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.
- Why this job: Make a real impact in the pharmaceutical industry while developing your 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 Bristol 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 Bristol
✨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. Confidence is key, so let your expertise shine!
✨Tip Number 3
Showcase your hands-on experience! When discussing your past roles, highlight specific projects where you’ve led validation activities or managed cross-functional teams. We want to see how you’ve made an impact in previous positions.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive and engaged in their job search.
We think you need these skills to ace Validation Engineer in Bristol
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Validation Engineer role. Highlight your experience in validation and CQV within GMP-regulated environments, and don’t forget to mention any project lead experience you have!
Showcase Your Skills:In your cover letter, showcase your strong communication and problem-solving skills. We want to see how you can effectively work across cross-functional teams and manage project risks.
Be Specific About Your Experience:When detailing your past roles, be specific about the validation documentation you've authored and executed. Mention any hands-on execution experience with equipment, utilities, or facilities that aligns with our needs.
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 this exciting opportunity in our busy engineering environment.
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 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.
