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 and travel within the role.
- Why this job: Join a dynamic team making a real impact in laboratory setups and expansions.
- Qualifications: Scientific degree, validation experience, and knowledge of GMP regulations.
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?
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
- Understanding of SHE, ensuring compliance with regulatory and legislative requirements
- Good understanding of research & pharmaceutical manufacturing regulations - GMP
- Membership of relevant professional body
- Familiar with Cross contamination control strategies & Quality Risk assessments
- Experience in the Validation of systems, equipment, and environment
- Experience of project delivery
- Highly organised and methodical with attention to detail
- Able to maintain confidentiality of Company and clients' information
- Experience of working in a Clean Room or Laboratory environment
- Knowledge of GLP, GMP, biomedical, biocontainment, pharmaceutical manufacturing, or fumigation processes
- Understanding of cGMP Clean Rooms, cGMP related utilities maintenance, cGMP equipment engineering & maintenance, Validation, and warehousing for cGMP related materials/product storage
- Familiarity with the RIBA stages of design
- 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.
For more information or to apply, please contact Chris Vinter.
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 in Surrey employer: Network Scientific Recruitment
As a Validation Specialist at our rapidly growing life science and healthcare company, you will thrive in a supportive and inclusive work culture that values your expertise in clean rooms and biocontainment. We offer competitive salaries, opportunities for professional growth, and the chance to work on exciting projects with esteemed clients such as universities and the NHS, all while contributing to meaningful advancements in laboratory environments.
Contact Detail:
Network Scientific Recruitment Recruiting Team
StudySmarter Expert Advice🤫
We think this is how you could land Validation Specialist in Surrey
✨Tip Number 1
Network, network, network! Get in touch with people in the life sciences and healthcare sectors. Attend industry events or webinars, and don’t be shy about reaching out on LinkedIn. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for interviews like a pro! Research the company and its projects, especially those related to clean rooms and biocontainment. We want you to show them you’re not just another candidate, but someone who genuinely understands their mission and can contribute to their goals.
✨Tip Number 3
Practice your responses to common interview questions, especially those around validation processes and GMP regulations. We recommend doing mock interviews with friends or mentors to build your confidence and refine your answers.
✨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 take the initiative to connect directly with us.
We think you need these skills to ace Validation Specialist in Surrey
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Validation Specialist role. Highlight your experience in GMP Life Science or Healthcare environments, and don’t forget to mention any specific projects you've led that relate to clean rooms and biocontainment.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Mention your scientific qualifications and how they align with the responsibilities listed in the job description.
Showcase Relevant Experience:When filling out your application, be sure to showcase your relevant experience in validation engineering. Include details about your familiarity with regulatory standards and any specific methodologies you’ve used in past projects.
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you’re considered for the role as quickly as possible!
How to prepare for a job interview at Network Scientific Recruitment
✨Know Your GMP Inside Out
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Understand the regulations and standards that govern clean rooms and biocontainment. Being able to discuss these confidently will show that you're not just familiar with the terms, but that you can apply them in real-world scenarios.
✨Prepare for Technical Questions
Expect to be asked about specific validation protocols and quality risk assessments. Review your past experiences and be ready to share examples of how you've executed validation protocols or led projects. This is your chance to showcase your expertise and problem-solving skills.
✨Showcase Your Project Management Skills
Since the role involves leading projects, be prepared to discuss your project management experience. Highlight any tools or methodologies you’ve used to keep projects on track and within budget. Demonstrating your organisational skills will be key to impressing the interviewers.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions! Inquire about the company’s approach to continuous improvement or how they handle challenges in clean room environments. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
