Problem solving,Eye for details,should be flexible to work in pressure . Ensure that all administrative duties,checks,documentation,reports and returns (internal and external) are completed accurately
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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
Proficient in data analysis,interpretation,and documentation3 8 years of relevant experience in a pharmaceutical R&D or CRO environment
Key ResponsibilitiesAudit Planning and ExecutionDevelop and implement a risk-based annual audit plan in collaboration with the Head of Internal Audit.Lead and manage internal audit projects, ensuring
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
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
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