Senior QC Analyst – GMP & Validation in Abingdon
Senior QC Analyst – GMP & Validation

Senior QC Analyst – GMP & Validation in Abingdon

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

  • Tasks: Perform QC testing and maintain cell lines to ensure quality standards.
  • Company: Leading biotechnology company focused on innovative cancer treatments.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Why this job: Make a real difference in lives through groundbreaking cancer research.
  • Qualifications: 3+ years lab experience and a degree in Chemistry or related fields.
  • Other info: Join a dynamic team dedicated to excellence in quality control.

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

A leading biotechnology company in Abingdon is seeking a Quality Control (QC) Analyst to perform routine and non-routine QC testing and maintain various cell lines. The ideal candidate will have at least 3 years of laboratory experience, a degree in Chemistry or related fields, and excellent analytical skills. This role includes writing and updating SOPs and participating in audits, ensuring adherence to GMP practices. Join us to impact lives through innovative cancer treatments.

Senior QC Analyst – GMP & Validation in Abingdon employer: Replimune Group

As a leading biotechnology company in Abingdon, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to make a real difference in the fight against cancer. We offer competitive benefits, continuous professional development opportunities, and a supportive environment where your contributions are valued and recognised. Join us to be part of a mission-driven team dedicated to improving lives through cutting-edge science.
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Contact Detail:

Replimune Group Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior QC Analyst – GMP & Validation in Abingdon

Tip Number 1

Network like a pro! Reach out to professionals in the biotech field on LinkedIn or at industry events. We can’t stress enough how personal connections can lead to job opportunities.

Tip Number 2

Prepare for interviews by brushing up on your GMP knowledge and analytical skills. We recommend practising common interview questions related to QC testing and SOP writing to show you’re ready to hit the ground running.

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 match your expertise in QC and validation.

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 biotech industry.

We think you need these skills to ace Senior QC Analyst – GMP & Validation in Abingdon

Analytical Skills
Laboratory Experience
SOP Writing
GMP Practices
Cell Line Maintenance
Quality Control Testing
Attention to Detail
Audit Participation
Chemistry Knowledge
Problem-Solving Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your relevant experience in QC testing and GMP practices. We want to see how your background aligns with the role, so don’t be shy about showcasing your analytical skills and any lab work you've done.

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality control and how you can contribute to our mission of innovative cancer treatments. Keep it concise but impactful!

Showcase Your SOP Writing Skills: Since writing and updating SOPs is part of the job, include examples of your experience with this in your application. We love seeing candidates who can clearly communicate their understanding of compliance and quality standards.

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 shows you’re keen on joining our team!

How to prepare for a job interview at Replimune Group

Know Your GMP Inside Out

Make sure you brush up on Good Manufacturing Practices (GMP) before the interview. Be ready to discuss how you've applied these practices in your previous roles, especially in relation to QC testing and maintaining cell lines.

Showcase Your Analytical Skills

Prepare to provide specific examples of how your analytical skills have contributed to successful outcomes in your past laboratory work. Think about challenges you've faced and how you overcame them using your expertise.

Familiarise Yourself with SOPs

Since writing and updating Standard Operating Procedures (SOPs) is part of the role, be prepared to talk about your experience with SOPs. Bring examples of SOPs you've worked on and be ready to discuss how you ensure compliance during audits.

Passion for Impactful Work

This company is focused on innovative cancer treatments, so express your passion for making a difference in people's lives through your work. Share any relevant experiences that highlight your commitment to quality and patient safety.

Senior QC Analyst – GMP & Validation in Abingdon
Replimune Group
Location: Abingdon

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