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- Tasks: Lead quality assurance efforts and maintain ISO accreditations in a dynamic medical equipment environment.
- Company: Join a leading Medical Equipment Manufacturing organization focused on innovative patient sampling solutions.
- Benefits: Enjoy a hybrid working model with flexibility and opportunities for professional growth.
- Why this job: Be part of a team driving quality standards in healthcare, making a real impact on patient safety.
- Qualifications: 5+ years in Quality Assurance Management with strong ISO knowledge and medical device experience required.
- Other info: Collaborate with senior leadership to shape quality benchmarks and improve processes.
The predicted salary is between 48000 - 72000 £ per year.
CPL are working with a leading Medical Equipment Manufacturing organisation with a growing workforce and expanding requirements for remote patient sampling, they require a Senior Quality Assurance Manager to join the team to achieve their ambitious growth in the coming years.
This position is based out of Croydon operating on a hybrid working model.
Responsibilities
- Responsibility of the Management Representative for the ISO:13485 accreditation
- Maintain accreditations for ISO:13485, ISO: 9001, ISO:14001, ISO:27001, and FSC
- Oversee the business’ performance and activities to maintain GDP standards and maintain an MHRA WDA license
- Collaborate with the Senior Leadership Team to set quality benchmarks, the effectiveness of the quality management system and improvements required
- Identify and review Quality issues, develop proposals, and make decisions with input from the QA team
- Promote and approve processes and procedures in accordance with industry standards and customer expectations
Competency requirements
- Strong knowledge of ISO:13485, ISO:9001, ISO:27001
- Knowledge of GDP working practices
- Understanding of and ability to determine relevance of governmental regulatory processes and regulations.
- 5+ years of medical device industry experience, in Quality Assurance Management
- Broad knowledge of ISO 13485:2016, US FDA, and European Medical Device Regulations (MDD, MDR, IVDD, IVDR)
- Strong organization, communication, and problem-solving skills
If you are interested please apply or send your CV to
Senior Quality Assurance Manager employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Quality Assurance Manager
✨Tip Number 1
Familiarize yourself with the specific ISO standards mentioned in the job description, especially ISO:13485 and ISO:9001. Being able to discuss these standards in detail during your interview will demonstrate your expertise and commitment to quality assurance.
✨Tip Number 2
Research the company’s recent projects or initiatives related to remote patient sampling. Showing that you understand their current focus and challenges will help you stand out as a candidate who is genuinely interested in contributing to their growth.
✨Tip Number 3
Prepare examples from your past experience where you successfully maintained accreditations or improved quality management systems. Be ready to share these stories to illustrate your problem-solving skills and leadership capabilities.
✨Tip Number 4
Network with professionals in the medical device industry, particularly those with experience in quality assurance. Engaging with others in the field can provide valuable insights and potentially lead to referrals that could enhance your application.
We think you need these skills to ace Senior Quality Assurance Manager
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Senior Quality Assurance Manager position. Understand the key responsibilities and competencies required, especially regarding ISO standards and quality management.
Tailor Your CV: Customize your CV to highlight your experience in quality assurance management, particularly in the medical device industry. Emphasize your knowledge of ISO:13485, ISO:9001, and other relevant regulations.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for quality assurance and your ability to meet the company's ambitious growth goals. Mention specific examples of how you've maintained accreditations or improved quality systems in previous roles.
Highlight Relevant Experience: In your application, clearly outline your 5+ years of experience in the medical device industry. Discuss your familiarity with governmental regulatory processes and how you have successfully navigated them in past positions.
How to prepare for a job interview at Cpl Life Sciences
✨Showcase Your ISO Knowledge
Make sure to highlight your strong knowledge of ISO:13485, ISO:9001, and ISO:27001 during the interview. Be prepared to discuss specific examples of how you've maintained these accreditations in your previous roles.
✨Demonstrate Leadership Skills
As a Senior Quality Assurance Manager, you'll be collaborating with the Senior Leadership Team. Share experiences where you've successfully led teams or projects, focusing on how you set quality benchmarks and drove improvements.
✨Prepare for Regulatory Questions
Expect questions about governmental regulatory processes and regulations. Brush up on your understanding of GDP working practices and be ready to explain how you've navigated these in past positions.
✨Problem-Solving Examples
Be ready to discuss specific quality issues you've identified and resolved. Prepare a couple of case studies that demonstrate your problem-solving skills and how you collaborated with your QA team to implement effective solutions.
