At a Glance
- Tasks: Shape and deliver quality frameworks in a pioneering biotech environment.
- Company: Innovative UK-based biotech with strong funding and a novel therapeutic pipeline.
- Benefits: Flexible contract, competitive rate, and high autonomy.
- Other info: Dynamic role with exposure to end-to-end QMS build.
- Why this job: Join at a pivotal moment and make a real impact on clinical development.
- Qualifications: Experience in GCP QA and supporting early clinical studies.
The predicted salary is between 113 - 113 £ per hour.
Your new company
You will be supporting an innovative UK-based biotech entering first-in-human studies, backed by strong funding and progressing a novel therapeutic pipeline into early clinical development. The organisation is at a pivotal stage, building out its clinical and quality infrastructure as it transitions toward the clinic.
Your new role
As a GxP QA Consultant (GCP led), you will play a key role in shaping and delivering the organisation's quality framework, with a primary focus on GCP but with exposure across broader GxP disciplines (GLP / GMP depending on pipeline and scope).
Key responsibilities will include:
- Supporting the development and streamlining of GCP SOPs
- Providing QA oversight of CROs and clinical vendors
- Conducting and supporting GCP audits (internal/vendor/study-level)
- Driving inspection readiness (MHRA/FDA/EMA)
- Advising on phase appropriate QMS build without overengineering
This is a high-impact role, working closely with senior leadership in a growing biotech environment.
What you'll need to succeed
- Proven experience within GCP QA in biotech or pharma environments
- Strong background supporting early clinical / FIH studies
- Experience building or improving QMS frameworks and SOPs
- Hands-on experience with audits and vendor oversight
- Ability to work autonomously in a fast-paced, evolving environment
What you'll get in return
- Opportunity to support a biotech at a critical inflection point
- Exposure to end-to-end QMS build and FIH readiness
- Flexible, high-autonomy contract environment
- Competitive Rate
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
GCP QA Consultant (Contract) in London employer: Hays Life Sciences
Join a pioneering UK-based biotech at a transformative stage, where your expertise as a GCP QA Consultant will directly influence the development of groundbreaking therapies. With a strong emphasis on employee autonomy and flexibility, this role offers a unique opportunity to shape quality frameworks in a supportive environment that values innovation and professional growth.
StudySmarter Expert Advice🤫
We think this is how you could land GCP QA Consultant (Contract) in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the biotech and pharma sectors. Attend industry events or webinars, and don’t be shy about introducing yourself. You never know who might have the inside scoop on job openings!
✨Tip Number 2
Prepare for interviews by brushing up on GCP and QMS frameworks. Be ready to discuss your hands-on experience with audits and vendor oversight. Show them you’re not just a fit on paper but can bring real value to their team!
✨Tip Number 3
Tailor your approach! When applying through our website, make sure to highlight your relevant experience in early clinical studies and your ability to work autonomously. This will help you stand out as the ideal candidate for this high-impact role.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way. It shows your enthusiasm for the role and keeps you fresh in their minds. Plus, it’s a great opportunity to reiterate why you’re the perfect fit for their team.
We think you need these skills to ace GCP QA Consultant (Contract) in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your GCP QA experience and any relevant biotech or pharma roles. We want to see how your background aligns with the key responsibilities mentioned in the job description.
Craft a Compelling Cover Letter:Use your cover letter to tell us why you're the perfect fit for this role. Share specific examples of your experience with GCP audits and QMS frameworks, and how you can contribute to our innovative biotech journey.
Showcase Your Autonomy:Since this role requires working autonomously, give us examples of how you've successfully managed projects or tasks independently in fast-paced environments. We love seeing candidates who can take initiative!
Apply Through Our Website:To make sure your application gets the attention it deserves, apply directly through our website. It’s the best way for us to keep track of your application and get back to you quickly!
How to prepare for a job interview at Hays Life Sciences
✨Know Your GCP Inside Out
Make sure you brush up on your Good Clinical Practice (GCP) knowledge. Be ready to discuss specific examples from your past experiences where you've implemented GCP guidelines, especially in early clinical studies. This will show that you’re not just familiar with the theory but have practical insights to offer.
✨Showcase Your QMS Experience
Since the role involves building and improving Quality Management Systems (QMS), prepare to talk about your previous work in this area. Bring concrete examples of how you've contributed to QMS frameworks or SOPs, and be ready to discuss any challenges you faced and how you overcame them.
✨Prepare for Audit Scenarios
Audits are a big part of this role, so think about your audit experiences. Prepare to discuss how you’ve conducted audits, what you look for, and how you ensure compliance. You might even want to role-play some common audit scenarios to get comfortable with articulating your approach.
✨Demonstrate Adaptability
This position requires working autonomously in a fast-paced environment, so be ready to share examples of how you've adapted to changing situations in your previous roles. Highlight your problem-solving skills and your ability to thrive under pressure, as this will resonate well with the hiring team.
