At a Glance
- Tasks: Support site validation and capital projects in a dynamic engineering environment.
- Company: Leading global pharmaceutical manufacturer with a focus on innovation.
- Benefits: Competitive pay, hands-on experience, and opportunities for professional growth.
- Other info: Fast-paced role with exposure to diverse projects and career advancement opportunities.
- Why this job: Make a real impact in the pharmaceutical industry while developing your engineering skills.
- Qualifications: Experience in validation within GMP-regulated environments and strong teamwork skills.
The predicted salary is between 40000 - 50000 £ per year.
A leading, global pharmaceutical manufacturing business is seeking an experienced Validation Engineer to support delivery of a major site validation and capital programme on a 12-month contract. This is a high-impact role within a busy engineering environment, offering exposure across equipment, utilities, facilities, and laboratory systems, with a need for hands-on execution specialists. If this capability brings with it project lead experience, this will also be valued.
The Role
Working as part of the Engineering function, you will support delivery of a structured site-wide validation programme, alongside capital project activity. Responsibilities will include:
- Supporting delivery of the Site Validation Master Plan (SVMP)
- Generating and reviewing validation / qualification documentation (IQ/OQ/PQ, FAT/SAT, etc.)
- Leading or supporting execution of validation activities across manufacturing, lab, and utility systems
- Working closely with internal stakeholders to ensure GMP and regulatory compliance
- Reviewing vendor documentation and supporting supplier-led validation activities
- Participating in FATs and site-based commissioning activities where required
- Managing or supporting third-party contractors and vendors
- Owning change controls, deviations, and CAPAs linked to validation activities
- Supporting requalification, new equipment introduction, and decommissioning activities
Project / Programme Exposure
In addition to core validation delivery, there is scope to contribute at a more strategic level:
- Supporting or leading capital project delivery (GxP and non-GxP)
- Defining project scope, timelines, and deliverables
- Managing project risks, budgets, and progress reporting
- Coordinating cross-functional stakeholders and teams
- Driving project governance, change management, and close-out activities
What We’re Looking For
We’re open to a range of profiles, from strong delivery-focused CQV engineers to more senior, project-led professionals:
- Experience in validation / CQV within GMP-regulated environments (pharma / biotech / related)
- Strong understanding of validation principles across equipment, utilities, or facilities
- Experience authoring and executing validation documentation
- Ability to work effectively across cross-functional teams and stakeholders
- Confidence operating in a fast-paced, project-driven environment
- Strong communication and problem-solving skills
Validation Engineer in Shrewsbury employer: RBW Consulting
As a leading global pharmaceutical manufacturing business, we pride ourselves on fostering a dynamic work environment that encourages innovation and collaboration. Our Validation Engineers benefit from a structured site-wide validation programme, ample opportunities for professional growth, and the chance to work on high-impact projects that directly contribute to improving healthcare outcomes. With a strong commitment to employee development and a culture that values teamwork and excellence, we offer a rewarding career path in a fast-paced industry.
StudySmarter Expert Advice🤫
We think this is how you could land Validation Engineer in Shrewsbury
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know that can land you that Validation Engineer role.
✨Tip Number 2
Prepare for those interviews by brushing up on your validation principles and project management skills. We recommend practising common interview questions and even doing mock interviews with friends or mentors. The more confident you are, the better you’ll perform!
✨Tip Number 3
Showcase your hands-on experience! When you get the chance to chat with potential employers, highlight your practical skills in executing validation activities and managing projects. We want to see how you’ve tackled challenges in fast-paced environments.
✨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 passionate individuals who can contribute to our validation efforts, so make sure you put your best foot forward!
We think you need these skills to ace Validation Engineer in Shrewsbury
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to highlight your experience in validation and CQV within GMP-regulated environments. We want to see how your skills match the role, so don’t be shy about showcasing relevant projects and achievements!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the Validation Engineer role. We love seeing enthusiasm and a clear understanding of the responsibilities outlined in the job description.
Showcase Your Communication Skills:Since this role involves working closely with internal stakeholders, make sure to highlight your strong communication skills in your application. We appreciate candidates who can convey complex information clearly and effectively.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at RBW Consulting
✨Know Your Validation Principles
Make sure you brush up on your validation principles, especially in GMP-regulated environments. Be ready to discuss your experience with IQ/OQ/PQ documentation and how you've applied these in past roles. This will show that you understand the core of what the role entails.
✨Showcase Your Project Management Skills
If you've led projects before, be prepared to share specific examples. Talk about how you defined project scopes, managed risks, and coordinated with cross-functional teams. This will demonstrate your ability to handle the strategic aspects of the role.
✨Prepare for Technical Questions
Expect technical questions related to validation activities across manufacturing, lab, and utility systems. Brush up on your knowledge of FAT/SAT processes and be ready to explain how you've executed these in previous positions. Confidence in your technical expertise can set you apart.
✨Communicate Effectively
Strong communication skills are key in this role. Practice articulating your thoughts clearly and concisely. Be ready to discuss how you've worked with internal stakeholders and managed third-party contractors, as this will highlight your collaborative approach and problem-solving abilities.
