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- Tasks: Ensure compliance in clinical trials by reviewing documentation and conducting audits.
- Company: Join a leading global biopharmaceutical company with a commitment to excellence.
- Benefits: Gain valuable experience in a dynamic industry with opportunities for career growth.
- Why this job: Make a real impact in the pharmaceutical field while developing your skills.
- Qualifications: Bachelor’s degree in a scientific field; QA experience preferred but not required.
- Other info: Be part of an award-winning team that values diversity and innovation.
The predicted salary is between 36000 - 60000 £ per year.
An exciting opportunity has arisen for an experienced Quality Assurance (QA) professional to join a leading global biopharmaceutical company within their Global Development Quality function.
Key Responsibilities
- Review clinical batch records and associated documentation to verify compliance with GMP and regulatory standards.
- Compile and approve QP data packs to support release of clinical trial materials.
- Conduct or support audits of data, systems, and facilities to ensure ongoing compliance.
- Review and approve analytical and production documentation prior to release.
- Communicate audit findings, prepare reports, and coordinate corrective actions with relevant departments.
- Partner with internal and external global teams to maintain compliance across the clinical supply chain.
Experience & Skills
- Previous experience in pharmaceutical, biotechnology, or regulatory QA roles with a solid understanding of cGMP requirements.
- Exceptional attention to detail, with strong written and verbal communication skills.
- Ability to work autonomously and manage issue resolution efficiently.
- Proficiency in documentation review, audit preparation, and regulatory compliance activities.
Qualifications
- Bachelor’s degree (or higher) in a relevant scientific field such as Chemistry, Biology, or Pharmacy.
- Prior QA or GMP experience preferred; however, applications are also welcomed from motivated science graduates eager to develop a career in pharmaceutical quality.
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
Please click ‘apply’ or contact Finlay Keyworth at Planet Pharma for more information: E: fleyworth@planet-pharma.co.uk
Quality Auditor employer: Planet Pharma
Contact Detail:
Planet Pharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Auditor
✨Tip Number 1
Network like a pro! Reach out to your connections in the biopharmaceutical industry and let them know you're on the lookout for QA roles. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of cGMP requirements and quality assurance processes. Be ready to discuss your previous experiences and how they relate to the role. Practice common interview questions with a friend to boost your confidence!
✨Tip Number 3
Showcase your attention to detail during the interview. Bring along examples of documentation you've reviewed or audits you've conducted. This will demonstrate your expertise and give the hiring team a taste of what you can bring to the table.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us. Good luck!
We think you need these skills to ace Quality Auditor
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Auditor role. Highlight your experience in QA, GMP compliance, and any relevant scientific qualifications. We want to see how your background fits with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance in the biopharmaceutical industry. We love seeing enthusiasm and a clear understanding of the role.
Showcase Your Attention to Detail: As a Quality Auditor, attention to detail is key. In your application, make sure to demonstrate this skill. Whether it's through your writing style or the way you present your experiences, we want to see that you can spot the finer points!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us that you’re proactive and keen to join our team!
How to prepare for a job interview at Planet Pharma
✨Know Your GMP Inside Out
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge before the interview. Familiarise yourself with the latest regulations and standards, as well as any recent changes in the industry. This will show that you're not just qualified but also genuinely interested in the field.
✨Prepare for Scenario Questions
Expect to be asked about specific situations you've encountered in previous roles. Think of examples where you had to resolve compliance issues or conduct audits. Use the STAR method (Situation, Task, Action, Result) to structure your answers clearly and effectively.
✨Showcase Your Attention to Detail
As a Quality Auditor, attention to detail is crucial. During the interview, highlight instances where your meticulous nature made a difference in your work. Bring along examples of documentation you've reviewed or audits you've conducted to demonstrate your thoroughness.
✨Communicate Clearly and Confidently
Strong communication skills are key in this role. Practice articulating your thoughts clearly and confidently. You might even want to do a mock interview with a friend to get comfortable discussing your experiences and findings, especially when it comes to audit results and corrective actions.
