. Bachelors or Masters degree in IT,Engineering,or a related. field. Proven domain experience in the Pharmaceutical or regulated Manufacturing industry is preferred. . Certifications such as PMP,Pg
All Jobs : (1-7 out of 7)
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
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
*Pharma Exp is mandatory . * Required previous Law Firm Exp as well Qualifications & Skills: . Bachelors degree in Law (LL.B.)8 years of experience in corporate legal roles,preferably within the phar
Employee : Overall responsibility of supply chain,warehouse & Logistics. Material requirement & planningPreferred candidate profile Having rich experience in Pharma (API) industry. .
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