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Urgent Requirement – Nootan Pharmaceuticals
(WHO–GMP Certified Plant, Baddi, HP)
We are expanding our team and looking for passionate professionals in the Cephalosporin – All Formulations segment:
QA – QMS
▪️ Exp: 7–10 years
▪️ regulatory compliance, audits & QMS improvement.
QA – Documentation
▪️ Exp: 3–6 years
▪️ Review & control of SOPs, BMR, validation, change control, deviation & CAPA.
QA – Stability
▪️ Exp: 3–6 years
▪️ Manage stability studies, protocols, reports & ICH compliance.
QC Executive (GLP & Analysis)
▪️ Exp: 4–8 years
▪️ Perform analysis of RM, intermediates & FPP as per GLP.
QA Executive
▪️ Exp: 4–8 years
▪️ IPQA, compliance checks, batch record review & audit readiness.
Microbiology Officer
▪️ Exp: 2–4 years
▪️ Micro analysis, environmental monitoring & sterility testing.
Location: Baddi, Himachal Pradesh
Plant Type: Cephalosporin – All Formulations
📧 Send CVs to: hrd1@nootanpharma.com
Join a growing team driven by Quality, Compliance & Career Growth!
