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For Companies At a Glance
- Tasks: Lead quality assurance efforts and maintain ISO accreditations in a dynamic medical equipment company.
- Company: Join a leading organisation focused on innovative medical solutions and remote patient sampling.
- Benefits: Enjoy a hybrid working model with flexibility and opportunities for professional growth.
- Why this job: Be part of a mission-driven team making a real impact in healthcare quality standards.
- Qualifications: 5+ years in Quality Assurance within the medical device industry and strong ISO knowledge required.
- Other info: Located in Croydon, this role offers a chance to shape quality benchmarks and processes.
The predicted salary is between 43200 - 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
Senior QA Manager employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior QA Manager
✨Tip Number 1
Familiarise yourself with the specific ISO standards mentioned in the job description, especially ISO:13485 and ISO:9001. Being able to discuss these standards confidently during an 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 can set you apart and highlight your genuine interest in the role.
✨Tip Number 3
Network with professionals in the medical device industry, particularly those who have experience with quality assurance management. Engaging in conversations can provide insights into the role and may even lead to referrals.
✨Tip Number 4
Prepare examples from your past experience that showcase your problem-solving skills and ability to maintain compliance with regulatory standards. Be ready to discuss how you've successfully navigated quality issues in previous roles.
We think you need these skills to ace Senior QA Manager
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly understand the responsibilities and requirements of the Senior QA Manager position. Familiarise yourself with ISO standards and the specific accreditations mentioned in the job description.
Tailor Your CV: Customise your CV to highlight your relevant experience in Quality Assurance Management, particularly in the medical device industry. Emphasise your knowledge of ISO:13485, ISO:9001, and other relevant regulations.
Craft a Compelling Cover Message: Use the cover message to express your enthusiasm for the role and the company. Mention specific experiences that align with the responsibilities outlined in the job description, showcasing your problem-solving skills and ability to collaborate with leadership teams.
Proofread Your Application: Before submitting, carefully proofread your CV and cover message for any errors or typos. A polished application reflects your attention to detail, which is crucial for a QA Manager role.
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 other relevant standards during the interview. Be prepared to discuss how you've applied these standards in your previous roles and how they can benefit the organisation.
✨Demonstrate Problem-Solving Skills
Prepare examples of how you've identified quality issues and developed proposals to resolve them. This will show your ability to think critically and make informed decisions, which is crucial for a Senior QA Manager.
✨Understand Regulatory Processes
Familiarise yourself with governmental regulatory processes and regulations related to medical devices. Being able to discuss these in detail will demonstrate your expertise and readiness for the role.
✨Communicate Effectively
Strong communication skills are essential for this position. Practice articulating your thoughts clearly and concisely, especially when discussing complex quality management concepts or collaborating with the Senior Leadership Team.
