Consultants – Regulatory Affairs
Brandwood Biomedical is a leading global consultancy headquartered on the lower north shore in Sydney and with offices in Greater China, USA 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 always seeking to expand both our Sydney and Beijing based offices. 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 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.
To apply for any of these positions, please send a resume and cover letter explaining why you would be a great fit for our team to Mieko@brandwoodbiomedical.com