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- Tasks: Manage regulatory requirements and coordinate audits in a global pharma environment.
- Company: Join a leading global pharmaceutical company focused on quality excellence.
- Benefits: Flexible working, competitive pay, and opportunities for professional growth.
- Why this job: Be part of impactful projects that enhance clinical operations and regulatory compliance.
- Qualifications: 3+ years in pharma, process improvement, and audit coordination experience.
- Other info: Work 2 days a week in Slough with a dynamic team.
The predicted salary is between 36000 - 60000 £ per year.
A global pharma is looking to hire a Process Quality Excellence Specialist on an initial 12 month contract. Working 2 days per week in Slough, the successful candidate will have the following responsibilities:
- Manage the Regulatory Intelligence Network requirements for the Global Clinical Sciences & Operations group.
- Act as the RIN coordinator and work with the relevant GCSO SMEs for regulatory/guidance requirements to controlled documents as needed.
- Review regulations and identify which SMEs should be assigned based on the topic.
- Act as a point of contact to confirm that CROs have assessed regulatory and country regulations that may impact their SOPs and studies.
- Act as an Audit Host. Work with the Auditing team to host and coordinate with relevant SMEs and functions on any internal Quality Audit.
- Assist the assigned SMEs in responding to queries by the auditees during the audit.
- Work with the SMEs on responses to findings, CAPAs, etc., until the audit is closed.
Preferred Experience:
- 3+ years in the pharmaceutical industry
- Process improvement experience
- RIN or RA experience preferred
- GCP experience needed
- GAP analysis experience preferred
- Audit awareness
- CAPA understanding
Please note: This is NOT a QA role - my client is not looking for candidates from a QA background.
For a confidential discussion, please get in touch - trish@warmanobrien.com
Process Quality Excellence Specialist in Slough employer: Warman O'Brien
Contact Detail:
Warman O'Brien Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Process Quality Excellence Specialist in Slough
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharma industry, especially those who have experience in regulatory intelligence or process improvement. Use platforms like LinkedIn to connect and engage with them; you never know who might have a lead on your dream job!
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GCP and CAPA. Be ready to discuss how your past experiences align with the responsibilities of the Process Quality Excellence Specialist role. We want to see you shine, so practice articulating your thoughts clearly and confidently!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a quick thank-you email to express your appreciation for the opportunity. It shows your enthusiasm for the role and keeps you fresh in their minds.
✨Tip Number 4
Apply through our website! We’ve got loads of resources to help you land that Process Quality Excellence Specialist gig. Plus, it’s a great way to ensure your application gets the attention it deserves. Let’s get you that job!
We think you need these skills to ace Process Quality Excellence Specialist in Slough
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Process Quality Excellence Specialist role. Highlight your experience in regulatory intelligence, process improvement, and any relevant audits you've been involved in. We want to see how your background fits 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 this role and how your skills align with the responsibilities mentioned in the job description. We love seeing genuine enthusiasm and a clear connection to the position.
Showcase Relevant Experience: When filling out your application, be sure to showcase your experience in the pharmaceutical industry, especially any roles related to GCP or CAPA. We’re keen on candidates who can demonstrate their understanding of these areas, so don’t hold back!
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep everything organised and ensures your application gets the attention it deserves. Plus, it’s super easy to do!
How to prepare for a job interview at Warman O'Brien
✨Know Your Regulations
Familiarise yourself with the latest regulations and guidance relevant to the pharmaceutical industry. Being able to discuss specific regulations and how they impact controlled documents will show your expertise and readiness for the role.
✨Highlight Your Coordination Skills
Since you'll be acting as a point of contact during audits, emphasise your experience in coordinating with various stakeholders. Prepare examples of how you've successfully managed communication between teams or facilitated processes in previous roles.
✨Prepare for Audit Scenarios
Think about potential audit scenarios you might encounter and how you would handle them. Be ready to discuss your understanding of CAPAs and how you've contributed to resolving findings in past experiences.
✨Showcase Process Improvement Experience
Be prepared to talk about specific instances where you've implemented process improvements. Highlight any tools or methodologies you've used, and how these changes positively impacted efficiency or compliance in your previous roles.
