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- Tasks: Lead strategic projects to enhance supplier quality in medical devices.
- Company: Convatec is a global leader in medical solutions, improving lives through innovative products.
- Benefits: Enjoy remote work options and a supportive team culture.
- Why this job: Make a real impact in healthcare while developing your project management skills.
- Qualifications: 3+ years in medical devices; strong project management and supplier quality experience required.
- Other info: Position may involve up to 20% travel; flexible working structure available.
The predicted salary is between 43200 - 72000 £ per year.
Senior Quality Engineer – Supplier Quality Projects
Convatec Paddington, England, United Kingdom
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Senior Quality Engineer – Supplier Quality Projects
Convatec Paddington, England, United Kingdom
Join to apply for the Senior Quality Engineer – Supplier Quality Projects role at Convatec
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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 more than 10,000 colleagues, we provide our products and services in around 90 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. Convatec’s revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit
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 more than 10,000 colleagues, we provide our products and services in around 90 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. Convatec’s revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit the role:
The Supplier Quality Senior Project Lead leads complex and strategic projects which support and enhance ConvaTec’s Global Supplier Quality program.
The purpose of the role is to lead, support and deliver on time execution of compliance, continuous improvement and new product development projects and initiatives in the scope of Global Supplier Quality.
Your key duties and responsibilities:
- Lead the development and maintenance of ConvaTec’s Global Supplier Quality program with a focus on New Product Development.
- Establish, maintain, and improve supplier performance metrics, policies, and procedures in administering quality relationships with suppliers globally.
- Be fully accountable for the identification, ownership, communication of progress, management, and on time execution of projects, quality plans and associated CAPAs.
- Build strong relationships with internal and external customers, suppliers, stakeholders, and support groups worldwide to meet the demands of a changing business environment.
- Support and lead, where appropriate, supplier selection, evaluation, and approval.
- Perform and support verification of effective implementation of quality systems to support ConvaTec product manufacturing outsourcing, e.g., by conducting supplier audits.
- Generate appropriate key performance indicators to assess supplier performance in a timely manner to drive resolution of corrective actions from the suppliers.
- Raise appropriate questions or concerns regarding regulatory compliance to appropriate authorities regarding Purchasing Control activities.
- Demonstrate high commitment to quality and customer service based on customer needs.
- Exhibit expert technical knowledge and principles in relation to medical devices and project management.
- Show strong project leadership skills for complex and strategic projects.
- Organize and present ideas with clear and concise verbal and written communication. Exhibit confidence when communicating issues, ideas, or subject matter expertise across all levels within the organization.
- Take personal responsibility for results and focus on setting clear expectations for key stakeholders and peers within the organization.
- Translate broad strategies into specific objectives and action plans.
- Generate alternatives and assess benefits and risks.
- Align personal goals and objectives with organization goals and business strategy and take actions to achieve them.
- Support a unified and seamless team.
- Provide direction to project teams that clarifies their expectations and roles.
- Communicate opinions, facts, and thoughts with clarity, transparency, and honesty.
- Seek multiple perspectives and listen openly to others’ points of view.
- Demonstrate the courage to speak up on issues and risks as well as on the good news.
- Demonstrate ownership of results within the area of responsibility.
- Set clear and high expectations and hold self and project team members accountable for decisions and results achieved.
- When required, lead and/or support supplier audits.
Skills & Experience:
- Minimum 3 years’ experience in the medical device industry.
- Supplier Quality experience
- String knowledge and understanding of project management methodologies and applying them to any assigned supplier quality related projects.
- Demonstrate ability to complete multiple, simultaneous projects with minimal supervision while motivating team members to achieve business objectives.
- Experience in TrackWise preferable
- Experience in internal and supplier related CAPA/ NC
- Knowledge and implementation of effective quality control for manufacturing and supply chain operations, particularly in supplier evaluation, selection, auditing, and supplier management programs.
- Ability to negotiate and partner with internal and external customers to enhance operational effectiveness.
- Knowledge of GxP and relative standards for manufacturing environments.
- Ability to work with people / teams across all levels within the organization in a complex, changing environment, to deliver value-added results to the business.
