6 10 years of experience in QC Pharma (OSD preferred) Experience: 610 Years
All Jobs : (1-13 out of 13)
Preparation and approval of URS (User Requirement Specifications) for production equipment and systems. Experience: 3 10 Years (depending on level)
and prepare reports. . Support regulatory department for product documentation,filing,etc. . Should have knowledge about SAPExperience: 10- 14 years (Apart from the QA functions,working on new proje
Qualifications: . BE / B Tech or ME / M Tech in Chemical Engineering Professional certification in process engineering or related areasProficiency in process analysis,process modelling and simulation
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
. API Production: Execute and oversee the manufacturing processes of active pharmaceutical ingredients,following approved batch records and standard operating procedures (SOPs)Technology Transfer and
Proficient in data analysis,interpretation,and documentation3 8 years of relevant experience in a pharmaceutical R&D or CRO environment
Provide administrative assistance to the schools management team and faculty as requiredTechnical Skills: Proficient in Microsoft Office Suite (Word,Excel,PowerPoint) and office management softwareExp
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
Experience Required: 3 to 6 years of hands-on experience in formulation IPR. . Qualification: M Pharm (Pharmaceutics / Pharmaceutical Chemistry or equivalent). Company name: Walter Bushnell. Work Loc
Walter Bushnell Pharmaceuticals is hiring a Senior Research Associate Analytical R&D for its OSD formulation facility in Roorkee.The ideal candidate should have hands-on experience in Analytical Metho
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