Qualified Person (QP) - GMP & Regulatory Lead (Onsite) in London
Qualified Person (QP) - GMP & Regulatory Lead (Onsite)

Qualified Person (QP) - GMP & Regulatory Lead (Onsite) in London

London Full-Time 43200 - 72000 Β£ / year (est.) No home office possible
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At a Glance

  • Tasks: Ensure compliance with GMP and regulatory standards for medicinal products.
  • Company: Leading pharmaceutical company in Greater London with a focus on patient safety.
  • Benefits: Opportunity to work in a globally recognised organisation with a strong commitment to quality.
  • Why this job: Make a real impact on patient safety and quality oversight in the pharmaceutical industry.
  • Qualifications: 4-5 years of QP experience and a degree in a relevant scientific discipline.
  • Other info: Join a dynamic team dedicated to excellence in pharmaceutical regulations.

The predicted salary is between 43200 - 72000 Β£ per year.

A leading pharmaceutical company in Greater London is seeking a Qualified Person (QP) to ensure compliance with GMP and regulatory standards for medicinal products. The role involves:

  • Batch certification
  • Quality oversight
  • Liaising with regulatory authorities

Candidates must have:

  • At least 4-5 years of experience as a QP
  • A degree in a relevant scientific discipline
  • Strong knowledge of pharmaceutical regulations

This position offers the opportunity to act within a globally recognized organization with a focus on patient safety.

Qualified Person (QP) - GMP & Regulatory Lead (Onsite) in London employer: Salve.Inno Consulting

Join a leading pharmaceutical company in Greater London, where we prioritise patient safety and compliance with GMP and regulatory standards. Our collaborative work culture fosters professional growth, offering employees the chance to develop their skills within a globally recognised organisation. With a commitment to innovation and excellence, we provide a supportive environment that values your contributions and encourages career advancement.
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Contact Detail:

Salve.Inno Consulting Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land Qualified Person (QP) - GMP & Regulatory Lead (Onsite) in London

✨Tip Number 1

Network like a pro! Reach out to professionals in the pharmaceutical industry on LinkedIn or at local events. We can’t stress enough how valuable personal connections can be in landing that QP role.

✨Tip Number 2

Prepare for interviews by brushing up on GMP and regulatory standards. We recommend creating a cheat sheet of key topics and questions you might face, so you can showcase your expertise confidently.

✨Tip Number 3

Don’t just apply anywhere; focus on companies that align with your values and career goals. We suggest checking out our website for tailored job listings that fit your qualifications and aspirations.

✨Tip Number 4

Follow up after interviews! A quick thank-you email can set you apart from other candidates. We believe it shows your enthusiasm and professionalism, which are key in the pharmaceutical field.

We think you need these skills to ace Qualified Person (QP) - GMP & Regulatory Lead (Onsite) in London

GMP Compliance
Regulatory Knowledge
Batch Certification
Quality Oversight
Liaising with Regulatory Authorities
Pharmaceutical Regulations
Scientific Degree
Experience as a Qualified Person (QP)
Attention to Detail
Problem-Solving Skills
Communication Skills
Patient Safety Focus

Some tips for your application 🫑

Tailor Your CV: Make sure your CV highlights your experience as a Qualified Person and showcases your knowledge of GMP and regulatory standards. We want to see how your background aligns with the role, so don’t hold back on those relevant details!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about ensuring patient safety and how your experience makes you the perfect fit for our team. Keep it engaging and personal – we love to see your personality!

Showcase Your Regulatory Knowledge: Since this role involves liaising with regulatory authorities, make sure to highlight any specific experiences you have in this area. We’re looking for candidates who can demonstrate a strong understanding of pharmaceutical regulations, so don’t be shy about sharing your expertise!

Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from our team!

How to prepare for a job interview at Salve.Inno Consulting

✨Know Your GMP Inside Out

Make sure you brush up on Good Manufacturing Practice (GMP) regulations before the interview. Be prepared to discuss specific examples from your experience where you've ensured compliance, as this will show your expertise and commitment to quality.

✨Showcase Your Regulatory Knowledge

Familiarise yourself with the latest pharmaceutical regulations relevant to the role. During the interview, highlight your experience liaising with regulatory authorities and how you've navigated complex compliance issues in the past.

✨Prepare for Scenario-Based Questions

Expect scenario-based questions that assess your problem-solving skills in real-world situations. Think of a few challenging scenarios you've faced as a QP and how you resolved them, focusing on your decision-making process and outcomes.

✨Emphasise Patient Safety

Since the role focuses on patient safety, be ready to discuss how your work has directly contributed to this aspect. Share specific instances where your actions have positively impacted patient outcomes, demonstrating your dedication to the core values of the company.

Qualified Person (QP) - GMP & Regulatory Lead (Onsite) in London
Salve.Inno Consulting
Location: London

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