At a Glance
- Tasks: Lead a team in quality control and ensure product compliance in a regulated environment.
- Company: Join Aurora Lifesciences, a partner of an established medtech manufacturer.
- Benefits: Competitive salary, career growth, and a chance to make a real impact.
- Other info: Dynamic role with opportunities for continuous improvement and teamwork.
- Why this job: Be at the forefront of quality assurance in medical device manufacturing.
- Qualifications: Experience in quality control and knowledge of ISO standards required.
Aurora Lifesciences is partnered with an established medtech manufacturer who is now seeking a Quality Control Lead to support its inspection and quality control operations. This hands-on role will provide daily leadership, technical guidance, and workload coordination for a team responsible for incoming inspection, product inspection, and final release activities. The role is suited to an experienced quality professional with strong knowledge of regulated manufacturing environments and applicable quality system requirements, including ISO 13485, EU MDR, and FDA 21 CFR Part 820.
Key Responsibilities
- Lead and support a team of Quality Control and Receiving Inspection personnel.
- Allocate daily workload, provide technical guidance, and support shift priorities.
- Act as a technical escalation point for inspection queries, specification interpretation, and non-conformance decisions.
- Ensure incoming materials, components, sub-assemblies, and finished products are inspected, tested, documented, and dispositioned in line with approved procedures.
- Review and authorise inspection records within delegated authority.
- Support final product inspection, testing, verification, and release activities.
- Review supplier documentation and support receiving inspection requirements.
- Conduct first article inspections against specifications, drawings, and engineering requirements.
- Identify training needs and support team qualification activities.
- Monitor inspection performance, resource needs, and non-conformance trends.
- Contribute to continuous improvement across inspection, manufacturing, and quality processes.
- Promote a culture of compliance, accountability, safety, and continuous improvement.
- Work closely with Manufacturing, Engineering, Quality Assurance, Supply Chain, and other business functions.
Required Experience
- Experience in quality control, receiving inspection, product inspection, or incoming quality within a regulated manufacturing environment.
- Experience in medical device manufacturing is desirable.
- Previous experience in a team leader, supervisory, or shift leadership role.
- Working knowledge of ISO 13485, EU MDR, and FDA 21 CFR Part 820.
- Formal quality system or regulatory training would be advantageous.
Key Skills
- Strong people leadership and team coordination skills.
- Good technical judgement and attention to detail.
- Ability to interpret specifications, inspection criteria, and technical drawings.
- Clear written and verbal communication skills.
- Ability to prioritise work and deploy resources effectively.
- Confident working with cross-functional teams.
- Hands-on, proactive, and comfortable working in a regulated manufacturing environment.
- Strong commitment to quality, compliance, safety, and continuous improvement.
Ideal Candidate Profile
The ideal candidate will be a practical and detail-focused quality professional with proven experience in regulated manufacturing and inspection environments. They will combine strong technical inspection knowledge with the ability to lead people, manage priorities, and support a culture of compliance and continuous improvement. They will be confident working in a cleanroom and office-based environment, comfortable interpreting specifications and technical drawings, and able to act as a trusted escalation point for inspection-related decisions. Above all, they will demonstrate a strong commitment to quality, safety, teamwork, and delivering products that meet the highest regulatory and customer expectations.
QC Lead in Bradford employer: Aurora Life Sciences
Aurora Lifesciences is an exceptional employer, offering a dynamic work environment where quality and compliance are at the forefront of our operations. Our culture promotes continuous improvement and teamwork, providing employees with ample opportunities for professional growth and development in the medtech sector. Located in a state-of-the-art facility, we ensure that our team members thrive in a supportive atmosphere that values safety, accountability, and innovation.
StudySmarter Expert Advice🤫
We think this is how you could land QC Lead in Bradford
✨Tip Number 1
Network like a pro! Reach out to your connections in the medtech industry, especially those who work in quality control. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ISO 13485 and FDA regulations. Be ready to discuss how your experience aligns with the role's responsibilities, especially around inspection and compliance.
✨Tip Number 3
Showcase your leadership skills! During interviews, share examples of how you've successfully led teams or improved processes in previous roles. This will highlight your fit for the QC Lead position.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace QC Lead in Bradford
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the specific skills and experiences mentioned in the job description. Highlight your experience in quality control and any relevant regulatory knowledge, like ISO 13485 or FDA standards. We want to see how you fit into our world!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for the QC Lead role. Share specific examples of your leadership experience and how you've contributed to quality improvements in past roles. Let us know why you’re excited about joining our team!
Showcase Your Technical Skills:In your application, don’t forget to mention your technical judgement and attention to detail. We love candidates who can interpret specifications and technical drawings, so give us some examples of how you've done this in your previous roles.
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 us you’re keen on being part of our team at StudySmarter!
How to prepare for a job interview at Aurora Life Sciences
✨Know Your Standards
Make sure you brush up on ISO 13485, EU MDR, and FDA 21 CFR Part 820 before the interview. Being able to discuss these standards confidently will show that you understand the regulatory environment and can lead a team effectively.
✨Showcase Your Leadership Skills
Prepare examples of how you've successfully led teams in the past. Think about specific situations where you allocated workloads or provided technical guidance. This will demonstrate your ability to manage and inspire a team.
✨Be Ready for Technical Questions
Expect questions that test your technical judgement and attention to detail. Brush up on interpreting specifications and inspection criteria, as well as discussing non-conformance decisions you've made in previous roles.
✨Emphasise Continuous Improvement
Be prepared to talk about how you've contributed to continuous improvement in your past roles. Share specific examples of initiatives you've led or participated in that enhanced quality processes or team performance.
