ASEA
  • 05-Nov-2018 to 04-Jan-2019 (MST)
  • Quality / R&D
  • Pleasant Grove, UT, USA
  • DOE
  • Hourly
  • Full Time

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


QUALITY CONTROL LAB LEAD / SUPERVISOR

 

ASEA is looking for a talented and enthusiastic Quality Control Lab Lead / Supervisor to join our team. ASEA, a global leader in cellular health, is dedicated to providing a sustainable lifestyle by delivering high-quality health products through a direct-selling distribution model. ASEA offers first-to-market products that affect health at the genetic level. We're regularly included on Utah's Best Places to Work and have a tight knit team that work hard and play hard. Perks include working in a brand new, very cool, office space (complete with on-site gym / fitness center and company-provided snacks) coupled with great opportunities for personal and professional growth.

 

SUMMARY:

The QC Lab Lead/Supervisor is responsible for the ensuring the quality of the product by ensuring the quality of incoming materials, in-process materials, bulk and finished product, and verifying operations are performed correctly.  This position will regularly inspect and test product and materials on and off the production line.   The QC Lab Lead/Supervisor will be integral in ensuring that quality controls are being maintained for production operations and incoming materials inspection, verifying that documentation is correct, and other quality requirements as needed. 

 

WHAT YOU'LL DO - RESPONSIBILITIES:

  • Perform Bulk/Finished product testing, in-process testing, and environmental monitoring testing.
  • Keep accurate laboratory notebooks and document according to good documentation practices (GDP).
  • Maintain lab cleanliness, personnel hygiene, lab equipment and reagents, as well as reordering supplies as needed.
  • Write, review, verify and as needed approve analytical methods and SOPs.
  • Report OOS, process deviations, nonconformance, and customer complain investigations in Quality Database.
  • Collect retain samples and lab samples and maintains sample retention room.
  • All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed.

 

WHAT YOU HAVE - QUALIFICATIONS: 

  • 4-year degree in a science related discipline or equivalent work experience.
  • At least 2-years Experience in cGMP environment preferred.
  • Attention to accuracy and detail, and ability to document and record critical quality processes.
  • Background in food, cosmetic, dietary supplement, medical device or pharmaceutical industry required.
  • Knowledge of cGMP Regulations required.
  • Excellent eye for detail - must be detail-oriented and possess strong organizational skills.
  • Must have strong time management skills with the ability to prioritize and manage completion of multiple tasks/projects with a variety of company personnel.
  • Ability to work with cross-functional teams and to follow instructions.
  • Bilingual Spanish speaking a plus.

 

OTHER - PHYSICAL REQUIREMENTS: 

  • Ability to stand and move around for the entire shift (10 hours+ per day; usual schedule is M-T, 10-hour days).
  • Frequent and repetitive: bending, crouching, stooping, and reaching throughout entire shift.
  • Occasionally lift 35-75 pounds, frequently lift 25-35 pounds.
  • Ability to work in warehouse condition; little heating or cooling.

ASEA is an equal employment opportunity employer, who maintains a drug-free workplace, and participates in e-Verify.

If you'd like to be part of a great team, are ready to take on a challenge and make a difference within our company, apply today. We offer a competitive wage and excellent benefits package including 401(k), medical, dental, vision, life, disability, supplemental insurance, paid time off, and free company products.

ASEA
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