6 to12 Years
1,50,000 - 2,00,000 Per Month
Minimum 8 years of experience in Computer System Validation within the
pharmaceutical/life sciences industry.
Proven experience in handling global implementation/rollout projects.
Strong knowledge of GxP, FDA 21 CFR Part 11, GAMP 5, Annex 11, and
other relevant regulatory guidelines.
Experience with validated systems such as SAP, LIMS, MES, QMS (e.g.,
TrackWise) is highly desirable.
Excellent documentation, analytical, and communication skills.
Experience with risk-based validation approaches and ALCOA+ data
integrity principles.
Ability to manage multiple validation projects and lead cross-functional teams.
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