Principal Engineer, Design Validation

You will collaborate closely with a diverse team, allowing you to gain exposure to various areas of our organisation. This unique aspect of the role offers exceptional prospects for career progression within our world-class company.

This role is Monday-Friday with the flexibility to work 08:00-16:00/08:30-16:30/09:00-17:00.

We offer a competitive salary and some fantastic benefits listed below.

• 25 days annual leave + bank holidays
• Subsided canteen
• Excellent career progression opportunities
• Blue light card
• Employee discount scheme
• Westfield healthcare
• Up to 8% pension contribution
• Employee assistance programme

Duties & Responsibilities

• Ensure Site Validation Master Plan (SVMP) is strictly adhered to and that all validation activities are conducted in accordance with established protocols and procedures by executing validation work and a variety of equipment. (Sometimes to support the operational status of the facilities there may be a small amount of weekend work)
• Develop and implement validation documents and protocols for a variety of processes, equipment, facilities, and systems, with a particular emphasis on aseptic manufacturing.
• Work closely with the validation team and teams from various departments to assist with the implementation of new processes, products, and equipment at the site. This involves developing detailed documentation, including Validation Plans (VP), User Requirement Specifications (URS), Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
• Actively participate in the assessment, review, and approval of changes that may impact the validation status of our facilities, equipment, processes, and systems. This involves ensuring the correct operation of our change control process.
• Conduct thorough reviews of validation execution and equipment changes carried out by external contractors and internal project team members to ensure compliance with validation requirements.
• Take ownership of project management and execution for Capital Expenditure and Process Improvement Projects within the EMEA Validation project portfolio.
• Work with Quality Assurance to react to adhoc validation requirements.

What experience are we looking for?

• You will have a Scientific/Engineering Degree or equivalent qualification or the right experience within a validation role.
• You will be able to demonstrate working knowledge of validation in a pharmaceutical/FMCG/medical devices environment preferably.
• Approach tasks with a logical and practical perspective, and have a proactive approach to problem-solving.
• Display analytical thinking and innovative problem-solving abilities to successfully implement validation strategies.
• Self-motivated and driven to complete projects/tasks efficiently and effectively.
• Excellent teamwork skills to contribute effectively as a member of a diverse team and effectively communicate with individuals involved in the project.

What happens next?

Please apply via workday with your up to date CV and a member of Talent Acquisition will be in touch within 2 weeks.