GxP QA Lead — GMP/GLP Compliance & Audits in Guildford
GxP QA Lead — GMP/GLP Compliance & Audits

GxP QA Lead — GMP/GLP Compliance & Audits in Guildford

Guildford Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Ensure compliance with GLP, GMP, and MHRA regulations while overseeing QA activities.
  • Company: Leading pharmaceutical company in Guildford with a focus on quality assurance.
  • Benefits: Full-time position with opportunities for training and occasional travel.
  • Why this job: Join a vital role in ensuring safety and compliance in the pharmaceutical industry.
  • Qualifications: Bachelor’s degree and 3+ years of experience in a GMP environment required.
  • Other info: Strong communication skills and knowledge of GMP standards are essential.

The predicted salary is between 36000 - 60000 £ per year.

A pharmaceutical company in Guildford is seeking a QA Specialist to ensure compliance with GLP, GMP, and MHRA regulations. The role demands oversight of QA activities, batch release processes, and regulatory audits.

Candidates should possess a Bachelor’s degree and 3+ years of experience in a GMP environment. Strong knowledge of GMP standards and excellent communication skills are essential.

This is a full-time on-site position with occasional travel for training or audits.

GxP QA Lead — GMP/GLP Compliance & Audits in Guildford employer: MEDPHARM LTD

Join a leading pharmaceutical company in Guildford that prioritises employee development and fosters a collaborative work culture. With a strong commitment to compliance and quality, we offer comprehensive training opportunities and support for career advancement, ensuring that our team members thrive in their roles. Enjoy the benefits of working in a dynamic environment where your contributions directly impact patient safety and product excellence.
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Contact Detail:

MEDPHARM LTD Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land GxP QA Lead — GMP/GLP Compliance & Audits in Guildford

Tip Number 1

Network like a pro! Reach out to professionals in the pharmaceutical industry, especially those who work in QA. LinkedIn is a great place to connect and engage with them; you never know who might have a lead on that perfect GxP QA Lead role.

Tip Number 2

Prepare for interviews by brushing up on your knowledge of GMP and GLP regulations. We recommend creating a cheat sheet of key points and examples from your experience that demonstrate your expertise. This will help you stand out when discussing compliance and audits.

Tip Number 3

Don’t underestimate the power of follow-ups! After an interview, send a thank-you email to express your appreciation and reiterate your interest in the position. It shows professionalism and keeps you fresh in their minds.

Tip Number 4

Apply through our website for the best chance at landing that QA Specialist role. We make it easy for you to showcase your skills and experience directly to hiring managers. Plus, it’s a great way to stay updated on new opportunities!

We think you need these skills to ace GxP QA Lead — GMP/GLP Compliance & Audits in Guildford

GMP Compliance
GLP Compliance
MHRA Regulations
QA Oversight
Batch Release Processes
Regulatory Audits
Bachelor’s Degree
3+ Years of Experience in GMP Environment
Strong Knowledge of GMP Standards
Communication Skills
Attention to Detail
Problem-Solving Skills
Team Collaboration
Adaptability
Training Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in GMP environments and any relevant qualifications. We want to see how your background aligns with the role, so don’t be shy about showcasing your skills!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about QA and how your experience meets the job requirements. We love seeing genuine enthusiasm for the role.

Showcase Your Communication Skills: Since excellent communication is key for this position, make sure your application reflects that. Use clear and concise language, and don’t forget to proofread for any typos or errors before hitting send!

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy to do!

How to prepare for a job interview at MEDPHARM LTD

Know Your GMP and GLP Inside Out

Make sure you brush up on your knowledge of GMP and GLP standards before the interview. Be prepared to discuss specific regulations and how they apply to the role. This will show that you’re not just familiar with the terms, but that you truly understand their importance in ensuring compliance.

Showcase Your Audit Experience

Since the role involves regulatory audits, be ready to share examples from your past experiences. Talk about the audits you've participated in, what your role was, and how you contributed to successful outcomes. This will demonstrate your hands-on experience and problem-solving skills.

Communicate Clearly and Confidently

Excellent communication skills are essential for this position. Practice articulating your thoughts clearly and confidently. You might want to prepare answers to common interview questions, focusing on how you can effectively communicate complex information to different stakeholders.

Prepare Questions About the Company

Research the pharmaceutical company and prepare thoughtful questions to ask during the interview. This shows your genuine interest in the role and helps you assess if the company culture aligns with your values. Ask about their approach to compliance and how they support their QA team.

GxP QA Lead — GMP/GLP Compliance & Audits in Guildford
MEDPHARM LTD
Location: Guildford
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  • GxP QA Lead — GMP/GLP Compliance & Audits in Guildford

    Guildford
    Full-Time
    36000 - 60000 £ / year (est.)
  • M

    MEDPHARM LTD

    50-100
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