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- Tasks: Shape and maintain high-quality systems in clinical operations.
- Company: Global biopharmaceutical organisation with a focus on quality excellence.
- Benefits: Competitive salary, professional development, and a dynamic work environment.
- Why this job: Make a real impact on clinical quality and compliance in a leading organisation.
- Qualifications: 8+ years in pharmaceuticals, strong GCP knowledge, and SOP writing experience.
- Other info: Initial 12-month contract with opportunities for growth.
The predicted salary is between 36000 - 60000 ÂŁ per year.
A global biopharmaceutical organisation are looking for an experienced Quality professional as they expand their Process Quality Excellence team! This role sits at the heart of clinical quality, helping to shape and maintain high‑quality systems across global clinical operations and ensuring teams stay inspection‑ready and fully aligned with GCP, GLP, and PV expectations. You’ll work closely with the Head of Process Quality Excellence, supporting the development of policies, SOPs, and best practices, while also helping colleagues navigate quality, compliance, and regulatory requirements across clinical programmes.
What you’ll be doing:
- Supporting the Head of Process Quality Excellence in building and maintaining the clinical operation’s quality and compliance framework.
- Creating and revising quality policies, SOPs, processes, and guidance.
- Working with Global Quality, Patient Safety, Regulatory Affairs, external partners, and wider stakeholders to maintain compliance with ICH GCP, GLP, PV and relevant global/local regulations.
- Leading and coordinating inspection readiness across all clinical operation functions.
- Taking part in audit and inspection planning alongside Global Quality.
- Representing, or ensuring representation for, clinical operations during internal and external audits/inspections.
- Supporting teams with audit and inspection responses, including CAPAs and follow‑up actions.
What you’ll bring:
- 8+ years’ experience in the pharmaceutical sector, ideally within global QA or Clinical Development.
- Strong working knowledge of GCP and GVP, with hands‑on experience of global audits and/or inspections.
- At least two years’ experience writing SOPs.
- Strong experience of conducting Regulatory Intelligence.
- A proactive, solutions‑focused approach and the confidence to work cross‑functionally.
This role is offered on an initial 12 month contract.
Senior Process Quality Excellence Specialist in Slough employer: VRS UK
Contact Detail:
VRS UK Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Process Quality Excellence Specialist in Slough
✨Tip Number 1
Network like a pro! Reach out to your connections in the biopharmaceutical sector and let them know you're on the hunt for a Senior Process Quality Excellence Specialist role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on GCP, GLP, and PV regulations. Make sure you can discuss how your experience aligns with the role's requirements. We recommend practising common interview questions related to quality assurance and compliance to boost your confidence.
✨Tip Number 3
Showcase your expertise! During interviews, be ready to share specific examples of how you've developed policies, SOPs, or handled audits in the past. This will demonstrate your hands-on experience and proactive approach, which are key for this role.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to engage directly with us. Good luck!
We think you need these skills to ace Senior Process Quality Excellence Specialist in Slough
Some tips for your application 🫡
Tailor Your CV: Make sure your CV speaks directly to the role of Senior Process Quality Excellence Specialist. Highlight your experience in quality assurance, GCP, and any relevant audits or inspections you've been involved in. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality in clinical operations and how your skills can help us maintain high standards. Be sure to mention specific experiences that relate to the job description.
Showcase Your Achievements: Don’t just list your responsibilities; showcase your achievements! Whether it's leading a successful audit or developing a new SOP, we want to know how you've made an impact in your previous roles. Numbers and outcomes can really make your application stand out.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of applications and ensures you get all the updates directly from us. Plus, it shows you're keen on joining our team at StudySmarter!
How to prepare for a job interview at VRS UK
✨Know Your GCP and GLP Inside Out
Make sure you brush up on your knowledge of Good Clinical Practice (GCP) and Good Laboratory Practice (GLP). Be ready to discuss how these regulations impact clinical operations and share examples from your past experiences where you've ensured compliance.
✨Showcase Your SOP Writing Skills
Since the role involves creating and revising SOPs, come prepared with specific examples of SOPs you've written or improved. Highlight the challenges you faced and how you overcame them to ensure clarity and compliance.
✨Demonstrate Your Audit Experience
Be ready to talk about your experience with audits and inspections. Share stories that illustrate your role in preparing for these events, how you handled findings, and any CAPAs you implemented to address issues.
✨Emphasise Cross-Functional Collaboration
This position requires working closely with various teams. Prepare to discuss how you've successfully collaborated with different departments in the past, focusing on your proactive approach to problem-solving and maintaining quality standards.
