Advisor Senior Advisor (GMP Audit)

• Wellington based Permanent Full time
• Influence regulatory decisions and provide trusted technical advice
• Midpoints of $92874 & $106849 dependent on experience

Ko tōu ake mahi - What youll do

This is a handson technical role at the frontline of medicines regulation where your expertise directly protects public health. As an Advisor (GMP Audit) youll play a critical role in ensuring medicines supplied in New Zealand are manufactured to the highest quality standards. Youll work with industry travel to manufacturing sites influence regulatory decisions and provide trusted technical advice in a fastmoving highimpact environment that balances rigour judgement and collaboration

• Lead and deliver GMP audits of medicine manufacturing and packing sites in New Zealand and overseas independently or as part of an audit team.
• Assess compliance and drive regulatory decisions evaluating audit findings corrective actions and making recommendations on licences approvals and GMP certification.
• Be a trusted technical authority providing clear GMP advice to industry supporting regulatory decisions and contributing to investigations and medicine recalls.
• Support continuous improvement and delivery contributing to projects process improvements and highquality advice across the Directorate.
• Build strong relationships and work with integrity collaborating across the Ministry and with external stakeholders while upholding equity priorities and Te Tiriti o Waitangi obligations.

Ko ngā pūkenga ōu - What youll bring

• A tertiary qualification in a relevant field for example a pharmacy qualification or a science or engineering-based qualification.
• Hold a full New Zealand drivers license and be comfortable driving in different areas of New Zealand.
• Strong technical foundation with a relevant tertiary qualification and handson experience in medicines manufacturing and GMP environments.
• Proven quality and audit expertise including experience working within pharmaceutical quality systems and contributing to or leading GMP audits.
• Clear and confident communicator able to engage effectively with industry regulators and stakeholders across a range of technical and nontechnical settings.
• Highly organised and detaildriven with the judgement and foresight to manage competing priorities meet deadlines and handle sensitive information.
• Analytical and digitally capable applying critical thinking sound judgement and practical data skills (including Excel) to inform advice and decision

Ngā hua o tō mātou whare - What we bring

Discover a world of opportunities for personal and professional growth. Were not just a workplace; were a whanau that values your well-being and the importance of work-life balance. At Manatū Hauora we value the authentic you ensuring that every voice is heard and every perspective matters. Your wellness is our priority with comprehensive support and resources to keep you thriving. Join us today and be part of a team dedicated to improving healthcare.

We are committed to fostering an inclusive and respectful environment welcoming applicants from diverse backgrounds. We value the unique perspectives and experiences each individual brings. Please contact us if you require any support to ensure the recruitment process is accessible.

Me pēhea te tono mai - How to apply

Applications close on Tuesday 10th March.

Please note that you must have full time legal working rights and be based in Wellington to be eligible for this role. If you plan to relocate please state your plans in your cover letter.

Click here to view the position description. Please follow the online process at our Careers Website. Please ensure you upload a CV and covering letter with all applications. If you have any questions email the recruitment team at .