IQA Specialist

Posted 8 Days Ago
Be an Early Applicant
United States of America
Junior
Digital Media • Sales
The Role
The IQA Specialist at Elevate Health Sciences is responsible for ensuring compliance with quality control standards by reviewing labels and managing inventory. Key tasks include inspecting incoming materials, maintaining documentation, conducting sampling, and participating in audits. Attention to detail and adherence to regulations are essential.
Summary Generated by Built In

Company:

Elevate Health SciencesIQA Specialist

This crucial role demands meticulous attention to detail and a commitment to safeguarding our brand and consumer safety. You'll be responsible for the label control and inventory oversight, while also assisting with incoming materials sampling and inspection.

Position Details:

Time: 40 hours/week (Monday-Friday)

Employment Type: Full-time

SHIFT: 8am-4:30pm

PAY:

Start Date: ASAP

Work Objectives:

  • Meticulously review all incoming materials and finished product labels for accuracy, completeness, and adherence to regulations and internal standards.
  • Proactively identify and address any label discrepancies or potential regulatory concerns.
  • Manage label inventory and destruction process.
  • Assist with incoming materials inspection as needed.
  • Oversee the inventory of held and rejected materials within the quality cage, ensuring accurate documentation and adherence to established procedures.
  • Conduct regular inspections of the quality cage to verify proper storage and segregation of materials.
  • Implement and adhere to established sampling protocols for all incoming raw materials.
  • Conduct visual inspections to identify potential discrepancies or damage.
  • Collect representative samples using appropriate techniques and equipment.
  • Maintain accurate and detailed records of all sampling activities and collaborate with the laboratory team for timely analysis.
  • Maintain comprehensive documentation of all activities, including sampling logs, label control records, and quality cage inventory records.
  • Stay updated on relevant regulations, quality control procedures, and GMP guidelines.
  • Participate in internal audits and process improvement initiatives.
  • Provide support to other Quality Assurance team members.
  • Assist the Testing & IQA Supervisor and the Senior Quality Manager with other projects as needed.

Qualifications:

  • Minimum 1-2 years of experience in a manufacturing or quality control setting, preferably within the nutraceutical or a similar industry.
  • Demonstrated understanding of good manufacturing practices and current regulatory requirements.
  • Exceptional attention to detail and a commitment to accuracy in all tasks.
  • Proficiency in Microsoft Office Suite and basic data management tools.
  • Excellent communication and interpersonal skills, with the ability to work independently and collaboratively.
  • Experience with raw material sampling, label control, and quality cage management is a strong plus.

Our Benefits & Perks:

You will be part of an engaged, inclusive, global community that values family, giving back, beauty, and sustainability. We offer competitive benefits to eligible employees with comprehensive medical, vision, and dental coverage; supplemental life, voluntary short-term, and disability insurance; free access to therapists; a health savings account and 401k. You'll also be empowered to prioritize what's important to you through our vacation policy.

The Company
Provo, UT
1,357 Employees
On-site Workplace
Year Founded: 1984

What We Do

Nu Skin Enterprises, Inc. is a global direct selling company with operations in 53 markets worldwide

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