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- Tasks: Lead quality assurance and compliance at a pharmaceutical manufacturing site.
- Company: Ferring Pharmaceuticals, dedicated to improving lives through innovative healthcare solutions.
- Benefits: Inclusive family support policies, competitive salary, and opportunities for professional growth.
- Other info: Join a diverse team committed to innovation and patient safety.
- Why this job: Make a real impact on patient lives while ensuring top-notch product quality.
- Qualifications: Degree in relevant sciences and extensive GMP experience required.
The predicted salary is between 48000 - 72000 £ 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.
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 Glasgow employer: Ferring Pharmaceuticals
Contact Detail:
Ferring Pharmaceuticals Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Director/Qualified Person – On Site in Glasgow
✨Tip Number 1
Network like a pro! Reach out to current or former employees at Ferring Pharmaceuticals on LinkedIn. A friendly chat can give us insider info about the company culture and maybe even a referral!
✨Tip Number 2
Prepare for the interview by diving deep into Ferring's mission and values. Show us how your experience aligns with their commitment to quality and patient safety. We want to see that passion shine through!
✨Tip Number 3
Practice your answers to common interview questions, especially around quality assurance and compliance. We need to hear how you’ve tackled challenges in the past and what you learned from them.
✨Tip Number 4
Don’t forget to follow up after your interview! A quick thank-you email can keep you top of mind. Plus, it shows us that you’re genuinely interested in the role and the company.
We think you need these skills to ace Quality Director/Qualified Person – On Site in Glasgow
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Director role. Highlight your experience in GMP environments and any relevant qualifications, like being a Fully Qualified Person (QP). We want to see how your background aligns with our mission at Ferring!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality assurance and how you can contribute to our team. Don’t forget to mention your commitment to patient safety and product quality – that’s super important to us!
Showcase Your Leadership Skills: As a Quality Director, leadership is key. In your application, share examples of how you've led teams or projects in the past. We love seeing candidates who can inspire and drive a strong quality culture within their teams.
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 shows you’re keen on joining the Ferring family!
How to prepare for a job interview at Ferring Pharmaceuticals
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of UK/EU GMP regulations and the specific requirements for pharmaceutical manufacturing. Being able to discuss these in detail will show that you're not just familiar with the rules, but that you can apply them effectively in a real-world setting.
✨Showcase Your Leadership Skills
As a Quality Director, you'll need to demonstrate strong leadership capabilities. Prepare examples from your past experiences where you've successfully led teams or initiatives, particularly in quality assurance or compliance. This will help illustrate your ability to foster a culture of quality and safety.
✨Prepare for Regulatory Inspections
Since you'll be acting as the primary contact for MHRA inspections, it's crucial to prepare for questions about your experience with regulatory audits. Think of specific instances where you managed inspections and what the outcomes were. This will highlight your readiness and confidence in handling such situations.
✨Engage with Cross-Functional Teams
Ferring values collaboration across departments. Be ready to discuss how you've partnered with QA, QC, Operations, and other teams in the past. Highlight any successful projects that required cross-functional teamwork, as this will demonstrate your ability to drive a strong quality culture throughout the organisation.