At a Glance
- Tasks: Manage regulatory filings and ensure compliance in a dynamic pharmaceutical environment.
- Company: Join Ferring Pharmaceuticals, a leader in reproductive and women's health innovation.
- Benefits: Inclusive family support policies, parental leave, and hybrid working arrangements.
- Other info: Collaborative culture with opportunities for professional growth and learning.
- Why this job: Make a real impact on people's lives while advancing your career in regulatory affairs.
- Qualifications: Life Science degree and 3-5 years of regulatory experience required.
The predicted salary is between 40000 - 50000 £ per year.
About Ferring Pharmaceuticals
At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in reproductive and women’s health, gastroenterology and urology. Ferring + You is all about working together and sharing ideas, so that we can bring science to life for patients around the world.
About Ferring+You
You will take responsibility for a range of tasks across Regulatory Affairs, Compliance, Good Distribution Practice (GDP) and Good Pharmacovigilance Practices (GVP), working closely with regulatory, quality, and safety colleagues. In this role, you will bring an innovative, solutions‑driven mindset, demonstrating curiosity, entrepreneurial spirit, and a strong desire to create opportunities while confidently challenging established norms. We will support you and ensure you have the learning support you need.
Your day at Ferring
- Prepare, review and submit variations, renewals, new product authorisations and other regulatory filings, including packaging material.
- Maintain and update the local UK Pharmacovigilance System Master File (PSMF).
- Monitor and update data in the Regulatory Information Management System (RIMS).
- Manage the assessment and response process for Parallel Trade Import Notifications for the UK and Ireland.
- Handle requests for Certificates of Pharmaceutical Products (CPP) and special statements.
- Monitor regulatory changes for the UK and Ireland, assess impact and record updates in internal systems.
- Contribute to monthly Regulatory Affairs and Pharmacovigilance reports.
- Act as Document Owner for assigned SOPs, policies and regulatory/PV documentation.
- Provide backup support for Regulatory Affairs, Pharmacovigilance, and the reporting of adverse events and product quality complaints.
- Ensure full compliance with GDP, GVP and all applicable regulatory requirements.
Qualifications
- Life Science degree or equivalent.
- Minimum of 3 years of Regulatory experience in a pharmaceutical company (preferably 5 years).
- Knowledge of the UK Regulatory environment is mandatory (including post‑Brexit requirements).
- Preferable to have experience or knowledge in the UK Pharmacovigilance environment.
- Preferable to have direct experience communicating with the UK Health Authority (MHRA).
Benefits
- Inspiration from our commitment to advocate for everyone’s right to build a family, no matter who you are or who you love.
- Inclusive support package – "Building Families at Ferring" provides equal and accessible policies for all employees who wish to start their family journey, ensuring a global standard, irrespective of location and role. Subject to a minimum period of employment at Ferring.
- Parental leave for both birthing and non‑birthing parents.
- Extended support on family building journey.
Working Arrangement
We operate a hybrid working arrangement with employees expected to work from the office for a minimum of 3 days each week – for this reason you should live within a reasonable commutable distance.
Regulatory Affairs and Pharmacovigilance Specialist in West Drayton employer: Ferring
Ferring Pharmaceuticals is an exceptional employer that prioritises innovation and collaboration, fostering a work culture where employees are encouraged to share ideas and challenge the status quo. With a strong commitment to employee growth, Ferring offers comprehensive support for professional development and a unique inclusive family-building policy, ensuring all employees feel valued and empowered. Located in the UK, the company promotes a hybrid working model, allowing for flexibility while maintaining a vibrant office environment that enhances teamwork and creativity.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Affairs and Pharmacovigilance Specialist in West Drayton
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching Ferring Pharmaceuticals and their work in regulatory affairs. Show them you’re not just another candidate; demonstrate your passion for their mission and how you can contribute to their goals.
✨Tip Number 3
Practice your responses to common interview questions, especially those related to compliance and pharmacovigilance. We recommend doing mock interviews with friends or mentors to build your confidence.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in being part of the Ferring team.
We think you need these skills to ace Regulatory Affairs and Pharmacovigilance Specialist in West Drayton
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the role of Regulatory Affairs and Pharmacovigilance Specialist. Highlight your relevant experience in regulatory affairs, compliance, and pharmacovigilance, especially any work with the UK Health Authority.
Craft a Compelling Cover Letter:Your cover letter should reflect your passion for the role and the company. Share specific examples of how you've demonstrated an innovative mindset and solutions-driven approach in your previous roles.
Showcase Your Knowledge:Demonstrate your understanding of the UK regulatory environment and any post-Brexit requirements. This will show us that you’re not just qualified, but also genuinely interested in the field.
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and ensure it gets the attention it deserves!
How to prepare for a job interview at Ferring
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of the UK regulatory environment, especially post-Brexit requirements. Familiarise yourself with the specific regulations and guidelines that Ferring Pharmaceuticals adheres to, as this will show your genuine interest and preparedness for the role.
✨Show Your Curiosity
Ferring values an innovative and solutions-driven mindset. Prepare examples from your past experiences where you’ve challenged established norms or come up with creative solutions in regulatory affairs or pharmacovigilance. This will demonstrate your entrepreneurial spirit and fit with their culture.
✨Be Ready to Discuss Compliance
Since compliance is a big part of the role, be prepared to discuss how you've ensured adherence to Good Distribution Practice (GDP) and Good Pharmacovigilance Practices (GVP) in your previous positions. Specific examples will help illustrate your expertise and commitment to regulatory standards.
✨Engage with Questions
Prepare thoughtful questions about Ferring’s approach to regulatory affairs and how they handle changes in the regulatory landscape. This not only shows your interest in the company but also gives you insight into their operations and culture, making it a two-way conversation.
