Oversee preparation,review,and alignment of technical documents including PDRs,AMVs,validation protocols,batch records,and regulatory filing modulesMinimum Education Requirement . Masters degree in Ph
All Jobs : (1-11 out of 11)
Recommend and coordinate external development and manufacturing partners (CMO / CDMO) where requiredMinimum Education Requirement Educational and Experience Requirements . Utilize portfolio experience
Employee : Overall responsibility of supply chain,warehouse & Logistics. Material requirement & planningPreferred candidate profile Having rich experience in Pharma (API) industry. .
Education Qualifications Required: . Graduate/ Masters degree in Human Resources Management or a relevant degree with a professional HR qualification
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
. 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
Regulatory compliance: Ensure all work complies with Good Manufacturing Practices (GMP),ICH guidelines,and other relevant regulatory standardsExperience: 5 to 12 years
- Graduate Freshers can Also Apply
Candidates only from Pharma company would be given preference Should have minimum of 2+ years experience in Pharma companyMust be proactive,self-driven,and energeticMust be a quick thinker,Extrovert,t
Preference: Candidate must be from Pharma Industry Must be proactive,self-driven and energetic Must be a quick thinker,Extrovert,team player,enthusiastic,active listener,learning attitude Qualificatio
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