Regulatory compliance: Ensure all work complies with Good Manufacturing Practices (GMP),ICH guidelines,and other relevant regulatory standardsExperience: 5 to 12 years
All Jobs : (1-7 out of 7)
. 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
Candidate should address scientific queries received from sales / marketing/doctors with sound scientific back-up Candidate should be from well recognized Reputed Govt InstituteShould be proficient in
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
Employee : Overall responsibility of supply chain,warehouse & Logistics. Material requirement & planningPreferred candidate profile Having rich experience in Pharma (API) industry. .
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