Quali Tech, LLC is a manufacturer of plant nutrition, animal nutrition, and food ingredients products and services. Found in 1967, Quali Tech has been developing new techniques to formulate specialized combinations of ingredients resulting in high quality, cost-effective and innovative products and services guided by our values. World Class Customer Service Uncompromising Quality Family Feel/Professionally Run Qualitech is seeking experienced Quality Assurance Tech for 3rd shift to ensure product safety and the quality of all products in the Food Divisions as well as ensuring regulatory compliance with regulatory bodies, customers and QualiTech.
Shift Hours: 9pm to 5.30am (Sunday - Thursday) $3/hr shift differential.
Essential Duties and Responsibilities:
Responsible for monitoring, evaluating, and reporting analytical results of products and raw materials including alerting out of compliance results
Assist in administering the Company's Quality Program in accordance with customer and company requirements. This includes:
- Review and assist in development of QA procedures
- Regular review of production and receiving records
- Sensory evaluation, visual inspection and analyses (Organoleptic, Moisture, Water Activity) of raw ingredient and finished product samples
- Maintain sample retain library
- Conduct final wash inspections of all production rooms
- Assist in troubleshooting product discrepancies
- Internal audits of cGMP areas and premises, including glass and brittle inventories
- Maintain lab safety
- Conduct Monthly/Quarterly/Bi-Annual/Annual tasks as required by the Food Safety Calendar
- Conduct environmental analyses, i.e. swabbing
- Conduct titration analysis of sanitation chemicals
- Participate in finished goods hold/release system
- Conduct tasks in accordance with Good Laboratory Practices.
- Lend technical support to R&D and Operations as appliable
- Assist in customer complaint investigations
- Assist in the compliance with all appropriate third-party audits such as BRC, Safe Food/Safe Feed and HACCP.Create & Maintain production documents including archival storage & organization, master document storage, certificates of analysis.
Education and Experience:
High School Diploma or GED required and 3 years experience in quality control and assurance in an FDA regulated industry or Bachelor's Degree in a science related field preferred.
A background in manufacturing and processing environments is desired.
Proven analytical strengths and experience.
Compensation details: 25-28 Hourly WagePI-0537
