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- Tasks: Lead GxP validation projects and ensure compliance across systems and facilities.
- Company: Join a pioneering biopharmaceutical organisation at the forefront of advanced therapeutics.
- Benefits: Enjoy a full-time role with opportunities for professional growth and collaboration.
- Why this job: Be part of a science-led team shaping the future of pharmaceutical innovation.
- Qualifications: Degree in life sciences or engineering; experience in validation within pharma or biopharma.
- Other info: Opportunity to influence internal procedures and contribute to audits.
The predicted salary is between 36000 - 60000 ÂŁ per year.
Get AI-powered advice on this job and more exclusive features.Direct message the job poster from Allerton Bishop SearchFounder & Director – Allerton Bishop SearchAre you a Senior Validation Specialist ready to make your mark in the next chapter of pharmaceutical innovation?Allerton Bishop is working with a pioneering biopharmaceutical organisation specialising in advanced therapeutics to appoint a Senior Validation Specialist who will take ownership of key validation activities across GxP systems, facilities, and computerised systems.This is more than just another validation role – it’s a chance to be part of a science-led business pushing boundaries in advanced therapies. You’ll play a central role in ensuring GMP and regulatory compliance, with the opportunity to contribute to audits, influence internal procedures, and help shape future validation strategy.ROLE RESPONSIBILITIES:Acting as the go-to Senior Validation Specialist for GxP validation projects – equipment, systems, facilities, and CSV (Computer System Validation).Supporting the delivery of compliant, inspection-ready validation documentation and reviewing protocols in line with EU, UK, and FDA requirements.Partnering with QA, Operations, Labs, IT, Facilities, and Engineering to drive validation excellence across a multi-site function.Representing the business as a validation SME during audits and regulatory inspections – influencing outcomes with confidence and clarity.Playing a hands-on role in CAPA, change controls, deviation management, and ensuring GMP activities are closed in a timely, compliant manner.CANDIDATE REQUIREMENTS:Degree in a life sciences or engineering discipline.Work experience in validation roles within the pharmaceutical or biopharma sector.Strong background in GxP environments, Computer System Validation (CSV) or Process Validation would be highly desirable.Up-to-date knowledge of GMP, GEP, GDocP, and international regulatory frameworks.Keywords:Senior Validation Specialist | CSV | GMP | GxP | Engineering Validation | Biopharmaceuticals | Life Sciences | FDA Compliance | EU Annex 11 | Pharmaceutical Engineering Jobs | Inspection Readiness | Validation SME | Computerised Systems | Quality Assurance | Change Control | CAPA | Data IntegritySeniority levelSeniority levelMid-Senior levelEmployment typeEmployment typeFull-timeJob functionJob functionQuality Assurance, Science, and EngineeringIndustriesPharmaceutical Manufacturing and Biotechnology ResearchReferrals increase your chances of interviewing at Allerton Bishop Search by 2xSign in to set job alerts for “Validation Specialist” roles.London, England, United Kingdom 1 day agoHead of Validation for AI Non-Model – CitiLondon, England, United Kingdom 16 hours agoTechnology Director – Strategic Remediation Validation TestingLondon, England, United Kingdom 1 week agoTechnology Specialist – Strategic Remediation Validation Testing (Hybrid)London, England, United Kingdom 1 week agoLondon, England, United Kingdom 1 week agoLondon, England, United Kingdom 2 weeks agoSittingbourne, England, United Kingdom 1 day agoChiswick, England, United Kingdom 5 days agoLondon, England, United Kingdom 16 hours agoLondon, England, United Kingdom 2 weeks agoResearch Engineer/Research Scientist, Pre-Training Evaluation and Validation, UKLondon, England, United Kingdom 2 days agoLondon, England, United Kingdom 2 weeks agoSenior / Scientist – Project Biology – Target ValidationLondon, England, United Kingdom 2 months agoWe’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr
Senior Validation Specialist employer: JobLeads GmbH
Contact Detail:
JobLeads GmbH Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Validation Specialist
✨Tip Number 1
Network with professionals in the pharmaceutical and biopharma sectors. Attend industry conferences or webinars where you can meet people who work in validation roles. This can help you gain insights into the company culture and expectations, making you a more attractive candidate.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in GxP and Computer System Validation. Being well-versed in current guidelines from the FDA and EU will not only boost your confidence but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Prepare to discuss specific examples of your past validation projects. Highlight your role in ensuring GMP compliance and how you handled audits or inspections. This will showcase your expertise and ability to influence outcomes effectively.
✨Tip Number 4
Research the biopharmaceutical organisation you're applying to. Understand their products, values, and recent developments. Tailoring your conversation to align with their mission can set you apart as a candidate who is genuinely interested in contributing to their success.
We think you need these skills to ace Senior Validation Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in validation roles, particularly within the pharmaceutical or biopharma sector. Emphasise your knowledge of GxP environments and any specific projects you've worked on that align with the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for pharmaceutical innovation and your understanding of GMP and regulatory compliance. Mention specific examples of how you've contributed to validation projects and influenced outcomes during audits.
Highlight Key Skills: In your application, clearly outline your skills related to Computer System Validation (CSV), CAPA, and change control processes. Use keywords from the job description to ensure your application stands out to hiring managers.
Showcase Collaborative Experience: Demonstrate your ability to work with cross-functional teams by providing examples of past collaborations with QA, Operations, Labs, IT, and Engineering. This will show that you can drive validation excellence across a multi-site function.
How to prepare for a job interview at JobLeads GmbH
✨Showcase Your Validation Expertise
Make sure to highlight your experience in GxP validation projects, especially in equipment and computerised systems. Be prepared to discuss specific examples where you ensured compliance with GMP and regulatory standards.
✨Understand the Regulatory Landscape
Familiarise yourself with EU, UK, and FDA requirements relevant to the role. Demonstrating your up-to-date knowledge of these regulations will show that you're serious about compliance and can contribute effectively to audits.
✨Collaborative Mindset
Emphasise your ability to work with cross-functional teams, such as QA, Operations, and IT. Share examples of how you've successfully partnered with different departments to drive validation excellence and improve processes.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world situations, such as handling CAPA or change controls. Prepare to discuss how you've managed deviations and ensured timely closure of GMP activities.
