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- Tasks: Oversee batch certification and ensure GMP compliance for sterile products.
- Company: Join a leading UK biopharmaceutical organization focused on vaccine safety and efficacy.
- Benefits: Enjoy competitive pay and a supportive, growth-focused work environment.
- Why this job: Make a real impact in biopharmaceuticals while working with cutting-edge products.
- Qualifications: Must have QP status and extensive experience in sterile manufacturing.
- Other info: Full-time on-site role with opportunities for leadership and collaboration.
The predicted salary is between 48000 - 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
Familiarize yourself with the latest GMP standards and regulations, as well as any recent changes in the biopharmaceutical industry. Being knowledgeable about current practices will help you stand out in discussions.
✨Tip Number 3
Prepare to discuss your experience with internal and external audits. Share specific examples of how you've led these processes and ensured compliance, as this is a key responsibility of the role.
✨Tip Number 4
Showcase your leadership and stakeholder management skills by providing examples of how you've driven collaboration and excellence in previous roles. This will align with the company's focus on a supportive and growth-oriented environment.
We think you need these skills to ace Qualified Person- Sterile Manufacturing
Some tips for your application 🫡
Highlight Relevant Experience: Make sure to emphasize your experience in sterile manufacturing and your QP status. Use specific examples that demonstrate your expertise in GMP compliance and operational quality initiatives.
Showcase Leadership Skills: Illustrate your leadership and stakeholder management skills. Provide examples of how you've driven collaboration and excellence in previous roles, especially in audit situations.
Tailor Your Application: Customize your CV and cover letter to align with the job description. Address the key responsibilities and requirements mentioned, showing how you meet or exceed them.
Proofread Your Documents: Before submitting your application, carefully proofread your documents for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial in the biopharmaceutical industry.
How to prepare for a job interview at AssureBio
✨Showcase Your QP Experience
Make sure to highlight your experience as a Qualified Person, especially in sterile manufacturing. Be prepared to discuss specific examples of how you've ensured GMP compliance and the impact of your work on product safety.
✨Demonstrate Leadership Skills
Since the role requires strong leadership and stakeholder management skills, come ready to share instances where you've successfully led teams or initiatives. Emphasize your ability to foster collaboration and drive quality culture.
✨Prepare for Technical Questions
Expect technical questions related to GMP standards and inspection readiness. Brush up on current regulations and be ready to discuss how you have implemented these standards in previous roles.
✨Express Your Commitment to Quality
Convey your passion for maintaining high levels of product safety and efficacy. Discuss how you stay updated with industry trends and your proactive approach to ensuring compliance and quality oversight.
