. 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
All Jobs : (1-11 out of 11)
Preparation and approval of URS (User Requirement Specifications) for production equipment and systems. Experience: 3 10 Years (depending on level)
6 10 years of experience in QC Pharma (OSD preferred) Experience: 7-12 Years
. API Production: Execute and oversee the manufacturing processes of active pharmaceutical ingredients,following approved batch records and standard operating procedures (SOPs)Technology Transfer and
Job Title: Mid-Level Legal Manager Location: Gurugram . *Pharma Exp is mandatory . * Required previous Law Firm Exp as well Qualifications & Skills: . Bachelors degree in Law (LL.B.)
Knowledge of scale-up processes,and familiarity with Good Manufacturing Practices (GMP) and ICH-guideline. . Hands-on experience with bench-scale and pilot-scale synthesis is essential. Preferred ca
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
Knowledge of regulatory expectations for APIs and CMC documentation preferredExperience: . 1 to 3 years (Research Associate Entry level) . Strong hands-on experience in peptide API process developme
Greenfield project experience preferred (lab setup,equipment qualification,method validation / transfer) Experience: 4 6 Years4 6 years of QC experience in a pharma OSD facility
Ideal Candidate Profile: . 6-10 years of relevant experience in pharma project managementExperience in tech transfer will be an added advantage
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