Get in touch with G&L Scientific today!

Warren, NJ   |   Boston, MA   |   San Diego, CA   |   Los Angeles, CA  |  Boca Raton, FL
London   |   Belfast   |   Marlow

Director/Senior Director Regulatory Affairs

About Us:

G&L Scientific is the world’s fastest-growing independent scientific consultancy providing Pharmaceutical and Biotechnology clients throughout the world with expert Regulatory Affairs consultancy and Quality Assurance solutions.

As demand for our services and solutions continues to increase, we have an exciting new opportunity for a Senior Regulatory Affairs professional to join our team in Canada.

Flexible working with regular meetings at our offices in Montreal or Toronto.

The Role:

  • We are looking for a dynamic and flexible individual who has a truly consultative approach to their work.
  • As part of our elite team, you will be working with a variety of our global pharmaceutical, biotechnology and device clients on a range of bespoke project engagements.
  • You will form an integral part of G&L’s RA team – supporting clients and colleagues alike, to ensure that all projects are delivered, and expectations are surpassed.
  • You will be expected to be an active member of G&L’s leadership team to create and participate in the overall vision, mission, values and strategic goals of our business.
  • Our ideal candidate will have excellent communication skills – covering all aspects of communication; your role may see you travelling to client sites to meet with our clients, or you may have to work intensively on TC or VC – using diplomacy, influencing and negotiation skills.
  • Your role will involve interacting with a broad spectrum of G&L’s clients – both existing and new, domestic and international.
  • This role can involve scoping out new projects, guiding our clients and explaining complex regulatory options, managing expectations on timelines and budgets.
  • You will also be working closely with G&L’s global team of staff – from junior colleagues to the leadership team; ensuring consistent performance and quality of work.
  • You will ensure your team is utilised and on target to meet or exceed financial targets for revenue and operating margins.
  • You will have to develop an organization of highly productive staff ensuring they have the required processes and tools to deliver their project work with quality, on time and on budget.
  • You will be expected to lead, coach and develop your direct reports to create a positive employee experience and build team capacity.
  • As part of our senior team, you will also be expected to assist with business development including networking and being mindful of upcoming industry opportunities.
  • You will be required to take part in strategic consulting in relation to client opportunities, actively participating with our clients, attending industry conferences, identifying new business opportunities and potentially working with the Client Services team to generate proposals and bids.
  • You may be required to speak at conferences or webinars, where there is the opportunity.

Candidate Requirements:

  • 15+ years experience in the pharmaceutical, biotechnology and ATMP industry.
  • Experience of Regulatory Affairs Strategy for Canadian, EU and RoW Markets.
  • Broad experienced in therapeutic areas.
  • Proven experience of building teams and line management of staff.
  • Prior experience working with global RA teams and direct contact with Regulatory Agencies / Health Authorities.
  • Extensive experience preparing for inspections.
  • A background in Regulatory Affairs consulting would be beneficial.
  • Contract Type:

    Full time career opportunity

  • Location:


submit your CV

Upload your CV

To apply for the Director/Senior Director Regulatory Affairs job position please complete the form below.

Upload CV Single Post
Upload your CV
Maximum upload size: 385.88MB

Keep up to date with the latest industry news and trends
Newsletter Signup

Worldwide Locations

G&L Scientific G&L Scientific G&L Scientific G&L Scientific G&L Scientific