Quality Inspector

Growve•Ogden, UT

5d•Onsite

About The Position

In this role, The Quality Inspector will be managing and maintaining the quality control compliance, reviewing batch records, inspecting production including blending, encapsulation and packaging. This role is for second shift at our Ogden location.

Requirements

1+ year of experience in Quality and/or Manufacturing in a cGMP environment.
1+ years of QA Inspection experience.
Knowledge of quality systems, cGMP, and GDP (Good Documentation Practice).
Proficient with MS Office.
Ability to identify deficiencies and lead continuous improvement initiatives in cooperation with other members of the quality team.
Ability to interact efficiently with a multidisciplinary team.
Excellent written and verbal communication skills.
Knowledge and understanding of the Dietary Supplement Industry.

Nice To Haves

Bachelor’s degree in science is a plus, but not necessary if proven industry skills.

Responsibilities

Responsible for accurately inspecting raw materials, in-process products, and finished goods throughout the manufacturing process to verify product quality and safety.
Adhere to the Standard Operating Procedures (SOP’s) and Good Manufacturing Practices.
Responsible for Implementation and upkeep of documentation per QC procedures.
Inspect incoming materials by confirming specifications; conduct visual and measurement tests; initial review for potential rejection and return of unacceptable materials.
Review the batch record and the batch record reconciliation from beginning to end of the manufacturing process.
Meticulously document in -process checks, results of inspection, and any deviations from approved standards.
Create and maintain up-to-date records of all quality assurance activities; temperature logs, sample logs, retains, cleaning logs.
Ensure all documentation of inspection and sample retention of processes are retained correctly on the proper forms.
Provide any information or retain samples required to complete any investigations, complaints, or deviations.
Adhere to quality systems to ensure compliance with industry standards, regulatory requirements for dietary supplements and nutritional products (cGMP, GDP, 21 CFR 111, HACCP, FSMA, SQF, NSF, GFCO, TGA, etc).
Responsible for communicating any quality defects with management.
Ability to work in different areas of production as needed.