Education: MSc / B Pharma + IT Certification. Industry Benchmarks: Experience in USFDA approved plants Experience & Education . Experience: 15+ Years specialized in Pharma R&D Quality IT
All Jobs : (1-20 out of 35)
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
Recommend and coordinate external development and manufacturing partners (CMO / CDMO) where requiredMinimum Education Requirement Educational and Experience Requirements . Utilize portfolio experience
Education: BTech / BE in Instrumentation,Electronics,CS . Industry Benchmarks: Must have led at least one end-to-end implementation of an MES (Werum,Rockwell,or similar) or a plant-wide Data Historian
Experience & Education . Bachelors or Master s degree in IT,Engineering,or a related. field. Proven domain experience in the Pharmaceutical or regulated Manufacturing industry is preferred. . Certif
Key Skills: Proficiency in requirements gathering tools (e.g.,Jira,Azure DevOps),strong understanding of process mapping tools,and working knowledge of GxP / CSV documentation standards. Education: BT
Qualification:- B Pharma Proficient in MS Office and quality management software. Minimum of 3-5 years of experience in IPQA within the pharmaceutical industry,preferably in API manufacturing. Experie
Employee : Overall responsibility of supply chain,warehouse & Logistics. Material requirement & planningPreferred candidate profile Having rich experience in Pharma (API) industry. .
Job Title: Sr. Executive / Assistant Manager Warehouse (Greenfield Project) Location: Roorkee Industry: Pharmaceuticals OSD Experience: 510 YearsJob Description:Walter Bushnell Pharmaceuticals is h
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
Job Description of AM ProductionKey Responsibilities1. Greenfield Project & Equipment Readiness Provide production user inputs for URS preparation of manufacturing equipment,utilities, and production
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
Work in shifts Perform line clearance,cleaning,and batch documentationRelevant OSD pharma experience in the applied roleMonobloc experience mandatory for Liquid Filling role. WhatsApp CV: 9650111639
Educational Qualification: M Pharm from a reputed universityWork experience 2-3 years in a reputed pharmaceutical company /Medical Publishing house/KPOs catering to Pharmaceutical Company /CROPrefe
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
from Pharma Background only. Preferred candidate profile
Graduate in any discipline .Experience of having worked any Trading / Pharmaceutical / FMCG CompanyThose who have worked in similar capacity in a Depot,Branch,CFA ( preferably) Distributor of FMCG,PHA
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