Play a key role in the setup and growth of a new company, managing a cross-disciplinary team and actively contributing to the development of this company’s strategy.
Using your previous operational experience, you will ensure the company meets its strict regulatory requirements whilst progressing towards more ambitious commercial targets.
You will also act as a main contact for government stakeholders and regulatory authorities, whilst managing customer relationships and identifying new business development opportunities using market research.
Responsibilities will include:
Designing and implementing regulatory strategies to obtain product approvals and market access
Overseeing the facility design and delivery work to ensure the company can successfully obtain the relevant certifications
Supervising the cultivation and production team to ensure the product is in line with regulatory requirements and client expectations
Developing client relationships and supply contracts
Managing the lifecycle of regulatory activities, including licence renewal, maintenance of certifications, product registrations and developing operational/transport logistics in multiple jurisdictions
Experience and skills required:
Minimum 3 years’ operational or management experience
At least 10 years’ professional experience, ideally within management functions
Good technical knowledge of Jersey and international laws relating to the manufacturing and supply of pharmaceuticals
Ability to confidently lead, direct, motivate and develop project teams
Previous experience of successful regulatory approvals relating to production licences, facility inspections and related operational permits
We are an equal opportunity employer and value diversity at all times.