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Validation Lead

Novartis
hybrid
Tuas South Avenue, Singapore Posted Aug 19, 2026

About this role

Validation Lead

Summary This role will be responsible for executing and managing process, shipping, and cleaning validation activities (and ongoing/continuous in the aforementioned areas) and associated change management activities to meet cGMP requirements on time without compromise to quality ensuring site validation programs are compliant with global regulatory expectations.

About the Role

Major accountabilities:

  • Support site validation planning by writing and maintaining master plans for process, cleaning, shipping processes and ongoing verification activities (as applicable).
  • Support process validation lifecycle activities by ensuring a state of control is maintained through ongoing process verification (OPV). Ensure that appropriate variables are identified for on-going monitoring as a contributor to quality risk management activities.

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