- Demonstrated ability to establish and respond to metrics related to supplier and contract manufacturers performance.
- Knowledge of quality control principles and their relationship to relevant regulatory requirements.
- Knowledge of regulatory requirements that affect the medical device manufacturing business and put policies and systems in place to achieve conformance: QSR Part 820, ISO 13485, MDD 93/42, ISO 9001, GMP Parts 201 and 211, EU MDR.
Qualifications/Education:
- BS/BA degree in medical engineering or life sciences
- Certified Quality Auditor – must have.
- Preferably, project management / lean six sigma qualifications.
Travel Requirements:
- Position may involve travel up to 20% of the time to Convatec and supplier locations globally. Some trips may include overnight travel.
Working Conditions:
- This role may be based in the UK with a remote working structure.
Ready to join us?
At Convatec, we’re pioneering trusted medical solutions to improve the lives we touch. If you’re ready to make a real impact, apply today and help us bring our Forever Caring promise to life.
Beware of scams online or from individuals claiming to represent Convatec
A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.
If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at
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.
Notice to Agency and Search Firm Representatives
Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Already a Convatec employee?
If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View \”Convatec Internal Career Site – Find Jobs\”. Thank you!
Seniority level
-
Seniority level
Not Applicable
Employment type
-
Employment type
Full-time
Job function
-
Job function
Quality Assurance
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Industries
Medical Equipment Manufacturing
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Senior Quality Engineer - Supplier Quality Projects employer: Convatec
Contact Detail:
Convatec Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Quality Engineer - Supplier Quality Projects
✨Tip Number 1
Familiarise yourself with the specific quality standards and regulations relevant to the medical device industry, such as ISO 13485 and QSR Part 820. This knowledge will not only help you in interviews but also demonstrate your commitment to quality and compliance.
✨Tip Number 2
Network with professionals in the medical device sector, especially those involved in supplier quality management. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and challenges in supplier quality.
✨Tip Number 3
Prepare to discuss your experience with project management methodologies, particularly how you've applied them in previous roles. Be ready to share specific examples of projects you've led that align with the responsibilities of the Senior Quality Engineer position.
✨Tip Number 4
Research Convatec's Global Supplier Quality program and understand their approach to supplier relationships. Tailor your discussions during interviews to reflect how your values and experiences align with their mission of improving patient outcomes.
We think you need these skills to ace Senior Quality Engineer - Supplier Quality Projects
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in the medical device industry, particularly in supplier quality and project management. Use specific examples that demonstrate your ability to lead projects and improve supplier performance.
Craft a Compelling Cover Letter: In your cover letter, express your passion for quality engineering and how it aligns with Convatec's mission. Mention your experience with CAPA and NC processes, and how you can contribute to their Global Supplier Quality program.
Highlight Relevant Skills: Clearly outline your skills related to project management methodologies, supplier evaluation, and quality control principles. Make sure to mention any certifications like Certified Quality Auditor or Lean Six Sigma qualifications.
Showcase Communication Skills: Since the role requires strong communication abilities, provide examples of how you've effectively communicated with stakeholders at all levels. This could include leading meetings, presenting ideas, or resolving conflicts.
How to prepare for a job interview at Convatec
✨Understand the Company and Its Values
Before your interview, take some time to research Convatec's mission and values. Understanding their commitment to improving lives through medical solutions will help you align your answers with their goals and demonstrate your genuine interest in the role.
✨Showcase Your Project Management Skills
As a Senior Quality Engineer, you'll need strong project management skills. Be prepared to discuss specific projects you've led, focusing on how you managed timelines, resources, and team dynamics. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Prepare for Technical Questions
Expect technical questions related to quality control principles, regulatory requirements, and supplier management. Brush up on relevant standards like ISO 13485 and QSR Part 820, and be ready to explain how you've applied these in your previous roles.
✨Demonstrate Strong Communication Skills
Effective communication is key in this role. Practice articulating your thoughts clearly and concisely, especially when discussing complex topics. Be ready to provide examples of how you've successfully communicated with stakeholders at various levels in your previous positions.
