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- Tasks: Conduct audits to ensure compliance with regulations and quality standards.
- Company: Join a leading global pharmaceutical company focused on health advancements.
- Benefits: Enjoy a hybrid work model and gain valuable industry experience.
- Why this job: Make a real impact in health while working in a dynamic team 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.
- 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:
Career Wallet 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 guidelines. Understanding these standards 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 industry, especially those working in quality assurance roles. Attend industry events or join relevant online forums to gain insights and potentially get referrals.
✨Tip Number 3
Prepare for potential technical questions by reviewing common audit scenarios and how you would handle them. This will showcase your problem-solving skills and readiness for the role.
✨Tip Number 4
Research the company’s recent projects and initiatives in the pharmaceutical sector. Being knowledgeable about their work will allow you to tailor your discussions and show genuine interest during interviews.
We think you need these skills to ace Quality Auditor
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Quality Auditor. Familiarise yourself with SOPs, GMP, and the specific requirements mentioned in the job description.
Tailor Your CV: Highlight your relevant experience in the pharmaceutical or chemical industry, especially any roles involving audits or compliance. Use keywords from the job description to ensure your CV aligns with what the company is looking for.
Craft a Strong Cover Letter: In your cover letter, express your passion for quality assurance and compliance. Mention specific experiences that demonstrate your ability to conduct audits and resolve findings, as well as your familiarity with regulatory standards.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any 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 Career Wallet
✨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
Collaboration is key in this role. Be ready to discuss how you've worked with operational teams in the past to resolve audit findings and improve processes. Highlight your ability to communicate effectively across departments.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's quality assurance processes and their approach to compliance. This demonstrates your genuine interest in the role and helps you assess if the company aligns with your career goals.
