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 hands-on 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 Sittingbourne employer: RBW Consulting
As a leading global pharmaceutical manufacturing business, we pride ourselves on fostering a dynamic and inclusive work culture that prioritises employee growth and development. Our Validation Engineers benefit from hands-on experience in a high-impact environment, with opportunities to lead significant projects while ensuring compliance with GMP standards. Located in a vibrant area, we offer competitive benefits and a collaborative atmosphere that encourages innovation and professional advancement.
StudySmarter Expert Advice🤫
We think this is how you could land Validation Engineer in Sittingbourne
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.
✨Tip Number 2
Prepare for interviews by practising common questions related to validation engineering. Think about your past experiences and how they align with the role. We recommend doing mock interviews with friends or using online resources to boost your confidence.
✨Tip Number 3
Showcase your hands-on experience! When discussing your background, highlight specific projects where you’ve executed validation activities. Use examples that demonstrate your problem-solving skills and ability to work under pressure.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive and engaged with our company. Let’s get you that Validation Engineer role!
We think you need these skills to ace Validation Engineer in Sittingbourne
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 how you've applied these principles in past roles, particularly around equipment and utilities.
✨Prepare for Technical Questions
Expect technical questions related to IQ/OQ/PQ documentation and validation activities. We recommend reviewing your previous projects and being prepared to explain your role in generating and executing validation documentation.
✨Showcase Your Project Management Skills
If you've led projects before, be ready to share specific examples. Discuss how you defined project scope, managed risks, and coordinated with cross-functional teams. This will demonstrate your ability to handle the strategic aspects of the role.
✨Communicate Effectively
Strong communication skills are key in this role. Practice articulating your thoughts clearly and concisely. Be prepared to discuss how you've worked with internal stakeholders and managed third-party contractors in the past.
