Regulatory & Scientific Affairs Manager for a prestigious market-leader based in Ontario.
Our award-winning client is currently looking for a regulatory expert to work on an international role.
You will have regional responsibility for the Americas region (US and Canada), filing submissions to the FDA and delivering presentations to senior leadership teams.
In this role you will be responsible for regional product compliance including submission planning and preparation. You will also be responsible for regulation tracking, review and assessment and compliance trend monitoring. Additionally you will be expected to implement global Scientific Regulatory Affairs (SRA) and Worldwide Product Regulatory Affairs (WPRA) regulatory policies.
This key role also involves some travel to offices throughout the US, Canada and to Geneva in Switzerland. It is an outstanding opportunity to gain exposure to many facets of the business, such as legal counsel.
For this role you will be expected to have experience in managing regulatory submissions with 3-5 years professional experience in a product-related scientific and regulatory environment, such as a pharmaceutical or other regulated industry. Additionally you must have strong communication and presentation skills with a fluency in English and a working knowledge of French or Spanish.
This job was posted over 30 days ago, and has expired.