Manager - 2

**Title**:Manager-2**: - Date: Jan 16, 2023- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd1. Exposure to routine Microbiology tests with hand on experience 2. Method development, Method Verification and routine analysis in Orals and Non-orals Formulations 3. Area of Experience: - Microbial Enumeration Test - Test for specified...

**Title**:Manager-2**: - Date: Jan 17, 2023- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd1. Exposure to routine Microbiology tests with hand on experience 2. Method development, Method Verification and routine analysis in Orals and Non-orals Formulations 3. Area of Experience: - Microbial Enumeration Test - Test for specified...

**Title**:Manager-2**: - Date: Jan 16, 2023- 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:Manager-2**: Date: Jan 16, 2023 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. Should be proficient...

Job Title:Manager 2Job Grade:G11ADepartment:India Regulatory AffairsSub-function:Corporate RelationsManager’s Job Title:Senior Manager - 1Skip Level Manager’s Title:Senior General ManagerNo. of Direct Reports (if any)Location:Tandalja-BarodaJob SummaryRegulatory submissions of drugs and medical devices in India.Area Of ResponsibilityEvaluation of...

Job Title: Manager 2 Job Grade: G11A Department: India Regulatory Affairs Sub-function: Corporate Relations Manager’s Job Title: Senior Manager - 1 Skip Level Manager’s Title: Senior General Manager No. of Direct Reports (if any) Location: Tandalja-Baroda Job Summary ...

Job Title: Manager 2 Job Grade: G11A Department: India Regulatory Affairs Sub-function: Corporate Relations Manager’s Job Title: Senior Manager - 1 Skip Level Manager’s Title: Senior General Manager No. of Direct Reports (if any) Location: Tandalja-Baroda Job Summary ...

Job Title: Manager 2 Job Grade: G11A Department: India Regulatory Affairs Sub-function: Corporate Relations Manager's Job Title: Senior Manager - 1 Skip Level Manager's Title: Senior General Manager No. of Direct Reports (if any) Location: Tandalja-Baroda Job Summary Regulatory submissions of drugs and medical...

1. Exposure to routine Microbiology tests with hand on experience 2. Method development, Method Verification and routine analysis in Orals and Non-orals Formulations 3. Area of Experience: - Microbial Enumeration Test - Test for specified Micro-organisms - Bio-burden Test , - Antimicrobial Effectiveness Test, - Sterility Test , - Bacterial Endotoxin...

**Department: F R&D (Non-oral), SPIL, Baroda** **Position: Manager-II (G11)** **Requirements**: - M. Pharm or Ph.D in Pharmaceutics from renounced institute. - Industrial experience from major pharma industries in Non-oral Products: Parenteral product (injection). - Experience in end-to-end parenteral product (injection) product development activities for...

Department: F R&D (Non-oral), SPIL, BarodaPosition: Manager-II (G11)Requirements: M. Pharm or Ph.D in Pharmaceutics from renounced institute. Industrial experience from major pharma industries in Nonoral Products: Parenteral product (injection). Experience in endtoend parenteral product (injection) product development activities for generic product...

Position: Executive/ Sr. Executive – Regulatory Affairs (API) Location: Baroda Education : M.Sc. (Organic Chemistry/Chemistry/Analytical Chemistry) Job Description: Minimum 5-6 years of experience in regulatory affairs/quality assurance of API Plant or corporate. Good understanding of DMF compilation and lifecycle management...

Position: Sr. Executive/Manager-II – Regulatory Affairs (API) Location: Mumbai Education : M.Sc. (Organic Chemistry) Job Description: Expertise in Control strategy and DMF preparations for US / Europe and other regulated/ emerging markets. Expertise in understanding the deficiencies received and to prepare appropriate response for...

Position: Sr. Executive/Manager-II – Regulatory Affairs (API) Location: Mumbai Education : M.Sc. (Organic Chemistry) Job Description: Expertise in Control strategy and DMF preparations for US / Europe and other regulated/ emerging markets. Expertise in understanding the deficiencies received and to prepare appropriate response for...

Position: Sr. Executive/Manager-II – Regulatory Affairs (API) Location: Mumbai Education : M.Sc. (Organic Chemistry) Job Description: Expertise in Control strategy and DMF preparations for US / Europe and other regulated/ emerging markets. Expertise in understanding the deficiencies received and to prepare appropriate...

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. Job Responsibilities: Responsible for study sample analysis for all pipeline products. Isolation of PBMC from whole blood and maintenance of commercial...

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. Job Responsibilities: Responsible for study sample analysis for all pipeline products. Isolation of PBMC from whole blood and maintenance of...

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. - Expertise in downstream...

Handling of filter validation activities including review of PPQ form, filterability trial documents, filter validation protocol and report. - To keep track of filter validation activity. - To review risk assessment reports for extractable and leachable study. - Review of product development documents - Review of tech-transfer documents. - Review of...

Executive and Sr. Executive Review all data and documents related to product registrations for various health authorities. Compile registration dossiers for submission to various health authorities like – China , Canada, Europe, Australia/New Zealand, Japan and Israel. Prepare responses to deficiency letters received from various...