Are you ready to take the next step in your regulatory affairs career?
We are partnering with a leading pharmaceutical organisation to find a skilled Regulatory Affairs Specialist who is passionate about ensuring compliance and safeguarding patient safety.
This exciting role offers the opportunity to work across UK, EU, and global markets.
Key Responsibilities Regulatory Compliance : Ensure adherence to regulatory requirements across UK, EU, and global regions, managing license submissions, variations, renewals, and inspections.
Interaction with Regulatory Authorities: Acting as a key contact with regulatory bodies for inspections, audits or clarifications regarding services Stakeholder Support : Provide strategic guidance on regulatory requirements to senior management, liaise with regulatory authorities, and foster strong relationships with stakeholders.
Licensing and Accreditation: Managing regulatory requirements for licenses, such as WDA and GDP compliance, ensuring the safe handling, storage and transport of medicines Qualifications and Skills A Life Science degree or equivalent professional qualification.
Strong interpersonal and communication skills (written, oral, and presentational).
Proven ability to influence stakeholders and drive service improvements.
3+ Years experience in within regulatory affairs Experience in regulatory strategy for importing and exporting in EU countries Strong problem-solving and analytical skills with a track record of delivering results in GDP environments.
Experience leading change management projects and implementing business improvements.
What We Offer This role is primarily remote, with occasional travel to London and very infrequent trips to the Netherlands.
Join a forward-thinking team in a dynamic organisation committed to excellence in pharmaceutical compliance.
Interviews will take place in November, with a planned start date in January.
For any questions, feel free to reach out directly.