AssureBio | Qualified Person (QP) - Sterile Manufacturing Apply now
AssureBio | Qualified Person (QP) - Sterile Manufacturing

AssureBio | Qualified Person (QP) - Sterile Manufacturing

England Full-Time 43200 - 72000 £ / year (est.) No home office possible
Apply now
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At a Glance

  • 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.

AssureBio | Qualified Person (QP) - Sterile Manufacturing employer: AssureBio

At AssureBio, we pride ourselves on being an exceptional employer in the pharmaceutical industry, offering a dynamic work culture that fosters collaboration and innovation. Our commitment to employee growth is evident through continuous training and development opportunities, ensuring that our team members thrive in their careers while making a significant impact on the quality and safety of sterile products. Located in the UK, we provide a competitive compensation package and a supportive environment where your expertise as a Qualified Person will be valued and recognized.
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Contact Detail:

AssureBio Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land AssureBio | 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 assurance and 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 interviews by practicing how you would lead operational quality initiatives. Think of specific examples from your past experiences where you successfully ensured inspection readiness and compliance.

Tip Number 4

Showcase your leadership and stakeholder management skills by discussing collaborative problem-solving scenarios. Be ready to explain how you have effectively worked with teams to achieve quality goals in a sterile manufacturing environment.

We think you need these skills to ace AssureBio | Qualified Person (QP) - Sterile Manufacturing

Qualified Person (QP) status
Experience in sterile manufacturing
Operational quality expertise
Inspection readiness knowledge
Regulatory compliance understanding
Leadership skills
Stakeholder management
Collaborative problem-solving
Audit preparation and hosting
Attention to detail
Strong communication skills
Ability to work on-site
Passion for quality assurance
Adaptability in a fast-paced environment

Some tips for your application 🫡

Understand the Role: Make sure to thoroughly read the job description for the Qualified Person (QP) position. Understand the key responsibilities and requirements, especially the importance of quality and compliance in sterile manufacturing.

Highlight Relevant Experience: In your application, emphasize your experience as a Qualified Person and any specific achievements in operational quality and inspection readiness within the pharmaceutical industry. Use concrete examples to demonstrate your expertise.

Showcase Leadership Skills: Since strong leadership and stakeholder management skills are crucial for this role, provide examples of how you've successfully led teams or initiatives in the past. Highlight your collaborative problem-solving abilities.

Tailor Your Application: Customize your CV and cover letter to reflect the specific requirements of the job. Use keywords from the job description to ensure your application stands out and aligns with what the company is looking for.

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 the role requires strong leadership, 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 role, 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 the Company’s Quality Standards

Research AssureBio's quality standards and recent initiatives in sterile manufacturing. Being knowledgeable about their practices will show your genuine interest in the company and help you align your answers with their values.

AssureBio | Qualified Person (QP) - Sterile Manufacturing
AssureBio Apply now
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  • AssureBio | Qualified Person (QP) - Sterile Manufacturing

    England
    Full-Time
    43200 - 72000 £ / year (est.)
    Apply now

    Application deadline: 2027-01-20

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    AssureBio

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