Demo

In-Process Quality Supervisor

Greiner
Monroe, MI Full Time
POSTED ON 4/24/2025
AVAILABLE BEFORE 5/21/2025

Your challenge

  • Active leadership, supervision, and mentoring of direct reports. Tasks include goal setting and regular performance review for direct reports.
  • Coordinating daily operational activities to meet departmental Safety, People, Quality, Responsiveness, and Cost KPI’s.
  • Coordinating and performing IPQ inspection and release for semi-finished and finished goods inspections according to valid procedure(s). This includes injection molding and final assembly departments.
  • Providing direct oversight for the identification and handling of nonconforming product according to valid procedure(s).
  • Performing timely compliance review and closure of production batch records.
  • Establishing clear procedures and documents compliant to Good Manufacturing Practice.
  • Supporting timely execution of Quality Assurance and Engineering validation activities including IQ, OQ, PQ, Product Verifications, Engineering Studies, Measurement Requests, etc.
  • Supporting Regulatory Affairs by performing customer complaint investigations, change control, internal / external audits, and corrective actions.
  • Supporting maintenance of testing equipment including troubleshooting, scheduling, and / or the performance of internal / external calibrations as required.
  • Performing periodic cycle counting and ordering of IPQ supplies as needed.
  • Performing other administrative duties to ensure IPQ operational readiness as required.

Authority includes :

  • The recruiting, hiring, training and retraining for IPQ Leads and Inspectors.
  • The direct monitoring and management of employee compliance in accordance to GBO NA Safety, Quality, HR, and payroll policies.
  • The evaluation of products, control of non-conforming products, and IPQ release according to valid procedures.
  • Responsible for ERP transactions such as stock transfers, quality hold and releases (SAP).
  • Responsible for the creation, revision, and distribution of IPQ documents.
  • Responsible for the creation, revision, and distribution of testing plans in the IPQ Laboratory Information Management System (Babtec).
  • Your Profile

  • Associate’s Degree in Science, life sciences, or related field; Bachelor’s Degree is preferred
  • 7 years of experience in an ISO 9001, ISO 13485, or similar regulated manufacturing environment; relevant leadership experience preferred.
  • 5 years of direct Quality Control work experience
  • Intermediate-level experience with laboratory testing equipment, instrumentation, and analysis, as well as laboratory data processing and review
  • Intermediate-level MS office skills
  • Intermediate-level knowledge of statistics, calculations, and reporting
  • Physical Requirements :

  • Must be able to stand and walk for up to 8-12 hours
  • Must be able to lift up to 50 lbs
  • Must have appropriate vision to perform detailed quality inspections as outlined in SOP’s or TP’s
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