At a Glance
- Tasks: Lead quality assurance activities and ensure compliance in pharmaceutical operations.
- Company: Dynamic pharmaceutical organisation in Essex with a focus on quality.
- Benefits: Competitive salary, career development opportunities, and a supportive work environment.
- Other info: Opportunity to mentor junior team members and grow within the industry.
- Why this job: Make a real impact on the quality of medicinal products and lead a passionate team.
- Qualifications: Experience in GMP/GDP quality management and leadership skills.
The predicted salary is between 50000 - 60000 £ 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.
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
Quality Assurance Manager/RP in Essex employer: Cranleigh STEM, Sustainability Recruitment
Join a leading pharmaceutical organisation in Essex that prioritises quality and compliance, offering a dynamic work environment where your expertise in GMP and GDP will be valued. With a strong focus on employee development, you will have the opportunity to mentor junior team members while continuously improving the Pharmaceutical Quality System. Enjoy a collaborative culture that supports regulatory excellence and fosters professional growth in a critical role that impacts the health and safety of patients.
Contact Details:
Cranleigh STEM, Sustainability Recruitment Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Quality Assurance Manager/RP in Essex
✨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 your GMP and GDP knowledge. Be ready to discuss how you've improved quality systems in the past. We want to see you shine and show that you're the right fit for leading quality activities!
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Check out our website for roles that excite you and match your expertise in quality assurance.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you top of mind. Share your enthusiasm for the role and reiterate how your experience aligns with their needs. It shows you're genuinely interested!
We think you need these skills to ace Quality Assurance Manager/RP in Essex
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the specific skills and experiences that match the Quality Assurance Manager role. Highlight your GMP and GDP experience, as well as any leadership roles you've had in quality management.
Craft a Compelling Cover Letter:Use your cover letter to tell us why you're passionate about quality assurance in the pharmaceutical industry. Share specific examples of how you've improved quality systems or led teams in past roles.
Showcase Your Achievements:Don’t just list your responsibilities; showcase your achievements! Use metrics where possible to demonstrate how you’ve positively impacted quality processes or compliance in previous positions.
Apply Through Our Website:We encourage you to apply directly through our website for a smoother application process. This way, we can easily track your application and get back to you quicker!
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 Practice (GMP) and Good Distribution Practice (GDP) knowledge. Be ready to discuss how you've applied these principles in your previous roles, as this will show your expertise and readiness for the Quality Assurance Manager position.
✨Showcase Your Leadership Skills
This role is all about leadership within quality systems. Prepare examples of how you've led teams or projects in the past, especially in a GxP environment. Highlight your ability to mentor junior team members and drive continuous improvement initiatives.
✨Familiarise Yourself with Regulatory Standards
Since you'll be hosting regulatory inspections and audits, it's crucial to know the relevant regulations inside out. Research the specific standards that apply to the pharmaceutical industry and be prepared to discuss how you've ensured compliance in your previous roles.
✨Prepare for Scenario-Based Questions
Expect questions that ask how you'd handle specific situations, like deviation investigations or change controls. Think through potential scenarios and how you would approach them, demonstrating your problem-solving skills and attention to detail.
