Validation Engineer
6 days ago
As a key member of our team, you will play a critical role in driving world-class manufacturing within the bio-pharmaceutical industry. Your expertise will be essential in identifying opportunities for improvement and collaborating across production and business units to ensure the effectiveness and efficiency of our manufactured products.
Key Responsibilities:- Verification Planning: Lead the planning of verification activities for systems and equipment.
- Validation Life Cycle Management: Manage the validation life cycle for all projects.
- Test Planning and Execution: Create detailed test plans, execute testing activities, analyze results, and compile documentation and reports.
- Collaboration and Communication: Work closely with Engineering and Quality departments to ensure test methods, equipment, and materials are available in line with company timelines.
- Data Analysis and Interpretation: Analyze and interpret data with precision and contribute to design reviews and collaborative discussions.
- Timeline Management: Work with planning and operations to schedule validation timelines to ensure business requirements are met.
Requirements:
- Proven experience as a Validation Engineer, ideally in the pharmaceutical, Medical Devices, or biotechnology industry.
- Qualification in Engineering or a related technical field and/or qualified by experience.
- Excellent technical writing and communication skills.
- Training or experience in GAMP5.
- Any experience with Injection Molding and Automation is advantageous, although not essential.
About Spirax-Sarco Engineering:
We are a FTSE 50 company, comprising ten established brands, each with their area of expertise. Together, we offer our customers unrivalled solutions for their pumping and fluid transfer applications. Our company values efficiency and sustainability, and we strive to be a leader in our industry.
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