Job Details

• Trainee Regulatory Affairs Officer
• Based in Worthing, West Sussex
• Biological science degree (or similar) is essential
• Experience of working in a Pharmaceutical environment as strong advantage
• Salary negotiable depending on experience (ideally £15k - £20k but could be slightly higher for the right candidate)
• Immediate start preferred

Summary

An exciting opportunity for a Science Graduate with excellent organisation skills and attention to detail, to join one of the most innovative companies in the South East.

The Company

A pioneering Europe-based Pharmaceutical company specialising in the treatment and prevention of allergies. Their unique focus is on the vaccination and prevention of conditions such as hay fever and asthma, and their groundbreaking work has recently been in the UK press.

The Role

Based in a fairly quiet but very busy office, you will be responsible for maintaining regulatory documentation, reviewing product labels, preparing and reviewing documentation for New Product Licences, variations, renewals and annual updates. This role has a large administrative element and will require excellent time management, the ability to learn new things quickly, strong IT skills and the genuine desire to further your career in the Pharmaceutical industry.

Regulatory Affairs is a fascinating part of any Pharmaceutical company and is ultimately responsible for the success of new and existing drug products. This role offers a lot of initial training and a structured career path for someone with genuine drive and commitment.

Benefits

• 25 days’ holiday
• Stakeholder pension plan (5% of salary)
• Life insurance scheme
• Long term disability scheme
• BUPA medical plan

Experience

The successful candidate will have a life science background (ideally to degree level), ideally with some experience gained in a Pharmaceutical office environment (preferable Reg Affairs). You must have an analytical mind and first-rate communication skills, being able to work on your own initiative.

Keywords

Reg Affairs, Graduate, Regulatory Affairs, CTD, eCTD, Drug Safety, Clinical Safety, PSUR, Clinical Trial, Pharmacovigilance, MHRA, FDA, Project Management

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