Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Join a dynamic team to manage regulatory compliance and guide post-approval activities.
- Company: A growing pharmaceutical company focused on innovation and compliance.
- Benefits: Gain valuable experience in a supportive environment with career advancement opportunities.
- Other info: Fully office-based role with no hybrid working options.
- Why this job: Make a real impact in the pharmaceutical industry while developing your regulatory expertise.
- Qualifications: Degree in Pharmacy/Chemistry and 2+ years of Regulatory Affairs experience required.
The predicted salary is between 35000 - 45000 £ per year.
An exciting opportunity has become available with my client, a growing pharmaceutical company, for an experienced and enthusiastic Regulatory Affairs professional wishing to expand their experience and knowledge in a growing Regulatory team. With a focus on post-approval activities, the successful candidate will gain exposure to many aspects of Regulatory compliance as well as the opportunity to supervise and guide a team.
Please note that this role is fully office based (5 days per week) and hybrid working is not available.
Responsibilities:- Converting an existing application to eCTD format.
- Preparation and submission of Sunset clause, MA cancellation applications, MA transfers, remediation dossiers as required by the Company.
- Ensure completion of post-approval commitments, if any.
- Compilation and maintaining Product license files.
- Co-ordinate regulatory activities with QPPV and QP (Quality/GMP) for management of MAs.
- Process and communicate regulatory approvals internally and to external stakeholders.
- Participate in the review of process/product changes, deviations, product complaints, adverse drug reactions, medical information, and batch recall to determine the need for any regulatory activities and to ensure compliance with regulatory requirements.
- Maintain regulatory files/database and chronologies in good order. Maintain system for tracking changes in documents submitted to agencies or partners.
- Publishing activities including converting/binding of pdf files, resolve validation issues.
- Compile and submit variations.
- Working in accordance with Company’s working Instructions and SOPs.
- Carrying out other activities which contribute to the effective performance of the Regulatory Affairs Department.
- Pharmacy/Chemistry degree.
- 2+ years Regulatory Affairs experience.
- Understanding of the current UK and European regulations, laws, guidelines, and industry requirements.
- Exposure to NeeS/eCTD format and electronic submission gateways is preferable.
- Experience with Generic products and MRP/DCP submissions is advantageous.
Regulatory Affairs Officer in Maidenhead employer: Select Pharma Recruitment
Contact Detail:
Select Pharma Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Officer in Maidenhead
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those in Regulatory Affairs. Attend industry events or webinars to meet potential employers and get your name out there.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of UK and European regulations. Be ready to discuss how your experience aligns with the responsibilities listed in the job description, especially around post-approval activities.
✨Tip Number 3
Showcase your skills! Create a portfolio that highlights your previous work in Regulatory Affairs, particularly any experience with eCTD formats or submissions. This will give you an edge during interviews.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can sometimes give you a better chance of standing out to hiring managers.
We think you need these skills to ace Regulatory Affairs Officer in Maidenhead
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Regulatory Affairs role. Highlight your relevant experience, especially in post-approval activities and any exposure to eCTD formats. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your enthusiasm for the role and the company. Share specific examples of your past experiences that relate to the responsibilities listed in the job description. Let us know why you're the perfect fit!
Showcase Your Knowledge: Demonstrate your understanding of UK and European regulations in your application. Mention any relevant qualifications or experiences that show you’re up-to-date with industry requirements. We love candidates who are knowledgeable and proactive!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re serious about joining our team at StudySmarter!
How to prepare for a job interview at Select Pharma Recruitment
✨Know Your Regulations
Make sure you brush up on the current UK and European regulations, laws, and guidelines relevant to the role. Being able to discuss these confidently will show your potential employer that you're not just familiar with the basics but are genuinely engaged with the field.
✨Showcase Your Experience
Prepare specific examples from your past roles that highlight your experience in Regulatory Affairs. Whether it’s about converting applications to eCTD format or managing post-approval commitments, having concrete examples ready will help you stand out.
✨Teamwork Makes the Dream Work
Since this role involves supervising and guiding a team, be ready to discuss your leadership style and how you’ve successfully collaborated with others in the past. Share instances where you coordinated regulatory activities or worked with Quality teams to demonstrate your teamwork skills.
✨Stay Organised
Regulatory Affairs requires a keen eye for detail and excellent organisational skills. Be prepared to talk about how you maintain regulatory files and databases, and any systems you use to track changes in documents. This will show that you can handle the responsibilities of the role effectively.