Qc/qa Associate Iii - Rancho Cucamonga, United States - Amaxi Nutrition Products

Description

Amaxi Nutritional Products is a USDA and FDA food manufacturing facility with the goal to providing nutritious, safe, and healthy food products. We serve both domestic and international markets.


Reporting Structure:
Report directly to the Quality Supervisor/Manager and have specific responsibilities outlined below.


Duties and responsibilities

• Sample materials, bulks and finished goods when necessary.
• Perform sanitation verification and allergen testing on equipment and other areas required.
• Organize, file, and maintain the Quality management system and its corresponding files.
• Participate with internal site audits.
• Ensure the quality records are prepared and collated in accordance with project requirements.
• Prepare and maintain test data for review.
• Correct recording and filling of all relevant record logs and documentation.
• Review all batch productionrelated records, including but not limited to all records for packaging and labeling operations, ensuring that production records are reviewed for completion and errors.
• Always assure use of the most current revision of all documentation.
• Review all receiving records for components, packaging, and labels.
• Determine whether all components, packing, and labels conform to specifications.
• Conduct incoming and inprocess inspection, sampling, final testing and inspection of finished products.
• Perform appropriate tests and examinations of manufacturing batches.
• Perform appropriate tests and examinations of manufacturing batches at points, steps, or stages identified in the master manufacturing record where control is necessary to prevent adulteration.
• Create requests for testing and follow up with outside laboratories for 3rd party tests and results.
• Develop, improve, and customize analytical methods and standard procedures to improve quality and efficiency.
• Maintain all analytical equipment according schedule and to standard.
• Resolve problems with instruments, test methods, lab chemicals, standards, and samples with direct support from Management.
• Assure calibrations, chemicals, analysis and other cGMP compliance activities are performed in the laboratory as applicable.
• Train, coordinate, and advise personnel in test procedures for analyzing components and physical properties of materials.
• Instrumentation experience including Micro, FTIR, and other applicable testing methods to ensure product validity.
• Perform quality control and calibrate equipment if necessary.
• Maintain equipment in proper working order and maintain a clean work area.
• Perform routine and nonroutine tests and analyses using the appropriate technical equipment and instruments.
• Perform miscellaneous tasks within the department as required.
• Effectively manage a documented sample retention program for raw materials/ingredients, Inprocess materials, and finished products.
• Adhere and follow all guidelines prudent to CFR 111, FDA, and applicable governing agencies such as the NSF, SQF, Halal, Kosher, etc.
• Perform other duties as assigned.

Qualifications

• Ability to lift 50lbs.
• Flexible schedule
• Able to work with mínimal supervision.
• Minimum of 4year experience in the Quality or Quality Control Department of a food manufacturing company or related field.
• 2+ years of experience working in a Laboratory
• Competent knowledge of FDA, and cGMP regulations
• Proficiency in document control and organization.
• Highly responsible, selfmotivated and must be able to work in a team environment.
• Proficient in Computer skills.

Pay:
$ $34.00 per hour

Expected hours: 40 per week


Experience level:

• 4 years

Schedule:

• 8 hour shift
• Monday to Friday
• Overtime
• Weekends as needed

Work setting:

• Inperson

Ability to Commute:

• Rancho Cucamonga, CA (required)

Work Location:
In person