Line clearance for production operations.
Review of BMR, BFR, BPR.
In - process QA functions.
Control sample management.
Collection of In process / Finished product and customer samples.
Compilation of APQR data with trend analysis.
Participation in process validation, hold time studies etc.
Co-ordination for batch release.
Routine GMP verification in production and warehouse, production and all other departments.
Co-ordination and review of vendor management documents, compilation of vendor assessment reports.
Document Archival management as on when required.
Issuance and control Formats, SOPs, Specifications and Batch Records.
In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth.
Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices.
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