Manager - 1

**Title**:Manager-1**: - Date: Jan 14, 2023- Location: Tandalja - R&D- Company: Sun Pharmaceutical Industries Ltd- As a Central Investigation Team member, primary role is statistical analysis of manufacturing data for the probable root cause and for other technical issues at site. - Assessment for Dissolution similarity as part of submission requirements. -...

Title:Manager-1**: Date: Jan 14, 2023 Location: Tandalja R&D Company: Sun Pharmaceutical Industries Ltd As a Central Investigation Team member, primary role is statistical analysis of manufacturing data for the probable root cause and for other technical issues at site. Assessment for Dissolution similarity as part of submission requirements. Statistical...

Title:Manager-1**: Date: Jan 13, 2023 Location: Tandalja R&D Company: Sun Pharmaceutical Industries LtdManager of Corporate Quality Compliance Responsible for review of. Responsible for identification and preparation of Best practice Guide documents to enhancement of Lab efficiency/Error reduction. Support to sites for conduct of regulatory inspections;...

1. Characterization of RLD pack samples. 2. Finalization of packing configuration for Exhibit batch packing of new generic product/NDA as per requirement. 3. Identification of new packaging material & new vendor development for packaging materials. 4. Mold development for primary packaging material & secondary packaging material & its validation. 5....

1. Characterization of RLD pack samples. 2. Finalization of packing configuration for Exhibit batch packing of new generic product/NDA as per requirement. 3. Identification of new packaging material & new vendor development for packaging materials. 4. Mold development for primary packaging material & secondary packaging material & its validation. ...

1. Characterization of RLD pack samples. 2. Finalization of packing configuration for Exhibit batch packing of new generic product/NDA as per requirement. 3. Identification of new packaging material & new vendor development for packaging materials. 4. Mold development for primary packaging material & secondary packaging material & its validation. 5....

1. Characterization of RLD pack samples. 2. Finalization of packing configuration for Exhibit batch packing of new generic product/NDA as per requirement. 3. Identification of new packaging material & new vendor development for packaging materials. 4. Mold development for primary packaging material & secondary packaging material & its validation. 5....

Manages Project from Pre PIF till filing and approval for US and OAM , in coordination with CFT comprising of Formulation, Analytical, Regulatory, API, plant teamsKnowledge of PM tools ( MS projects, CCPM )Maintains project plans and regularly updates in softwareManages project timelines, cost and scopePrepares and Updates project status for management...

Manages Project from Pre PIF till filing and approval for US and OAM , in coordination with CFT comprising of Formulation, Analytical, Regulatory, API, plant teams Knowledge of PM tools ( MS projects, CCPM ) Maintains project plans and regularly updates in software Manages project timelines, cost and scope  Prepares and Updates project status for...

Manages Project from Pre PIF till filing and approval for US and OAM , in coordination with CFT comprising of Formulation, Analytical, Regulatory, API, plant teams Knowledge of PM tools ( MS projects, CCPM ) Maintains project plans and regularly updates in software Manages project timelines, cost and scope  Prepares and Updates project status...

JD for – R&D QA biotechnologyReview of product development documents such as process development reports, process descriptions, process control strategy documents etc.Review of analytical developments such as method development reports, method qualification/validation protocols and reports and ensure compliance as per latest quality and regulatory...

JD for – R&D QA biotechnology  Review of product development documents such as process development reports, process descriptions, process control strategy documents etc. Review of analytical developments such as method development reports, method qualification/validation protocols and reports and ensure compliance as per latest quality and...

Qualification: M. PharmaMinimum Experience: 10-15 yearsRole: Manager – Regulatory & Business ContinuityIndustry Preference: PharmaJob Description:Preparation of registration strategy for various health authorities like Russia, Belarus, Kazakhstan, Ukraine, AzerbaijanReview of documents related to product registration and dossier submission leading to...

Qualification: M. Pharma Minimum Experience: 10-15 years Role: Manager – Regulatory & Business Continuity Industry Preference: Pharma Job Description: Preparation of registration strategy for various health authorities like Russia, Belarus, Kazakhstan, Ukraine, Azerbaijan Review of documents related to product registration and...

Qualification: M. Pharma Minimum Experience: 10-15 years Role: Manager – Regulatory & Business Continuity Industry Preference: Pharma Job Description: Preparation of registration strategy for various health authorities like Russia, Belarus, Kazakhstan, Ukraine, Azerbaijan Review of documents related to product registration...

Job Title: Sr. Manager Location: Vadodara Function:  Human Resources Sub-function: IR & Compliance Job Summary Centralized Statutory Compliances related to : The Code on Social Security ,Central labour legislations.ie., The Employees’ Compensation Act, , The Employees’ State Insurance Act, ,The Employees’...

Job Title: Sr. Manager Location: Vadodara Function:  Human Resources Sub-function: IR & Compliance Job Summary Centralized Statutory Compliances related to : The Code on Social Security ,Central labour legislations.ie., The Employees’ Compensation Act, , The Employees’ State Insurance Act, ,The Employees’ Provident...

Title:Manager-1**: Date: Jun 25, 2023 Location: Tandalja R&D Company: Sun Pharmaceutical Industries Ltd Responsible for designing advance workflows to measure & characterize process related impurities at different stages of product development such as Host cell protein (HCPs), Host Cell DNA (HCD) & Leachable. Responsible for routine in process sample...

Characterization of RLD pack samples Finalization of packing configuration for Exhibit batch packing of new generic product/NDA as per requirement Identification of new packaging material & new vendor development for packaging material Mold development for primary packaging material & secondary packaging material & its validation. Support to Regulatory team...

To design formulation strategy development and verify experiments, lab notebooks and online documents  To do literature search, project evaluation, ideation, IP development, summary evaluation and prepare proposal  To prepare product development, new requirements and proposals Inter department activity coordination, cross functional team...