At a Glance
- Tasks: Lead global QA projects for medical devices and ensure quality standards are met.
- Company: Ferring Pharmaceuticals, a leader in reproductive and women's health innovation.
- Benefits: Inclusive family support policies, parental leave, and career development opportunities.
- Other info: Empowering culture that values collaboration and continuous growth.
- Why this job: Make a real impact on patients' lives through innovative medical device quality assurance.
- Qualifications: 10 years in the pharmaceutical/medical device industry with project management experience.
The predicted salary is between 70000 - 90000 £ 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 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.
As Global QA Senior Manager, Medical Devices & Drug/Device Combined Products, you will lead Major Global QA Medical Device projects and support the Ferring Manufacturing sites as the main point of contact regarding Medical Devices and device constituents of combination/medicinal products. The role may require travel of approximately 10–20% of your time, mainly within Europe.
Your day at Ferring:
- Contribute to QMS improvements for medical device and device constituent of combination products and support ISO 13485, MDSAP & MDR certification.
- Own key Medical Devices Process/SOPs.
- Ensure the corporate QMS for device activities at Manufacturing Sites, in Operation and in Central functions is implemented.
- Support the Manufacturing sites dealing with Medical Devices and Combination Products by providing guidance, coordination and escalation on topics such as complaints, Deviation/CAPA, Change Request, vendor assessments or during audits Notified Bodies, FDA and Competent Authorities.
- Support the Commercial Medical Devices/Combination Products Projects as QA representative, ensure inputs from sites are considered and transfer properly organized.
- Lead assigned GQA Projects and audits.
Nice to have a scientific degree, preferably Master (pharmacy, chemistry, biology or equivalent). 10 years of experience in the Pharmaceutical and Medical Device Industry (development, manufacturing, packaging, QC, QA) and cGMP environment or equivalent. Standards such as 21 CFR part 4, part 820, MDR and ISO13485 regulations (MDSAP is a plus). Design control / Design & Development process for Medical Devices and Drug/Device Combination product. Experienced in Project Management. Vendors/Customers relationships and you have the ability to set up links between external and internal partners. Medical Device / Drug Device Combination Product company auditing (as a lead auditor). You are accountable, collaborative and entrepreneurial, with a curious mindset.
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.
Location: Ferring Controlled Therapeutics UK
Global QA Senior Manager, Medical Devices & Combo Products in Glasgow employer: Ferring
Ferring Pharmaceuticals is an exceptional employer that prioritises innovation and collaboration, fostering a culture where employees are empowered to contribute to life-changing advancements in healthcare. With a strong commitment to employee growth, our inclusive support package ensures that all team members have access to family-building resources and policies, making Ferring a supportive workplace for everyone. Located in the UK, we offer a dynamic environment where your expertise in quality assurance can thrive, alongside opportunities for meaningful impact on global health.
StudySmarter Expert Advice🤫
We think this is how you could land Global QA Senior Manager, Medical Devices & Combo Products in Glasgow
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those at Ferring. A friendly chat can open doors and give you insights that a job description just can't.
✨Tip Number 2
Prepare for interviews by knowing your stuff! Brush up on ISO 13485 and MDSAP regulations, and be ready to discuss how your experience aligns with Ferring's mission of improving lives through innovative medical devices.
✨Tip Number 3
Show your passion for quality assurance! During interviews, share examples of how you've contributed to QMS improvements or led successful projects in the past. Let them see your commitment to getting it right the first time.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you're serious about joining the Ferring team and contributing to our mission.
We think you need these skills to ace Global QA Senior Manager, Medical Devices & Combo Products in Glasgow
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the specific skills and experiences that match the Global QA Senior Manager role. Highlight your experience in the Pharmaceutical and Medical Device Industry, especially around QMS improvements and compliance with ISO standards.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to tell us why you're passionate about quality assurance in medical devices and how your background aligns with our mission at Ferring. Be sure to mention any relevant projects you've led or contributed to.
Showcase Your Project Management Skills:Since this role involves leading major global QA projects, make sure to highlight your project management experience. Share specific examples of how you've successfully managed projects in the past, particularly in a cGMP environment.
Apply Through Our Website:We encourage you to apply directly through our website. This ensures your application gets to the right people and shows us you're serious about joining our team. Plus, it's super easy!
How to prepare for a job interview at Ferring
✨Know Your Stuff
Make sure you brush up on the key regulations like ISO 13485, MDR, and MDSAP. Familiarise yourself with the latest trends in medical devices and combination products. This will not only show your expertise but also your genuine interest in the field.
✨Showcase Your Experience
Prepare to discuss your past experiences in QA and project management. Be ready to share specific examples of how you've led projects or improved processes in a cGMP environment. This will help demonstrate your capability to handle the responsibilities of the role.
✨Emphasise Collaboration
Ferring values teamwork, so be prepared to talk about how you've worked with cross-functional teams in the past. Highlight instances where you've successfully collaborated with manufacturing sites or external partners to achieve quality goals.
✨Ask Insightful Questions
Prepare thoughtful questions that show your understanding of Ferring's mission and culture. Inquire about their approach to QMS improvements or how they support their teams in dealing with regulatory challenges. This shows you're not just interested in the job, but in contributing to their vision.
