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- Tasks: Support clinical trials by ensuring compliance with GCP regulations and conducting audits.
- Company: Join a renowned research facility in Manchester focused on lifesaving drug development.
- Benefits: Part-time hours, competitive salary, and the chance to make a real impact.
- Why this job: Be part of a mission-driven team improving patients' lives while gaining valuable experience.
- Qualifications: Degree in Science or equivalent experience in a regulated QA environment required.
- Other info: Flexible part-time role at 17.5 hours per week, perfect for students.
The predicted salary is between 26000 - 29000 £ per year.
Part time (17.5 hours per week) in Central Manchester. Salary: £26,000 - £29,000 DOE (£13,000 - £14,500 pro rata).
We are working on behalf of a well-known research facility based in Manchester that carries out important research into lifesaving and life extending drugs. They are looking to add a part time QA Officer to their busy QA department to support their clinical trial activities by ensuring they comply with GCP regulations.
Responsibilities include but are not limited to:
- Ensuring all QA documentation is completed and up to date
- Supporting the completion of Non-Conformances (NCs) and Corrective and Preventative Actions (CAPA)
- Conducting internal audits and supporting preparations for external audits and regulatory inspections
- Keeping up to date with current regulatory requirements and developments for GCP
- Supporting the timely delivery of QA activities
- Interacting with specialist teams and core groups on all matters of GCP compliance
Suitable candidates for this role should be qualified to degree level (or equivalent) in Science or related subject or have equivalent relevant experience working as a QA officer in a highly regulated environment.
If you are interested in contributing to an organisation that is actively working towards improving patients' quality of life and curing life threatening illnesses then please contact Dave Cattell at Reed for more information or apply via this site.
Contact Detail:
Reed Specialist Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Officer
✨Tip Number 1
Familiarise yourself with Good Clinical Practice (GCP) regulations and guidelines. Understanding these will not only help you in interviews but also demonstrate your commitment to quality assurance in clinical trials.
✨Tip Number 2
Network with professionals in the QA field, especially those working in clinical research. Attend relevant industry events or webinars to make connections that could lead to valuable insights or referrals.
✨Tip Number 3
Prepare to discuss specific examples of how you've handled Non-Conformances (NCs) and Corrective and Preventative Actions (CAPA) in past roles. This will showcase your practical experience and problem-solving skills.
✨Tip Number 4
Stay updated on the latest developments in regulatory requirements for GCP. Being knowledgeable about current trends and changes can set you apart from other candidates during the interview process.
We think you need these skills to ace Quality Assurance Officer
Some tips for your application 🫡
Understand the Role: Read the job description carefully to understand the responsibilities and qualifications required for the Quality Assurance Officer position. Tailor your application to highlight relevant experience in QA and compliance with GCP regulations.
Highlight Relevant Experience: In your CV and cover letter, emphasise any previous roles or projects where you ensured compliance with regulatory standards, conducted audits, or managed QA documentation. Use specific examples to demonstrate your expertise.
Craft a Strong Cover Letter: Write a compelling cover letter that explains why you are passionate about the role and how your skills align with the organisation's mission of improving patients' quality of life. Mention your degree or equivalent experience in Science or related fields.
Proofread Your Application: Before submitting, thoroughly proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a QA Officer role.
How to prepare for a job interview at Reed Specialist Recruitment
✨Know Your GCP Regulations
Make sure you have a solid understanding of Good Clinical Practice (GCP) regulations. Be prepared to discuss how these regulations impact QA processes and your previous experiences in ensuring compliance.
✨Showcase Your Audit Experience
Highlight any experience you have with conducting internal audits or preparing for external audits. Be ready to provide examples of how you've identified non-conformances and implemented corrective actions in past roles.
✨Demonstrate Team Collaboration
Since the role involves interacting with specialist teams, be prepared to discuss how you've successfully collaborated with others in a QA context. Share specific examples that showcase your communication skills and teamwork.
✨Stay Updated on Regulatory Changes
Research recent developments in GCP and related regulatory requirements. Showing that you are proactive about staying informed will demonstrate your commitment to the role and the importance of compliance in clinical trials.
