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Quality Supervisor

GREEN RIVER, WY Jul 6, 2026 to Jul 10, 2026

Job Number

  • Job Number R2026-15180

Description

The Supervisor will be responsible for managing and directing a staff of lab analysts and all related quality-testing activities, as well as the day-to-day affairs of the QC/QA Laboratory.

DUTIES AND RESPONSIBILITIES (*denotes essential job functions):

  • Directing the activities of the QC/QA analysts in order to assure the completion of the following:
    • Appropriate validation and accuracy of USP testing, SPD logbook results, and all other finished product inspections/testing.
    • Conduction of Test Method Reviews and collaboration with Corporate R&D to improve method efficiencies and/or costs.
    • Compliance with all GMP, FDA and other regulatory standards by Lab Analysts and in all laboratory SOP's and procedures.
    • Maintenance of JIT inventory of chemicals, reagents, glassware, etc. as needed for the day-to-day lab operations, within budget.
  • Working closely with corporate representatives regarding new or revised product specifications
  • to effectively manage the site's BOM process as well as facilitate the successful completion of test plans.
  • Establishing and maintaining efficient procedures for tracking plant costs incurred to produce quality finished goods in support of a corporate initiative, the "Cost of Quality" program.
  • Verifying and approving timecards for the non-exempt Lab Analysts,
  • Ensuring the Lab Analysts' time away from work is covered, utilizing a consistent method for distribution overtime.
  • As a fully trained auditor, conducting internal ISO and sanitation audits of the facility.
  • Conducting external inspections of suppliers; and
  • Making recommendations for hiring and terminations within the department.

MINIMUM EDUCATION, TRAINING, AND EXPERIENCE REQUIREMENTS:

  • Bachelor's degree in a relevant field, a minimum of five years of applicable experience.

PREFERED EDUCATION, TRAINING, AND EXPERIENCE REQUIREMENTS:

  • Preference will be given to candidates with experience in FDA requirements/inspections, ISO, and Good Manufacturing Practices.

KNOWLEDGE, SKILLS, AND ABILITIES:

  • Computer literacy.
  • Demonstrated ability to reason and make timely and quality decisions.
  • Proven interpersonal skills and leadership ability with strong communication skills.

REQUIRED TRAINING:

  • OSHA Safety Training

WORKING CONDITIONS:

  • Must be able to work and be comfortable in an industrial environment and chemical processing facility.
  • Must possess the ability to work in a standard office setting and to use standard office equipment.
  • Must possess the ability to maintain attention to detail despite interruptions

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