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- Tasks: Lead quality initiatives and oversee batch certification for sterile products.
- Company: Join a high-performing team in the dynamic pharmaceutical industry.
- Benefits: Enjoy an excellent compensation package and career advancement opportunities.
- Why this job: Make a meaningful impact on cutting-edge pharmaceutical products in a supportive environment.
- Qualifications: Must have Qualified Person (QP) 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.
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 the role of a Qualified Person.
✨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 possible, attend industry conferences or workshops related to pharmaceutical quality and compliance. These events can provide valuable insights and networking opportunities that may lead to job referrals.
We think you need these skills to ace Qualified Person (QP) - Sterile Manufacturing
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly understand the responsibilities and requirements of the Qualified Person (QP) position. Highlight your relevant experience in sterile manufacturing and operational quality in your application.
Tailor Your CV: Customize your CV to emphasize your qualifications as a QP, focusing on your expertise in batch certification, compliance, and leadership in the pharmaceutical industry. Use specific examples that demonstrate your problem-solving skills and experience with audits.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality and compliance in sterile manufacturing. Mention your QP status and how your background aligns with the company's goals. Be sure to express your enthusiasm for the opportunity to contribute to their high-performing team.
Proofread and Submit: Before submitting your application, carefully proofread all documents to ensure there are no errors. Make sure your application is complete and accurately reflects your qualifications. Submit your application through our website to ensure it reaches the hiring 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 setting.
✨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.
