Consultant – Regulatory Affairs
Brandwood Biomedical is a leading global consultancy headquartered on the lower north shore in Sydney and with offices in China and New Zealand – providing technical, regulatory and commercial advisory services to the Medical Devices and IVD industry. We are a committed, supportive and family oriented team.
Due to a continuing growth in our client base, we are seeking to expand our Sydney based team. We are looking for team players who bring to us both a well-grounded practical knowledge of regulatory practice, the flexibility to apply their skills across a diverse range of client projects and who have a hunger to learn and grow with the business. A background in managing compliance at a global or regional level would be particularly well regarded but above all you must be able to operate in a commercially focused, client service environment. In this role, you will have the opportunity for personal growth and professional development in a challenging and energetic environment.
We take pride on our services ranging from support the whole product life-cycle, to investment readiness and due diligence to development and implementation of global regulatory strategies. Key service areas include Australian and International medical device sponsorship, agency services, post-market reporting, advertising and labelling compliance, clinical evaluations, expert technical reports, quality systems compliance and reimbursement.
This is an exciting opportunity to join a leading Consultancy with considerable opportunity for future development and for international experience. If you present with the skills and qualities above, please apply now by sending your resume and contact details to Denise Souza at HR@brandwoodbiomedical.com