Quality Inspector Growve - 3.7 Ogden, UT Job Details Full-time 1 day ago Benefits Health insurance 401(k) Qualifications Quality control experience within consumer goods industry Raw material quality management Performance improvement leadership Quality records maintenance Laboratory document review Good documentation practices (GDP) Inspection reporting and documentation Manufacturing standard operating procedures Laboratory quality control records management Bachelor's degree HACCP Quality assurance standard operating procedures Compliance documentation Visual inspection as testing technique Regulatory/legal compliance standards in production Operational excellence initiatives Productivity software Production batch record review Quality control communication 1 year Standard operating procedures (SOPs) Manufacturing company experience Communication skills Entry level FDA regulations

Full Job Description Company Overview:

Growve is a leading health and wellness company specializing in acquiring, operating, and growing world-class brands within the active nutrition, dietary supplement, and beauty verticals. Our portfolio includes 16+ brands and thousands of unique products.

Position Title:

Quality Inspector Position Overview:

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.

Objectives & 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.

Skills & Qualifications:

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. Bachelor's degree in science is a plus, but not necessary if proven industry skills. Knowledge and understanding of the Dietary Supplement Industry.

Additional Information & Benefits:

Full Time with Competitive Pay. Health Benefits Package DTO 401(k) Progressive Working Environment Located in Ogden, Utah Notice to Recruiters — We do not work with outside recruiting agencies. Please do not solicit. This description is not intended to be an exhaustive list of responsibilities and qualifications. The position, duties, and qualifications are subject to change at any time.