• 25-Sep-2017 to 24-Nov-2017 (MST)
  • Quality / R&D
  • Pleasant Grove, UT, USA
  • DOE
  • Salary
  • Full Time

Generous 401(k), medical, dental, and vision benefits; Life, disability, and supplemental insurance; Holiday and paid time off; Continuing training and education; Advancement opportunities


The Director of Quality Assurance is responsible for strategic development and implementation of all Quality initiatives and ensuring strict adherence to FDA and all other applicable regulations. The position provides leadership and direction to the Quality Assurance/Quality Control team.   



  • Establish quality and reliability standards of raw materials, in-process product, and disposition of finished products.
  • Maintain product quality by collaborating with other members of management and contributing to team results.
  • Prepare product and process quality reports, analyze information and trends, and establish documentation system.
  • Complete quality assurance operational requirements by scheduling and assigning employees, following up on work results, and maintaining the Quality Database.
  • Manage quality assurance staff by recruiting, training, coaching, planning, and appraising employees.
  • Develop Standard Operating Procedures (SOPs) and implement other quality assurance policies and procedures.
  • Maintain professional and technical quality knowledge.
  • Achieve financial objectives by preparing the quality assurance budget; scheduling expenditures, and analyzing variances.



  • Vocational or B.S. in a science related discipline or H.S Diploma and equivalent work experience required.
  • 3+ years of experience in quality leadership position required.
  • Experience in a cGMP dietary supplement, pharmaceutical, food, or medical device manufacturing environment required.
  • Previous audit experience required.
  • Strong computer skills (Microsoft Office products) required.
  • Electronic document management systems preferred.
  • Possess strong verbal and written communications.
  • Knowledge of cGMP regulations required.
  • Knowledge of documentation control requirements for cGMP regulated industries to meet FDA regulations desired.
  • Excellent eye for detail and strong organizational skills.
  • Strong time management skills with the ability to prioritize and manage completion of multiple tasks/projects.
  • Ability to work with cross-functional teams.
  • Experience with Direct Sales, MLM, or Network Marketing industry a plus.



ASEA, an emerging global leader in cellular health, is dedicated to providing a sustainable lifestyle by delivering high-quality cellular health products through a principle-based, direct-selling distribution model. Harnessing science, ASEA offers first-to-market products that utilize molecules native to the human body that enhance vital cellular functions. ASEA's cornerstone, patented redox signaling technology boosts the body's natural cellular renewal and communication processes, improving total body health and allowing every system of the body to function better.


Currently, redox signaling technology is available in two first-to-market product lines: ASEA Redox Supplement, the company's flagship liquid supplement, and RENU ADVANCED, a revitalizing whole-body skincare system. Founded in 2010, ASEA currently operates in the United States and 30 international markets.



  • Salary (DOE)
  • Generous 401(k), medical, dental, and vision benefits
  • Life, disability, and supplemental insurance
  • Holiday / paid time off
  • Continuing training and education
  • Advancement opportunities
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