Biotech QA Specialist - GMP Compliance & Audit Lead in London
Biotech QA Specialist - GMP Compliance & Audit Lead

Biotech QA Specialist - GMP Compliance & Audit Lead in London

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

  • Tasks: Manage quality systems and ensure compliance with regulatory standards in a fast-growing biotech company.
  • Company: Join a dynamic biotech firm making waves in the UK.
  • Benefits: Competitive salary, career advancement, and a chance to shape quality assurance practices.
  • Why this job: Be a key player in ensuring product safety and quality in the biotech industry.
  • Qualifications: 5 years of QA experience in pharmaceuticals and a minimum HND in a Biological subject.
  • Other info: Excellent opportunity for growth in a supportive and innovative environment.

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

A fast-growing Biotech company in the UK seeks a Quality Assurance Specialist to manage quality systems and ensure compliance with regulatory standards. The ideal candidate will have at least 5 years of QA experience in the pharmaceuticals industry, a minimum HND in a Biological subject, and excellent communication and leadership skills.

Responsibilities include:

  • Document review
  • Supporting audits
  • Maintaining quality programs

A strong understanding of GMP and GLP systems is essential for success in this role.

Biotech QA Specialist - GMP Compliance & Audit Lead in London employer: RRxCo.TM

Join a dynamic and rapidly expanding Biotech company in the UK, where your expertise as a Quality Assurance Specialist will be valued and nurtured. We offer a collaborative work culture that prioritises employee growth through continuous training and development opportunities, alongside competitive benefits that support your well-being. With a commitment to innovation and excellence in the pharmaceuticals industry, this is an ideal environment for those seeking meaningful and rewarding employment.
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Contact Detail:

RRxCo.TM Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land Biotech QA Specialist - GMP Compliance & Audit Lead in London

✨Tip Number 1

Network like a pro! Reach out to your connections in the biotech and pharmaceuticals industry. Attend relevant events or webinars to meet potential employers and get your name out there.

✨Tip Number 2

Prepare for interviews by brushing up on GMP and GLP systems. We recommend creating a list of common interview questions related to quality assurance and practising your responses to show off your expertise.

✨Tip Number 3

Showcase your leadership skills! During interviews, share examples of how you've led teams or projects in the past. This will demonstrate your ability to manage quality systems effectively.

✨Tip Number 4

Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.

We think you need these skills to ace Biotech QA Specialist - GMP Compliance & Audit Lead in London

Quality Assurance
GMP Compliance
GLP Systems
Document Review
Audit Support
Leadership Skills
Communication Skills
Quality Program Management
Regulatory Standards Knowledge
Biological Subject Knowledge
Pharmaceuticals Industry Experience
Attention to Detail
Problem-Solving Skills
Team Collaboration

Some tips for your application 🫑

Tailor Your CV: Make sure your CV highlights your QA experience in the pharmaceuticals industry. We want to see how your skills align with the GMP and GLP systems mentioned in the job description.

Showcase Your Communication Skills: Since excellent communication is key for this role, include examples of how you've effectively communicated in past positions. We love seeing candidates who can lead and collaborate well!

Be Specific About Your Experience: When detailing your responsibilities, be specific about your involvement in document review and audits. We’re looking for concrete examples that demonstrate your expertise in managing quality systems.

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 don’t miss out on any important updates from us!

How to prepare for a job interview at RRxCo.TM

✨Know Your GMP and GLP Inside Out

Make sure you brush up on your knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Be ready to discuss how you've applied these standards in your previous roles, as this will show your expertise and commitment to quality assurance.

✨Prepare for Document Review Questions

Since document review is a key responsibility, expect questions about your experience with quality documentation. Think of specific examples where you identified issues or improved processes, and be prepared to explain your thought process during those situations.

✨Showcase Your Leadership Skills

As a QA Specialist, you'll need to lead audits and support teams. Prepare to share instances where you've successfully led a team or project, highlighting your communication skills and ability to motivate others. This will demonstrate that you're not just a technical expert but also a capable leader.

✨Research the Company Culture

Understanding the company's values and culture can give you an edge. Look into their recent projects, achievements, and any news related to their growth. This will help you tailor your responses and show that you're genuinely interested in being part of their team.

Biotech QA Specialist - GMP Compliance & Audit Lead in London
RRxCo.TM
Location: London

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