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What you will be doing

This role, as a quality representative, plays a crucial role in ensuring compliance with World Courier policies and procedures at the local level. They are responsible for overseeing quality-related activities within the Clinical Trial, Commercial, and Transport divisions of the organization. They provide guidance to office, depots and divisional associates on matters of quality and compliance. Additionally, they are responsible for ensuring compliance with local regulatory requirements related to operations and may have regulatory responsibilities in front of local authorities.

Tasks and Key Areas of Responsibility

1) Quality Management System (QMS)

1. a) QMS Management: Developing and maintaining a robust QMS that defines the organization's quality objectives, policies, procedures, and performance metrics. This includes acting as a first contact for the Country Manager and local team for quality related topics and ensuring that quality aspects for CCS and Transport are adequately represented during local and global meetings as well as local and general projects and initiatives.
2. b) Organize and support management review meetings in accordance with applicable SOP.
3. c) Quality Agreements: Review and negotiate quality agreements and Confidentiality Disclosure Agreements (CDAs/NDAs). This includes carefully examining the terms and conditions outlined in these agreements, ensuring alignment with company policies and regulatory requirements.
4. d) Internal / External Audits, Inspections and certification audits: Be the main auditor contact and communicate with relevant parties within the organization. Initiate and oversee the audit organization, respond promptly to auditor inquiries by providing accurate information, supporting documentation or clarification as needed,



and work with management teams to develop and follow up action plans for addressing any identified non‑compliance issues and provide audit responses in due time.
5. e) Incident Management: Review and manage documentation on incidents. Actively participate in investigations of non‑conformities or deviations from established quality standards. Provide quality input for investigations, root cause analysis and CAPA, and support corrective and preventive action initiatives to address root causes. Assist in the creation of comprehensive reports and diligently monitor deviations and subsequent actions as outlined in the specific internal guidelines. Report to integral QA and local leadership any deviations or potential problems and ensure that relevant customer complaints are dealt with effectively.
6. f) Risk Management and Change Control: Assist in setting up and participating in Risk Management and Change Control processes. Ensure that clients are contacted whenever required to communicate changes such as expansions, depot moving process, regulatory updates clarifications, etc.
7. g) Pest Control and Facility Cleaning: Ensure that pest control and cleaning programs are properly implemented and documented following applicable SOPs.
8. h) Technical Quality Support: Overview and verify technical change controls, calibration, maintenance and qualification/validation program according to internal guidelines, supporting the local facility representative and QA manager technical compliance. Support the review of temperature graphs as defined in applicable SOP.
9. i)



Documentation Management: Ensure accurate documentation of all quality-related activities such as SOPs, work instructions, test records, audit reports, etc. Organize regular reviews of e.g. Local Standard Operating Procedures (SOPs) and Work Instructions (WIs) with the process owner/author. Support the review of these documents to ensure that they align with established service standards as well as quality and regulatory requirements.
10. j) Quality Data Management: Execute all tasks using dedicated software tools such as Master Control and SharePoint (or other applicable software tools). Accurately input and timely update data, attach relevant documents, track progress, document actions taken, and adhere to any specific workflows or process as outlined in the standard operating procedures.

2) Quality Control

1. a) Quality Checks and Control: Implement processes to monitor product or service quality throughout the entire lifecycle from design to delivery. This may involve conducting inspections and analyzing data to ensure accuracy and quality of records, to identify defects or areas for improvement.
2. b) Self Inspection and Quality Checks: Responsible for quality related activities related to the Self‑Inspection Report as well as quality checks as defined in standard procedure.
3. c) Manufacturing (CSS only):
- Ensure that the batch processing and final records related to the relabeling operation are reviewed through QA spot checks and documented appropriately.

Legal and Non-Discriminatory Statement

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status.

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Postúlate en Kit Empleo: kitempleo.cl/empleo/1djnfq

📌 QA Supervisor (Santiago)
🏢 Cencora
📍 Santiago