Senior Group Quality Manager - Medical Devices - New Zealand
- Posted 29 May 2024
- SalaryUp to €110000 per annum
- Location
- Job type Permanent
- DisciplineLife Sciences & Engineering Technologies, Science Leaders & Specialists
- ReferenceBBBH30327_1716994528
- 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 into the General Manager, 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 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 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.
