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Research Associate - Documentation
Greetings from Macleods Pharma
Role: Research Associate - Documentation
Qualification: M.Sc. / M.Pharm
Exp: 2-4 years
Location: Mumbai - Andheri
Job Description:
- Preparation of analytical specifications and protocols for API, Intermediate, IPQC and raw materials.
- Preparation of Certificate of Analysis and Result of Analysis
- Documentation for standard qualification and its characterization.
- Maintaining standards and its records
- Resolving queries from Plant and Regulatory Affairs regarding documentation.
Preparation of SOPs
Role: Research Associate - Documentation
Qualification: M.Sc. / M.Pharm
Exp: 2-4 years
Location: Mumbai - Andheri
Job Description:
- Preparation of analytical specifications and protocols for API, Intermediate, IPQC and raw materials.
- Preparation of Certificate of Analysis and Result of Analysis
- Documentation for standard qualification and its characterization.
- Maintaining standards and its records
- Resolving queries from Plant and Regulatory Affairs regarding documentation.
Preparation of SOPs
- Knowledge of analysis on HPLC, GC & Pharmacopoeia such as USP/EP/BP/IP
monograph
- Other documentation
Role: Research Associate
- GC
Qualification: M.Pharm / M.Sc
Experience: 02 - 06 Years
Location: Mumbai Andheri
Job Description:
- Method Development of Residual Solvent of given drug product.
- Gas Sample Analysis by Gas Chromatography
- Excipient Sample Analysis by Gas Chromatography.
- Analysis of stability batches as per ICH guidelines by Gas Chromatography..
- Analysis of in process, routine product as per specification by Gas Chromatography..
- Handle & operate the instrument as per standard operating procedure.
- Calibration of instrument such as GC.
- Reporting and documentation of results as per SOP.
- Preparation of Protocol and Report for Method Validation and Method
Development.
- Trouble Shooting for given development
- Solving Plant Issues or any Query.
Kindly share your updated CV: mayurim@macleodspharma.com
- Gas Sample Analysis by Gas Chromatography
- Excipient Sample Analysis by Gas Chromatography.
- Analysis of stability batches as per ICH guidelines by Gas Chromatography..
- Analysis of in process, routine product as per specification by Gas Chromatography..
- Handle & operate the instrument as per standard operating procedure.
- Calibration of instrument such as GC.
- Reporting and documentation of results as per SOP.
- Preparation of Protocol and Report for Method Validation and Method
Development.
- Trouble Shooting for given development
- Solving Plant Issues or any Query.
Kindly share your updated CV: mayurim@macleodspharma.com
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