Regulatory Specialist
9 hours ago
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.
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