Website Asset Recruitment

Asset Recruitment


Validation Engineer

The successful candidate will need to have demonstrated experience in one or more of these areas –
(1) Sterilisation – Autoclaves, SIP of vessels
(2) Cleaning – Parts Washer and CIP of vessels
(3) Vial and Syringe filling operations –Glass handling, Tray & Tub handling, Drug Product Filling and Parenteral Product Visual Inspection.
(4) Vial and Syringe Sterility operations – Isolators, VHP, E-Beam and Depyrogenation systems.

Each role will be involved in the project from the vendor Factory Acceptance Test (FAT), at the earliest, through to the Performance Qualification. Levels of responsibility will vary during this timeframe as outlined below –

• Factory Acceptance Test – Attendance, hands-on support and C&Q Oversight
• Installation to Mechanically Complete – C&Q Oversight
• Commissioning & Qualification – Hands-on support & Oversight throughout project lifecycle
• Cycle Development – Execution of Cycle Development pre and post OQ phases
• Performance Qualification – Responsibility for / Execution of all Performance Qualification testing.

Within your chosen role you will be acting as a senior engineer reporting within the Technical Engineering department, the role will include –

• Engage in the early stages of the project, giving input into design by working with equipment vendors and global engineering teams, attending FAT and design reviews to represent client validation interests. Oversee equipment C&Q within the assigned area with a view to ensuring right first-time C&Q and Validation effort.
• Act as validation SME on the equipment within the area assigned. As such you will be leveraging testing from

Commissioning and Qualification.
• Providing technical and validation oversight to process, design and project delivery teams and coaching to associate staff within the assigned suite.
• Implementing the requirements as outlined in the site / project Validation Master Plan.
• Coordination of engineering sub-teams in the assigned suite during execution of Cycle Development & Validation activities.
• Authoring and reviewing standard operating procedures and technical reports including PQ protocols.
• Technical review and approval of Commissioning protocols, Qualification protocols and Validation protocols executed by vendors, cross functional groups and/ or validation counterparts.
• Supporting regulatory submissions as required.
• Owning Change Management process for Equipment introduction within the assigned suite for qualification / validation up to PQ stage.
• Effective application of LeanSixSigma and Change Management tools in the Validation group

• Bachelor’s degree in Engineering, Computer Science or equivalent
• Minimum of 5 years directly related experience in academia, pharmaceutical or biotechnology industry – along with a working knowledge of current regulatory requirements and current Good Manufacturing Practices.
• Minimum 3 years process equipment C&Q/ Validation experience on Large Scale Projects
• SME on Equipment Validation on any of; CIP & Parts Washer / SIP / Autoclaves / DHT & Electron Beam sterilisation / Vaporised Hydrogen Peroxide Sterilising Isolators / Clean Utilities Transfer Panels & Formulation Vessels
• Working knowledge of ASTM E2500 / Eudralex / FDA / ISPE guidelines
• Experience with liaising with other departments – engineering, technical, operations and QA
• Experience with sterile processing and sterilisation technologies
• Experience with cleaning and process validation, technology transfer, regulatory filing, and commercial drug product manufacturing of biologics is a plus.
• Prior experience in drug product processing equipment, PQ, Process Performance Qualification and Validation, site readiness, batch record reviews, authoring documents subject to regulatory inspection.
• SIP and CIP subject matter extensive experience
• Autoclave Qualification and Sterilisation Loads Cycle Development experience
• Use of temperature mapping equipment such as Lives/ Kaye etc. and trending, analysing and interpreting complex data
• Warehouse and CTU qualification


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