At a Glance
- Tasks: Join our team to manage regulatory compliance and documentation for innovative products.
- Company: We're a leading UK company in pharmaceuticals and medical devices, dedicated to patient value.
- Benefits: Enjoy a competitive salary and an extensive benefits package, including flexible work options.
- Why this job: Be part of a growing company that values innovation and compliance in healthcare.
- Qualifications: A degree in a scientific field and 1-2 years of regulatory experience are essential.
- Other info: Ready to advance your career? Click 'Easy Apply' or contact us for more info!
The predicted salary is between 30000 - 42000 £ per year.
An exciting opportunity to join the Regulatory Affairs team, in charge of maintenance and compliance of approved products, including contact with the relevant stakeholders for information as required to ensure timelines are adhered to, to meet business needs.
Company Overview:
Our client is an established UK based company that provides an extensive portfolio of pharmaceuticals and medical devices that offer bespoke value to patients and Healthcare Professionals (HCPs). Through continued success, they have achieved enormous growth in the past five years. Devoted to delivering value to patients and Healthcare Professionals.
Job Overview:
- Submission, maintenance, and control of regulatory information and documentation for products.
- Coordinate with internal and external stakeholders to prepare responses to requests for information from regulatory authorities within stated timelines.
- Assist with regulatory due diligence of new products using knowledge of current regulations and guidance.
- Maintain awareness of existing and new legislation/guidance relating to role and products within the region as required.
- Maintain awareness of new and existing legislation and guidance from regulatory competent authorities.
To be successful:
- Degree in a scientific or similar discipline.
- 1-2 years regulatory experience.
- Highly organised with good attention to detail.
- Task orientated and diligent.
- Scientific writing.
How to apply:
If you like the sound of this opportunity and you’re ready to take the next step in your career, we would love to hear from you! Please click the 'Easy Apply' button or contact Elaine Plunkett on 01225 336 335 for more information.
Regulatory Affairs Specialist employer: Star People
Contact Detail:
Star People Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Specialist
✨Tip Number 1
Familiarise yourself with the latest regulations and guidelines in the pharmaceutical and medical device sectors. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in the field.
✨Tip Number 2
Network with professionals in regulatory affairs through platforms like LinkedIn. Engaging with industry groups can provide insights into the role and may even lead to referrals, increasing your chances of landing the job.
✨Tip Number 3
Prepare for potential interview questions by practising responses that highlight your organisational skills and attention to detail. Use specific examples from your past experiences to illustrate how you've successfully managed regulatory tasks.
✨Tip Number 4
Research the company’s portfolio and recent developments in their products. Being knowledgeable about their offerings will allow you to tailor your conversation during interviews and show genuine interest in their mission.
We think you need these skills to ace Regulatory Affairs Specialist
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Regulatory Affairs Specialist. Familiarise yourself with the key tasks mentioned in the job description, such as submission and maintenance of regulatory information.
Tailor Your CV: Highlight your relevant experience in regulatory affairs, especially any scientific writing or compliance work. Make sure to emphasise your organisational skills and attention to detail, as these are crucial for the role.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for the pharmaceutical industry and your understanding of regulatory processes. Mention specific examples from your past experience that demonstrate your ability to meet deadlines and coordinate with stakeholders.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors. A well-presented application reflects your attention to detail, which is essential for a Regulatory Affairs Specialist.
How to prepare for a job interview at Star People
✨Know Your Regulations
Familiarise yourself with the current regulations and guidance relevant to the role. Being able to discuss specific legislation will demonstrate your expertise and commitment to compliance.
✨Showcase Your Organisational Skills
Prepare examples that highlight your organisational abilities. Discuss how you manage timelines and coordinate with stakeholders, as these are crucial for the role of a Regulatory Affairs Specialist.
✨Demonstrate Scientific Writing Skills
Be ready to showcase your scientific writing skills. You might be asked to explain how you would prepare regulatory documents or responses, so having examples or experiences to share will be beneficial.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's products and regulatory processes. This shows your genuine interest in the role and helps you understand how you can contribute to their success.