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- Tasks: Ensure equipment and systems meet regulatory standards in biotechnology.
- Company: Join Hobson Prior, a leading life sciences recruiter shaping healthcare's future.
- Benefits: Gain experience in a dynamic team with opportunities for growth and learning.
- Why this job: Make a real impact in healthcare while working in a collaborative environment.
- Qualifications: Experience in cGMP environments and knowledge of validation processes required.
- Other info: Must have the right to work in London; apply now to join our mission!
The predicted salary is between 36000 - 60000 £ per year.
Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that\’s shaping the future of healthcare and science.
Hobson Prior is seeking an Engineering Validation Specialist to join a dynamic team in London.
In this role, you will ensure that all equipment, facilities, and computerized systems used in regulated processes meet the required standards. You will act as a subject matter expert on validation, ensuring compliance with EU, UK, and FDA regulations while supporting quality management activities.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Ensure all equipment, facilities, and systems are validated and compliant with regulatory requirements.
- Review and approve validation documents, protocols, and reports.
- Collaborate with various departments to align validation plans with business objectives.
- Support audits and inspections by acting as a subject matter expert.
- Address and resolve issues related to validation and compliance.
- Maintain inspection readiness and ensure documentation meets quality standards.
- Manage changes and deviations effectively, ensuring timely resolution.
- Stay updated on industry regulations and best practices.
Key Skills and Requirements:
- Experience working within a cGMP pharmaceutical/biotechnology manufacturing environment
- Knowledge of computerized system validation and engineering validation
- Experience working on utilities/equipment/facilities
For more information, please contact William Hay.
If you are interested in applying to this exciting opportunity, then please click \’Apply\’ or to speak to one of our specialists visit the \’Contact Us\’ page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you\’ve read and understood our privacy policy, which informs you how we process and safeguard your data – .
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Engineering Validation Specialist employer: Hobson Prior
Contact Detail:
Hobson Prior Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Engineering Validation Specialist
✨Tip Number 1
Familiarise yourself with the latest EU, UK, and FDA regulations related to engineering validation. Being well-versed in these standards will not only boost your confidence but also demonstrate your commitment to compliance during any discussions.
✨Tip Number 2
Network with professionals in the biotechnology and pharmaceutical sectors. Attend industry events or webinars where you can meet people who work in validation roles. This can provide you with insights into the role and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples from your past experience that showcase your skills in validation and compliance. Think about challenges you've faced and how you resolved them, as this will highlight your problem-solving abilities.
✨Tip Number 4
Stay updated on the latest trends and technologies in the biotechnology field. Showing that you are proactive about learning and adapting to new developments can set you apart from other candidates.
We think you need these skills to ace Engineering Validation Specialist
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Engineering Validation Specialist position. Familiarise yourself with the key skills mentioned in the job description, such as experience in cGMP environments and knowledge of validation processes.
Tailor Your CV: Customise your CV to highlight relevant experience and skills that align with the job description. Emphasise your background in biotechnology or pharmaceutical manufacturing, and include specific examples of your work with validation and compliance.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for biotechnology and your understanding of the role. Mention how your expertise can contribute to the company's goals and demonstrate your familiarity with EU, UK, and FDA regulations.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial for a role focused on compliance and quality management.
How to prepare for a job interview at Hobson Prior
✨Know Your Regulations
Familiarise yourself with EU, UK, and FDA regulations related to validation. Being able to discuss these in detail will demonstrate your expertise and show that you are serious about compliance.
✨Showcase Your Experience
Prepare specific examples from your past work in cGMP environments. Highlight your experience with computerized system validation and how you've ensured compliance in previous roles.
✨Collaborative Mindset
Emphasise your ability to work with various departments. Discuss how you’ve successfully aligned validation plans with business objectives in the past, showcasing your teamwork skills.
✨Stay Current
Demonstrate your commitment to professional development by discussing recent industry trends or changes in regulations. This shows that you are proactive and dedicated to staying informed.
