QP/RP

Full-Time 48000 - 72000 £ / year (est.) No home office possible
Apply now
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At a Glance

  • Tasks: Ensure quality processes and compliance in consumer health products.
  • Company: Join a pioneering force enhancing global health with trusted brands.
  • Benefits: Enjoy a hybrid work environment and be part of an innovative culture.
  • Why this job: Shape the future of health with a collaborative team and impactful work.
  • Qualifications: Must be a Qualified Person with 5+ years in pharma/healthcare.
  • Other info: This role is based in London, UK, and offers a chance to lead quality practices.

The predicted salary is between 48000 - 72000 £ per year.

Our key client is a pioneering force in consumer health. Our mission is to enhance the everyday health of billions worldwide. We achieve this by expanding and innovating our diverse portfolio of leading brands. Our success is driven by a unique blend of profound human insight and trusted scientific expertise. We take pride in our autonomy, collaborative environment, and distinctive culture. Are you ready to be part of our journey? This is your invitation.

With renowned brands, underpinned by trusted science and deep human understanding, combined with our passion, knowledge, and expertise, we are uniquely positioned to grow a robust and successful business.

This is a thrilling time to join us and help shape the future. Be part of something extraordinary.

About the Role

As a Qualified Person (QP) and Responsible Person (RP), you will play a crucial role in ensuring the implementation of robust quality processes and systems across all business activities, in line with standards, policies, and full compliance with GMP, GDP, and regulatory requirements. Reporting to the GBI Quality Lead, you will lead best quality practices to ensure the safety of our products for patients and customers in Europe. This hybrid role is based at our London, United Kingdom office.

Key Responsibilities

  • Qualified Person (QP) and Responsible Person (RP) Duties : Fulfill QP and RP responsibilities in accordance with GMP/GDP requirements, marketing authorization, and local regulations.
  • License Maintenance : Ensure all necessary licenses are maintained and the business is always inspection-ready.
  • Batch Review and Disposition : Oversee timely batch review and disposition of products to meet supply demands and ensure timely review of PQP.
  • Supplier Management : Oversee suppliers and third parties, ensure audits are conducted, and quality agreements are reviewed and approved.
  • Risk Management : Implement the risk management strategy for all GxP risks.
  • Training : Ensure relevant personnel are trained, monitor KPIs, and drive action plans as needed. Maintain the training matrix and curricula.
  • QMS Implementation : Implement the QMS strategy, assist in documentation assessment, and ensure relevant personnel are trained.
  • Complaint Management : Ensure complaints are raised and addressed promptly and review trends.
  • New Product Introduction (NPI) : Ensure timely implementation of new product introduction projects.
  • Customer Qualification : Ensure customers are qualified and annual bonafides are completed.
  • Distribution Management : Handle distribution issues, queries, and product returns.
  • Additional Responsibilities : Support and take accountability for team projects and day-to-day activities, including incident management, PIRC, recalls, internal audits, quality council, and quality team meetings.

Qualifications and Skills

  • Essential :
  • Qualified Person (QP) practicing under an MIA License in the UK.
  • Minimum of 5 years' experience in the pharmaceutical/consumer healthcare industries.
  • Knowledge of GMP and GDP regulations and MHRA/HPRA expectations.

QP/RP employer: EPM Scientific

Join a pioneering force in consumer health that is dedicated to enhancing the everyday health of billions worldwide. Our London office offers a collaborative and autonomous work culture, where your expertise as a Qualified Person (QP) and Responsible Person (RP) will be valued and impactful. With a commitment to employee growth and a focus on innovation, this is an extraordinary opportunity to contribute to meaningful projects while being part of a passionate team that drives success through trusted science and deep human insight.
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Contact Detail:

EPM Scientific Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land QP/RP

✨Tip Number 1

Familiarize yourself with the latest GMP and GDP regulations, as well as MHRA/HPRA expectations. This knowledge will not only help you in interviews but also demonstrate your commitment to compliance and quality.

✨Tip Number 2

Network with professionals in the pharmaceutical and consumer healthcare industries. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and challenges in quality management.

✨Tip Number 3

Highlight your experience in batch review and supplier management during conversations. Be prepared to discuss specific examples of how you've ensured compliance and quality in previous roles.

✨Tip Number 4

Showcase your ability to implement training programs and manage risk effectively. Prepare to share instances where you've successfully trained teams or managed GxP risks, as this aligns closely with the responsibilities of the role.

We think you need these skills to ace QP/RP

Qualified Person (QP) Certification
Responsible Person (RP) Certification
GMP and GDP Knowledge
Regulatory Compliance
Batch Review and Disposition
Supplier Management
Risk Management
Training and Development
Quality Management Systems (QMS)
Complaint Management
New Product Introduction (NPI)
Customer Qualification
Distribution Management
Incident Management
Internal Audits

Some tips for your application 🫡

Understand the Role: Make sure to thoroughly read the job description for the QP/RP position. Understand the key responsibilities and qualifications required, as this will help you tailor your application effectively.

Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in the pharmaceutical or consumer healthcare industries, particularly any roles that involved GMP and GDP regulations. Use specific examples to demonstrate your expertise.

Showcase Your Skills: Clearly outline your skills related to quality management systems, risk management, and supplier oversight. Mention any relevant certifications or training that align with the role's requirements.

Craft a Compelling Cover Letter: Write a personalized cover letter that reflects your passion for consumer health and your understanding of the company's mission. Explain why you are excited about the opportunity to contribute to their success and how your background makes you a great fit.

How to prepare for a job interview at EPM Scientific

✨Show Your Expertise in GMP and GDP

Make sure to highlight your knowledge of Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) during the interview. Be prepared to discuss specific examples from your past experience where you ensured compliance with these regulations.

✨Demonstrate Your Leadership Skills

As a QP/RP, you'll be leading quality practices. Share instances where you've successfully led teams or projects, particularly in a regulatory environment. This will showcase your ability to manage and motivate others while ensuring compliance.

✨Prepare for Scenario-Based Questions

Expect scenario-based questions that assess your problem-solving skills in real-world situations. Think about challenges you've faced in batch review, supplier management, or complaint handling, and how you resolved them effectively.

✨Emphasize Your Collaborative Spirit

The company values a collaborative environment, so be ready to discuss how you've worked with cross-functional teams in the past. Highlight your communication skills and how you foster teamwork to achieve quality objectives.

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  • QP/RP

    Full-Time
    48000 - 72000 £ / year (est.)
    Apply now

    Application deadline: 2027-01-13

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    EPM Scientific

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