Essex Junction, VT 05452
Full-time

Full Job Description
Job Overview:
As an Associate Quality Assurance Specialist you will collect, analyze, and report performance data for the manufacturing site quality program. This includes standardizing documentation by participating with the development, completion and maintenance of the internal standards references. In addition, you will analyze data and documentation including but not limited to product and process specifications, policies, and other operational records to support the manufacturing site’s compliance to GFSI (Global Food Safety Initiative), corporate and regulatory requirements.

Shift & Schedule: This is a full time position on 1st shift, Monday-Friday, 8am-5pm. Flexibility to work overtime, weekends and holidays as scheduled is required.

Benefits: KDP offers a very competitive benefits package that includes medical, dental, vision, 401k, Beverage Benefit, & so much more! Benefits are available to new hires DAY 1!

What you will do:

Gather, calculate, audit, and report key information to ensure compliance specific to customer requirements and product specifications.
Record production data in appropriate database for customer, regulatory, and GFSI compliance. Analyze data and prepare weekly and/or monthly summary reports, including but not limited to trend analysis.
Work with operations and quality departments to ensure proper documentation is maintained to support activities related to traceability exercises, recalls, and stock recovery of manufactured products.
Assist in trials ensuring new products meet manufacturing standards.
Assist in preparing pertinent documentation and reports on quality and food safety issues by providing key data analysis.
Work with data streams to understand and communicate all potential impacts; identify priority opportunities for the Continuous Process Improvement teams.
Appropriately communicate to keep the relevant stakeholders aware of focus areas, including status of open issues and opportunities for improvement concerning electronic and manual data collection.
Ensures records are maintained to meet all site certification requirements.
Promote, support and guide the development of standardized documentation per corporate Keurig Dr Pepper policies and procedures.
Maintains the manufacturing site library system of standard’s documents, ensuring completeness, accuracy, and accessibility of reference information to operators, supervisors and other interdependent parties.
Interface with manufacturing site teams to ensure document standards are maintained in a manner that meets requirements.
Maintains change control processes for new documents and document revisions, including the process where approved copies of documents are circulated effectively, and obsolete versions of documents are destroyed.
Works with related departments to effectively ensure that requested policy, process and product standard changes are evaluated, approved, and documented appropriately.
Must work effectively in team environments, communicating and participating in a constructive manner.
Multitasking is required daily, and constant assessment of prioritization is required to best meet both the customer and business needs.
Must be proactive, anticipating and planning to meet objectives by finding ways to identify potential obstacles and improve processes and procedures to prevent occurrence.
Performs other duties as requested by management.
Responsibility to report food safety, quality and regulatory compliance to plant or division personnel with authority to initiate action.
Ensure the staff is aware of their responsibility to report food safety, quality and regulatory compliance to plant or division personnel with authority to initiate action.
Responsible for ensuring the production of a safe, wholesome and quality product and requires trained designees when applicable.
Performs other duties as requested by management.
Follow all Keurig Dr Pepper policies and procedures



Essex Junction, VT 05452 Full-time Full Job Description Job Overview: As an Associate Quality Assurance Specialist you will collect, analyze, and report performance data for the manufacturing site quality program. This includes standardizing documentation by participating with the development, completion and maintenance of the internal standards references. In addition, you will analyze data and documentation including but not limited to product and process specifications, policies, and other operational records to support the manufacturing site’s compliance to GFSI (Global Food Safety Initiative), corporate and regulatory requirements. Shift & Schedule: This is a full time position on 1st shift, Monday-Friday, 8am-5pm. Flexibility to work overtime, weekends and holidays as scheduled is required. Benefits: KDP offers a very competitive benefits package that includes medical, dental, vision, 401k, Beverage Benefit, & so much more! Benefits are available to new hires DAY 1! What you will do: Gather, calculate, audit, and report key information to ensure compliance specific to customer requirements and product specifications. Record production data in appropriate database for customer, regulatory, and GFSI compliance. Analyze data and prepare weekly and/or monthly summary reports, including but not limited to trend analysis. Work with operations and quality departments to ensure proper documentation is maintained to support activities related to traceability exercises, recalls, and stock recovery of manufactured products. Assist in trials ensuring new products meet manufacturing standards. Assist in preparing pertinent documentation and reports on quality and food safety issues by providing key data analysis. Work with data streams to understand and communicate all potential impacts; identify priority opportunities for the Continuous Process Improvement teams. Appropriately communicate to keep the relevant stakeholders aware of focus areas, including status of open issues and opportunities for improvement concerning electronic and manual data collection. Ensures records are maintained to meet all site certification requirements. Promote, support and guide the development of standardized documentation per corporate Keurig Dr Pepper policies and procedures. Maintains the manufacturing site library system of standard’s documents, ensuring completeness, accuracy, and accessibility of reference information to operators, supervisors and other interdependent parties. Interface with manufacturing site teams to ensure document standards are maintained in a manner that meets requirements. Maintains change control processes for new documents and document revisions, including the process where approved copies of documents are circulated effectively, and obsolete versions of documents are destroyed. Works with related departments to effectively ensure that requested policy, process and product standard changes are evaluated, approved, and documented appropriately. Must work effectively in team environments, communicating and participating in a constructive manner. Multitasking is required daily, and constant assessment of prioritization is required to best meet both the customer and business needs. Must be proactive, anticipating and planning to meet objectives by finding ways to identify potential obstacles and improve processes and procedures to prevent occurrence. Performs other duties as requested by management. Responsibility to report food safety, quality and regulatory compliance to plant or division personnel with authority to initiate action. Ensure the staff is aware of their responsibility to report food safety, quality and regulatory compliance to plant or division personnel with authority to initiate action. Responsible for ensuring the production of a safe, wholesome and quality product and requires trained designees when applicable. Performs other duties as requested by management. Follow all Keurig Dr Pepper policies and procedures
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