Responsible for following all aspects of company safety rules and procedures including helping informing management of any unsafe conditions. Follow all working guideline instructed by the Barcel USA including the 5’s protocol which is based on keeping the working areas clean and organized. Ensure Good Manufacturing Practices and Food safety and quality guidelines are being followed. Investigate customer complaints and non-conformance issues. Develop, recommend and monitor corrective and preventive actions. Prepare reports to communicate outcomes of quality activities and customer complaints reclassification.

Provide support documenting process improvement projects.

Provide support with administrative activities such as KPI’s reports on a weekly basis.

Responsible for the monitoring activities of the Microbiology program. Ability to work as an integral part of the team.

Ability to learn different analytical techniques; all laboratory procedures.

Proficiency in basic computer skills including Microsoft Office and its tools such as Planner, Teams, OneDrive, Share point, etc.

Excellent verbal and written communication skills. 

Demonstrated ability to maintain a positive work atmosphere by behaving and communicating professionally and effectively with others as well as being able to receive communication from others.

Must be organized and thorough with all lab procedures.

Must have excellent attention to detail and have accurate follow through. 

Must have thorough knowledge of the testing procedures and specifications for finished products, intermediates, and raw materials.

Must be able to do math computations and calculations.

Responsibilities in verification and validations, participation in internal audits.

Demonstrated knowledge of OSHA Laboratory Standards and requirements.

Design and manage fixed asset systems; create weekly managers reports monitoring KPI.

Assist with implementing new Vivaldi QMS system and integrate all plant documents into new system and manage new system when complete.

Lead cross functional project team to build user-friendly windows base customer support applications which interface with the OmniPlan/OmniPlus mainframe application.

Prepare reports using ProClarity for outstanding CAPA cases and tasks.

Participate in audits supporting GMP areas through an in-house training program.

Host GMP/GLP inspections and customer audits for market products and services and associate CAPA management.

Author QMS documents, specifications, and process guides to meet and maintain quality standards. Collect daily product audit and data for CMM operations, PPAP, tracking and reporting. Conduct GMP and GLP audits (internal and external) for Taconic departments, vendors and suppliers.

Develop quality meeting agendas, type and distribute meeting minutes, and update SharePoint with quality meeting records.

Create and complete the backbone of a HACCP plan for the crush mill along with step by step flow chart analysis. Handle this additional duty when need for a few hours daily while payroll are being process and during vacation for coverage.

Systematize records for reporting certify payroll. Provide explanation of all HACCP documentation to any auditor.