Senior Regulatory Affairs Associate - Pharmaceuticals
- Sydney
- Medical Device / Medical
- Pharmaceutical Regulatory experience required
- Work for a global organisation! Hybrid working arrangement
- Work in a highly collaborative and dynamic team
Bring your regulatory experience to this global medical devices company in the surgical ophthalmology portfolio.
- Medical Devices and Pharmaceutical Regulatory experience required
- Work for a global organisation
- Work in a highly collaborative and dynamic team
It's an exciting time to join this global medical technology company as part of a recent divestment, relaunch and development of their business, team and culture. A well recognised brand in their areas of specialisation, they pride themselves on innovative technology, broad product offering and focus on bringing value to their customers. Due to opportunities, they are in search of a senior regulatory affairs associate to join their team
Reporting to the Regulatory and Medical Affairs Manager your responsibilities include;
- Registering new Medicines and Medical Devices and the maintenance of approved products in order to ensure viability of these products in the marketplace.
- Developing quality registration dossiers, ensuring their timely submission.
- Providing accurate and timely regulatory advice to the business teams.
- Ensuring regulatory compliance for assigned products.
- Reviewing and approve advertising materials in compliance with regulation.
- Knowledge of Australian and New Zealand medicine and medical device regulatory requirements and processes
- Effective written and verbal communications
- Tertiary qualifications in a pharmacy or a life science discipline.
- At least 4 years pharmaceutical industry experience in a regulatory/medical affairs role
To apply for this role please submit your application in WORD format or contact Liz Miritis on 0447 273 551 for further enquiries. Confidentiality is assured.
For more information contact
0447 273 551liz.miritis@hengandhurst.com