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Regulatory affairs officer

Deeside
Regulatory affairs officer
£38,000 - £42,000 a year
Posted: 16 August
Offer description

​ Sunday Times Best Places to Work 2024 BioNow Business Growth Award Winner 2024 ​ The Opportunity: ​ We are seeking a motivated and detail-oriented Regulatory Affairs Officer to join our team. The successful candidate will assist in ensuring that our products meet relevant regulatory and quality standards. This role involves supporting the preparation of regulatory documentation, helping to maintain compliance with requirements, and assisting with client communications under guidance from the senior team. This is a great opportunity for the right individual to progress their career within the Regulatory Affairs function at Reacta Healthcare. ​ Key Accountabilities Support the preparation and maintenance of regulatory documentation for the company’s product portfolio. Maintain organised regulatory files and documentation according to company policies and relevant regulations. Assist in tracking and reporting the status of regulatory activities to the business. Monitor updates to regulatory requirements and help communicate important changes to internal teams. Keep up-to-date with industry trends and regulatory developments to support ongoing compliance. Help coordinate client communications related to regulatory submissions/ updates. ​ Skills, Qualifications and Experience Essential To be successful in this role, applicants need to have the following essential skills and experience: Bachelor’s degree in a scientific, healthcare, or related field. Proven experience of Regulatory Affairs in the Pharmaceutical Industry. Strong organisational skills and attention to detail. Effective written and verbal communication abilities. Willingness to learn and adapt to changing regulatory requirements. Ability to work collaboratively within a team environment. Basic proficiency with common office software (e.g., Microsoft Word, Excel, Outlook). Demonstrated initiative and eagerness to develop professionally in regulatory affairs. Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP). Desirable Experience with regulatory submissions for new product approvals and post-market changes. Do you want to feel inspired every day? We are future-focused, and our business is growing rapidly. We succeed together through passion, commitment, and teamwork, and so can you.

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