Prinova US LLC
At Prinova, our passion for food knows no bounds! With a rich history spanning over four decades in the food industry, we have established ourselves as a trusted global supplier and manufacturer of functional food ingredients, flavors, and aromas. With CUSTOMER FOCUS as our central core value, we put pride in our work to ensure the end user has a quality product.
For the past four years, Prinova has proudly received national acclaim as one of the Best and Brightest Companies to Work For® in the Nation, a testament to our status as an exceptional employer.
Guided by the renowned FISH® philosophy, we prioritize creating meaningful work interactions, fostering community engagement, and empowering professional growth, ensuring a remarkable and fulfilling experience for our team members.
Quality Systems Supervisor
Department:
Quality Admin Location:
Salt Lake City, UT
The Quality Systems Supervisor manages the QA functions that ensures the release and approval of the production work order according to internal and customer specifications. Also, oversee the duties of the QA Document Control Specialist, QA Specialist, Compliance Coordinator, and Quality Systems Specialists
Main Duties & Responsibilities
Ensures compliance with established regulations and customer requirements, including GMPs as listed in 21 CFR 111 and 117 and the Global Food Safety Initiative (GFSI) scheme; Coordinate the product lot release schedule with customer service and lab management to ensure efficient and on-time release of product batches; Monitor and track non-conformances that affects Positive Product Releases (i.e. OOS, NC's, rework, CCP failures); Reviews laboratory testing documents (QC Chemistry & Micro) ensuring all results conform to product specifications; Creation of all Certificate of Analysis, including those sent to the customer; Document retrieval from local files and archives, as required for submissions and customer requests. (i.e. Canada); Maintains deviation and change control records; E-File documents in quality management system and ERP system; Compiles all completed Batch Manufacturing Records/Filing; Support internal audits to ensure policies and regulations of FDA (cGMP), TDA, customer, third party certifiers and internal SOPs are followed; Assist with traceability and mock recall exercises; Assist in inter-departmental training and provide compliance guidance to personnel; Follow and enforce cGMP guidelines and processes as established in department SOPs; Perform other duties as deemed necessary. Requirements and Skills
1-3 years' experience in related field preferred (quality assurance, safety, regulatory, documentation control, etc.); High School Diploma or GED required; some college experience preferred; Attention to detail, strong organization, and record-keeping skills essential; Effective verbal and written communication skills; Advanced proficiency in Microsoft Office products including Excel, PowerPoint, and Word; Working knowledge of JD Edwards or other inventory tracking software; PCQI certification preferred; Ability to work without direct supervision. Ability to lift up to 15 lbs.; Ability to sit and stand for extended periods of time; Ability to view a computer screen and type for extended hours; Work environment is normally in an office setting. Must be able to make frequent rounds in a warehouse environment; Other physical requirements include moderate standing and occasional squatting, bending, and twisting; Ability to wear any required PPE; Ability to adjust work schedule as business needs require. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Benefits:
Medical, Dental, Vision Employer paid STD and LTD HSA and FSA PTO Employer paid Basic Life Insurance 401(k) & Roth with employer match Eight Paid Holidays + 2 Floating Holidays Voluntary - Critical Illness, Hospital Indemnity, Accident Personal growth including training and development opportunities
For the past four years, Prinova has proudly received national acclaim as one of the Best and Brightest Companies to Work For® in the Nation, a testament to our status as an exceptional employer.
Guided by the renowned FISH® philosophy, we prioritize creating meaningful work interactions, fostering community engagement, and empowering professional growth, ensuring a remarkable and fulfilling experience for our team members.
Quality Systems Supervisor
Department:
Quality Admin Location:
Salt Lake City, UT
The Quality Systems Supervisor manages the QA functions that ensures the release and approval of the production work order according to internal and customer specifications. Also, oversee the duties of the QA Document Control Specialist, QA Specialist, Compliance Coordinator, and Quality Systems Specialists
Main Duties & Responsibilities
Ensures compliance with established regulations and customer requirements, including GMPs as listed in 21 CFR 111 and 117 and the Global Food Safety Initiative (GFSI) scheme; Coordinate the product lot release schedule with customer service and lab management to ensure efficient and on-time release of product batches; Monitor and track non-conformances that affects Positive Product Releases (i.e. OOS, NC's, rework, CCP failures); Reviews laboratory testing documents (QC Chemistry & Micro) ensuring all results conform to product specifications; Creation of all Certificate of Analysis, including those sent to the customer; Document retrieval from local files and archives, as required for submissions and customer requests. (i.e. Canada); Maintains deviation and change control records; E-File documents in quality management system and ERP system; Compiles all completed Batch Manufacturing Records/Filing; Support internal audits to ensure policies and regulations of FDA (cGMP), TDA, customer, third party certifiers and internal SOPs are followed; Assist with traceability and mock recall exercises; Assist in inter-departmental training and provide compliance guidance to personnel; Follow and enforce cGMP guidelines and processes as established in department SOPs; Perform other duties as deemed necessary. Requirements and Skills
1-3 years' experience in related field preferred (quality assurance, safety, regulatory, documentation control, etc.); High School Diploma or GED required; some college experience preferred; Attention to detail, strong organization, and record-keeping skills essential; Effective verbal and written communication skills; Advanced proficiency in Microsoft Office products including Excel, PowerPoint, and Word; Working knowledge of JD Edwards or other inventory tracking software; PCQI certification preferred; Ability to work without direct supervision. Ability to lift up to 15 lbs.; Ability to sit and stand for extended periods of time; Ability to view a computer screen and type for extended hours; Work environment is normally in an office setting. Must be able to make frequent rounds in a warehouse environment; Other physical requirements include moderate standing and occasional squatting, bending, and twisting; Ability to wear any required PPE; Ability to adjust work schedule as business needs require. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Benefits:
Medical, Dental, Vision Employer paid STD and LTD HSA and FSA PTO Employer paid Basic Life Insurance 401(k) & Roth with employer match Eight Paid Holidays + 2 Floating Holidays Voluntary - Critical Illness, Hospital Indemnity, Accident Personal growth including training and development opportunities