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- Tasks: Oversee batch certification and ensure GMP compliance for sterile products.
- Company: Join a leading UK biopharmaceutical organization making a difference in vaccine safety.
- Benefits: Enjoy competitive pay and a supportive, growth-focused work environment.
- Why this job: Play a key role in delivering safe vaccines and work on cutting-edge biopharmaceutical products.
- Qualifications: Must have QP status and extensive experience in sterile manufacturing and GMP environments.
- Other info: Full-time on-site presence is required; UK residency is a must.
The predicted salary is between 43200 - 72000 £ per year.
We’re looking for an experienced Qualified Person (QP) with a strong background in sterile manufacturing to join a leading UK biopharmaceutical organisation.
This is an opportunity to play a key role in ensuring GMP compliance and the delivery of safe and effective vaccines .
Key Responsibilities:
- Act as a QP , overseeing batch certification for sterile products.
- Lead operational quality initiatives, ensuring inspection readiness and regulatory compliance.
- Provide expert guidance on GMP standards , maintaining the highest levels of product safety and efficacy .
- Take the lead in internal and external audits , ensuring robust quality oversight.
Requirements:
- QP status with extensive sterile manufacturing experience.
- Strong background in operational quality and inspection readiness within GMP environments .
- Proven leadership and stakeholder management skills, driving a culture of collaboration and excellence.
- Ability to be on-site full-time to provide hands-on support.
Why Join?
- Competitive compensation, recognising top industry talent.
- Work on cutting-edge biopharmaceutical products with a high-impact role.
- A supportive, growth-focused environment where your expertise makes a difference.
- UK residency required.
Contact us confidentially to explore this exclusive opportunity.
Qualified Person- Sterile Manufacturing employer: AssureBio
Contact Detail:
AssureBio Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person- Sterile Manufacturing
✨Tip Number 1
Make sure to highlight your QP status and any specific certifications related to sterile manufacturing during your conversations. This will demonstrate your qualifications and commitment to the role.
✨Tip Number 2
Prepare to discuss your experience with GMP compliance and inspection readiness in detail. Be ready to share specific examples of how you've led quality initiatives in previous roles.
✨Tip Number 3
Showcase your leadership skills by discussing how you've successfully managed teams or projects in a GMP environment. Highlight any collaborative efforts that led to improved quality outcomes.
✨Tip Number 4
Research the company’s recent projects and initiatives in biopharmaceuticals. Being knowledgeable about their work will help you engage in meaningful discussions and show your genuine interest in the role.
We think you need these skills to ace Qualified Person- Sterile Manufacturing
Some tips for your application 🫡
Highlight Your QP Status: Make sure to clearly state your Qualified Person status in your application. This is a crucial requirement for the role, so emphasize your qualifications and any relevant certifications.
Showcase Sterile Manufacturing Experience: Detail your experience in sterile manufacturing. Include specific examples of your responsibilities and achievements in previous roles, particularly those related to GMP compliance and batch certification.
Demonstrate Leadership Skills: Provide examples of your leadership and stakeholder management skills. Highlight instances where you have driven quality initiatives or led teams in a GMP environment, showcasing your ability to foster collaboration.
Tailor Your Application: Customize your CV and cover letter to align with the job description. Use keywords from the posting, such as 'GMP compliance', 'inspection readiness', and 'quality oversight' to ensure your application stands out.
How to prepare for a job interview at AssureBio
✨Showcase Your QP Experience
Be prepared to discuss your specific experiences as a Qualified Person, particularly in sterile manufacturing. Highlight any relevant projects or challenges you've faced and how you ensured GMP compliance.
✨Demonstrate Leadership Skills
Since the role requires strong leadership and stakeholder management, think of examples where you've successfully led teams or initiatives. Be ready to explain how you foster collaboration and drive quality culture.
✨Prepare for Regulatory Questions
Expect questions related to GMP standards and inspection readiness. Brush up on current regulations and be ready to discuss how you've implemented these in past roles to maintain product safety and efficacy.
✨Emphasize Hands-On Support
The job requires full-time on-site presence, so express your willingness and ability to provide hands-on support. Share examples of how your direct involvement has positively impacted quality outcomes in previous positions.
