Executive

**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...

**Department: F R&D (Non-oral), SPIL, Baroda** **Position: Executive (Replacement of Mr Ankit Soni)** **Requirements**: - M. Pharm in Pharmaceutics from renowned institute (Good Score in GPAT). - Good Academic Career **Responsibilities**: - Design, conduct and verify/review experiments to develop a robust formulation. - Literature search, patent search,...

Job Responsibilities: - Responsible to take training before execution of allotted work - Responsible to perform routine in-process sample analysis - Responsible to perform Method Development and Method Validation of various finished products - Responsible to prepare STPs, SOPs, Method Development Report, Method Validation Protocol and Report, Study Protocol...

**Job Description - Position - Executive** **Department: FRD-Orals** - Literature search, product understanding, data interpretation for product to be undertaken for development. - Design of primary product strategy, preparation of product strategy for discussion with group leader/team leader. - Planning and execution of product development work to achieve...

Literature search, product understanding, data interpretation for product to be undertaken for development. - Design of primary product strategy, preparation of product strategy for discussion with group leader/team leader. - Planning and execution of product development work to achieve desired product profile and data compilation - Scheduling the work plan...

**Title**:Executive**: - Date: Sep 11, 2024- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd1) Review all data and documents related to product registrations for various health authorities 2) Compile registration dossiers for submission to various health authorities like - US, Canada, Europe, Australia & China 3) Prepare responses to...

Literature search, product understanding, data interpretation for product to be undertaken for development. - Initiation of documents required for product development/movement like T-License, Import License for drug substance as well as reference product and bioequivalence study request. - Design of primary product strategy, preparation of product strategy...

**Title**:Executive**: - Date: Sep 10, 2024- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd**Position**: Exe / Sr. Exe (Regulatory Affairs, Baroda) **Grade **- G12A/G11B **Education** - B.Pharm / M. Pharm **Experience** - 4 to 6 years **Location** - R&D - Baroda - Review all data and documents related to product registrations for...

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,...

**Job Summary** Executive HR with passion for Hiring and having learning attitude. Understanding of pulse of the business and drive for the results. **Areas Of Responsibility** **Talent Acquisition** - Manage End to End Talent Acquisition for specific department. - Maintaining TAT of 85 days or below. - Keep the manpower fill ratio at 95%+ throughout the...

**Title**:EXECUTIVE**: - Date: Sep 3, 2024- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd**Position**: Exe / Sr. Exe (Regulatory Affairs, Baroda) **Grade **- G12A/G11B **Education** - B.Pharm / M. Pharm **Experience** - 4 to 6 years **Location** - R&D - Baroda - Review all data and documents related to product registrations for...

**Position **:Executive/Sr. Executive - Formulation Development (Orals) **Exp** : 2 to 5 years **Education** : M.Pharm **Job Summary** - As a Product Robustness Review and Compliance Team member, work profile would be product robustness assessment, review of technical documents for all markets, harmonization related activities, compliance related...

Proficiency in English - Assist managers and executives with their daily tasks - Coordinate and organize meetings, including agenda preparation and minute-taking - Manage incoming phone calls, providing information or routing to relevant individuals - Schedule appointments and maintain an updated calendar for effective time management - Develop spreadsheets...

**JOB DESCRIPTION**: **Job Title** G11 **Grade** G11 **Location Tandalja, Vadodara **Division** R&D-I **Department **Innovative Projects-Pharmacology **Reports to** Dhiren Joshi/Dr. Vinod Burade **Direct Reportees **No** **1. JOB PURPOSE/OBJECTIVE (2-3 lines on why does the job exist)** 1. For new NCE project (GLP-1 and Mito-Esc) 2. To manage...

**Responsibilities**: - To have thorough knowledge and understanding of QC workflows (Analysis/ Review/ Approve/ Investigation etc.), Analytical methods (Instrumental/ Pharmacopoeial chapters/ Monographs), QC instrumentation activities (operation, calibration, preventive maintenance etc.) and Analytical method validation/Method transfer activities and other...

**Key role**: Development of multiplex based cytokine release assay and Elispot/ flow cytometry based T cell assays to measure the innate and adaptive Immunogenicity of synthetic peptide products. **Responsibilities**: - Responsible for study sample analysis for all pipeline products. - Isolation of PBMC from whole blood and maintenance of commercial cell...

1) Review all data and documents related to product registrations for various health authorities 2) Compile registration dossiers for submission to various health authorities like - US, Canada, Europe, Australia & China 3) Prepare responses to deficiency letters received from various agencies. 4) Maintain life-cycle / post approval changes for drug...

**Key Responsibilities**: - Responsible for analytical method qualification for all pipeline products. - Characterization of innovator product batches sourced from different geographical region and preparation of quality target profile. - Analytical similarity assessment of in-house products. - Preparation and review of method development reports (MDR) and...

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...

**Position**: Exe / Sr. Exe (Regulatory Affairs, Baroda) **Grade **- G12A/G11B **Education** - B.Pharm / M. Pharm **Experience** - 4 to 6 years **Location** - R&D - Baroda - Review all data and documents related to product registrations for various health authorities. - Compile registration dossiers for submission to various health authorities like -...