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- Tasks: Join us as a Validation Engineer, working on diverse pharmaceutical projects.
- Company: Be part of a growing company known for promoting internal progression and skill development.
- Benefits: Enjoy a negotiable salary and opportunities for career advancement.
- Why this job: Gain hands-on experience in the full validation life cycle and enhance your expertise.
- Qualifications: Broad validation experience in GMP and familiarity with cGMP regulations required.
- Other info: Contact Simon Fowler at NGAGE Smart4Sciences to learn more and apply.
The predicted salary is between 36000 - 60000 £ per year.
Are you looking for your next step in Pharmaceutical Validation? This company is experiencing an exciting period of growth, known for internal progression & variation, making it a great place to progress your skills & expertise in Validation Engineering.
As the Validation Engineer, you will benefit from working on various projects including exposure to the full validation life from Design Qualification through to operational handover & inclusive of CSV.
Desirable Experience & Qualifications:
- Broad validation experience in GMP
- Experience in cGMP Annex 11, 21 CFR Part 11, GAMP 5
- Able to write URS and VMP (DQ, OQ, IQ, PQ)
If you would like to discuss this opportunity, please get in touch & apply now or contact Simon Fowler at NGAGE Smart4Sciences.
Validation Engineer employer: Smart4Sciences
Contact Detail:
Smart4Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Validation Engineer
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who work in validation. Attend industry events or join relevant online forums to connect with others and learn about potential job openings.
✨Tip Number 2
Familiarise yourself with the latest regulations and guidelines related to GMP, cGMP Annex 11, and 21 CFR Part 11. This knowledge will not only boost your confidence but also demonstrate your commitment to staying updated in the field.
✨Tip Number 3
Consider reaching out to current or former employees of the company to gain insights into their experiences. This can provide you with valuable information about the company culture and expectations for the Validation Engineer role.
✨Tip Number 4
Prepare to discuss specific projects where you've applied your validation skills, particularly in writing URS and VMP documents. Being able to share concrete examples will help you stand out during interviews.
We think you need these skills to ace Validation Engineer
Some tips for your application 🫡
Understand the Role: Familiarise yourself with the responsibilities of a Validation Engineer in the pharmaceutical sector. Highlight your understanding of GMP, cGMP Annex 11, and 21 CFR Part 11 in your application.
Tailor Your CV: Make sure your CV reflects your broad validation experience and any specific projects you've worked on that relate to Design Qualification, Operational Qualification, Installation Qualification, and Performance Qualification.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention your experience with writing User Requirement Specifications (URS) and Validation Master Plans (VMP), as these are key aspects of the job.
Proofread Your Application: Before submitting, carefully proofread your application for any errors or omissions. A well-presented application demonstrates attention to detail, which is crucial in validation engineering.
How to prepare for a job interview at Smart4Sciences
✨Know Your Validation Standards
Familiarise yourself with GMP, cGMP Annex 11, and 21 CFR Part 11. Be prepared to discuss how these regulations impact your work and provide examples of how you've applied them in previous roles.
✨Showcase Your Project Experience
Be ready to talk about specific projects you've worked on, especially those involving the full validation life cycle. Highlight your contributions during Design Qualification, Operational Qualification, and Performance Qualification phases.
✨Demonstrate Your Documentation Skills
Since writing URS and VMP is crucial for this role, prepare to discuss your experience in creating these documents. Bring examples if possible, and explain your approach to ensuring compliance and accuracy.
✨Emphasise Continuous Learning
This company values internal progression, so express your enthusiasm for professional development. Share any recent training or certifications you've completed that relate to validation engineering.
