Senior Group Quality Manager - Medical Devices - New Zealand

Posted 25 June 2024
SalaryUp to €110000 per annum
Job type Permanent
DisciplineLife Sciences & Engineering Technologies, Science Leaders & Specialists
ContactTrisha Bracken

Job description

Senior Group Quality Manager - Medical Devices - New Zealand (Visa sponsorship and Relocation fully covered)

Our client is one of New Zealand's largest Medical Device manufacturers employing 7000 professionals globally with revenues of 2 Billion NZD. With three manufacturing sites globally, and a sales team distributed across 65 locations the company has doubled in size over the past five years.

Due to their continued growth and expansion, they are now seeking a Senior Group Quality Manager to be based out of their Auckland, NZ, headquarters and report directly to the General Manager of group Quality.

This is a unique opportunity for an experienced quality manager to play a key role in the success of this medical device operation in a leadership capacity.

The Position

  • Plan, lead, and manage quality support for the product group to achieve quality objectives.
  • Lead, direct, and develop employees to foster a motivated team and high-performance culture.
  • Develop and implement strategies to achieve product group quality goals.
  • Prioritise quality objectives, plan activities, and allocate resources to meet business needs and achieve business plan goals.
  • Monitor and report on quality performance and the suitability of quality system elements within the product group.
  • Identify and implement strategies to improve quality performance.
  • Stay informed on regulatory and industry changes to ensure compliance and implement necessary adjustments.
  • Lead the resolution of quality or compliance issues effectively.
  • Build and maintain collaborative relationships with internal stakeholders to ensure awareness and compliance with regulations and standards.

The Person

  • Degree qualification is required, preferably in engineering, science, or a clinical discipline.
  • Minimum of 5 years working in the medical device industry.
  • Expert knowledge and experience in a range of quality processes.
  • Proven experience interpreting and complying with global medical device regulations.
  • Project management skills.

The Benefits

  • Full Relocation for you and your family is covered.
  • Visa sponsorship.
  • Bonus - Company & LT Shares.
  • Significant career growth and opportunities.

To learn more about this opportunity, apply online or contact Trisha Bracken at HRM Search Partners on +353 16321802, for a confidential discussion.