Medical Device Regulatory Professional
3 weeks ago
We are seeking a skilled Regulatory Affairs Officer to join our team at Aspire Pharma Ltd.
This is an exciting opportunity for someone who wants to build a career in the pharmaceutical industry and contribute to the development of innovative formulations and value-for-money products.
The successful candidate will be responsible for ensuring compliance with regulatory requirements, managing regulatory documentation, and collaborating with internal and external stakeholders.
About the Role:
- Submission, maintenance, and control of regulatory information and documentation.
- Compilation, review, and submission of new product dossiers and technical files.
- Ensuring all submissions to regulatory authorities are of high quality and correspondence is conducted in a professional and timely manner.
Key Responsibilities:
- Preparation and update of registered information for third parties to ensure products can be manufactured and released in accordance with approved regulatory information.
- Quality, maintenance, control, and distribution of internal sources of regulatory information.
- Responsible for ensuring compliance with regulatory requirements and managing regulatory documentation.
Requirements:
- A robust science degree relevant to working in the pharmaceutical industry.
- 1-2 years of regulatory experience (preferred).
- A strong ambition to build a career in this sector.
What We Offer:
- A competitive salary of around £42,000 per annum.
- A comprehensive benefits package, including a generous pension scheme, life assurance cover, and employee assistant program.
- Ongoing learning and development opportunities to support your career growth.
- An excellent company culture where employees are truly valued.
Location: This role is based in Petersfield, UK. We offer free parking and a pleasant working environment.
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