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- Tasks: Conduct audits to ensure compliance with regulations and review production documentation.
- Company: Join a leading global pharmaceutical company dedicated to improving health for all.
- Benefits: Enjoy a hybrid work model and gain valuable experience in a dynamic industry.
- Why this job: Make a real impact on health standards while working in a collaborative environment.
- Qualifications: Degree in a science-related field; prior experience in pharmaceuticals or QA 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.
Quality Auditor employer: S3 Science Recruitment
Contact Detail:
S3 Science Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Auditor
✨Tip Number 1
Familiarise yourself with the latest cGMP regulations and standards relevant to the pharmaceutical industry. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance and quality assurance.
✨Tip Number 2
Network with professionals in the pharmaceutical sector, especially those working in quality assurance roles. Attend industry events or join online forums to gain insights and potentially get referrals that could lead to job opportunities.
✨Tip Number 3
Prepare for potential interview questions by reviewing common scenarios related to audit findings and corrective actions. Being able to discuss how you've handled similar situations in the past can set you apart from other candidates.
✨Tip Number 4
Showcase your ability to work both independently and as part of a team. Be ready to provide examples of how you've successfully collaborated with others to implement quality improvements or resolve compliance issues in previous roles.
We think you need these skills to ace Quality Auditor
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 conducting audits, compliance with SOPs, and knowledge of GMP regulations.
Tailor Your CV: Customise your CV to reflect your experience in the pharmaceutical or chemical industry. Emphasise any previous roles related to quality assurance, audits, and regulatory compliance to make your application stand out.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality assurance and your understanding of the importance of compliance in the pharmaceutical industry. Mention specific examples of how you've successfully conducted audits or resolved compliance issues in the past.
Proofread Your Application: Before submitting, carefully 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 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 with operational teams in the past. Highlight instances where your teamwork led to successful outcomes in audits or quality assurance.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's quality assurance processes and how they handle audit findings. This shows your genuine interest in the role and helps you assess if the company aligns with your career goals.
