At a Glance
- Tasks: Lead quality assurance activities and ensure compliance in pharmaceutical operations.
- Company: Dynamic pharmaceutical organisation in Essex focused on quality and innovation.
- Benefits: Competitive salary, career development opportunities, and a supportive work environment.
- Other info: Join a collaborative team dedicated to continuous improvement and regulatory excellence.
- Why this job: Make a real impact in the pharmaceutical industry while developing your leadership skills.
- Qualifications: Experience in quality assurance within pharmaceuticals or biotechnology is essential.
The predicted salary is between 45000 - 55000 £ per year.
I’m currently supporting a pharmaceutical organisation in Essex 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, 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.
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.
- 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
- 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 within Quality Assurance in the pharmaceutical or biotechnology sector is required, along with experience operating within Quality Management Systems (QMS) or Pharmaceutical Quality Systems (PQS). Previous involvement in deviation management, change control and investigation processes is also necessary, as well as experience supporting regulatory inspections and audits.
If you’re interested in learning more about this opportunity, please get in touch to discuss the role in more detail or to submit your application.
Projects and Quality Supervisor in Essex employer: Cranleigh STEM, Sustainability Recruitment
As a leading pharmaceutical organisation in Essex, we pride ourselves on fostering a collaborative and innovative work culture that prioritises employee growth and development. Our commitment to quality assurance not only ensures compliance but also empowers our team members to take on meaningful leadership roles, with ample opportunities for professional advancement. Join us to be part of a dynamic environment where your contributions directly impact the health and well-being of patients worldwide.
Contact Details:
Cranleigh STEM, Sustainability Recruitment Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Projects and Quality Supervisor in Essex
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry and let them know you're on the hunt for a Quality Assurance Manager role. 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 GMP and GDP knowledge. Make sure you can discuss how you've managed quality systems in the past and be ready to share examples of your leadership in GxP activities. Confidence is key!
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Check out our website for openings that match your skills and interests, and tailor your approach to each one.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in showing your enthusiasm for the role. It’s also a great opportunity to reiterate why you’re the perfect fit for the Quality Assurance Manager position.
We think you need these skills to ace Projects and Quality Supervisor in Essex
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 role, so don’t be shy about showcasing relevant projects or 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 and how you can contribute to our team. Keep it engaging and personal!
Showcase Leadership Skills:Since this role involves leading quality activities, we’d love to see examples of your leadership experience. Whether it’s mentoring junior team members or managing cross-functional projects, let us know how you’ve made an impact!
Apply Through Our Website:We encourage you to submit your application through our website. It’s the easiest way for us to keep track of your application and ensures you’re considered for the role. Plus, it shows you’re keen to join our team!
How to prepare for a job interview at Cranleigh STEM, Sustainability Recruitment
✨Know Your GMP and GDP Inside Out
Make sure you brush up on your Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP). Be ready to discuss how you've applied these principles in your previous roles, as this will show your depth of knowledge and experience in quality management.
✨Showcase Your Leadership Skills
As a Projects and Quality Supervisor, you'll need to demonstrate your leadership capabilities. Prepare examples of how you've led teams or projects in the past, particularly in quality assurance settings. Highlight any mentoring experiences you've had with junior team members.
✨Prepare for Regulatory Inspections
Familiarise yourself with the regulatory inspection process and be ready to discuss your experience supporting audits. Think of specific instances where you contributed to successful inspections or audits, and how you ensured compliance across GxP activities.
✨Emphasise Continuous Improvement
Quality is all about improvement, so come prepared with examples of how you've managed or improved quality systems in the past. Discuss any initiatives you've led that resulted in enhanced compliance or efficiency within a Pharmaceutical Quality System.
