Working in partnership with our clients, we deliver major projects and programmes with skill and precision, by focusing on outcomes and driving high performance. 

Delivering innovative solutions and exceptional outcomes across our sectors, we drive the success of our client’s projects and programmes through effective planning, highly skilled teams, and rigorous controls

Our capabilities include asset management, controls and performance, cost and commercial management, digital, procurement and supply chain, programme advisory, project management and sustainability. Backed by our extensive experience, we focus on outcomes to transform client’s projects and programmes.

With over 133 offices across 47 countries, we are an organisation of over GBP 1.5 billion turnover and 12,000+ talented team members across the world.  In 2025, we are combining with CBRE’s Project Management business to create the premier, differentiated programme, project, and cost management capability globally.  Through this change, our profile in Asia will scale significantly, comprising a team of over 4000 staff across all major countries in region.  The combination of our programme management and project management and commercial management capabilities will provide a unique opportunity to do things for our clients.

We are seeking highly skilled and experienced validation consultants. The ideal candidates will provide specialized knowledge and expertise in validation processes during project construction, commissioning, and operational phases, ensuring compliance with relevant standards and regulations. This role requires effective coordination and collaboration with various stakeholders to ensure all assignments are delivered on time and meet high-quality standards.

• Lead BMS validation work, including preparing and reviewing DER, TMX, IT CARA, and SER to ensure all URS/ES requirements are met.
• Support the review of BMS design, FAT protocol/report, and SAT protocol/report.
• Assist with BMS calibration.
• Lead FMS validation work, including preparing and reviewing DER, TMS, IT CARA, and SER to ensure all URS/ES requirements are met.
• Support the review of FMS design, FAT protocol/report, SAT protocol/report, and IOV protocol/report.
• Lead IQCF preparation.
• Assist with OVM/PVM.
• Support FMS calibration.
• Collaborate with QA, suppliers, and cross-functional teams to ensure smooth validation activities and compliance with regulatory standards.

• Bachelor or above in pharmaceutical sciences, engineering, or a related field.
• At least 15 years of experience in pharmaceutical validation and compliance.
• Preferred experience in multinational enterprises, overseas projects, and large-scale validations.
• Knowledge of cGMP, USP, EMA and other relevant regulatory requirements.
• Understanding of risk and science-based validation systems.
• Extensive BMS/FMS validation experience.
• Strong communication and interpersonal skills.
• Proven ability to work collaboratively with various teams and suppliers.
• Proficient in English.

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It is strictly against Turner & Townsend policy for candidates to pay any fee in relation to our recruitment process. No recruitment agency working with Turner & Townsend will ask candidates to pay a fee at any time. 

Any unsolicited resumes/CVs submitted through our website or to Turner & Townsend personal e-mail accounts, are considered property of Turner & Townsend and are not subject to payment of agency fees. In order to be an authorised Recruitment Agency/Search Firm for Turner & Townsend, there must be a formal written agreement in place and the agency must be invited, by the Recruitment Team, to submit candidates for review.