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- Tasks: Conduct audits to ensure compliance with regulations and quality standards.
- Company: Join a leading global pharmaceutical company dedicated to health advancements.
- Benefits: Enjoy a hybrid work model and gain valuable industry experience.
- Why this job: Make an impact in health while developing your skills in a dynamic environment.
- Qualifications: Degree in a science-related field; prior experience in pharmaceuticals is a plus.
- Other info: This is a 6-month contract role with opportunities for growth.
The predicted salary is between 36000 - 60000 £ per year.
We are on the lookout for a Quality Auditor to join our client based in London – a global pharmaceutical company committed to advancing both animal and human health. In this role, you’ll support compliance by conducting audits across systems, data, procedures, equipment, and facilities to ensure alignment with SOPs, GMP, and international regulations. You’ll also review and approve production and analytical documentation for the release of clinical and safety assessment batches, identify and resolve audit findings, and collaborate with teams to implement corrective actions. This is a hybrid role offered on a 6-month contract basis.
Key responsibilities:
- Conduct routine audits of data, procedures, equipment, systems (including computer systems), and facilities to ensure compliance with SOPs, GMP, and global regulatory standards.
- Review and approve production and analytical documentation related to the release of API, Safety Assessment, and clinical supply lots (bulk and packaged).
- Assess conformance of documentation and processes to regulatory requirements and internal quality standards.
- Perform audits or inspections of assigned areas or systems independently or as part of a team.
- Identify, document, and communicate audit findings, ensuring timely resolution with relevant departments.
- Issue audit reports summarising observations, deficiencies, and required corrective actions.
- Collaborate with operational teams to implement and verify effectiveness of remedial actions.
- Escalate significant findings and inspection outcomes to appropriate management for review and follow-up.
Job requirements:
- Prior experience in the pharmaceutical or chemical industry or with a government drug-regulatory agency, ideally within a GMP-compliant environment.
- Knowledge of cGMP regulations.
- Previous experience with QA or similar GMP environment.
- Proven ability to conduct audits or inspections of systems, facilities, procedures, and documentation for compliance.
- Comfortable working independently or as part of a team, with moderate supervision.
- Degree qualified in a science-related field (Bachelor’s degree minimum); open to science graduates with a willingness to learn.
Contact Detail:
S3 Science Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Auditor (City of London)
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who have experience in quality assurance and compliance. Attend industry events or webinars to connect with potential colleagues and learn more about the role.
✨Tip Number 2
Familiarise yourself with the latest cGMP regulations and standards relevant to the pharmaceutical sector. This knowledge will not only boost your confidence but also demonstrate your commitment to the role during interviews.
✨Tip Number 3
Prepare for potential interview questions by reviewing common audit scenarios and how you would handle them. Think of examples from your past experiences that showcase your problem-solving skills and attention to detail.
✨Tip Number 4
Showcase your ability to work both independently and as part of a team. Be ready to discuss how you've successfully collaborated with others in previous roles to implement corrective actions and improve compliance.
We think you need these skills to ace Quality Auditor (City of London)
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 quality assurance, compliance, and auditing within the pharmaceutical or chemical industry.
Tailor Your CV: Customise your CV to reflect your experience with GMP regulations and any previous roles in quality auditing. Use specific examples that demonstrate your ability to conduct audits and resolve findings effectively.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality assurance and your understanding of the pharmaceutical industry. Mention how your skills align with the company's commitment to advancing health and compliance.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial for a Quality Auditor role.
How to prepare for a job interview at S3 Science Recruitment
✨Know Your Regulations
Familiarise yourself with cGMP regulations and any relevant international standards. Being able to discuss these confidently will show your understanding of the industry and its compliance requirements.
✨Prepare for Scenario Questions
Expect questions that ask you to describe how you would handle specific audit situations or findings. Prepare examples from your past experience where you successfully identified issues and implemented corrective actions.
✨Showcase Your Teamwork Skills
Since collaboration is key in this role, be ready to discuss how you've worked effectively within a team. Highlight instances where you’ve contributed to resolving audit findings alongside operational teams.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s auditing processes and how they ensure compliance. This demonstrates your genuine interest in the role and helps you assess if the company is the right fit for you.
