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- Tasks: Ensure compliance with clinical trial regulations and conduct internal audits.
- Company: Join a leading centre of excellence in cancer research.
- Benefits: Part-time role with flexible hours and the chance to make a real impact.
- Why this job: Be part of groundbreaking research that directly supports patient care.
- Qualifications: Experience in QA or compliance, with a science background preferred.
- Other info: Opportunity to work in a dynamic team focused on innovation.
The predicted salary is between 36000 - 60000 £ per year.
Join a Leading Centre of Excellence in Clinical Research. A unique part-time opportunity has opened up for a detail-oriented and proactive Quality Assurance Specialist to contribute to a world-renowned research hub driving breakthroughs in cancer diagnostics and treatment. In this pivotal role, you’ll be part of a specialised team ensuring compliance with Good Clinical Practice (GCP) in clinical trials. From managing internal audits and non-conformances to guiding teams on regulatory standards, you’ll be at the heart of initiatives that directly support patient-focused research.
The Role:
- Ensure compliance with GCP and clinical trial regulations
- Conduct internal audits and manage documentation reviews
- Handle non-conformances and support CAPA implementation
- Maintain and improve Quality Management System (QMS)
- Activate and track projects in the Laboratory Information Management System (LIMS)
- Provide QA guidance and basic training to staff
- Support external audit preparation and regulatory inspections
You’ll Bring:
- Experience in QA or compliance in GxP-regulated labs
- Working knowledge of GCP, CAPA, internal audits, and quality systems like LIMS and QPulse
- A science background (BSc or equivalent experience) and a meticulous eye for detail
Quality Assurance Specialist employer: S3 Science
Contact Detail:
S3 Science Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Specialist
✨Tip Number 1
Familiarise yourself with Good Clinical Practice (GCP) guidelines and any recent updates in clinical trial regulations. This knowledge will not only help you during interviews but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the clinical research field, especially those who work in quality assurance. Attend relevant webinars or local meetups to gain insights and potentially get referrals that could boost your application.
✨Tip Number 3
Prepare to discuss specific examples of how you've handled non-conformances or conducted internal audits in previous roles. Real-life scenarios can showcase your problem-solving skills and attention to detail, which are crucial for this position.
✨Tip Number 4
Stay updated on the latest trends and technologies in quality management systems like LIMS and QPulse. Being knowledgeable about these tools can set you apart from other candidates and show your proactive approach to continuous learning.
We think you need these skills to ace Quality Assurance Specialist
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to grasp the key responsibilities and requirements. Highlight your relevant experience in QA, compliance, and GCP to align with what the company is looking for.
Tailor Your CV: Customise your CV to reflect your experience in GxP-regulated labs and your knowledge of quality systems like LIMS and QPulse. Use specific examples that demonstrate your attention to detail and compliance expertise.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality assurance and your understanding of clinical trials. Mention how your background in science and your proactive approach make you a perfect fit for the role.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for any spelling or grammatical errors, and ensure that all information is clear and concise to make a strong impression.
How to prepare for a job interview at S3 Science
✨Showcase Your Attention to Detail
As a Quality Assurance Specialist, attention to detail is crucial. Be prepared to discuss specific examples from your past experiences where your meticulous nature helped identify issues or improve processes.
✨Demonstrate Your Knowledge of GCP and CAPA
Familiarise yourself with Good Clinical Practice (GCP) and Corrective and Preventive Actions (CAPA). During the interview, confidently explain how you have applied these principles in previous roles, showcasing your understanding of compliance in clinical trials.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving skills. Think of situations where you had to manage non-conformances or conduct internal audits, and be ready to explain your approach and the outcomes.
✨Highlight Your Team Collaboration Skills
Quality assurance often involves working closely with various teams. Share examples of how you've successfully collaborated with others to ensure compliance and improve quality systems, emphasising your ability to guide and train staff.
