Demo

Manufacturing Engineer

cGxPServe
MN Full Time
POSTED ON 2/26/2025
AVAILABLE BEFORE 5/22/2025

Roles & Responsibilities :

  • Review and approve the documents required to qualify through production process (Control Plan, Flow Charts, Process Drawings, Capability studies, Design Failure Mode Effect Analysis (DFMEA) and Process Failure Mode Effect Analysis (PFMEA).
  • Good experience in CAPA process.
  • Measurement System Analysis / Test method Validation.
  • Test protocol and report preparation.
  • Review and approve the documents required to qualify through production process (Control Plan, Flow Charts, Process Drawings, Capability studies, Design Failure Mode Effect Analysis (DFMEA) and Process Failure Mode Effect Analysis (PFMEA).
  • Good experience in CAPA process.
  • Measurement System Analysis / Test method Validation.
  • Test protocol and report preparation.
  • Supplier coordination in support of selection and qualification of new suppliers or changes to existing supplied products and processes.
  • Support, review, and approval of Process Validation (IQ / OQ / PQ), MSA and Control Plan.
  • Route PPAP Checklist in Agile.
  • Leverage GMP (Good Manufacturing Practices). Navigates the complexities of various industry regulations to include FDA Quality System Regulation (QSR 21 CFR 820), ISO 13485, and ISO 14971.
  • PPAP experience.
  • Supplier document review and approve per MDT process.
  • Supplier control and management.
  • Work closely with supplier.
  • Track wise and MAP agile experience.
  • Critical component identification and qualification.
  • Perform receiving inspection.
  • Driving supplier activities.
  • Leadership toward supplier activities and interaction.

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