise in injection molding processes to oversee validation activities documentation.
  • Candidates should have a Bachelor's degree in Science and at least 5 years of experience in FDA regulated industries performing validation lifecycle activities.
  • The role involves familiarity with IQ, OQ, and PQ validation phases, as well as developing inspection programs and updating Standard Operating Procedures (SOPs).
  • Additionally, knowledge of Gage R&R methodology and metrology equipment such as calipers and CMM is preferred.
  • Candidates must also possess technical writing skills and be proficient in English and Spanish.
Engineering Specialist with a strong knowledge of injection molding processes to support the development, execution, and documentation of validation activities (Protocols, Tests, Reports).
  • Familiarized with IQ, OQ and PQ validation phases for molds and equipment.
  • IQ: Confirmation of Drawings (including mold attributes), Equipment, and Procedures (mold setup and operating), mechanical assessment of mold and equipment.
  • Develop inspection programs and instructions for setup/positioning of tooling and parts.
  • Assuring that all product development processes and relevant applicable documentation are executed according to the agreed Product Specific Design and Development Plans.
  • Updating and defining Standard Operating Procedures (SOPs).
  • Familiarized with Gage R&R methodology preferable.
  • Preferably, familiarized with metrology equipment and methods such as calipers, micrometers, CMM, Programmable Vision Inspections Systems.


Requirements

  • Bachelor in Science
  • Experience in FDA regulated industry
  • 5 years of experience performing validation lifecycle activities
  • Techical writting skills
  • Read, write, speak and understand English and Spanish





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