Executive

**Title**:Executive**: - Date: May 14, 2024- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd**JD - GPNT/ TT- EXECUTIVE** - Monitor and compile data related of process Scale up studies in Lab/ Pilot plant to establish a robust process parameter for tech transfer & scale-up activity. - Map the right equipment for scale up and provide...

**JD - GPNT/ TT- EXECUTIVE** - Monitor and compile data related of process Scale up studies in Lab/ Pilot plant to establish a robust process parameter for tech transfer & scale-up activity. - Map the right equipment for scale up and provide support in the execution of scale up batches. - Map the equipment’s based on the volume calculations from Kilo lab...

**Title**:Executive**: - Date: Jan 25, 2024- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd- Expertise in downstream process development of large molecules recombinant protein and monoclonal antibodies. - Proficient in handling of chromatographic systems. - Should be conversant with interpretation of analytical and process data. -...

**Title**:Executive**: - Date: Mar 23, 2023- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries LtdExperience in Analytical Method Development and Characterisation using HPLC, GC, LCMS, GCMS, NMR, DSC, TGA, Raman Spectroscopy and XRD in drug substance and drug products. Experience in analytical method validations in GMP environment. Good...

**Title**:Executive**: - Date: Apr 16, 2024- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd- Regulatory submission/publishing activities for eCTD global submission dossiers according to Agency and ICH Guidance requirements. (US and other advanced markets). - Electronic Document Publishing (i.e. PDF file preparation as per eCTD...

**Title**:Executive**: - Date: Mar 20, 2024- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries LtdTo provide the value addition (technically) throughout the development process and to achieve successful on time filing. 2. To have strong execution skills and to interact cross functionally and ensure timely submission and approval of the...

**Title**:Executive**: - Date: Apr 15, 2024- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd- Review all data and documents related to product registrations for various health authorities. - Compile registration dossiers for submission to various health authorities like -** USA, **Canada, Europe, Australia and Israel. - Prepare...

**Title**:Executive**: - Date: Aug 11, 2023- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd**Primary Responsibilities**: - Analytical Method development for API/NCE sample. - Analysis of raw material, Intermediate, API/NCE samples on gas chromatography, liquid chromatography and chemical analysis. - Method validation for API/NCE...

This position is responsible for Sales and Business development across international markets. - Rich exposure of working in multi geographical regulated markets especially emerging markets. - End to End Execution, strategic and analytical thinking ability - Knowledge of business and management principles (budgeting, strategic planning, resource allocation,...

To provide the value addition (technically) throughout the development process and to achieve successful on time filing. 2. To have strong execution skills and to interact cross functionally and ensure timely submission and approval of the assigned projects as per agreed work plan. 3. To navigate the project technically and provide feasible technical...

**Title**:Executive**: - Date: Mar 20, 2024- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd- Experience in Formulation R&D product development with experience in Injectable product development in Novel drug delivery systems/ Lyophilized product/ Solution product. - To do literature search like Summary based approval (SBA), Patent...

**Title**:Executive**: - Date: May 14, 2024- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd**GLP Bioanalytical** To Access Study Plan and Standard Operating Procedures and to comply with instructions given in Study Plan and Standard Operating Procedures. To record raw data promptly and accurately and in compliance with the...

**Title**:Executive**: - Date: Mar 20, 2024- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd**GLP Bioanalytical** To Access Study Plan and Standard Operating Procedures and to comply with instructions given in Study Plan and Standard Operating Procedures. To record raw data promptly and accurately and in compliance with the...

**Title**:Executive (G12A)**: - Date: Oct 30, 2023- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd- List of Responsibilities / Job Functions: - To verify whether code creation request is initiated in compliance of Global SOP / Site SOP. - To evaluate the new code creation scenario against the Rule book referred in Global SOP / Site...

Review all data and documents related to product registrations for various health authorities. - Compile registration dossiers for submission to various health authorities like -** USA, **Canada, Europe, Australia and Israel. - Prepare responses to deficiency letters received from various agencies. - Maintain life-cycle / post approval changes for drug...

Regulatory submission/publishing activities for eCTD global submission dossiers according to Agency and ICH Guidance requirements. (US and other advanced markets). - Electronic Document Publishing (i.e. PDF file preparation as per eCTD requirement, bookmarking/linking, compilation/publishing in software) - Regulatory maintenance activities Skills/Knowledge...

**GLP Bioanalytical** To Access Study Plan and Standard Operating Procedures and to comply with instructions given in Study Plan and Standard Operating Procedures. To record raw data promptly and accurately and in compliance with the Principles of Good Laboratory Practice, review of raw data and are responsible for the quality of their data. Operation...

**GLP Bioanalytical** To Access Study Plan and Standard Operating Procedures and to comply with instructions given in Study Plan and Standard Operating Procedures. To record raw data promptly and accurately and in compliance with the Principles of Good Laboratory Practice, review of raw data and are responsible for the quality of their data. Operation...

Expertise in downstream process development of large molecules recombinant protein and monoclonal antibodies. - Proficient in handling of chromatographic systems. - Should be conversant with interpretation of analytical and process data. - Should be proficient in writing document such as BMR, SOPs, Investigational reports etc

Experience in Analytical Method Development and Characterisation using HPLC, GC, LCMS, GCMS, NMR, DSC, TGA, Raman Spectroscopy and XRD in drug substance and drug products. Experience in analytical method validations in GMP environment. Good knowledge of different guidelines and regulatory requirements, versed in different protocol and report preparations