At a Glance
- Tasks: Lead quality assurance activities in a dynamic pharmaceutical environment.
- Company: Reputable pharmaceutical organisation in Kent with a focus on quality.
- Benefits: Competitive salary, career growth, and the chance to make a real impact.
- Other info: Join a collaborative team dedicated to improving healthcare.
- Why this job: Step into a leadership role and enhance your expertise in quality management.
- Qualifications: Experience in GMP/GDP and a passion for quality assurance.
The predicted salary is between 50000 - 60000 £ per year.
I’m currently supporting a pharmaceutical organisation in Kent with the search for a Quality Assurance Manager to lead quality activities across GxP operations. This role would suit someone with strong GMP and GDP quality management experience, and could be particularly well suited to someone who already operates as a Responsible Person (RP) or is interested in stepping into a broader leadership role within a Pharmaceutical Quality System.
This is a key position within the quality function, responsible for overseeing quality systems, supporting regulatory inspections, and ensuring compliance across the import, storage, manufacture and distribution of medicinal products.
The Role
As QA Manager, you will take responsibility for maintaining and continuously improving the Pharmaceutical Quality System (PQS) while providing leadership across GxP‑related quality activities. You will work closely with cross‑functional teams to ensure regulatory compliance and support ongoing quality improvements across the organisation.
Key Responsibilities
- Provide quality leadership across GxP activities including the import, storage, manufacture and distribution of medicinal products
- Manage and continuously improve the Pharmaceutical Quality System (PQS)
- Oversee the self‑inspection programme and support both internal and external GMDP audits
- Host and support regulatory inspections and customer audits
- Support site validation activities and maintain the Validation Master Plan (VMP)
- Manage supplier qualification activities and progress Quality Technical Agreements (QTAs)
- Review batch records to ensure QA requirements are met prior to certification by the Qualified Person (QP)
- Lead or support deviation investigations, change controls and root cause analysis
- Mentor and support the development of junior quality team members
Experience & Background
- Experience within Quality Assurance in the pharmaceutical or biotechnology sector
- Strong working knowledge of GMP and GDP regulations
- Experience operating within Quality Management Systems (QMS) or Pharmaceutical Quality Systems (PQS)
- Previous involvement in deviation management, change control and investigation processes
- Experience supporting regulatory inspections and audits
- Excellent attention to detail and the ability to work collaboratively across departments
Candidates who already hold Responsible Person (RP) experience or are looking to step into a role with RP responsibilities are particularly encouraged to apply.
Package
Salary: £50k - £60k
Location: Essex
Sector: Pharmaceutical / Life Sciences
Quality Manager/RP in Rayleigh employer: Cranleigh Scientific Ltd
Join a leading pharmaceutical organisation in Kent that prioritises quality and compliance, offering a dynamic work culture where your expertise as a Quality Manager will be valued. With a strong focus on employee development, you will have the opportunity to mentor junior team members and enhance your leadership skills while contributing to meaningful improvements in the Pharmaceutical Quality System. Enjoy competitive salary packages and the chance to work in a collaborative environment that supports regulatory excellence and innovation in the life sciences sector.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Manager/RP in Rayleigh
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work in quality assurance. 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 and GDP regulations. Be ready to discuss how you've managed quality systems in the past. We want to hear your success stories and how you’ve tackled challenges!
✨Tip Number 3
Showcase your leadership skills! If you’ve mentored junior team members or led projects, make sure to highlight these experiences. We love seeing candidates who can inspire and guide others in quality assurance.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate individuals ready to step into key roles like QA Manager.
We think you need these skills to ace Quality Manager/RP in Rayleigh
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience in GMP and GDP quality management. We want to see how your background aligns with the responsibilities of the QA Manager role, so don’t be shy about showcasing relevant achievements!
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 pharmaceutical sector. We love seeing candidates who can connect their personal motivations to the role.
Showcase Your Leadership Skills:Since this role involves leading quality activities, make sure to highlight any previous leadership experiences. We’re looking for someone who can mentor others and drive improvements, so share examples of how you've done this in the past.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best 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 Cranleigh Scientific Ltd
✨Know Your GMP and GDP Inside Out
Make sure you brush up on your knowledge of Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP). Be ready to discuss how you've applied these regulations in your previous roles, as this will show your expertise and readiness for the Quality Manager position.
✨Showcase Your Leadership Skills
As a QA Manager, you'll be leading quality activities across GxP operations. Prepare examples of how you've successfully led teams or projects in the past. Highlight your mentoring experience with junior team members, as this is a key aspect of the role.
✨Prepare for Regulatory Inspections
Since you'll be hosting and supporting regulatory inspections, think about your past experiences with audits. Be ready to discuss specific instances where you ensured compliance and how you handled any challenges that arose during inspections.
✨Demonstrate Your Problem-Solving Skills
The role involves managing deviation investigations and change controls. Prepare to talk about a time when you identified a problem, conducted a root cause analysis, and implemented a solution. This will showcase your analytical skills and attention to detail, which are crucial for this position.
