Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Support and improve clinical quality systems in a global pharma company.
- Company: Join a leading global pharmaceutical company with a focus on quality excellence.
- Benefits: Competitive pay, hybrid working, and opportunities for professional growth.
- Why this job: Make a real impact on clinical programmes and ensure regulatory compliance.
- Qualifications: 8+ years in pharma, strong GCP expertise, and excellent communication skills.
- Other info: Dynamic role with a chance to lead inspection readiness activities.
The predicted salary is between 28 - 40 £ per hour.
Location: Slough/Remote (hybrid working)
Duration: 12 months initial (temporary role)
Rate (circa): £35 per hour (PAYE) / £47 per hour (Umbrella)
Overview
We are supporting a global pharma company who are seeking an experienced Senior Process Quality Excellence Specialist to support the development, maintenance, and continuous improvement of clinical quality systems within Global Clinical Sciences & Operations (GCSO). This role plays a key part in ensuring inspection readiness, regulatory compliance, and high-quality delivery across clinical programmes.
Responsibilities
- Support the creation, revision, and implementation of GCSO quality and compliance policies, SOPs, and processes.
- Collaborate with Global Quality, Patient Safety, Regulatory Affairs, and external partners to ensure compliance with ICH GCP, GLP, PV and global/local regulations.
- Lead and drive inspection readiness activities across GCSO, serving as a central coordinator with inspection teams.
- Represent GCSO during internal and external audits/inspections, supporting preparation and follow-up activities.
- Act as Regulatory Intelligence (RIN) Coordinator, reviewing regulations, identifying relevant SMEs, and ensuring CROs assess country-specific regulatory impacts.
Skills & Experience
- 8+ years’ experience in the pharmaceutical industry, ideally within global Quality Assurance or Clinical Development.
- Strong expertise in GCP and GVP, with hands-on experience in global audits and/or inspections.
- Minimum 2 years’ experience writing or revising SOPs.
- Demonstrated ability to interpret regulatory guidance and coordinate SME engagement across functions.
- Excellent communication and stakeholder-management skills, with experience supporting audits, inspection readiness, and CAPA follow-up.
To Apply
If you are interested and want to find out more about this role, please click to apply or contact Theo Charles to discuss further.
Senior Process Quality Excellence Specialist - SRG in Slough employer: Jobster
Contact Detail:
Jobster Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Process Quality Excellence Specialist - SRG in Slough
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharma industry, especially those who work in quality assurance or clinical development. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GCP and regulatory compliance. We recommend creating a list of common interview questions related to quality systems and practice your answers. Confidence is key!
✨Tip Number 3
Showcase your experience with audits and inspections during interviews. Use specific examples to highlight your expertise in leading inspection readiness activities. This will demonstrate your value to potential employers.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for talented individuals like you to join our team in making a difference in the pharma world.
We think you need these skills to ace Senior Process Quality Excellence Specialist - SRG in Slough
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Process Quality Excellence Specialist role. Highlight your experience in GCP, audits, and SOP writing, as these are key for us. 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 the perfect fit for this role. Mention specific experiences that relate to the responsibilities listed in the job description. We love seeing genuine enthusiasm!
Showcase Your Communication Skills: Since excellent communication is crucial for this role, make sure your application reflects that. Use clear and concise language, and don’t forget to proofread for any typos. We appreciate attention to detail!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re proactive, which we love!
How to prepare for a job interview at Jobster
✨Know Your Stuff
Make sure you brush up on your knowledge of GCP, GLP, and the specific regulations relevant to the role. Familiarise yourself with the company's quality systems and any recent changes in regulatory guidelines. This will show that you're not just interested but also well-prepared.
✨Showcase Your Experience
Prepare to discuss your 8+ years in the pharmaceutical industry, especially your hands-on experience with audits and inspections. Have specific examples ready that highlight your expertise in writing or revising SOPs and how you've contributed to inspection readiness in the past.
✨Communication is Key
Since this role involves collaboration with various teams, practice articulating your thoughts clearly. Be ready to demonstrate your stakeholder management skills and how you've effectively communicated with different departments during audits or compliance activities.
✨Ask Insightful Questions
Prepare a few thoughtful questions about the company’s current quality initiatives or challenges they face in compliance. This not only shows your interest but also gives you a chance to engage in a meaningful conversation, making you stand out as a candidate.
