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 a critical phase in biotech and make a real impact on clinical development.
- Qualifications: Proven GCP QA experience in biotech or pharma and strong audit skills.
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
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 Slough employer: Hays
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. Enjoy a flexible and autonomous work environment that fosters innovation and collaboration, while offering competitive rates and the chance to shape quality frameworks in early clinical studies. This role not only provides significant exposure to senior leadership but also presents unique opportunities for professional growth in a dynamic and supportive culture.
StudySmarter Expert Advice🤫
We think this is how you could land GCP QA Consultant (Contract) in Slough
✨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 researching the company thoroughly. Understand their pipeline and recent developments. This will help you tailor your answers and show that you're genuinely interested in their work.
✨Tip Number 3
Showcase your hands-on experience! Be ready to discuss specific examples of how you've improved QMS frameworks or conducted audits. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace GCP QA Consultant (Contract) in Slough
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.
Showcase Your Achievements:When writing your application, don’t just list your duties. We love to see specific examples of how you've improved QMS frameworks or successfully conducted audits. Numbers and outcomes can really make you stand out!
Keep It Professional Yet Personal:While we appreciate a professional tone, don’t be afraid to let your personality shine through. A bit of authenticity can go a long way in making your application memorable.
Apply Through Our Website:We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications and ensures you’re considered for this exciting opportunity!
How to prepare for a job interview at Hays
✨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.
✨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. This will show that you can thrive in a fast-paced setting.
