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2 weeks ago
This is a 12-month contract position with the potential to extend.
As part of our organization, you will contribute to business growth by providing regulatory expertise for a portfolio of products.
Our team is dedicated to delivering exceptional outcomes for patients and customers.
You will oversee a product portfolio, develop strategic regulatory plans, and manage local regulatory submissions for Australia and New Zealand.
Collaboration is key, and you will work closely with global, regional, and local colleagues throughout the submission and evaluation processes.
Responsibilities include leading cross-functional project teams, providing regulatory guidance, and ensuring compliance with relevant regulations.
Required Skills and Qualifications- Bachelor's Degree in Pharmacy or Science or a related field
- Previous experience in Regulatory Affairs, preferably in prescription medicines within Australia and New Zealand
- Proven technical expertise working with the TGA and Medsafe
- A natural growth mindset, positive attitude, and self-motivation
- Effective verbal and written communication skills, ability to lead from the front, and solid stakeholder management and negotiation skills
A competitive remuneration package, ongoing training, and award-winning leadership development programs.
Part of an organization that values diversity, inclusion, and accessible working arrangements.
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