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- Tasks: Lead quality assurance and compliance at a cutting-edge pharmaceutical manufacturing site.
- Company: Ferring Pharmaceuticals, dedicated to helping families and improving lives globally.
- Benefits: Inclusive family-building support, competitive salary, and extensive parental leave.
- Why this job: Make a real impact in healthcare while ensuring product quality and safety.
- Qualifications: Degree in relevant sciences and extensive GMP experience required.
- Other info: Join a diverse team committed to innovation and patient care.
The predicted salary is between 72000 - 84000 £ 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 Technical Operations division develops, manufactures and supplies high-quality products so our patients can live better lives. Creating and delivering life-changing products means getting it right first time is a shared responsibility, so our global manufacturing teams work closely together to ensure quality, accuracy and safety at all times. That means a culture of empowerment, where speaking up is valued, and growth and development are constant.
The Quality Director is responsible for ensuring excellence in Quality, Compliance and GMP at our MHRA-licensed pharmaceutical manufacturing site, ensuring full compliance with UK/ EU GMP requirements. The role holds strategic and operational accountability for Quality Assurance and Quality Control. In addition, the QP role ensures that all medicinal products are manufactured, tested, and released in accordance with UK/EU legislation, GMP requirements, and the conditions of relevant Marketing Authorisations.
Your day at Ferring:
- Ensure compliance with UK/EU GMP regulations
- Provide leadership of the site Quality function (QA, QC, QMS)
- Perform QP batch certification and release activities in accordance with UK Human Medicines Regulations
- Act as primary contact for MHRA inspections and other regulatory authority audits
- Ensure effective management of the Quality Management System
- Maintain robust data integrity systems (including Annex 11 compliance)
- Lead inspection readiness and continuous improvement initiatives
- Support regulatory submissions and lifecycle management activities
Cross‐Functional Quality Leadership: Partner with QA, QC, Operations, Supply Chain, and Engineering to drive a strong quality culture.
Shop‐Floor Presence & Continuous Improvement: Maintain operational visibility, identify risks and contribute to improvement initiatives.
Behind our innovation...There’s you:
- Degree in Pharmacy, Chemistry, Microbiology, Life Sciences, or related discipline
- Extensive experience in pharmaceutical quality within a GMP manufacturing environment
- Proven expertise in batch certification and regulatory compliance, with strong knowledge of EU/UK GMP, ICH guidelines, MHRA expectations, and Quality Risk Management Principles
- Confident supporting regulatory inspections and customer audits, demonstrating high standards of compliance and operational readiness
- Fully Qualified Person (QP) under UK legislation with strong GMP pharmaceutical manufacturing experience/close to completing VIVA with relevant oral solid dosage pharmaceutical experience
- Proven experience managing MHRA inspections with successful outcomes
Key Competencies:
- Strong regulatory leadership
- Skilled at interpreting data and making sound, risk‐based quality decisions
- Excellent stakeholder engagement and communication
- Commitment to patient safety and product quality
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.
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.
Quality Director/Qualified Person – On Site in East Kilbride employer: Ferring Holding SA
Contact Detail:
Ferring Holding SA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Director/Qualified Person – On Site in East Kilbride
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect with Ferring employees on LinkedIn. Building relationships can open doors that applications alone can't.
✨Tip Number 2
Prepare for interviews by researching Ferring's values and recent projects. Show us how your experience aligns with our mission to improve lives through innovative healthcare solutions.
✨Tip Number 3
Practice your pitch! Be ready to explain how your skills in quality assurance and compliance make you the perfect fit for the Quality Director role. Confidence is key!
✨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 genuinely interested in joining our team.
We think you need these skills to ace Quality Director/Qualified Person – On Site in East Kilbride
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Quality Director role. Highlight your experience in GMP compliance and quality assurance, as this will show us you understand what we're looking for.
Showcase Your Leadership Skills: We want to see how you've led teams or projects in the past. Share specific examples of how you've driven a quality culture or managed inspections, as this will demonstrate your fit for the role.
Be Clear and Concise: When writing your application, keep it straightforward. Use clear language and avoid jargon where possible. This helps us quickly grasp your qualifications and makes your application stand out.
Apply Through Our Website: Don’t forget to submit your application through our official website! This ensures we receive all your details correctly and gives you the best chance of being considered for the role.
How to prepare for a job interview at Ferring Holding SA
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of UK/EU GMP regulations. Ferring Pharmaceuticals places a strong emphasis on compliance, so be prepared to discuss how you've ensured quality and compliance in your previous roles.
✨Showcase Your Leadership Skills
As a Quality Director, you'll need to demonstrate your ability to lead cross-functional teams. Think of examples where you've successfully driven a quality culture or led continuous improvement initiatives, and be ready to share these during the interview.
✨Prepare for Regulatory Questions
Expect questions about your experience with MHRA inspections and regulatory audits. Be ready to discuss specific instances where you've managed these processes and achieved successful outcomes, as this will show your expertise and readiness for the role.
✨Emphasise Your Commitment to Patient Safety
Ferring is all about making a difference in patients' lives. Be prepared to talk about how your work has directly contributed to patient safety and product quality, and why this is important to you personally.