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United States, Salisbury, NC, Adhesive Technologies

Lead Quality Engineer

HENKEL IS FOR THOSE WHO STEP UP. DO YOU?

At Henkel, you can make a difference and craft your career. That’s why you own your projects and take full responsibility from an early stage. Our unique brands in markets around the world open up countless opportunities to follow your convictions and explore new paths. If you have an entrepreneurial mindset that allows you to always think out of the box - take the chance and shape the digital future together with us.

YOUR ROLE

  • The Lead Quality Engineer will be responsible for activities associated with ensuring and improving the overall quality levels of products manufactured at the Salisbury Plant. This position will oversee the day to day problem solving activities associated with process improvements leading to higher outgoing quality levels
  • Drive actions related to GMP product lines including determining root cause and corrective actions related to audit findings, process deviations, out of trend analysis and out of specification analysis.
  • Coordinator for plant Specification Review and PPAP activity
  • Design validation protocols, perform/coordinate validation testing, and analyze/assemble results to create a finished validation test protocol as required.
  • Lead projects for improvement within lab and between key functional groups for timely, correct sampling and reporting results.
  • Drive actions related to GMP product lines including determining root cause and corrective actions related to audit findings, process deviations, out of trend analysis and out of specification analysis.

 YOUR SKILLS 

  • Bachelor of science degree in Engineering or related field is required.
  • 5+ years' experience in manufacturing / chemical industry or within the quality profession is required.Understanding of TS 16949, ISO 9001, and PPAP requirements with practical application in manufacturing/chemical industry.
  • Analytical and problem-solving skills, Six Sigma or statistical experience preferred.
  • Ability to write and execute validation plans, protocols and reports per existing procedures and templates Knowledge of cGMP and SAP preferred.

Henkel is an equal opportunity employer.  We evaluate qualified applicants without regard to race, color, religion, sex, national origin, disability, veteran status and other legally protected characteristics.  Henkel does not accept unsolicited resumes from search firms or employment agencies.  Unsolicited referrals and resumes are considered Henkel property and therefore, Henkel will not pay a fee for any placement resulting from the receipt of an unsolicited referral.  At Henkel's request only, preferred vendors may be invited to refer talent for specific open positions.  In these cases, a fully-executed agreement with Henkel must be in place and current.        

JOB ID: 1900088Z
Contract & Job type: Full Time, Regular
Contact information for application-related questions: 1-866-836-7067
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