Mold Validation Engineer

Karwell Technologies

  • Minneapolis, MN
  • 2 days ago

    Highlights

    Primary Responsibilities: Executes mold trials (Functional Test, Gate Freeze, D3, Characterization). Please look for hands on experience in Mold Validation role in Medical Device Industries.

    Numbers & Facts

    LocationMinneapolis, MN

    Description

    Primary Responsibilities:
    • Executes mold trials (Functional Test, Gate Freeze, D3, Characterization)
    • Captures RJG data & defines validated process windows
    • Updates PODs & FW redlines
    • Prepares draft OQ/PQ plans
    • Coordinates daily with Healthcare ME, Ops, Quality, and Tooling
    • Approves POD redlines & validation documents
    • Ensures compliance with QMS & regulatory standards
    • Run trials, collect RJG data, set process windows
    • Prepare PODs, FW redlines, OQ/PQ drafts
    • Coordinate with Healthcare teams
    • Define mold validation scope
    • Approve validation approach, parameters, PODs
    • Provide templates (OQ, PQ, FW forms, POD format)
    • Confirm press allocation and trial windows
    • Review all trial results
    • Participate in technical decisions (e.g., process window changes)
    • Approve POD redlines
    • Approve OQ/PQ draft documents
    • Provide sign-off on validation readiness

    Qualification:

    • Mold engineer -Mold qualification skills required.
    • BE/master's in relevant to mechanical/Polymer/Industrial /Production .
    • Exp range: 8 -12 years

    Please look for hands on experience in Mold Validation role in Medical Device Industries.

    • Healthcare.
    • Client.
    • Boston Scientific.
    • Client.
    • Stryker.
    • Baxter.
    • Cardinal Health.

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