Senior Validation Engineer - Equipment and P

Job Type
Emp Type
Full Time
Functional Expertise
Countries, Regions
Salary Type

Job Description

Senior Validation Engineer – Process & Equipment Validation – Singapore – 18 Month Contract  

Start Date:   September / October 23  
Contract Duration 12 Month + 6 Month contract + Extensions 
Working week:    40 Hours / Week (Mon-Fri) OT maybe required dependent on operational requirement. 50+ Hour weeks during shutdown phases 
Offer:  Paid based on a competitive hourly rate: Estimated $130,000 - $140,000 (Estimates based on 40 hrs / week X 46 Weeks Work + Paid Annual Leave and Public Holidays)  

The Company 

A multinational pharmaceutical and nutrition manufacturer with state-of-the-art production facilities in Tuas. 

The Project

Supporting the validation relating to the installation and commissioning of new processing equipment relating to an evaporator plant. This is a new facility on the client existing production site.

Key Responsibilities 

•    Participates in the validation planning and supports the execution of medium- to large-size projects, requiring custom, risk-managed execution plans, investigations, and/or troubleshooting and meets deadlines. 
•    Designs and advises on testing strategies and engineering studies, often with multiple variables, and performs detailed analysis. Assesses relevance.
•    Coordinates with technical support personnel to conduct experimental qualification runs and engineering studies.
•    Directs the efforts of others such as technicians and outside resources.
•    Executes validation protocols. Influences validation strategy

Candidate Requirements 

•    Bachelor’s degree in engineering discipline (Chemical / Mechanical or similar) 
•    Min 6 years of related experience in Validation in a manufacturing plant, preferably in Pharma/Nutrition/Food industry
•    Right to live and work in Singapore (Singaporean or Permanent residents) 
•    Experienced in protocol writing and execution, closure of validation activities and validation strategy. 
•    Experience in process and equipment validation. 
•    Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP)
•    Experience in implementation validation master plans 
•    Experience in drafting of protocols and execution of validation activities. 
•    Knowledge of problem-solving tools (e.g. 6M Analysis, Fishbone, 5 Whys etc)


Tim Millington