Deep understanding of PLCs (Siemens S7,Rockwell Logix),SCADA & Industrial Protocols (OPC UA,Modbus) . Education: BTech / BE in Instrumentation,Electronics,CS . Industry Benchmarks: Must have led at le
All Jobs : (1-9 out of 9)
Regulatory compliance: Ensure all work complies with Good Manufacturing Practices (GMP),ICH guidelines,and other relevant regulatory standardsExperience: 5 to 12 years
. 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
Educational Qualification: M Pharm from a reputed universityWork experience 2-3 years in a reputed pharmaceutical company /Medical Publishing house/KPOs catering to Pharmaceutical Company /CROPrefe
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
Employee : Overall responsibility of supply chain,warehouse & Logistics. Material requirement & planningPreferred candidate profile Having rich experience in Pharma (API) industry. .
Preferred candidate profile . M Sc in Chemistry/ M Pharm/ PhD in PharmacyExperience . 15-20 years of experience (~3 years in senior leadership
. API Production: Execute and oversee the manufacturing processes of active pharmaceutical ingredients,following approved batch records and standard operating procedures (SOPs)Technology Transfer and
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