Regulatory Affairs Specialist

ARx Recruitment Services; Watford; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading pharmaceutical company near Watford is seeking experienced Regulatory Affairs professionals. You will ensure compliance with regulatory requirements and manage documentation. Ideal candidates have 5+ years in Pharmaceutical Regulatory Affairs and a strong working attitude. This site-based role fosters growth and a supportive culture within the company.

Qualifications

• 5+ years of experience in Pharmaceutical Regulatory Affairs.
• Familiar with global Regulatory requirements (MHRA, EMA, ICH).

Responsibilities

• Ensure compliance with regulatory requirements.
• Manage documentation related to regulatory affairs.

Skills

Attention to detail

Team collaboration

Hard working attitude

Tools

eCTD manager

Document management tools

Job description

What does 'family business' mean to you?

For some, it's code for small, for others it is a collaborative and friendly space. The truth - it's usually both.

Family, small to midsized pharmaceutical companies look after their staff. You become part of their community, their culture, and the way they do things.

In our experience, staff at family run SMEs experience longer levels of employment than at large global corporations, and are often compensated well over time for their rewards.

Job Opportunity

We are delighted to be representing a leading (family run) pharmaceutical manufacturing organisation based near Watford in the UK. This amazing company are going through a great transformation that should ensure the company's future for generations to come, and as part of that they are looking for reliable, professional and hard working Regulatory Affairs professionals.

As part of this expansion, our client is looking for someone with 5+ years experience in Pharmaceutical Regulatory Affairs (ideally in a similar style of company, but they are open to people from all different pharmaceutical organisations).

Responsibilities and Requirements

• Hard working attitude
• Good attention to detail
• Able to work well with your team
• Experience in eCTD manager and document management tools
• Knowledge of global Regulatory requirements and guidelines (MHRA, EMA and ICH)

This is a site based role near Watford (5 days per week) and would suit someone looking for a company they can grow with, and build with, and that will give them huge career trajectory in a culture that is supportive and dynamic.