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- Tasks: Lead quality assurance for clinical trials and support the Clinical Affairs team.
- Company: Join a cutting-edge organisation focused on molecular data analysis.
- Benefits: Enjoy a competitive salary, bonus, and hybrid work flexibility.
- Why this job: Make an impact in healthcare while working with innovative technologies and a supportive team.
- Qualifications: Experience in quality assurance and knowledge of IVD or medical device regulations required.
- Other info: This is a 12-month fixed-term contract covering maternity leave.
The predicted salary is between 32000 - 40000 £ per year.
Job Type: 12 months fixed-term contract, Maternity cover
Location: Manchester, UK (hybrid) 3x a week on site
Remuneration: £40,000 - £46,000 + 10% Bonus
Cpl Life Sciences is partnering with a leading organisation that uses technologies to help customers extract, analyse, and interpret molecular data from samples containing DNA, RNA, and proteins.
Due to maternity leave, we are looking for an experienced candidate to take responsibility for quality and compliance oversight of the activities performed by the Clinical Affairs team. The function supports the testing and registration of diagnostic tests/instruments covering a diverse portfolio of indications.
As a senior member of the Clinical QA team, you will take responsibility for:
- Overseeing division of workload
- Advising and supporting the team as required
Work with members of the Clinical Affairs team to ensure compliance during trial activities e.g. closure of deviations, complaints etc.
Review clinical relevant documentation throughout the clinical trial.
Desirable:
- Working knowledge of IVD or medical device regulations
- Experience in performing as a Subject Matter Expert in regulatory inspections and other formal audits
- Willingness to travel internationally up to 10%
This role will be a hybrid-based position with 3x a week required on site in Manchester.
Clinical QA Manager employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical QA Manager
✨Tip Number 1
Familiarise yourself with the latest IVD and medical device regulations. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to compliance, which is crucial for the Clinical QA Manager role.
✨Tip Number 2
Network with professionals in the clinical quality assurance field. Attend relevant industry events or join online forums to connect with others who may provide insights or even referrals for the position at StudySmarter.
✨Tip Number 3
Prepare to discuss your experience with regulatory inspections and audits in detail. Be ready to share specific examples of how you've successfully navigated these processes, as this will highlight your expertise and suitability for the role.
✨Tip Number 4
Showcase your leadership skills by preparing examples of how you've effectively managed teams in previous roles. As a senior member of the Clinical QA team, your ability to oversee and support your colleagues will be key to your success.
We think you need these skills to ace Clinical QA Manager
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the responsibilities and requirements of the Clinical QA Manager position. Highlight key skills such as quality oversight, compliance, and experience with IVD or medical device regulations.
Tailor Your CV: Customise your CV to reflect relevant experience in quality assurance and compliance within clinical settings. Emphasise any previous roles where you acted as a Subject Matter Expert during regulatory inspections or audits.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality assurance in the clinical field. Mention specific experiences that align with the job requirements, such as managing deviations or supporting clinical trial activities.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects attention to detail, which is crucial for a Clinical QA Manager.
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Regulations
Familiarise yourself with IVD and medical device regulations before the interview. Being able to discuss these regulations confidently will demonstrate your expertise and show that you are well-prepared for the role.
✨Showcase Your Experience
Prepare specific examples from your past roles where you successfully managed quality assurance processes or compliance oversight. Highlight any experience you have with regulatory inspections or audits, as this will be crucial for the position.
✨Understand the Company’s Mission
Research the organisation's technologies and how they impact molecular data analysis. Showing that you understand their mission and how your role fits into it can set you apart from other candidates.
✨Ask Insightful Questions
Prepare thoughtful questions about the Clinical Affairs team and their current projects. This not only shows your interest in the role but also gives you a chance to assess if the company culture aligns with your values.
