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Niche LabWare LIMS expertise and regulated pharma domain reduce applicant density.
Requires regulated LIMS and pharma quality experience, limiting cross-industry transferability.
Mandatory 5–10 years, LabWare LIMS experience and regulatory knowledge make filters strict.
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Own master data management and troubleshooting support for LabWare LIMS across multiple Piramal Pharma Solutions sites.
Monitor ticket queues and SLA adherence post LIMS go-live, coordinating with internal and external stakeholders to resolve issues and implement change requests.
Develop training materials and lead sessions for laboratory personnel on LIMS usage, while promoting cross-site standardization and continuous improvement in LIMS processes.
Graduate or Post-Graduate degree in Science, B. Pharm, M. Pharm, or relevant technical qualification.
5-10 years of relevant experience with QC laboratory workflows and LIMS, preferably LabWare.
Hands-on experience in LabWare LIMS master data management and troubleshooting, knowledge of GxP, 21 CFR Part 11, and data integrity standards.
Willingness to work flexi shifts to support India, US, UK time zones.
Experienced with LabWare LIMS administration including workflows and templates, ideally certified Admin-1 in LabWare.
Able to coordinate across multiple sites and functions including Quality, IT, and external OEMs, ensuring standardization and shared best practices.
Strong analytical and troubleshooting capability to resolve system issues and drive continuous process improvements within a Center of Excellence environment.