ASEA
  • 01-Jul-2019 to 30-Aug-2019 (MST)
  • Quality / R&D
  • Pleasant Grove, UT, USA
  • DOE
  • Hourly
  • Full Time

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.


 

QUALITY ASSURANCE DOCUMENT CONTROL SPECIALIST

 

ASEA is looking for a talented and enthusiastic Quality Assurance Document Control Specialist 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 works hard and plays hard. We provide great opportunities for personal and professional growth working in ASEA's Redox Manufacturing Center.

 

 

SUMMARY:

 

The Quality Assurance Document Control Specialist will, under the direction of the quality management team, oversee all document organization and storage relating to the regulatory requirements that govern our production activities. This position will also be front desk reception at the Redox Center, filling orders and greeting visitors.

 

 

RESPONSIBILITIES:

 

  • Scan and file all documents that support the Quality Management System for ASEA
  • Organize and name existing documents to comply with our strict document control system
  • Help us work toward as few paper documents as possible by optimizing digital document storage
  • Greet visitors and fill orders at the Redox Center
  • Weekly inventory of our Will Call inventory
  • Communicate inventory needs to our shipping team to stock product in Will Call
  • Assist in document reviews to assure completion and full compliance of GDP protocols
  • Route documents for process change order approvals
  • Assist in other organizational tasks as needed

 

 

QUALIFICATIONS: 

 

  • High school diploma or equivalent
  • Any college attendance or science background a plus
  • Extreme attention to detail
  • Familiarity of cGMP guidelines. GDP (good document control) and FDA requirements a plus
  • Excellent typing skills
  • Ability to read and write English at an outstanding level, to ensure document accuracy
  • Ability to work both independently and with team members
  • Self-motivated with a strong desire for excellence and accuracy

 

 

 

PHYSICAL REQUIREMENTS:

 

  • This is primarily a seated position, but will involve moving and storing stacks of documents, as well as processing orders
  • Ability to life 25 lbs while processing orders and moving inventory around

 

 

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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