At a Glance
- Tasks: Lead the strategy for Commissioning, Qualification, and Validation while collaborating with various teams.
- Company: Lonza is a global leader in life sciences, dedicated to improving lives through innovative solutions.
- Benefits: Enjoy a supportive work culture, opportunities for career ownership, and the chance to make a real impact.
- Why this job: Join a team that values creativity and problem-solving in a meaningful field that benefits millions.
- Qualifications: BSc/MSc in relevant engineering or science fields; expertise in CQV areas required.
- Other info: Be part of a company that prioritises ethical practices and environmental responsibility.
The predicted salary is between 48000 - 72000 £ per year.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
The Senior Validation Specialist at Lonza is responsible for working with the Head of Validation in defining the vision and strategy for the Commissioning, Qualification, and Validation (CQV) department. You will be working with colleagues and internal customers sharing knowledge and experience, in all technical areas and aspects of project work throughout the validation lifecycle and determining innovation and identifying compliance requirements in the validation lifecycle. Be a technical Subject Matter Expert for at least one area of competency (CSE, Sterilisation, Gas Testing, Clean Room, Equipment Qualification).
Key responsibilities:
- Cultivate positive relationships between QA, Manufacturing, Quality Control, Development Services, Project Management, business services, and maintenance departments.
- Support and successfully implement a risk-based approach to CQV.
- Drive updates to policies & procedures in line with current regulations and industry standards, continuously challenging and improving working practices and performance.
- Provide support and input for site projects and initiatives, ensuring that the CQV team is aligned.
- Manage changes aligned with business objectives and support the CQV Team through change to ensure positive outcomes.
- Troubleshoot technical issues to guarantee smooth operations.
- Contribute towards supporting Deviation, CAPA, Out Of Specification (OOS), and Out Of Trend (OOT) investigations.
Key requirements:
- BSc/MSc or equivalent experience in Mechanical Engineering, Chemical Engineering, Electronic/Electrical Engineering, Automation, Biological Sciences, or Chemistry.
- Be a technical Subject Matter Expert for at least one area of competency (CSE, Sterilisation, Gas Testing, Clean Room, Equipment Qualification).
- Proven knowledge of Regulatory and cGMP guidelines, contributing to quality records (Deviations, Investigations, CAPA, and Change Control).
- Proactively seeks to understand internal/external customer and market needs.
- Develops insights that can be used to improve customer happiness and other important measurements.
- Employs meticulous methods to track and analyse customer performance indicators for continuous improvement.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Senior Validation Specialist employer: Lonza
Contact Detail:
Lonza Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Validation Specialist
✨Tip Number 1
Familiarise yourself with the latest trends and regulations in the life sciences industry, particularly around CQV processes. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in a rapidly evolving field.
✨Tip Number 2
Network with professionals already working in validation roles or related fields. Attend industry conferences or webinars to connect with potential colleagues at Lonza, as personal connections can often lead to job opportunities.
✨Tip Number 3
Prepare to discuss specific examples of how you've successfully implemented risk-based approaches in previous roles. Highlighting your practical experience will set you apart as a candidate who can contribute immediately to the CQV team.
✨Tip Number 4
Showcase your ability to cultivate positive relationships across departments. Be ready to share instances where you've collaborated effectively with QA, Manufacturing, or Project Management, as this is crucial for the Senior Validation Specialist role.
We think you need these skills to ace Senior Validation Specialist
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the key responsibilities and requirements for the Senior Validation Specialist position. Tailor your application to highlight how your skills and experiences align with what Lonza is looking for.
Highlight Relevant Experience: In your CV and cover letter, emphasise your experience in Mechanical Engineering, Chemical Engineering, or related fields. Be specific about your technical expertise in areas like CSE, Sterilisation, or Equipment Qualification, as these are crucial for the role.
Showcase Problem-Solving Skills: Lonza values creativity in solving complex problems. Include examples in your application that demonstrate your ability to troubleshoot technical issues and implement innovative solutions within a validation lifecycle.
Emphasise Team Collaboration: The role involves cultivating positive relationships across various departments. Highlight your teamwork and communication skills in your application, providing examples of successful collaborations in past projects.
How to prepare for a job interview at Lonza
✨Understand the Role and Responsibilities
Make sure you have a clear understanding of the Senior Validation Specialist role. Familiarise yourself with the key responsibilities, such as working with the Head of Validation and supporting CQV processes. This will help you articulate how your skills and experiences align with what they are looking for.
✨Showcase Your Technical Expertise
As a technical Subject Matter Expert, be prepared to discuss your specific area of competency in detail. Highlight your knowledge of regulatory guidelines and how you've applied them in past roles. This will demonstrate your capability and confidence in handling the technical aspects of the job.
✨Emphasise Collaboration Skills
Lonza values positive relationships across various departments. Be ready to share examples of how you've successfully collaborated with QA, Manufacturing, and other teams in previous positions. This will show that you can work effectively in a team-oriented environment.
✨Prepare for Problem-Solving Scenarios
Expect to discuss how you've tackled technical issues or challenges in the past. Prepare specific examples that illustrate your problem-solving skills and your ability to drive improvements in processes. This will highlight your proactive approach and readiness to contribute to Lonza's mission.