At a Glance
- Tasks: Lead quality compliance efforts and ensure high standards in manufacturing processes.
- Company: Convatec is a global leader in medical products, dedicated to improving lives through innovative solutions.
- Benefits: Enjoy a supportive work culture, opportunities for growth, and the chance to make a real impact.
- Other info: Office-based role with flexible hours; be part of a dynamic and caring environment.
- Why this job: Join a mission-driven team focused on excellence and transforming healthcare for millions.
- Qualifications: 2-4 years in QA/QC within medical devices; ISO 13485 certification preferred.
The predicted salary is between 36000 - 60000 £ per year.
About Us
Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs.
At Convatec, we’re transforming our business for the better. Better products. Better ways of working. And better ways of delivering for our customers and each other. We’re aiming for nothing short of excellence. Join us on our journey to #ForeverCaring as Quality Compliance Lead, and you’ll do the same.
About the role:
This position will have the objective of maintaining high quality standards for the product manufacturing and compliance with all applicable regulatory requirements. The scope is focused on Manufacturing Quality Compliance.
Your key duties and responsibilities:
- Oversight & coordination of GMP inspections of controlled environments.
- Oversight & coordination of inspections / audits of business-critical processes.
- Education & training for production / engineering team members in compliance issues.
- Supporting GMP improvement projects.
- Develop the manufacturing site towards “Audit Ready At All Times”.
- Performs and lead GMP walks / process inspections.
- Track GMP issues identified and work with site management to correct and prevent.
- Provide leadership, support and guidance to drive successful execution of the Internal Audit Process at Deeside Manufacturing site.
- Generate the audit schedule for Deeside Manufacturing with appropriate input from site Quality Leadership and other stakeholders.
- Ensure that the Quality Management System is periodically evaluated and audited and appropriate CAPA is taken to meet the business and regulatory requirements.
- Gather and analyse data as an input to the Management Reviews to allow meaningful review.
- Support Internal Audit as required.
- Provide training & education activities to support induction activities & ongoing employee training / development.
- Maintenance of the Intra Company Quality Agreements as required.
- Support other projects as required by the business.
Skills & Experience:
- Internal Lead Auditor Certification and experience in executing audits.
- Excellent written and verbal communication skills, with an open, collaborative, interactive leadership style.
- Ability to build and nurture strong and positive relationships with other leaders to partner effectively.
- Balanced technical understanding of products and processes combined with business and compliance acumen.
Qualifications/Education:
- Two to Four (2-4) years’ experience in a QA/QC role in medical device and/or pharmaceutical industry.
- ISO 13485 Internal auditor (Lead auditor preferred).
Working Conditions:
Office based, predominantly on days, however flexibility is required to work with nights / weekends teams as required.
Our ambitions will bring the very best out in you. You’ll be pushed to aim higher and really own your work. You’ll be encouraged and supported to make things happen, too. It can be challenging. But, as the progress you make will help improve the lives of millions, it’ll be worth it.
This is stepping up to a challenge. This is work that’ll move you.
Equal opportunities
Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.
Quality Compliance Lead employer: ConvaTec Group
At Convatec, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation. As a Quality Compliance Lead, you will have the opportunity to contribute to meaningful projects that improve patient outcomes while enjoying comprehensive benefits and robust professional development opportunities. Located in Deeside, our facility is committed to maintaining high quality standards and provides a supportive environment where your contributions are valued and recognised.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Compliance Lead
✨Tip Number 1
Familiarise yourself with the latest regulations and standards in the medical device industry, particularly ISO 13485. This knowledge will not only help you during interviews but also demonstrate your commitment to quality compliance.
✨Tip Number 2
Network with professionals in the quality assurance field, especially those who have experience in the medical sector. Attend industry conferences or webinars to connect with potential colleagues and learn about best practices.
✨Tip Number 3
Prepare to discuss specific examples of how you've successfully managed compliance issues in previous roles. Highlight your leadership skills and ability to educate teams on compliance matters, as these are crucial for the Quality Compliance Lead position.
✨Tip Number 4
Research Convatec's products and their impact on patient care. Understanding their mission and values will allow you to align your answers during the interview, showing that you're genuinely interested in contributing to their goals.
We think you need these skills to ace Quality Compliance Lead
Some tips for your application 🫡
Understand the Role:Before applying, make sure you fully understand the responsibilities and requirements of the Quality Compliance Lead position. Tailor your application to highlight how your experience aligns with the key duties mentioned in the job description.
Highlight Relevant Experience:In your CV and cover letter, emphasise your experience in quality assurance within the medical device or pharmaceutical industry. Mention specific projects or roles where you demonstrated your skills in compliance, audits, and training.
Showcase Communication Skills:Since excellent written and verbal communication skills are essential for this role, ensure your application reflects this. Use clear, concise language and structure your documents well to demonstrate your ability to communicate effectively.
Tailor Your Cover Letter:Craft a personalised cover letter that not only expresses your interest in Convatec but also outlines how your values align with their mission of 'Forever Caring'. Mention specific aspects of the company that resonate with you and how you can contribute to their goals.
How to prepare for a job interview at ConvaTec Group
✨Understand the Company
Before your interview, take some time to research Convatec. Familiarise yourself with their products, values, and recent developments in the medical technology field. This will help you demonstrate your genuine interest in the company and align your answers with their mission.
✨Showcase Your Compliance Knowledge
As a Quality Compliance Lead, you'll need to exhibit a strong understanding of GMP and regulatory requirements. Be prepared to discuss your experience with audits and compliance processes, and how you've contributed to maintaining high-quality standards in previous roles.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills and ability to handle compliance issues. Prepare examples from your past experiences where you successfully managed audits or resolved quality-related challenges, highlighting your leadership and collaborative approach.
✨Ask Insightful Questions
At the end of the interview, take the opportunity to ask thoughtful questions about the role and the company's future plans. This not only shows your enthusiasm but also helps you gauge if Convatec is the right fit for you.
