Reporting Quality Assurance Management, the QC Inspection Specialist is responsible for quality control, raw material, in-process and finished goods inspection. This position works closely with Planning, Manufacturing, Supply chain, Strategic procurement and Operations internally and external suppliers and partners. The role will establish and maintain trackers for raw material, in-process and finished goods batch movement. Working to create and ensure Nordic Natural quality standards are met at all levels of production. Comply with Nordic Naturals quality standards as well as State, Federal, and international regulations. Other duties and responsibilities as assigned by the Quality Assurance Management.
ESSENTIAL FUNCTIONS
Reasonable Accommodations Statement
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable Accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.
Essential Functions Statement(s)
• Assist with establishment and maintenance of quality standards for raw materials, components, in-process and manufactured goods, including performance metrics and quality feedback for suppliers.
• Maintain quality control standards for incoming and in-process inspections, specifically working with and supervising QC inspectors.
• Manage quality data records and databases to establish and maintain quality metrics for review of material and goods.
• Assist with the development of or improve upon existing quality control inspection standards.
• Review supplier submitted documentation against internal specifications for raw materials, packaging, in-process and finished product.
• Working knowledge of food safety, food and supplements manufacturing supply chain, procurement and production process.
• Assist with corporate metrics around supplier quality, failures and on time rates and provide QA representation on the Material Review Board.
• Assist with internal audits of the quality control process to ensure continuous improvement and meet all regulatory standards for current Good Manufacturing Practices (cGMPs).
• Assist in FDA, CDPH, and third-party audits to meet 21 CFR Part 111. Ensure all findings are addressed appropriately to ensure continued certification and compliance to Federal and State regulations.
• Other duties as assigned.
POSITION QUALIFICATIONS
Competency Statement(s)
SKILLS & ABILITIES
Computer Skills
Other Requirements