Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead quality improvement initiatives and ensure compliance with quality management systems.
- Company: STERIS is a global leader in healthcare products, focused on infection prevention and patient care.
- Benefits: Enjoy opportunities for growth, learning, and making a real difference in the world.
- Why this job: Join a dynamic team driving innovation in healthcare and contribute to a safer world.
- Qualifications: 7-10 years in Manufacturing/Quality Engineering, with leadership experience in regulated industries required.
- Other info: This role offers autonomy and the chance to impact quality strategies at a senior level.
The predicted salary is between 48000 - 72000 £ per year.
HOW YOU WILL MAKE A DIFFERENCE
About you:
Do you want to spend your working time making a difference in the world around you? Are you motivated by impactful work? If so, then a career with STERIS team could be a great fit for you.
About Us:
At STERIS we are a leading global provider of products and services that support patient care with an emphasis on infection prevention. Our mission is to help our customers create a healthier and safer world. Working at STERIS, you GROW, LEARN and MAKE A DIFFERENCE.
We are currently recruiting for a Quality Manager vacancy. This is an excellent opportunity to join us at senior level in a division that drives the business forwards through innovation.
The Quality Manager will be responsible for leading quality improvement for a manufacturing or service facility/function. This position leads implementing and maintaining state-of-the-art quality practices for associated product and service lines
What is involved
- Lead the organization\’s Quality staff to ensure compliance to the overall Quality Management System and drive continuous improvement.
- Lead the organization\’s Quality staff to ensure alignment to manufacturing and servicing operations, support Lean efforts and drive quality improvement for products and services.
- Work closely with site senior management to provide strategic direction and development of the organization\’s quality strategies and tactics.
- Provide quality viewpoints and opinions on future product and service development.
- Provide coaching, mentoring and leadership to the Quality staff.
- Serve as the site\’s Management Representative and lead the organization\’s Management Review process.
- Ensure compliance with appropriate domestic regulatory and international standards and requirements.
- Lead the organization\’s continuous improvement process; including data analysis, improvement projects and process capability to improve key metrics as measured by the product/service quality dashboard.
- Lead and implement effective production and process controls.
- Manage the complaint handling processes to insure customer responsiveness and product and process improvements.
- Ensure compliance to the New Product Development process and assurance that the Product Requirements Document includes key quality performance metrics.
- Assess new designs for manufacturability, testability and reliability to ensure the Quality risks and deliverables of the New Product Development process meet the required application reliability and design intent.
- Determine supplier qualification risks based upon criticality of component and supplier process capability.
- The position requires a level of authority to conduct and direct required activities such as quality planning, personnel management and regulatory compliance.
- This individual has autonomy to perform the duties of Person Responsible for Regulatory Compliance (PRRC) on behalf of STERIS legal manufacturing entities under the EU MDR. This individual shall suffer no disadvantage within the organization in relation to proper fulfilment of his or her duties in lieu of article 15 of the EU MDR
Required Experience
- 7-10 years of combined Manufacturing/Quality Engineering and/or Quality Systems experience.
- 7-10 years of experience with medical device or other regulated industries preferred.
- 7-10 years of experience working in an ISO certified environment required.
- Minimum of 3 years in a Quality leadership role.
- Must fulfil the experience requirements listed in Article 15 of the EUMDR (PRRC).
- ASQ, QSR or familiarity with QSR/GMP regulations preferred
- Bachelor\’s degree
Skills
- Excellent problem-solving skills
- Focus on identification of potential issues and continuous improvement.
- Experience working on cross-functional teams and on own initiative.
- Demonstrated excellent organizational, oral and written communications skills.
- Must have PC experience, as well as working familiarity of desktop applications including Excel, Word, and PowerPoint.
- Experience with statistical analysis software and Visio preferred.
Equal Opportunities
STERIS plc provides employment and advancement opportunities without regard to age, disability, gender reassignment, marriage or civil partnership, pregnancy and maternity, race, religion/belief, sex (gender), sexual orientation or any other legally protected characteristic as defined by UK employment law. The Company bases all employment decisions on merit, qualifications, skills, and abilities with the intention that the best candidate is selected for each position.
STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare, life sciences and dental products and services. STERIS is a $5 billion, publicly traded (NYSE: STE) company with approximately 18,000 associates and Customers in more than 100 countries.
STERIS strives to be an Equal Opportunity Employer.
#J-18808-Ljbffr
Manager, Quality employer: STERIS Corporation
Contact Detail:
STERIS Corporation Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Manager, Quality
✨Tip Number 1
Familiarise yourself with STERIS's mission and values. Understanding their commitment to infection prevention and patient care will help you align your responses during interviews, showcasing how your experience and values resonate with theirs.
✨Tip Number 2
Highlight your experience in ISO certified environments and any specific quality management systems you've worked with. Be prepared to discuss how you've led quality improvement initiatives in previous roles, as this is crucial for the Quality Manager position.
✨Tip Number 3
Prepare examples of how you've successfully managed cross-functional teams and driven continuous improvement projects. This role requires collaboration across various departments, so demonstrating your leadership and teamwork skills will be key.
✨Tip Number 4
Research current trends and challenges in the medical device industry, particularly around regulatory compliance and quality assurance. Being knowledgeable about these topics will show your commitment to staying informed and your readiness to tackle the challenges faced by STERIS.
We think you need these skills to ace Manager, Quality
Some tips for your application 🫡
Tailor Your CV: Make sure to customise your CV to highlight your experience in quality management, particularly in manufacturing or regulated industries. Emphasise your leadership roles and any specific achievements related to quality improvement.
Craft a Compelling Cover Letter: Write a cover letter that reflects your passion for making a difference in the healthcare sector. Discuss how your skills align with STERIS's mission and how you can contribute to their quality management goals.
Highlight Relevant Experience: In your application, clearly outline your 7-10 years of experience in Quality Engineering and any familiarity with ISO standards. Mention specific projects where you led quality improvements or compliance initiatives.
Showcase Problem-Solving Skills: Provide examples in your application that demonstrate your excellent problem-solving skills. Discuss situations where you identified potential issues and implemented successful solutions in a quality management context.
How to prepare for a job interview at STERIS Corporation
✨Understand the Company Mission
Before your interview, make sure you understand STERIS's mission to create a healthier and safer world. Be prepared to discuss how your values align with this mission and how you can contribute to their goals.
✨Showcase Your Quality Management Experience
Highlight your 7-10 years of experience in Manufacturing/Quality Engineering and your leadership roles. Be ready to provide specific examples of how you've led quality improvement initiatives and ensured compliance with quality management systems.
✨Prepare for Technical Questions
Expect questions related to ISO standards, regulatory compliance, and quality metrics. Brush up on your knowledge of QSR/GMP regulations and be ready to discuss how you've applied these in previous roles.
✨Demonstrate Problem-Solving Skills
Prepare to discuss specific challenges you've faced in quality management and how you approached solving them. Use the STAR method (Situation, Task, Action, Result) to structure your responses and showcase your analytical skills.
