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- Tasks: Manage regulatory affairs and pharmacovigilance tasks to ensure compliance and safety.
- Company: Ferring Pharmaceuticals, a global leader in reproductive and women's health.
- Benefits: Inclusive family support policies, parental leave, and hybrid working arrangements.
- Why this job: Join a mission-driven team making a real difference in people's lives.
- Qualifications: Life Science degree and 3-5 years of regulatory experience in pharmaceuticals.
- Other info: Collaborative culture with opportunities for personal and professional growth.
The predicted salary is between 36000 - 60000 ÂŁ per year.
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 the areas of 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.
Our Commercial teams collaborate as trusted partners with patient groups, clinicians, policy makers and the scientific community to identify and develop new opportunities to help patients. Customer centric, we offer an empowering, entrepreneurial culture – and a place to thrive and grow.
You will take responsibility for a range of tasks across Regulatory Affairs, Compliance, and Good Distribution Practice (GDP) as well as Good Pharmacovigilance Practices (GVP), working closely with your regulatory, quality, and safety colleagues. In this role, you will be expected to 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.
Behind our innovation… There’s you.
Life Science degree or equivalent.
Minimum of 3 years Regulatory experience in a pharmaceutical company (ideally 5 years experience).
Knowledge of the UK Regulatory environment is mandatory (this should include the current post-Brexit requirements).
Preferable to have experience or knowledge in the UK Pharmacovigilance environment (ideally to have some work experience in Pharmacovigilance).
Preferable to have direct experience of communicating with the UK Health Authority (the MHRA).
People come first at Ferring. Get inspired from our commitment to advocate for everyone’s right to build a family, no matter who you are, where you live or who you love.
Our 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.
Making a difference in the life of millions of people means we succeed by working together. Our diverse backgrounds, experiences, expertise, and perspectives enable us to find solutions to even the most challenging problems, and our success is tied to each team member’s contributions. Imagine the power of your career when it’s Ferring + You.
If our mission and your vision are aligned, please apply! We strive to build and maintain an inclusive and diverse workplace with equal opportunities and mutual respect for all employees regardless of their backgrounds and socioeconomic status.
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 Pharmaceuticals
Contact Detail:
Ferring Pharmaceuticals Recruiting Team
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 professionals in the Regulatory Affairs and Pharmacovigilance field on LinkedIn. Join relevant groups, attend webinars, and don’t be shy to ask for informational interviews. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for your interviews by researching Ferring Pharmaceuticals thoroughly. Understand their mission, values, and recent developments in the industry. This will help you tailor your answers and show that you’re genuinely interested in being part of their team.
✨Tip Number 3
Practice common interview questions related to Regulatory Affairs and Pharmacovigilance. Think about how your experience aligns with the job description and be ready to share specific examples. We want you to shine and show off your skills!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re proactive and really keen on joining the Ferring family. Let’s get you that dream job!
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 Regulatory Affairs and Pharmacovigilance role. Highlight relevant experience, especially in the UK regulatory environment and any pharmacovigilance knowledge you have. We want to see how your background aligns with our mission!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your passion for the role and how your innovative mindset can contribute to our team. Don’t forget to mention why you’re excited about working at Ferring – we love hearing what inspires you!
Showcase Your Curiosity: In your application, demonstrate your curiosity and entrepreneurial spirit. Share examples of how you've challenged norms or brought new ideas to the table in previous roles. We value those who think outside the box and are eager to learn!
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates. Let’s get started on this journey together!
How to prepare for a job interview at Ferring Pharmaceuticals
✨Know Your Regulatory Stuff
Make sure you brush up on the UK regulatory environment, especially post-Brexit requirements. Familiarise yourself with the specifics of Good Distribution Practice (GDP) and Good Pharmacovigilance Practices (GVP) as these will likely come up in your interview.
✨Show Your Curiosity
Ferring values an innovative mindset, so be prepared to discuss how you've challenged norms in your previous roles. Think of examples where your curiosity led to solutions or improvements in regulatory processes.
✨Communicate Effectively
Since you'll be working closely with various stakeholders, practice articulating your thoughts clearly. Be ready to explain complex regulatory concepts in simple terms, as this will demonstrate your ability to collaborate effectively with non-experts.
✨Prepare Questions
Have a few thoughtful questions ready about Ferring's approach to regulatory affairs and pharmacovigilance. This shows your genuine interest in the role and helps you assess if the company culture aligns with your values.
