Reed Scientific are working with a global healthcare provider based in the North West of the UK, and are currently seeking an experienced Regulatory Affairs Manager to oversee and manage the regulatory affairs team.
Main Responsibilities:
Regulatory Strategy: Develop and implement regulatory strategies aligned with the companies' strategic objectives.
Team Leadership: Lead, support, and develop the regulatory affairs team.
Regulatory Submissions: Oversee the filing and approval of regulatory submissions for licensed and unlicensed products.
Compliance: Ensure promotional materials, product labelling, and regulatory submissions comply with current legislation and guidelines.
Budget Management: Agree and review local regulatory budgets.
License Maintenance: Ensure all licenses, including specials licenses, are up to date.
Resource Management: Manage resourcing requirements within the regulatory affairs team.
Skills & Experience:
Proven experience in regulatory affairs within the pharmaceutical or medical device industry.
Strong leadership and team management skills.
Excellent knowledge of regulatory requirements and guidelines.
Ability to develop and implement effective regulatory strategies.
Strong communication and interpersonal skills.
If this looks like a position of interest and you possess the required skills and experience then please follow the link to apply.