Quality Manager I

4 weeks ago


Huntington, United States Ecolab Full time

Quality Manager I

Ecolab is seeking a Quality Manager I to ensure quality priorities and improvement plans are integrated into Site Master Plans. This role will act as the first point of contact for the deployment of effective Plant to Plant and RD&E to Plant transfers.

The Quality Manager I will be responsible for maintaining excellence in Quality Management and fostering talent in the associates to develop the talent pipeline.

This role will also have a leadership role in auditing and assuring that the Ecolab quality system requirements are being met by all production sites, that complaints have a timely and satisfactory resolution, and that FDA/GMP requirements are being met by the sites.

The Quality Manager I will establish quality control guidelines and testing procedures, ensuring that raw material and finished product quality and reliability are in compliance with engineering and product specifications.

This role will also maintain an effective quality system including QMS structure, quality planning, execution of all QMS processes.

The Quality Manager I will manage interactions with external agencies (FDA, EPA, ISO, Kosher, HALAL, or similar) including internal and external audits.

This role will apply and mentor/coach the application of quality principles, concepts, and tools to complex systems and processes.

The Quality Manager I will oversee site level quarterly Quality Steering Committee Meetings and Annual Management Review for facility compliance and assurance of policies and procedures as well as associated inputs and outputs of the meeting (site level metrics).

This role will address quality, service, and cost issues at site level to assure customer satisfaction and compliance to regulations.

The Quality Manager I will be responsible for developing/revising applicable standard operating procedures and work instructions specific to responsibilities within the Quality department as needed.

This role will also be responsible for compliance with regulatory and ISO training requirements.

The Quality Manager I will oversee any investigations into process deviations and determine appropriate disposition as needed and assure compliance with quality system requirements.

Requirements:

  • Bachelor's degree
  • ~7 years quality experience in manufacturing or RDE (research, development, and engineering)
  • ~ Expertise in ISO 9001, cGMP's and managing quality optimization projects
  • ~ Strong Knowledge of manufacturing of regulated products including medical devices, cosmetics, pharmaceutical products
  • Bachelor's degree in a technical field, including engineering, biology, microbiology, or chemistry
  • ~ Project management experience
  • ~ Certified Quality Auditor Certification (ASQ CQA)
  • ~ Certified Manager of Quality Certification (ASQ CQM/OE)
  • ~2 years' experience in a continuous improvement environment (Lean, Six Sigma, TPM, and/or 5S experience - certification preferred)


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