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- Tasks: Lead quality validation processes in a dynamic pharmaceutical environment.
- Company: Join a top UK employer known for innovation and career growth.
- Benefits: Enjoy a competitive salary, 15% bonus, and hybrid work options.
- Why this job: Be part of a culture that prioritises quality and compliance while making a real impact.
- Qualifications: 5+ years in GMP validation; degree in science or engineering preferred.
- Other info: Opportunity to collaborate with global stakeholders and drive process improvements.
The predicted salary is between 36000 - 60000 £ per year.
Location: Surrey, UK (Hybrid)
Package: Salary plus 15% bonus and Car or Car Allowance
My client is a world-renowned pharmaceutical organisation recognised as a top employer in the UK. They offer an excellent working environment with competitive benefits and outstanding opportunities for career development.
They now have a pivotal role in ensuring the highest standards of quality at an innovative pharmaceutical manufacturing site. As a Quality Validation Engineer, you will be at the forefront of the Quality Validation program, focusing on key areas such as Process Validation, Control Strategy, Cleaning Validation, and Hold Time Validation. You will also manage the planning and execution of overall Validation processes for the site.
You will ensure validation documentation meets GMP Regulations and company procedures/policies, fostering a culture of compliance throughout the organisation. You will author, review, and execute validation and qualification lifecycle documentation while overseeing site validation activities.
Key Responsibilities
- Drive process improvements and support operations in delivering projects aligned with business needs
- Collaborate across all site functions to ensure compliance with local and company directives
- Create and maintain validation documents and quality strategic documentation
- Manage validation documentation including protocols and reports (URS, FAT, SAT, IOPQ, etc.)
- Generate monthly, quarterly, and annual KPI adherence reports
- Work with all departments to maintain validated status of processes
- Establish strong connections with local validation SMEs and global stakeholders
- Support Quality Management System activities (audits, CAPA, Deviation, Change Control)
- Develop and modify SOPs, Work Instructions, and guidelines for validation policies
About You
- 5+ years in equipment and process validation within a GMP pharmaceutical environment
- Strong understanding of GMP, Risk assessment, and Data Integrity
- Extensive knowledge of validation and qualification processes
- Degree in a related science or engineering field, or formal qualification in validation or quality
- Experience in aseptic production and biologics and/or Project management experience are desirable
If you're interested in the above role then please click apply or get in touch to discuss further. Consult will endeavour to contact candidates within 14 days of application. However, if you do not hear back after 2 weeks then please assume on this occasion, unfortunately, you have not been successful.
Quality Validation Engineer employer: Consult
Contact Detail:
Consult Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Validation Engineer
✨Tip Number 1
Familiarise yourself with the latest GMP regulations and validation processes. Being well-versed in these areas will not only boost your confidence during interviews but also demonstrate your commitment to quality standards.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who work in quality validation. Attend relevant conferences or webinars to make connections and gain insights that could give you an edge in your application.
✨Tip Number 3
Prepare to discuss specific examples of how you've driven process improvements in previous roles. Highlighting your hands-on experience with validation documentation and compliance will resonate well with hiring managers.
✨Tip Number 4
Research the company culture and values of the organisation you're applying to. Tailoring your conversation to align with their mission and demonstrating how you can contribute to their goals will set you apart from other candidates.
We think you need these skills to ace Quality Validation Engineer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in equipment and process validation, particularly within a GMP pharmaceutical environment. Emphasise any relevant projects or roles that demonstrate your understanding of GMP, risk assessment, and data integrity.
Craft a Compelling Cover Letter: Write a cover letter that specifically addresses the key responsibilities mentioned in the job description. Discuss how your skills and experiences align with the role of Quality Validation Engineer, particularly in areas like process validation and compliance.
Highlight Relevant Qualifications: In your application, clearly state your degree in a related science or engineering field, or any formal qualifications in validation or quality. If you have experience in aseptic production or project management, make sure to include that as well.
Showcase Collaboration Skills: Since the role involves collaboration across various site functions, provide examples in your application of how you've successfully worked with different teams to ensure compliance and drive process improvements in previous positions.
How to prepare for a job interview at Consult
✨Know Your GMP Regulations
As a Quality Validation Engineer, it's crucial to have a solid understanding of Good Manufacturing Practices (GMP). Brush up on the latest regulations and be prepared to discuss how you've applied them in your previous roles.
✨Showcase Your Validation Experience
Highlight your experience with validation processes, especially in areas like Process Validation and Cleaning Validation. Be ready to provide specific examples of projects you've managed and the outcomes achieved.
✨Demonstrate Collaboration Skills
This role requires working closely with various departments. Prepare to discuss how you've successfully collaborated with cross-functional teams in the past and how you can foster strong connections with stakeholders.
✨Prepare for Technical Questions
Expect technical questions related to validation documentation and quality management systems. Review key concepts and be ready to explain your approach to managing validation documentation and compliance.
