At a Glance
- 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: Join a team that values quality and offers real impact on product standards.
- Qualifications: Experience in Quality Assurance within a GMP environment and strong attention to detail.
- Other info: Dynamic role with opportunities for growth and development 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.
About the Opportunity
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.
About You
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.
Why Join?
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.
QA Specialist - Pharmaceutical (6 Month FTC) in Manchester employer: Radar Recruitment
Contact Detail:
Radar Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Specialist - Pharmaceutical (6 Month FTC) in Manchester
✨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 interview questions related to QA and thinking of examples from your past experiences that showcase your skills.
✨Tip Number 3
Show your passion for quality! During interviews, share why you care about maintaining high standards in pharmaceuticals. This will help you stand out as someone who genuinely values the role.
✨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 QA Specialist - Pharmaceutical (6 Month FTC) in Manchester
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 background aligns with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your passion for quality assurance and how you can contribute to our team. Be sure to mention specific experiences that demonstrate your skills and mindset.
Showcase Your Attention to Detail: In QA, attention to detail is key. Make sure your application is free from typos and errors. We appreciate candidates who take the time to present their best selves, so double-check everything before hitting send!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Radar Recruitment
✨Know Your GMP Inside Out
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge before the interview. Be ready to discuss how you've applied GMP principles in your previous roles, as this will show your understanding of the industry's standards and expectations.
✨Showcase Your Documentation Skills
Since strong documentation skills are crucial for this role, prepare examples of how you've managed quality documentation in the past. Bring along samples or be ready to discuss specific situations where your attention to detail made a difference.
✨Prepare for Cross-Functional Collaboration
This position requires working closely with various departments, so think of examples that highlight your ability to communicate and collaborate effectively. Be prepared to share how you've successfully worked with different teams to improve processes or resolve issues.
✨Emphasise Continuous Improvement
The company values continuous improvement, so come equipped with ideas or experiences that demonstrate your proactive approach to enhancing quality systems. Discuss any initiatives you've led or participated in that resulted in measurable improvements.