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- Tasks: Coordinate and execute validation of facilities, processes, and equipment in the pharma sector.
- Company: Join a leading life science organisation making a difference in healthcare.
- Benefits: Enjoy a permanent role with opportunities for professional growth and development.
- Why this job: Be part of a dynamic team ensuring quality and compliance in life sciences.
- Qualifications: Relevant experience in validation within the pharma or biopharma industry is essential.
- Other info: Located in the South East, this role offers a chance to impact patient safety.
The predicted salary is between 36000 - 60000 £ per year.
Our client is a leading life science organisation. At present, they are seeking a Validation Specialist on a permanent basis at their site in the South East, UK.
Responsibilities:
- To co-ordinate and execute the validation and re-qualification of facilities, processes, equipment, and Computer Systems (including cleaning validation) where required, to meet the site operations business needs.
Deliverables:
- Ensure review and update of validation procedures (Policies, Master plans, SOP’s etc.) for equipment and facilities.
- Establish and maintain Validation Plans as applicable.
- Prepare, execute and report validation protocol including cleaning validation in accordance with EU GMP.
- Perform qualification and requalification temperature mapping activities of storage locations, i.e. refrigerators, freezers and incubators.
- Perform qualification studies on other equipment and processes.
- Establish and maintain the re-qualification schedule for validated equipment.
- Liaise with Engineering, Quality Assurance and User Departments to ensure that validation is conducted in a timely manner according to the Validation Plan and with minimal disruption to production.
- Attend meetings, both internal and external, representing the department in a professional manner.
- Participate in audits by customers and regulatory authorities.
- Ensure that safe working methods and practices are followed.
Validation Specialist employer: Click To Hired
Contact Detail:
Click To Hired Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Validation Specialist
✨Tip Number 1
Familiarise yourself with EU GMP guidelines and validation processes specific to the pharma and biopharma sectors. This knowledge will not only help you understand the role better but also demonstrate your commitment and expertise during interviews.
✨Tip Number 2
Network with professionals in the life sciences industry, especially those working in validation roles. Attend relevant conferences or webinars to make connections and gain insights that could give you an edge when applying for the Validation Specialist position.
✨Tip Number 3
Prepare to discuss specific examples of past validation projects you've worked on. Be ready to explain your role, the challenges faced, and how you ensured compliance with validation protocols, as this will showcase your practical experience.
✨Tip Number 4
Research the company’s current projects and initiatives in the validation space. Tailoring your conversation to align with their goals can show that you're genuinely interested in contributing to their success as a Validation Specialist.
We think you need these skills to ace Validation Specialist
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the responsibilities and deliverables of a Validation Specialist. Tailor your application to highlight relevant experience in validation, compliance with EU GMP, and any specific skills related to facilities and equipment.
Highlight Relevant Experience: In your CV and cover letter, emphasise your previous experience in validation within the pharma or biopharma sectors. Include specific examples of projects where you coordinated validation processes, prepared protocols, or liaised with different departments.
Showcase Your Skills: Make sure to showcase skills that are crucial for the role, such as attention to detail, project management, and knowledge of regulatory requirements. Use bullet points to make these skills stand out in your CV.
Craft a Strong Cover Letter: Write a compelling cover letter that not only summarises your qualifications but also expresses your enthusiasm for the role and the company. Mention why you want to work for this particular life science organisation and how you can contribute to their success.
How to prepare for a job interview at Click To Hired
✨Know Your Validation Standards
Familiarise yourself with EU GMP guidelines and validation protocols relevant to the pharma industry. Being able to discuss these standards confidently will show your expertise and understanding of the role.
✨Prepare for Technical Questions
Expect questions about specific validation processes, equipment qualification, and cleaning validation. Brush up on your technical knowledge and be ready to provide examples from your past experiences.
✨Demonstrate Team Collaboration Skills
Since the role involves liaising with various departments, be prepared to discuss how you have successfully worked in teams before. Highlight any experiences where you coordinated with engineering or quality assurance teams.
✨Showcase Your Problem-Solving Abilities
Validation can often present unexpected challenges. Be ready to share examples of how you've tackled issues in previous roles, particularly those that required quick thinking and effective solutions.
