Senior Validation Engineer

2 weeks ago


Singapore No deviation Pte Ltd Full time

Responsibilities:

  • Responsible for planning, executing and closing out the validation activities within the assigned area.
  • Develop required validation documents, including Risk Assessments, plans, protocols, and reports.
  • Review, analyse, interpret and summarise data of executed studies.
  • Investigate or support the investigating of deviations or nonconformities raised during validation studies.
  • Provide SME input wherever required.
  • Ensure safety, quality and delivery of the validation projects.
  • Effectively collaborate with all identified stake holders. Wherever required, collaborate with Global/Corporate functions.
Required Experience & Knowledge

  • Minimum Bachelor's degree in science or engineering discipline
  • Minimum 5 years of experience in pharmaceutical CQV.
  • Indepth knowledge in the assigned area and of Validation Lifecycle approach (URS, FAT/SAT, commissioning, I/O/PQ Protocols, etc), guidelines, international regulatory requirements and other industry best practices.
  • Fluency in written and spoken English
  • Ability to work in a fast paced / dynamic work environment
  • A fast learner with "Cando" attitude
  • Good time management skill and great attention to detail.
  • Proficient presentation and facilitation skill is a plus.

EA License No: 19C9587

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