Quality Assurance Specialist

Growve•Ogden, UT

19d•Onsite

About The Position

In this onsite role based in Ogden, UT, we are seeking a quality-focused, motivated and detail-oriented Quality Assurance Specialist to join our NutraSelf team! This position will be responsible for managing and maintaining the release of goods into market as well as the release of WIP from/to the various facilities. This position requires exceptional attention to detail, strong organizational skills, and commitment to maintaining high-quality standards.

Requirements

A bachelor’s degree in science is a plus, but not necessary if proven industry experience.
3+ years in an administrative role required.
Accurate data entry skills
Detail oriented
Excellent interpersonal/communication skills
Experience in a Quality Control environment strongly preferred.
Experience with Office (Word/Excel)
Excellent written and verbal communication.
Ability to interact efficiently with a multidisciplinary team.
Ability to identify deficiencies and lead continuous improvement initiatives in cooperation with the other members of the quality team.
Knowledge and understanding of the Dietary Supplements Industry.

Responsibilities

Responsible for good documentation practices surveillance at the manufacturing facility along with the other QA/QC team members.
Implement and continue to upkeep documentation via Quality Control procedures.
Inspect incoming materials by confirming specifications; conducting visual and measurement tests; initial review for potential rejection and return of unacceptable materials.
Manages and maintains the release of goods into market as well as the release of WIP from/to the various facilities in collaboration with the Operations Department and Quality Unit.
Maintain quality systems and improve programs to ensure compliance with industry standards, regulatory requirements for dietary supplements and nutritional products (cGMP, GDP, 21 CFR111, HACCP, FSMA, SQF, NSF, GFCO, TGA, etc.)
Organize, file, and maintain controlled document files such as Certificates of Analysis, Sanitation logs, Pest Control records and other cGMP logs/documents.
Communicate with contract manufacturers to obtain Certificates of Analysis
Assist with cGMP training and adherence to cGMP compliance.
Work with Sanitation Supervisor
Keep measurement equipment operating by following calibration and PM schedules.
Authority for acceptance/rejection of finished products based on their compliance with current specifications and government standards.
Assists in establishing supplier quality requirements and rating system for critical vendors.
Performs root-cause analysis and other problem-solving activities to identify effective corrective actions and process improvement opportunities.
Evaluates and develops CAPAS when non-conformances are identified.
Assists in the development of special projects and works in conjunction with distribution and other departments as needed.
Additional duties as needed.