Internal QSE Auditor

General Purpose

Contribute to achieving the objectives of the integrated management system, through audits with a systematic and professional approach to assess compliance with the requirements, standards, and applicable laws regulatory requirements as well as the administration of document control and effective corrective actions of the organization's Integrated Management System.

Duties and Responsibilities

• Perform scheduled/assigned internal audits and assigned inspections scheduled during the month (GMP verification), inspections of the following process:  production, packaging, reception of  raw material and packaging materials, sanitation, mixing & blending, water treatment,  prevention of foreign matter, verify compliance with the storage conditions of allergenic products, finished products, ingredients and packaging materials and  fleet area; mapping of the conditions of starting lines and generate report of findings found, as well as the corresponding actions.
• Comply with periodic tours in the facilities.
• Review the documents and records in the areas to verify compliance with the compliance calendar.
• Provide advice and establish communication with the managers, coordinators and supervisors of areas for the implementation of policies, programs, work instructions or SOP’s, and training for the improvement of the integrated management system.
• Communicate the results of the internal reviews (audits/inspections) to the Plant Manager, Quality Management and Management Systems Facilitator.
• Support facility activities to follow up on the results of walkthroughs and audits through the corrective action program.
• Support facility activities to carry out the calculation of the Corrective Action Plan Effectiveness Indicator.
• Support facility activities to communication communicating the progress of the Corrective Action Plan Effectiveness Indicator to the Management Team.
• Jointly review with the users when the agreements of the Plans are not reached.
• Make an analysis of effectiveness for the evidence presented to comply with the Corrective Action Plans.
• Perform and document the effective closure of the Corrective Action Plans.
• Support facility activities for managing the document control software (SIGO).
• Advise staff on any required updating of documentation.
• Support facility activities to receive and publish external documentation that has a potential impact on the plant.
• Verify that the documentation is up to date and enforced during audits and inspections.

Qualifications

Minimum Education: Professional

Desirable Education: Master's Degree or Postgraduate

Bachelor's Degree:

• Chemical Sciences
• Food Science/Food Engineering
• Industrial Engineering

Career Experience:

2 Years Quality Analyst

1 Year Quality Assistant