We are on the lookout for a competitive Coord QA Document to join our stellar team at Milk Specialties Global in Wautoma, WI.
Growing your career as a Full Time Coord QA Document is an incredible opportunity to develop exceptional skills.
If you are strong in leadership, creativity and have the right drive for the job, then apply for the position of Coord QA Document at Milk Specialties Global today!
At Milk Specialties Global, our focus is to create high-quality ingredients designed to optimize health and nutrition. We are passionate and dedicated people. Each day, we collectively explore new, innovative ways to enhance product performance and value through our broad human and animal nutrition portfolios. The human nutrition division focuses on industry leading whey and milk protein isolates, concentrates, and hydrolysates - backed by the speed, execution, and passion it takes to exceed the expectation of our customers.
The MMR Document Coordinator has the responsibility for building and maintaining product Master Manufacturing Records (MMR) at Milk Specialties Global – Wautoma. This includes creating the set of instructions for every product through every stage of the process to ensure successful product realization. Responsibilities include reviewing, maintaining, developing, and correcting controlled documents and the data within those documents or electronic records.
Communicate with internal departments; our customers and suppliers, to gather information supporting product MMRs. Collaborate with Corporate R&D teams to access and verify: Label proofs Master formulas Product routes (Bill of Materials) Request corrections as needed to build accurate MMRs before circulation. Identify pallet configurations with case vendors to meet customer's shipping specifications. Seek approvals when onboarding new customers with an existing internal form: Inkjets Case labels Pallet tags Sampling needs Assist stakeholders in the development, testing, and maintenance of automation projects. Automation projects strive to ensure data accuracies and improve documentation change management: Inkjets Case labels Pallet tags MMR templates Execute attention to detail in System21 to accurately update data fields Follow site's change management program to update all targeted MMRs as customer's needs and/or specifications evolve. Set up item parameters in electronic databases (Redzone). Communicate regularly with our customers to ensure MMRs are approved prior to scheduling requiring the documents for work order releases. Customers may require final MMR approval signoffs before circulation. As a result, effective time management, attention to detail, and prioritization are critical skills in this role. Assist with item maintenance inquiries, investigations, and potential customer complaint reviews related to commercialization. Be instrumental in streamlining the QA process. Give input on ways to improve the QA process within GMP parameters. Look for ways to improve efficiency Complete special projects as assigned in an accurate and timely manner, reporting all data and observations. Provide assistance as needed to ensure that information is conveyed in a timely manner. Communicate with internal departments; our customers and suppliers, to gather information supporting product MMRs. Collaborate with Corporate R&D teams to access and verify: Label proofs Master formulas Product routes (Bill of Materials) Request corrections as needed to build accurate MMRs before circulation. Identify pallet configurations with case vendors to meet customer's shipping specifications. Seek approvals when onboarding new customers with an existing internal form: Inkjets Case labels Pallet tags Sampling needs Assist stakeholders in the development, testing, and maintenance of automation projects. Automation projects strive to ensure data accuracies and improve documentation change management: Inkjets Case labels Pallet tags MMR templates Execute attention to detail in System21 to accurately update data fields Follow site's change management program to update all targeted MMRs as customer's needs and/or specifications evolve. Set up item parameters in electronic databases (Redzone). Communicate regularly with our customers to ensure MMRs are approved prior to scheduling requiring the documents for work order releases. Customers may require final MMR approval signoffs before circulation. As a result, effective time management, attention to detail, and prioritization are critical skills in this role. Assist with item maintenance inquiries, investigations, and potential customer complaint reviews related to commercialization. Assist Quality Manager in evaluating and improving existing quality documentation systems. OTHER RESPONSIBILITIES: Provide assistance as needed to ensure that information is conveyed in a timely manner. Complete special projects as assigned in an accurate and timely manner, reporting all data and observations. Be instrumental in streamlining the QA process. Give input on ways to improve the QA process within GMP parameters. Look for ways to improve efficiency Be ready to step into any situation to help problem solve and to provide solutions. OPEN
Benefits of working as a Coord QA Document in Wautoma, WI:
? Company offers great benefits
? Opportunities to grow
? Competitive salary
