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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 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 continuous learning in a supportive team.
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 Bolton 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 Bolton
✨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 referrals that could give you an edge.
✨Tip Number 2
Prepare for interviews by brushing up on GMP regulations and quality systems. We recommend practising common QA interview questions and scenarios so you can showcase your expertise and confidence when it counts.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation. It keeps you fresh in their minds and shows your enthusiasm for the role.
✨Tip Number 4
Apply through our website for the best chance at landing that QA Specialist role! We’re always looking for passionate individuals who care about quality, and applying directly can help us see your application faster.
We think you need these skills to ace QA Specialist - Pharmaceutical (6 Month FTC) in Bolton
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 your application 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 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 your commitment to quality.
✨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.
