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- Tasks: Ensure compliance and oversee engineering processes for animal health equipment.
- Company: Join Elanco, a global leader in animal health with a commitment to innovation.
- Benefits: Diverse work environment, career growth opportunities, and a chance to make a real impact.
- Why this job: Be part of a mission that enriches the lives of animals and their owners.
- Qualifications: Engineering or Science degree with experience in pharmaceutical cGMPs required.
- Other info: Collaborate with dynamic teams and develop your expertise in a supportive culture.
The predicted salary is between 28800 - 43200 £ per year.
At Elanco (NYSE: ELAN) – it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Your role:
- Engineering and compliance oversight for equipment at Speke Site. Custodian of processes and systems that maintain the qualified state of Direct Impact equipment, facilities and utilities on site – specifically Controlled Temperature Storage (Temperature Mapping), Autoclaves, and Fume cupboard & safety cabinet qualification.
- Additional support for Process Filtration, Direct Impact Utilities (e.g. high-grade water, steam and compressed gases).
Your responsibilities:
- Technical knowledge
- Maintain a knowledge and understanding of regulatory expectations, industry best practices and global standards relating to temperature mapping and autoclave qualification.
- Know and understand the fundamental theory of applicable equipment/systems.
- Incorporate this knowledge into governing Standard Operating Procedures, and validation master plan.
- Review updates to corporate quality and Engineering standards and develop plans to address any identified site gaps.
- Represent the site in areas of responsibility at internal and external regulatory inspections.
- Support Manufacturing
- Co-ordinate annual re-qualification programs and communicate standards and expectations to Product and support teams.
- Author qualification protocols and reports for applicable systems.
- Communicate compliance gaps/deviations to senior management. Raising deviations as required.
- Liaise with customers/key stakeholders to improve systems.
- Safety and Environment
- Perform regular active monitoring to drive standards/expectations and identify safety issues.
- Drive system improvement in close co-operation with customers/key stakeholders
- Identify need and opportunities for improvement and work with Product teams to develop and implement solutions.
- Raise Change controls when required.
- Support capital projects.
- Define/agree commissioning and qualification requirements.
- Review C&Q documents for applicable new equipment/facilities.
- Establish internal corporate network and external contacts and develop professional expertise
- Belong to subject groups within Elanco.
- Become point person/subject matter expert within Speke site for applicable systems.
- Develop external focus, links to appropriate industry forums (e.g. ISPE, etc.).
What You Need to Succeed (minimum qualifications):
- Engineering or Science Degree.
- At least 3 years' experience in pharmaceutical cGMPs.
- Formal training in sterilisation principles and practices.
What will give you a competitive edge (preferred qualifications):
- Experience and/or training in HVAC systems and clean room standards.
- Experience and/or training in GMP Facility Temperature Mapping.
Validation Engineer in London employer: Elanco Tiergesundheit AG
Contact Detail:
Elanco Tiergesundheit AG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Validation Engineer in London
✨Tip Number 1
Network like a pro! Reach out to current or former employees at Elanco on LinkedIn. A friendly chat can give us insider info about the company culture and maybe even a referral!
✨Tip Number 2
Prepare for the interview by brushing up on your technical knowledge. Make sure we can confidently discuss temperature mapping and autoclave qualification, as these are key areas for the Validation Engineer role.
✨Tip Number 3
Show off our passion for animal health! During interviews, share why we care about making animals' lives better. This aligns perfectly with Elanco's mission and will help us stand out.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure our application gets noticed. Plus, it shows we’re serious about joining the Elanco team.
We think you need these skills to ace Validation Engineer in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Validation Engineer role. Highlight relevant experience and skills that match the job description, especially your knowledge of regulatory expectations and industry best practices.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about animal health and how your background makes you a great fit for Elanco. Don’t forget to mention any specific projects or achievements that relate to the role.
Showcase Your Technical Skills: Since this role requires technical knowledge, be sure to include any relevant certifications or training in sterilisation principles, HVAC systems, or GMP Facility Temperature Mapping. This will help us see your expertise at a glance!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining our team at Elanco!
How to prepare for a job interview at Elanco Tiergesundheit AG
✨Know Your Stuff
Make sure you brush up on your technical knowledge related to validation engineering, especially around temperature mapping and autoclave qualification. Familiarise yourself with the regulatory expectations and industry best practices so you can confidently discuss them during the interview.
✨Showcase Your Experience
Prepare to talk about your previous experience in pharmaceutical cGMPs and any formal training you've had in sterilisation principles. Be ready to provide specific examples of how you've applied this knowledge in past roles, particularly in relation to compliance and system improvements.
✨Ask Smart Questions
Demonstrate your interest in the role by preparing thoughtful questions about Elanco's processes, culture, and future projects. This not only shows that you're engaged but also helps you assess if the company is the right fit for you.
✨Emphasise Teamwork
Elanco values collaboration, so be sure to highlight your ability to work with diverse teams. Share examples of how you've successfully liaised with stakeholders or improved systems through teamwork, as this aligns with their commitment to innovation and inclusivity.
