Quality Manager (GCP/GVP) in Northampton

Quality Manager (GCP/GVP) in Northampton

Northampton Temporary 70000 - 85000 £ / year (est.) Home office (partial)
Cpl Life Sciences

At a Glance

  • Tasks: Drive quality improvements and compliance in a global biotech environment.
  • Company: Innovative biotechnology company focused on quality excellence.
  • Benefits: Competitive salary, fully remote work, and exposure to global functions.
  • Other info: Join a dynamic team dedicated to continuous improvement and quality culture.
  • Why this job: Make a real impact on medicine development while enhancing your quality management skills.
  • Qualifications: 6+ years in pharma/biotech with strong GCP/GVP knowledge.

The predicted salary is between 70000 - 85000 £ per year.

  • Temporary Quality Manager (GCP/GVP)
  • Location: Uxbridge, London, UK – Hybrid/Remote
  • Contract: Temporary
  • About the Opportunity

We are seeking an experienced Temporary Quality Manager (GCP/GVP) to support a global development quality function within an innovative, science-led biotechnology environment.

This is an exciting opportunity for a quality professional with expertise in Good Clinical Practice (GCP) and/or Good Pharmacovigilance Practice (GVP) to play a key role in quality system governance, quality event oversight, compliance activities, and continuous improvement initiatives across a global organisation.

Key Responsibilities

  • Partner with Global Development stakeholders to drive process improvements, standardisation, and regulatory compliance.
  • Manage quality metrics and trend reporting to support continuous improvement activities.
  • Oversee the Quality Event portfolio and provide subject matter expertise to functional teams.
  • Lead quality data analysis, root cause investigations, and CAPA development and implementation.
  • Manage Quality System Metrics, including reporting, thresholds, actions, and effectiveness measures.
  • Facilitate governance meetings and present Quality Management System performance data to stakeholders.
  • Coordinate procedural document reviews and impact assessments.
  • Support and promote a strong quality culture across the organisation.
  • Collaborate with cross-functional teams to strengthen Quality Management System effectiveness and compliance.

About You

To be successful in this role, you will have

  • Bachelor's degree and a minimum of 6 years' experience within the pharmaceutical, biotechnology, or healthcare industry.
  • Experience within Quality Management, Quality Assurance, or Clinical Development environments.
  • Strong working knowledge of GCP and/or GVP regulations and compliance requirements.
  • Experience managing or supporting Quality Management Systems (QMS), quality events, governance processes, and continuous improvement activities.
  • Experience conducting investigations, root cause analyses, and CAPA management.
  • Experience acting as a Subject Matter Expert, Process Owner, or Business Process Owner within a quality-related function.
  • Experience supporting regulatory inspections and audit readiness activities.
  • Previous experience training, mentoring, or supervising colleagues.
  • Strong project management, organisational, and prioritisation skills.
  • Excellent communication, stakeholder management, and presentation abilities.
  • A proactive approach with strong attention to detail and the ability to manage multiple priorities effectively.

What's on Offer?

  • Fully remote working arrangement.
  • Opportunity to work within a highly innovative and science-driven environment.
  • Exposure to global quality and development functions.
  • A chance to contribute to quality excellence and continuous improvement initiatives that support the development of medicines for patients worldwide.
  • For more information, please reach out to

You must be based and living in the UK to apply for this role. With prior QA experience in a biotech environment.

Quality Manager (GCP/GVP) in Northampton employer: Cpl Life Sciences

Cpl Life Sciences is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration within the vibrant streaming and entertainment sector. Employees benefit from immediate project impact opportunities, comprehensive training, and career growth in a cloud-oriented environment, making it an ideal place for those looking to advance their skills in data engineering while working with cutting-edge technologies.

Cpl Life Sciences

Contact Details:

Cpl Life Sciences Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Quality Manager (GCP/GVP) in Northampton

Join Biotechnology Meetups

Get yourself into the loop by joining local biotech meetups or workshops. These events are perfect for making connections with professionals in the field and can often lead to temporary gigs through word-of-mouth. Plus, you'll get to hear about the latest trends and developments directly from the source.

Showcase Your Passion in Science

Consider starting a blog or social media channel to showcase your interest in biotechnology. Share the latest research, your insights, and even your projects. This will not only enhance your visibility in the community but also attract potential employers like Cpl Life Sciences who might be scrolling through for talent.

Tap into University Resources

If you’re still in school or recently graduated, don’t forget to use your university’s career services. They often have exclusive connections with companies looking for temporary staff. Reach out to them for internship listings and networking opportunities tailored to the biotech sector.

Apply Directly on Our Website

When you spot that perfect temporary role at Cpl Life Sciences, make sure to apply directly through our website. This way, you’ll be in the best position to get noticed quickly and can show your enthusiasm for the role while filling out the application.

We think you need these skills to ace Quality Manager (GCP/GVP) in Northampton

Good Clinical Practice (GCP)
Good Pharmacovigilance Practice (GVP)
Quality Management Systems (QMS)
Quality Assurance
Regulatory Compliance
Continuous Improvement
Root Cause Analysis

Some tips for your application 🫡

Showcase Relevant Lab Skills:In the biotech world, your lab skills are paramount. Make sure your CV highlights specific techniques and equipment you’ve used, such as PCR, gel electrophoresis, or cell culture. This will give us a clear picture of what you can bring to Cpl Life Sciences as a temporary teammate.

Highlight Your Research Experience:If you’ve worked on any research projects — whether during your studies or in previous positions — make sure to detail these in your application. Include the objective, your role, and what you achieved. This will help us see your potential and fit for the temporary position at Cpl Life Sciences.

Keep It Concise and Relevant:Especially for a temporary role, we want to see a clear and focused application. Tailor your CV and cover letter to emphasise the qualifications and experiences that are most relevant to the biotech field and the specific role at Cpl Life Sciences. This shows us you’re genuinely interested and capable.

Be Clear About Your Availability:Since it’s a temporary role, let us know right away when you’re available to start and how long you can commit. Include this in your cover letter — this kind of transparency saves us all time and helps us find the right fit quickly at Cpl Life Sciences.

How to prepare for a job interview at Cpl Life Sciences

Brush Up on Your Biotech Basics

Understanding the fundamental concepts in biotechnology is crucial. Be ready to discuss core topics like genetics, molecular biology, or bioinformatics, especially if you're asked technical questions. We suggest revisiting your coursework or recent projects to refresh your memory.

Demonstrate Your Adaptability

Since this is a temporary role, they’re likely looking for someone who can jump in and get up to speed quickly. Share experiences where you’ve adapted to new environments, tools, or teams in a short space of time. It shows you're ready to tackle the challenge head-on!

Emphasise Your Lab Experience

If you’ve got hands-on experience in lab settings, now’s the time to showcase it. Talk about specific techniques you’ve mastered, like PCR or chromatography, and any relevant safety protocols you’ve followed. These details help paint you as an effective team member from day one.

Be Prepared to Explain Your Passion

Hiring managers want to see your motivation, especially for a temporary position in a fast-paced field like biotechnology. Be ready to discuss what excites you about the industry, your career goals, and how this role at Cpl Life Sciences aligns with them. It’s all about showing that you’re not just looking for a job, but a stepping stone in your biotech journey.