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- Tasks: Join our team as a Qualified Person overseeing sterile product batch certification.
- Company: Be part of a high-performing team in the pharmaceutical industry focused on quality and compliance.
- Benefits: Enjoy an excellent compensation package and a supportive work environment.
- Why this job: Make a meaningful impact on cutting-edge products while advancing your career.
- Qualifications: Must have Qualified Person status and experience in sterile manufacturing.
- Other info: On-site work required five days a week; UK residency is necessary to apply.
The predicted salary is between 43200 - 72000 £ per year.
We are seeking an experienced Qualified Person (QP) to join a high-performing team within the pharmaceutical industry. This is a confidential opportunity for a driven professional who is passionate about ensuring quality and compliance in a sterile manufacturing environment. Make sure to apply with all the requested information, as laid out in the job overview below. Key Responsibilities: Serve as a Qualified Person with oversight of batch certification for sterile products. Lead operational quality initiatives to support inspection readiness and maintain compliance with regulatory requirements. Provide expert advice on quality standards, ensuring the safety, efficacy, and compliance of products. Play a pivotal role in preparing and hosting internal and external audits. Requirements: Qualified Person (QP) status with substantial experience in sterile manufacturing. Proven expertise in operational quality and inspection readiness within the pharmaceutical industry. Strong leadership and stakeholder management skills, with a focus on collaborative problem-solving. Ability to work on-site five days a week to provide hands-on support. Why Join? This role offers an excellent compensation package , reflecting the importance of attracting the best talent in the industry. You’ll have the opportunity to make a meaningful impact, working on cutting-edge pharmaceutical products while advancing your career in a supportive environment. Contact us in confidence to discuss this exclusive opportunity further. You must be a UK resident to apply.
Qualified Person (QP) - Sterile Manufacturing employer: AssureBio
Contact Detail:
AssureBio Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person (QP) - Sterile Manufacturing
✨Tip Number 1
Make sure to highlight your experience in sterile manufacturing during any networking opportunities. Connect with professionals in the pharmaceutical industry on platforms like LinkedIn and engage in discussions about quality compliance.
✨Tip Number 2
Stay updated on the latest regulatory requirements and quality standards in the pharmaceutical sector. This knowledge will not only help you in interviews but also demonstrate your commitment to maintaining high-quality practices.
✨Tip Number 3
Prepare for potential interview questions by practicing how you would lead operational quality initiatives. Think of specific examples from your past experiences that showcase your leadership and problem-solving skills.
✨Tip Number 4
If you have experience with audits, be ready to discuss your role in preparing for and hosting them. Highlight any successful outcomes or improvements you implemented as a result of audit findings.
We think you need these skills to ace Qualified Person (QP) - Sterile Manufacturing
Some tips for your application 🫡
Understand the Role: Make sure you fully understand the responsibilities of a Qualified Person in sterile manufacturing. Highlight your relevant experience and how it aligns with the key responsibilities mentioned in the job description.
Tailor Your CV: Customize your CV to emphasize your qualifications, particularly your QP status and experience in operational quality within the pharmaceutical industry. Use specific examples that demonstrate your leadership and compliance expertise.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality and compliance in sterile manufacturing. Discuss your approach to maintaining inspection readiness and your experience with audits, as these are crucial for the role.
Highlight Collaborative Skills: Since the role requires strong stakeholder management skills, be sure to include examples of how you've successfully collaborated with teams or led initiatives in previous positions. This will show your ability to work effectively in a high-performing team.
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 certifications and how you've ensured compliance with regulatory requirements in your previous roles.
✨Demonstrate Leadership Skills
Since strong leadership is crucial for this role, think of examples where you've led quality initiatives or managed teams. Be ready to explain how you foster collaboration and solve problems effectively within a team.
✨Prepare for Audit Scenarios
Given the importance of audits in this position, prepare to discuss your experience with internal and external audits. Share specific instances where you played a key role in preparing for an audit and how you ensured inspection readiness.
✨Understand Regulatory Standards
Brush up on the latest regulatory standards relevant to sterile manufacturing. Be ready to discuss how you stay informed about changes in regulations and how you implement these standards in your work.
