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- Tasks: Ensure top-notch quality in pharmaceutical operations and maintain GMP compliance.
- Company: Forward-thinking GMP-licensed pharmaceutical business with a collaborative culture.
- Benefits: Competitive salary, potential for contract extension, and meaningful contributions from day one.
- Why this job: Make a real impact on product quality and regulatory readiness in a dynamic environment.
- Qualifications: Experience in Quality Assurance within a GMP pharmaceutical setting and strong documentation skills.
- Other info: Great opportunity for career growth and stability in the pharmaceutical industry.
The predicted salary is between 36000 - 60000 £ per year.
Are you a hands-on QA Specialist who enjoys being right at the heart of GMP operations? Looking for a role where Quality genuinely matters - not just on paper, but in everything the site does? This is a fantastic opportunity to join a forward-thinking, GMP-licensed pharmaceutical business on an initial 6-month FTC, with a strong chance of extension or permanent placement for the right person. You’ll be part of a collaborative Quality team where standards are high, voices are heard and continuous improvement is encouraged every day.
As QA Specialist, you’ll play a key role in maintaining and strengthening GMP compliance across the site. From batch record review and QMS activities to audit support and investigations, you’ll be trusted to make a real impact on product quality and regulatory readiness. Working closely with QA leadership and cross-functional teams, you’ll help ensure the site remains inspection-ready, compliant, and continuously improving.
Key Responsibilities:- Promoting and fostering a strong GMP and Quality compliance culture across the site.
- Reviewing Finished Batch Records and supporting GMP release ahead of final QP certification.
- Supporting ongoing regulatory licence readiness and inspection preparation.
- Managing and contributing to QMS activities, including deviations, non-conformances, CAPAs, and change controls.
- Maintaining and improving Quality documentation - SOPs, forms, BMRs, reports, and controlled documents.
- Coordinating and closing quality investigations, ensuring robust root cause analysis and effective actions.
- Managing Quality databases, metrics, logs, and master lists to ensure data integrity and audit readiness.
- Supporting product enquiries, customer complaints, recalls, and supplier documentation approvals.
- Taking part in internal and external audits, including participation in the internal audit programme.
- Collaborating with all departments to improve processes, service levels, and quality performance.
- Maintaining personal training records and continually developing your Quality skill set.
This role offers real exposure across the full QA lifecycle, which is perfect for someone who enjoys variety, ownership and being close to operations.
You’re organised and comfortable working in a busy GMP environment. You care deeply about doing things the right way and take pride in maintaining high standards. The ideal candidate for the QA Specialist role will have the following background:
- Experience working in Quality Assurance within a GMP pharmaceutical environment.
- A solid understanding of pharmaceutical quality systems and regulatory expectations.
- Strong documentation skills and attention to detail.
- Confidence working cross-functionally and communicating with stakeholders at all levels.
- A positive, collaborative mindset with a desire to learn and grow.
This is a company that genuinely values Quality and the people who deliver it. You’ll be well supported and given the opportunity to contribute meaningfully from day one. Whether you’re looking for your next FTC challenge or hoping to secure a longer-term move within a strong pharmaceutical business, this role offers both stability and opportunity.
Quality Assurance Specialist - Pharmaceutical (6 Month FTC) employer: Radar Recruitment
Contact Detail:
Radar Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Specialist - Pharmaceutical (6 Month FTC)
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those in QA roles. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on GMP regulations and quality systems. We recommend practising common QA interview questions and scenarios to show you’re ready to tackle real-world challenges.
✨Tip Number 3
Showcase your passion for quality! During interviews, share specific examples of how you've contributed to quality improvements in past roles. This will demonstrate your commitment to maintaining high standards.
✨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 are proactive about their job search.
We think you need these skills to ace Quality Assurance Specialist - Pharmaceutical (6 Month FTC)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the QA Specialist role. Highlight your experience in GMP environments and any relevant quality systems you've worked with. We want to see how your skills match 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 and how you can contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your Attention to Detail: As a QA Specialist, attention to detail is key. Make sure your application is free from typos and errors. This shows us that you take pride in your work and understand the importance of quality.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of applications and ensures you don’t miss out on any important updates. Plus, it’s super easy!
How to prepare for a job interview at Radar Recruitment
✨Know Your GMP Inside Out
Make sure you brush up on Good Manufacturing Practices (GMP) before your interview. Understand the key principles and how they apply to the role of a QA Specialist. Being able to discuss specific examples of how you've maintained or improved GMP compliance in previous roles will show that you're not just familiar with the concepts, but that you can apply them effectively.
✨Showcase Your Documentation Skills
Since strong documentation skills are crucial for this role, prepare to discuss your experience with Quality Management Systems (QMS) and any relevant documentation you've worked on. Bring examples of SOPs, batch records, or reports you've created or improved. This will demonstrate your attention to detail and your ability to maintain high standards.
✨Prepare for Cross-Functional Collaboration
This position requires working closely with various departments, so be ready to talk about your experience collaborating with different teams. Think of specific instances where you’ve successfully communicated with stakeholders at all levels. Highlighting your collaborative mindset will show that you’re a team player who values input from others.
✨Emphasise Continuous Improvement
The company values continuous improvement, so come prepared with examples of how you've contributed to process enhancements in your past roles. Discuss any CAPAs or change controls you've managed and the impact they had on quality performance. This will illustrate your proactive approach and commitment to fostering a quality culture.