At a Glance
- Tasks: Lead validation projects in clean room and biocontainment environments.
- Company: Rapidly growing life science and healthcare company with a collaborative culture.
- Benefits: Competitive salary, inclusive environment, and exciting career opportunities.
- Other info: Opportunity for professional growth in a supportive and friendly workplace.
- Why this job: Join a dynamic team making a real impact in laboratory setups and expansions.
- Qualifications: Scientific degree and experience in validation engineering required.
The predicted salary is between 40000 - 50000 € per year.
Do you have validation engineering experience working in a GMP Life Science or Healthcare environment? Do you have expertise in clean rooms and biocontainment? Are you looking for an exciting and unique challenge with a rapidly growing business? Apply below after reading through all the details and supporting information regarding this job opportunity.
Our client is a specialist life science and healthcare company who work with a range of clients including universities, pharmaceutical manufacturers and the NHS. They provide expert advice and knowledge in relation to clean room environments, biocontainment and laboratory set-up, providing a high level of service in order to support their clients achieve their goals with relation to establishing new laboratories and expanding existing ones. Due to growth, they are now looking to recruit a Validation Engineer to join their team.
Responsibilities will include:
- Lead Projects through all stages of design and development
- Working with a project team of end users, designers and contractors to deliver high quality projects to timescale
- Provide detailed consultancy to project stakeholders in line with regulatory and engineering standards for clean room design and construction
- Execution of validation protocols at customer and vendor facilities
- Generation of Quality Risk assessments
- Lead project meetings including site visits
- Generation of Validation Protocols for a full validation life cycle
- Producing documentation specific to customer requirements: URS, VMP VP, RTM, DQ, IQ, OQ, & VSR
- Responsible for the review, creation and maintenance of project progress reports including internal reports on project progress against budget and costs
- Implement continuous improvement suggestions on process, procedures and documentation
To be considered for the role you will:
- Have scientific graduate and post-graduate qualifications in applied biology, biochemical/biomedical engineering
- Have an understanding of SHE, ensuring compliance with regulatory and legislative requirements
- Have a good understanding of research & pharmaceutical manufacturing regulations - GMP
- Be a member of a relevant professional body
- Be familiar with cross contamination control strategies & Quality Risk assessments
- Have experience in the validation of systems, equipment, and environment
- Have experience of project delivery
- Be highly organised and methodical with attention to detail
- Be able to maintain confidentiality of Company and clients’ information
- Have experience of working in a Clean Room or Laboratory environment
- Have knowledge of GLP, GMP, biomedical, biocontainment, pharmaceutical manufacturing, or fumigation processes
- Have an understanding of cGMP Clean Rooms, cGMP related utilities maintenance, cGMP equipment engineering & maintenance, Validation, and warehousing for cGMP related materials/product storage
- Be familiar with the RIBA stages of design
- Have a willingness to travel on a regular basis
You will be rewarded with a friendly, inclusive working environment and competitive salary, as well as the opportunity to join a great business at an exciting time.
Please note that all applicants for this role should be able to prove that they are legally entitled to work in the UK.
Validation Specialist employer: Network Scientific Recruitment
Join a rapidly growing specialist life science and healthcare company that values innovation and collaboration. With a focus on clean room environments and biocontainment, we offer a friendly and inclusive work culture, competitive salaries, and ample opportunities for professional growth. Be part of a team that supports prestigious clients like universities and the NHS, while contributing to meaningful projects that make a difference in the scientific community.
Contact Detail:
Network Scientific Recruitment Recruiting Team
StudySmarter Expert Advice🤫
We think this is how you could land Validation Specialist
✨Tip Number 1
Network, network, network! Reach out to your connections in the life sciences and healthcare sectors. We all know someone who knows someone, so don’t be shy about asking for introductions or advice.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GMP regulations and clean room standards. We want you to feel confident discussing your experience and how it aligns with the role of a Validation Specialist.
✨Tip Number 3
Showcase your project management skills! Be ready to discuss specific projects you've led, especially those involving validation protocols and quality risk assessments. We love hearing about real-life examples.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets the attention it deserves. Plus, we’re always looking for passionate candidates like you to join our growing team.
We think you need these skills to ace Validation Specialist
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to highlight your validation engineering experience, especially in GMP Life Science or Healthcare environments. We want to see how your skills match the job description, so don’t hold back on showcasing your expertise in clean rooms and biocontainment!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re excited about this role and how your background makes you the perfect fit. We love seeing genuine enthusiasm, so let your personality come through while keeping it professional.
Showcase Relevant Projects:If you've led projects or worked on relevant tasks, make sure to include those details in your application. We’re looking for someone who can hit the ground running, so highlight any experience with project delivery and validation protocols that aligns with our needs.
Apply Through Our Website:We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications better and ensures you don’t miss out on any important updates. Plus, it’s super easy to do!
How to prepare for a job interview at Network Scientific Recruitment
✨Know Your Stuff
Make sure you brush up on your validation engineering knowledge, especially in GMP Life Science and Healthcare environments. Familiarise yourself with clean room standards and biocontainment protocols, as these will likely come up during the interview.
✨Showcase Your Experience
Prepare to discuss specific projects you've led or contributed to, particularly those involving clean room design and validation protocols. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your achievements.
✨Ask Smart Questions
Demonstrate your interest in the role by preparing insightful questions about the company's projects, challenges they face in validation, or their approach to continuous improvement. This shows you're not just interested in the job, but also in how you can contribute to their success.
✨Be Organised and Methodical
Since the role requires a high level of organisation and attention to detail, make sure to convey this during your interview. Bring along any relevant documentation or reports that showcase your ability to manage projects effectively and maintain compliance with regulatory standards.
