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For Companies At a Glance
- Tasks: Ensure regulatory compliance and manage license submissions across UK, EU, and global markets.
- Company: Join a leading pharmaceutical organization dedicated to patient safety and compliance excellence.
- Benefits: Enjoy remote work flexibility with occasional travel and a dynamic team environment.
- Why this job: Make a real impact in regulatory affairs while working with top stakeholders and authorities.
- Qualifications: Life Science degree, 3+ years in regulatory affairs, strong communication, and problem-solving skills required.
- Other info: Interviews in November, with a start date planned for January.
The predicted salary is between 36000 - 60000 £ per year.
Role: Senior or Principal Regulation Engineer
Location: Birmingham
Salary: Senior level: £45,000–£55,000, Principal level: £55,000–£65,000
Onsite working is 4 days, 1 day from home
About the Role:
This position involves providing strategic analysis of regulations in global markets and delivering regular status updates.
Requirements:
- BS/MS or higher in Science, Engineering, or a related field.
- Minimum of three years’ R&D experience in relevant industries.
- Strong understanding of automotive regulations worldwide.
- Experience with regulation trend analysis and vehicle homologation processes.
- Automotive industry experience is preferred.
Duties & Responsibilities:
- Conduct in-depth analysis of the global automotive regulations landscape.
- Deliver regular reports on key regulation trends, particularly in Europe.
- Support the development of overseas marketing strategies.
- Assist in creating products suitable for international markets.
- Collaborate with headquarters and regional organisations involved in homologation.
- Research new standards, regulations, and market-specific requirements.
- Represent the company in the UK and potentially the EU on regulation-related matters.
Other Features:
- Based primarily at Birmingham Business Park.
- Some travel may be required depending on project needs.
- Candidates must be eligible to work in the UK.
Benefits:
- Pension scheme
- Private medical insurance
- Income protection insurance
- Life assurance
- Free lunch for all employees/workers
- Enhanced company sick pay
- Company bonus scheme
- Free on-site parking
- Company car allowance for senior grades
- Relocation allowance
- Company events
- Reward gateway – offering discounts and savings from hundreds of retailers
How to apply?
Please send a CV to danielle.chapman@experis.co.uk
Regulatory Specialist employer: People Source Consulting trading as Experis
Contact Detail:
People Source Consulting trading as Experis Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Specialist
✨Tip Number 1
Familiarize yourself with the specific regulatory frameworks in the UK, EU, and global markets. Understanding the nuances of these regulations will not only help you in interviews but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the regulatory affairs field. Attend industry conferences or webinars to connect with others who may have insights into the company or the role, which can give you an edge during the application process.
✨Tip Number 3
Prepare to discuss your experience with regulatory compliance and stakeholder management in detail. Be ready to share specific examples of how you've influenced stakeholders or improved processes in previous roles.
✨Tip Number 4
Stay updated on current trends and changes in pharmaceutical regulations. This knowledge will not only prepare you for potential interview questions but also show your proactive approach to staying informed in a rapidly evolving field.
We think you need these skills to ace Regulatory Specialist
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Regulatory Specialist position. Highlight key responsibilities and qualifications that resonate with your experience and skills.
Tailor Your CV: Customize your CV to reflect your relevant experience in regulatory affairs, particularly focusing on compliance, stakeholder interaction, and any specific licenses you have managed. Use keywords from the job description to align your application with what the company is looking for.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for regulatory affairs and patient safety. Mention specific examples of how you've ensured compliance and improved processes in previous roles, and express your enthusiasm for working in a dynamic pharmaceutical environment.
Highlight Your Skills: In your application, emphasize your strong interpersonal and communication skills, as well as your problem-solving abilities. Provide concrete examples of how you've influenced stakeholders and driven service improvements in past positions.
How to prepare for a job interview at People Source Consulting trading as Experis
✨Know Your Regulations
Make sure you are well-versed in the regulatory requirements across the UK, EU, and global markets. Be prepared to discuss specific regulations and how they impact compliance and patient safety.
✨Showcase Your Communication Skills
Since strong interpersonal and communication skills are crucial for this role, practice articulating your thoughts clearly. Prepare examples of how you've effectively communicated with stakeholders or regulatory authorities in the past.
✨Demonstrate Problem-Solving Abilities
Be ready to share instances where you've successfully navigated challenges in regulatory affairs. Highlight your analytical skills and how you've delivered results in GDP environments.
✨Prepare for Change Management Questions
Given the emphasis on leading change management projects, think of examples where you've implemented business improvements. Discuss your approach to managing change and influencing stakeholders positively.
