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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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
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
Hands-on experience in URS preparation,equipment qualification,SOP writing,and QMS . .
This includes completing the required coursework,projects,internships,and examinations and are verified through SCMs Student education verification: Verification of education documents of the passed-o
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