Regulatory compliance: Ensure all work complies with Good Manufacturing Practices (GMP),ICH guidelines,and other relevant regulatory standardsExperience: 5 to 12 years
All Jobs : (1-8 out of 8)
. To prepare Master documents of Analytical Method Development / Analytical reports for submission & validation batches. . Material Master creation of Material code/ Vendor code in ERP of MIC creati
Work in shifts Perform line clearance,cleaning,and batch documentationRelevant OSD pharma experience in the applied roleMonobloc experience mandatory for Liquid Filling role. WhatsApp CV: 9650111639
Qualification:- Bachelors degree or higher in Computer Science,Information Technology or related field. :- Must possess basic knowledge about server and client architecture setup (preferably from Pha
To prepare Master documents of MFC / MFR / BMR / BPR /PVP / Development reports for submission & validation batches. . Material Master creation of Material code/ Vendor code in ERP. . MIC creation o
To prepare Master documents of MFC / MFR / BMR / BPR /PVP / Development reports for submission & validation batches. . Material Master creation of Material code/ Vendor code in ERP. . MIC creation o
Minimum Education Requirement . ITI / Diploma engineering/ BSc in mechanical branch Adhere to required standards during all maintenance activities to ensure safety,operation & complianceEducational an
Employee : Overall responsibility of supply chain,warehouse & Logistics. Material requirement & planningPreferred candidate profile Having rich experience in Pharma (API) industry. .
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