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Quality Lead Inspector

Freudenberg Group
Posted 3 days ago, valid for 10 days
Location

Jeffersonville, IN, US

Salary

Competitive

Contract type

Full Time

By applying, a Freudenberg Group account will be created for you. Freudenberg Group's Privacy Policy and Terms & Conditions will apply.

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Sonic Summary

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  • Freudenberg is seeking a Quality Department Lead with at least 8 years of experience in quality-related roles to oversee inspection functions and ensure adherence to quality standards.
  • The role involves training QC inspectors, maintaining timecards, and scheduling quality inspection activities to support operations.
  • Candidates should possess comprehensive knowledge of medical device regulations and quality systems, along with strong leadership and communication skills.
  • Experience with SAP and MasterControl systems is preferred, as well as the ability to perform physical tasks in cleanroom environments.
  • The position offers a competitive salary, commensurate with experience, and emphasizes the company's commitment to diversity and inclusion.

Working at Freudenberg: We will wow your world!

Responsibilities:

  • Leads and directs the daily activities of all inspection functions within the Quality department & coordinate inspector’s workload.
  • Maintain QC inspector timecards and approve payroll.
  • Place purchase requests for QC operating supplies and office equipment.
  • Train QC inspectors making sure standard work is being followed.
  • Determine training targets, update and maintain versatility matrix.
  • Applies sampling standards. Ensures team is cross-trained.
  • Performs operational checks, preventative maintenance checks and accuracy verifications of measurement and test equipment used in production, Engineering and other areas.
  • Oversee the inspection and testing of materials, parts and products to ensure adherence to established requirements and quality standards.
  • Oversight of non-conforming materials and ensuring that product is properly segregated dispositioned per MRB.
  • Tests and controls WIP, raw material and finished product quality, ensuring compliance with company standards and applicable government regulations.
  • Interprets and executes inspection requirements according to company requirements.
  • Responsible for scheduling quality inspection activities to support operations in meeting required schedules or to resolve complex problems.
  • Analyzes and corrects issues with system performance, and identifies and drives system improvements.

Qualifications:

  • High school diploma or equivalent (GED).

  • At least 8 years in quality-related roles.

  • Comprehensive knowledge of medical device regulations and quality systems (e.g., ISO 13485, FDA 21 CFR Part 820).

  • Proven ability to lead teams, drive quality initiatives, and mentor inspectors on procedures, standards, and tools. 

  • Strong leadership, coaching, and communication skills; ability to anticipate quality risks and implement preventive actions. 

  • Experience with SAP and MasterControl systems to ensure data integrity and compliance. 

  • Ability to stand for long periods, perform fine motor tasks, lift up to 50 lbs., and work in cleanroom environments. 

‎ ‎

The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.

Freudenberg Medical LLC



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By applying, a Freudenberg Group account will be created for you. Freudenberg Group's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.