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: Fast-paced environment with opportunities for professional growth.
- Why this job: Join at a critical stage and make a real impact on clinical development.
- Qualifications: Experience in GCP QA and early clinical studies required.
The predicted salary is between 50000 - 65000 £ per year.
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
GCP QA Consultant (Contract). Job in London LilyLifestyle Jobs employer: United Cerebral Palsy of Georgia
Join a pioneering UK-based biotech firm at the forefront of innovative therapeutic development, where you will have the opportunity to shape the quality framework in a dynamic and supportive environment. With a strong focus on employee growth, this role offers exposure to critical clinical processes and the chance to work closely with senior leadership, all while enjoying a flexible contract structure that promotes autonomy and work-life balance.
Contact Details:
United Cerebral Palsy of Georgia Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land GCP QA Consultant (Contract). Job in London LilyLifestyle Jobs
✨Tip Number 1
Network like a pro! Reach out to your connections in the biotech and pharma sectors. Attend industry events or webinars to meet potential employers and get your name out there. Remember, it’s all about who you know!
✨Tip Number 2
Prepare for interviews by brushing up on your GCP knowledge and understanding the specific challenges faced by the company. Tailor your responses to show how your experience aligns with their needs. We want to see that you can hit the ground running!
✨Tip Number 3
Don’t just apply and wait! Follow up on your applications through our website. A quick email or message can show your enthusiasm and keep you on their radar. It’s all about making that personal connection!
✨Tip Number 4
Showcase your hands-on experience! Be ready to discuss specific audits or QMS frameworks you've worked on. We love hearing about real-life examples that demonstrate your skills and how you can contribute to their success.
We think you need these skills to ace GCP QA Consultant (Contract). Job in London LilyLifestyle Jobs
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. Mention specific experiences that demonstrate your ability to support early clinical studies and improve QMS frameworks.
Showcase Your Autonomy:Since this role requires working autonomously, share examples of how you've successfully managed projects or tasks independently in fast-paced environments. We love seeing initiative!
Apply Through Our Website:For the best chance of getting noticed, apply directly through our website. It helps us keep track of applications and ensures you’re considered for this exciting opportunity!
How to prepare for a job interview at United Cerebral Palsy of Georgia
✨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 standards, 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.
✨Demonstrate Your Audit Skills
Audits are a big part of this role, so be prepared to share your audit experiences. Discuss the types of audits you've conducted, what you learned from them, and how you ensured compliance. This will highlight your hands-on experience and ability to maintain high standards.
✨Be Ready for Fast-Paced Questions
Given the dynamic nature of the biotech environment, expect questions that assess your adaptability and problem-solving skills. Think of scenarios where you had to make quick decisions or adapt to changes in project scope, and be ready to share those stories.