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: 12-month contract with competitive pay and valuable industry experience.
- Other info: Opportunity for career growth and exposure to strategic project management.
- Why this job: Make a real impact in the pharmaceutical industry while developing your skills.
- Qualifications: Experience in validation within GMP-regulated environments is essential.
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 Northampton employer: RBW Consulting
Join a leading global pharmaceutical manufacturing business that prioritises employee growth and development in a dynamic engineering environment. With a strong focus on collaboration and compliance, this role offers the chance to work on high-impact projects while benefiting from a supportive culture that values hands-on expertise and strategic input. Enjoy competitive benefits and the opportunity to make a meaningful impact in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Validation Engineer in Northampton
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about letting people know you’re on the hunt for a Validation Engineer role. You never know who might have the inside scoop on an opportunity!
✨Tip Number 2
Prepare for interviews by brushing up on your validation principles and project management skills. Be ready to discuss your hands-on experience with IQ/OQ/PQ documentation and how you've tackled challenges in past roles. Confidence is key!
✨Tip Number 3
Showcase your problem-solving skills during interviews. Think of specific examples where you’ve navigated complex validation scenarios or managed cross-functional teams. This will demonstrate your ability to thrive in a fast-paced environment.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got a range of exciting opportunities waiting for you, and applying directly can give you a better chance of standing out. Let’s get you that Validation Engineer role!
We think you need these skills to ace Validation Engineer in Northampton
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 Project Experience:If you’ve got project lead experience, make sure to highlight it! We’re looking for candidates who can manage project risks and timelines effectively, so share specific examples of your past successes in this area.
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and get you on our radar quickly!
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.
✨Showcase Your Project Management Skills
If you've led projects before, highlight this experience! Talk about how you defined project scopes, managed risks, and coordinated with cross-functional teams. This will show that you're not just a hands-on engineer but also a strategic thinker.
✨Prepare for Technical Questions
Expect some technical questions related to validation activities across manufacturing, lab, and utility systems. Brush up on your knowledge of FAT/SAT processes and be prepared to explain how you've executed these in previous roles.
✨Communicate Effectively
Strong communication skills are key in this role. Practice articulating your thoughts clearly and concisely. Be ready to discuss how you've collaborated with internal stakeholders and managed third-party contractors in the past.
