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Country Quality Lead Australia & New Zealand

悉尼, 澳大利亞 Regular 发布于   Jun. 19, 2026 申请截止于   Jul. 20, 2026
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Job Title: Country Quality Lead Australia & New Zealand

Location:   Barangaroo, Australia

Job Type: Full time

About the Job

Our Team/ Overview:

Lead and manage the implementation and maintenance of the Country Quality system for GxP transversal process and new product introduction embarking all concerned country functions (responsible for Good Practices - GxP and health-regulated activities), ensuring quality of safe and effective products, information and services made available to meet patients and customers’ needs.

Main Accountabilities

1.   Commercial Operations

  • Develops and implements the quality program in alignment with local and corporate objectives.
  • Provides leadership and in the identification delivery of strategic quality initiatives across the business.
  • Establishes effective working relationships across the local business, other country organizations, key customers, and suppliers
  • Foster a sense of quality throughout the business.
  • Established tracking systems to understand the health of the Quality System.
  • Demonstrates a strong knowledge of local TGA and MEDSAFE GxP regulations and is able to lead local teams in projects impacted by these regulations.
  • Establish and maintain quality across the local organization. This system must be complaint with the ISO9001:2015.
  • Manage the product quality complaints process in accordance with local GxP and company procedures.
  • Develops and carries out an audit program for the detection, and rectification of anomalies within the quality system, in accordance with the GMP, GWP, GLP, ISO and company procedures.
  • Maintain an appropriate level of supervision of third-party manufacturing sites mitigates risk of the production of non-conforming products. Supervision may include the review of master production documentation, stability, and validation programs.
  • Product is released for distribution in conformance to the registered specification. Maintain hold statuses appropriately
  • Ensures an effective document management system is on place and works with others on the development of documentation.
  • Provides leadership in the management of critical quality events such as recalls.
  • Participates in the use of Quality Management techniques in the improvement of company processes.
  • Work with key customers and suppliers to improve processes.
  • Is involved in continued learning through participation in associations, conference, outside meetings and involvement within the Quality network.
  • Ensures an effective management of repackaging systems is in place for some products sold in Australia and New Zealand.
  • Provide support (as needed) to internal customers (Supply, Reg Affairs, Medical) relating to manufacturing and quality.
  • Support product launches and transfers through developing a technical understanding of the products and manufacturing process to aid in the knowledge transfer, as well as creation of the technical transfer package.
  • Provide training on quality systems as required.
  • Provide support to other functions of the Quality team as required.
  • Participate in local and global projects as required.

2.     People Management

  • Recruit, develop and coach for high performance.
  • Conduct and document regular performance reviews and an annual review as well as regular personal / career development discussions with direct reports, in line with agreed Sanofi Performance Management Process
  • Build, guide, and coach teams to deliver work output within timeline & budget constraint

3.     MCO (Multi Country Organization) Leadership & Support

  • Provide leadership and support with the South Korea and Australia New Zealand MCO as required and act as subject matter expert on assigned topics
  • Serve as a technical reference for the assigned quality processes and promote best practices,
  • Facilitate knowledge sharing and continuous improvement among quality teams

Candidate Profile

Essential Skills and Experience

  • Essential Qualifications
  • 5-10 years in the pharmaceutical industry in a similar role
  • Medical terminology
  • Product knowledge
  • Knowledge of relevant codes of GxP
  • Knowledge of Manufacturing and warehousing operations
  • Knowledge of quality systems
  • Document management
  • Tertiary qualifications in life sciences or related field

Desirable Skills and Experience

Desirable Qualifications

  • Presentation skills
  • Negotiation skills
  • Leading Teams / People Management
  • Knowledge of SAP & Digital QMS Systems (VEEVA)\
  • Registration with relevant Professional Association / Government Board
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