Date: Aug 30, 2023 Location: Airoli, IN Company: Lupin Brief JD -
Collaborate with leadership from Production, Quality, Engineering, Subject Matter Experts (SMEs) for effective and successful application implementation in defined timelines.
Experience in facing regulatory inspections like USFDA, MHRA, EMA etc.
Excellent skills of resource handling and people management
Good understanding on handling of GxP Applications/software implementation
IPC/HMI/Scada based System.
PC based systems in manufacturing and quality domain
QMS system like caliber, Track-wise. etc
LIMS (Laboratory Information Management Systems
C-DAS (Central Data acquisition systems)
Chromeleon
Good understanding of Enterprise & site-specific software new implementations & upgrades.
Good understanding on handling of IT infrastructure/tools
Network components
Servers/database
Operating systems
Security tools
Harmonization and Implementation of best-in-class practices & procedure to improve IT efficiency and compliance.
Management of application vendors, implementation partners and other support teams.
Stakeholder and Conflict management.
IT Compliance Handling:
Knowledge of CSV as per GAMP, 21 CFR Part 11, EU Annexure-11 and compliance practices.
Excellent skills in investigation report & SOP writing
Good understanding of QC and manufacturing systems in line with Data integrity aspect.
Ensure IT application activities are executed according to regulatory compliance standards and IT security norms.
Excellent Understanding on IT related change control, CAPA, deviations and incident etc.
Good Skills to deliver training across the IT domain.
Participating in periodical SOP reviews and facilitating for various internal/External audits.
Budget management and cost monitoring.
Any additional responsibilities as assigned
Experience - 15+ Years in Pharma IT Qualification - B.E / B.Tech
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