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 work environment.
- Other info: Work closely with senior leadership in a fast-paced, evolving setting.
- Why this job: Join a critical phase in biotech and make a real impact on clinical development.
- Qualifications: Experience in GCP QA and supporting 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
Contract GCP Quality Assurance Consultant. Job in London LilyLifestyle Jobs employer: United Cerebral Palsy of Georgia
Join a pioneering UK-based biotech firm in London, where you will be instrumental in shaping the quality framework for innovative therapies entering first-in-human studies. With a strong emphasis on employee growth and a flexible, high-autonomy work culture, this role offers a unique opportunity to make a significant impact while collaborating closely with senior leadership in a dynamic environment.
Contact Details:
United Cerebral Palsy of Georgia Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Contract GCP Quality Assurance Consultant. Job in London LilyLifestyle Jobs
✨Tip Number 1
Network like a pro! Reach out to people in the biotech and pharma sectors, especially those who have experience with GCP QA. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your GCP knowledge and understanding the specific challenges faced by companies in early clinical development. We want you to show off your expertise and how you can help shape their quality framework!
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Check out our website for tailored opportunities that match your skills in GCP QA – we’ve got your back!
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you top of mind and show your enthusiasm for the role. Plus, it’s a great chance to reiterate why you’re the perfect fit for their team.
We think you need these skills to ace Contract GCP Quality Assurance Consultant. Job in London LilyLifestyle Jobs
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience in GCP QA 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 work with GCP SOPs, audits, and QMS frameworks to show us what you can bring to the table.
Showcase Your Autonomy:Since this role requires working autonomously in a fast-paced environment, make sure to highlight instances where you've successfully managed projects or tasks independently. 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 your details are in the right hands!
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, especially those related to early clinical studies. This will show that you’re not just familiar with the concepts 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 along any relevant documentation or examples of SOPs you've developed or improved, as this will demonstrate your hands-on experience.
✨Prepare for Scenario-Based Questions
Expect questions that put you in hypothetical situations, like how you would handle a GCP audit or manage vendor oversight. Practise articulating your thought process and decision-making skills, as this will highlight your ability to work autonomously in a fast-paced environment.
✨Research the Company and Its Pipeline
Take some time to understand the biotech's therapeutic pipeline and their current projects. Being able to discuss how your skills align with their goals will show your genuine interest in the role and help you stand out as a candidate who’s invested in their success.
