Job Description:
PAT Vitamins was founded in 1995, by Dr. Steve Huang, PHD in Chemistry (Rensselaer Polytechnic Institute). PAT Vitamins started by supplying Chinese manufactured Ascorbic Acid to the Nutritional Industry here in North America. By emphasizing product quality, technical support, on-time delivery, and manufacturer selections, we are proud to provide a set of value-added services to all our customers. Within the past decades PAT Vitamins has established close relationships with its original manufacturers. The company chooses to work with manufacturers that care about the health of the consumers and can produce high-quality raw ingredients to enhance wellness and support our mission. With a comprehensive quality agreement in place and a thorough risk assessment completed, PAT Vitamins has managed to work with the most reputable manufacturers such as the following: Xinfa Pharmaceutical, Hubei Guangji, and Wilmar Springfruit, to name a few.
PAT Vitamins believes in this industry and is passionate about growing to the next level and is currently looking for a QA, Regulatory Specialist and Technical Support.
Description
PAT Vitamins believes in this industry and is passionate about growing to the next level and is currently looking for a QA, Regulatory Specialist and Technical Support.
Description
- Oversee all quality functions in the facility and ensure systems adhere to Quality Master Plan;
- Provide direction, support, and communication to all employees in the facility regarding quality systems, guidelines, and standards compliance, such as QA Inspectors at all locations;
- Lead product incident problem solving and resolution. Identify causes to product quality incidents by using direct staff and collaborating with operations peers to quickly understand issue. Lead to control product and prevent further incident by implementing effective solutions. Document and track incident reports, corrective actions, and material reviews;
- Complete final review and approval of product specifications, production batch records, laboratory raw data, labels, and COAs for raw materials and finished products;
- Complete internal audits to ensure policies and regulations of FDA (cGMP), TDA, third party certifiers and internal SOPs are followed;
- Maintain and monitor HACCP Program to insure plant sanitation requirements are met;
- Interface with outside governmental agencies, such as: USDA, FDA, TDA, etc. and to consumers and customers through investigation and response to complaints;
- Interface with customers for their audit requirements and provide technical support through continuous monitoring of the Supplier Qualification Program;
- Maintain records of internal and external deviations, incident reports, corrective/preventative actions and employee training; Ensure staff follows all safety procedures;
- Perform any other related duties assigned.
Compensation/Salary:
DOE
Category:
Confidential Job:
0
Last Resume Date:
Thursday, June 16, 2022 - 5:15am
Contact First Name:
Steve