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Known pharma brand and mid-level title but LIMS niche reduces candidate pool.
LIMS expertise and GxP/21 CFR Part 11 regulatory knowledge are highly industry-specific.
Explicit 5-10 years, mandatory LabWare/LIMS experience and GxP compliance makes filters stringent.
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Accountable for LIMS master data management and troubleshooting post-implementation across PPL sites.
Monitor ticket and SLA adherence, coordinate with business and LabWare for change requests and recurring issues.
Develop training modules and conduct sessions for laboratory personnel and new LIMS users, facilitating cross-site communication and process standardization.
Graduate or Post-Graduate in Science, B.Pharm, M.Pharm, or relevant technical qualification.
5-10 years of relevant experience in QC laboratory workflows and LIMS (preferably LabWare).
Hands-on experience with LabWare LIMS platforms and master data management; Admin-1 certification preferred.
Flexi shift covering support for India, US, and UK time zones.
Experience working with cross-functional teams in quality and IT environments supporting LIMS.
Strong knowledge of GxP, 21 CFR Part 11, and data integrity standards relevant to pharmaceutical QC environments.
Ability to lead continuous improvement initiatives within a LIMS Center of Excellence and promote cross-site best practices.