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- Tasks: Ensure compliance with regulations and manage submissions for new drug applications.
- Company: Join a global pharmaceutical leader with a forward-thinking approach.
- Benefits: Gain valuable experience in a dynamic industry with potential for career growth.
- Why this job: Make a real impact in the pharmaceutical field while working on exciting projects.
- Qualifications: B.S. in Chemistry, Biology, or related fields; experience in Cosmetic Regulatory affairs required.
- Other info: Opportunity to work independently and lead key regulatory projects.
The predicted salary is between 36000 - 60000 £ per year.
Do you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring the expertise of an experienced Regulatory Affairs Specialist.
Responsibilities:
- Ensures compliance with regulatory agency regulations and interpretations.
- Prepares responses to regulatory agencies' questions and other correspondence.
- Gathers and assembles information necessary for submissions in accordance with regulations and relevant guidelines.
- Develops timelines for submissions under the direction of senior regulatory affairs staff.
- Provides solutions to extreme complex problems in which data analysis requires an evaluation of intangible variables.
- Provides regulatory advice to project teams.
- Organises and maintains reporting schedules for new drug application and investigations new drug applications.
Requirements:
- Minimum B.S. Chemistry, Biology, or related fields.
- Significant experience in Cosmetic Regulatory affairs mainly with promotional material and artwork review/approval at all stages of life cycle management, with demonstrated accountability of managing multiple brands.
- Well versed with UK ASA, CAP, BCAP Guidance for Advertising, proven record of successful project management of dossiers with ClearCast.
- Strong knowledge and application of the UK & EU Cosmetic Product Regulation.
- Excellent leadership, communication, and organisational skills.
- Attention to detail, effective in written and oral communication.
- Works independently to plan, conduct, and manage regulatory projects to meet department and company objectives.
- Responsible for identifying, implementing and managing key RA Departmental projects and/or strategies based on both short- and long-term RA Department objectives.
If this role is of interest to you, please apply now!
Regulatory Affairs Specialist employer: Quanta part of QCS Staffing
Contact Detail:
Quanta part of QCS Staffing Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Specialist
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory affairs field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of UK & EU Cosmetic Product Regulations. We recommend creating a cheat sheet of key points to discuss, so you can impress your interviewers with your expertise.
✨Tip Number 3
Showcase your project management skills! Be ready to share examples of how you've successfully managed multiple brands and projects. We love hearing about real-life experiences that demonstrate your capabilities.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. We’re here to help you every step of the way, so let’s get you that Regulatory Affairs Specialist role!
We think you need these skills to ace Regulatory Affairs Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Regulatory Affairs Specialist role. Highlight your experience in cosmetic regulatory affairs and any relevant projects you've managed. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about regulatory affairs and how your background makes you a perfect fit for our team. Keep it concise but impactful – we love a good story!
Showcase Your Attention to Detail: In regulatory affairs, attention to detail is key. Make sure your application is free from typos and errors. We appreciate candidates who take the time to double-check their work, so show us you care!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at Quanta part of QCS Staffing
✨Know Your Regulations
Make sure you brush up on the UK & EU Cosmetic Product Regulation and the ASA, CAP, and BCAP guidelines. Being able to discuss these regulations confidently will show that you're not just familiar with them but can apply them in real-world scenarios.
✨Showcase Your Project Management Skills
Prepare examples of how you've successfully managed multiple brands and projects in the past. Use the STAR method (Situation, Task, Action, Result) to structure your responses, highlighting your leadership and organisational skills.
✨Be Ready for Complex Problem-Solving
Expect questions that assess your ability to tackle complex regulatory issues. Think of specific instances where you provided solutions to challenging problems, especially those involving data analysis and intangible variables.
✨Communicate Effectively
Since communication is key in this role, practice articulating your thoughts clearly and concisely. Prepare to discuss how you've effectively communicated with project teams and regulatory agencies in the past, showcasing your attention to detail.
