Sun Pharmaceutical Industries Ltd

Title: Regional Medical Advisor (RMA) Date: Jun 6, 2025 Location: Delhi - Office Company: Sun Pharmaceutical Industries Ltd YOUR TASKS AND RESPONSIBILITIES: Primary scientific face of the organization to Key Opinion Leaders (KOLs) & physicians for a given therapy area Responsible for Identification, mapping and profiling of KOLs of given geography and therapy area, on an ongoing basis Engagement of identified KOLs through medical affairs activities, in alignment with the overall strategic plan Responsible to execution of strategic medical affairs plan including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects A therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, patients treatment trends and studies in the therapeutic areas in which the Company is involved, with defined audience of leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other Stakeholders) and to be considered a trusted scientific counterpart Jointly responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals Representing the organization in various internal & external scientific platforms Gathering deep insights on disease trends and treatment patterns from key thought leaders and conveying them back to the therapy lead and commercial teams Proactively conduct disease trend analysis in identified disease segments and contribute effectively to the development of annual Medical Affairs Strategy Plan Ability to handle complex questions from health care professionals related to Sun Pharma products or disease area to satisfaction Receiving and processing scientific information requests received from physicians Ensure that all activities in the region are conducted in alignment to Sun Pharmas Global Code of Conduct and compliance guidelines Primary scientific resource for the sales team of a given therapy area, responsible for regular training and flow of latest medical developments in the given field Collaborating with KOLs to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in journals of repute WHO YOU ARE: Prefer 2 years working experience in the pharmaceutical industry or research company and with competency in a project management capacity Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data Experience with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship Experience with complex business environments preferred Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards Experience in medical writing preferred Integrity driven decision making skills Collaboration and teaming with ability to work in a matrix environment Strategic thinking & sound analytical skills Big picture orientation with attention to detail Sense of urgency & desire to excel Intellectual curiosity Self-awareness and adaptability Result oriented and performance drive Excellent interpersonal & communication skills to effectively interact with a broad range of audience NOTE: The role is field-based and involves extensive travel (12 days a month) for interaction with leading KOLs and driving medical affairs activities including medical education programs, advisory board meetings, clinical studies and publications

Title: Regional Medical Advisor (RMA) Date: Jun 6, 2025 Location: Not Applicable Company: Sun Pharmaceutical Industries Ltd YOUR TASKS AND RESPONSIBILITIES: Primary scientific face of the organization to Key Opinion Leaders (KOLs) & physicians for a given therapy area Responsible for Identification, mapping and profiling of KOLs of given geography and therapy area, on an ongoing basis Engagement of identified KOLs through medical affairs activities, in alignment with the overall strategic plan Responsible to execution of strategic medical affairs plan including but not limited to medical education, product education, medical evidence generation, advisory boards, pre-license activities and special projects A therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, patients treatment trends and studies in the therapeutic areas in which the Company is involved, with defined audience of leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other Stakeholders) and to be considered a trusted scientific counterpart Jointly responsible with therapy area lead to support optimal patient outcomes through communication of data, information, knowledge and insights in support of healthcare professional needs and organizational goals Representing the organization in various internal & external scientific platforms Gathering deep insights on disease trends and treatment patterns from key thought leaders and conveying them back to the therapy lead and commercial teams Proactively conduct disease trend analysis in identified disease segments and contribute effectively to the development of annual Medical Affairs Strategy Plan Ability to handle complex questions from health care professionals related to Sun Pharma products or disease area to satisfaction Receiving and processing scientific information requests received from physicians Ensure that all activities in the region are conducted in alignment to Sun Pharmas Global Code of Conduct and compliance guidelines Primary scientific resource for the sales team of a given therapy area, responsible for regular training and flow of latest medical developments in the given field Collaborating with KOLs to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in journals of repute WHO YOU ARE: Prefer 2 years working experience in the pharmaceutical industry or research company and with competency in a project management capacity Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data Experience with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer relationship Experience with complex business environments preferred Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards Experience in medical writing preferred Integrity driven decision making skills Collaboration and teaming with ability to work in a matrix environment Strategic thinking & sound analytical skills Big picture orientation with attention to detail Sense of urgency & desire to excel Intellectual curiosity Self-awareness and adaptability Result oriented and performance drive Excellent interpersonal & communication skills to effectively interact with a broad range of audience NOTE: The role is field-based and involves extensive travel (12 days a month) for interaction with leading KOLs and driving medical affairs activities including medical education programs, advisory board meetings, clinical studies and publications

Title: MES Team Member-Digital Transformation Date: Jun 9, 2025 Location: Sun House - Corporate Office Company: Sun Pharmaceutical Industries Ltd Job Summary We are looking for a seasoned professional with 10-15 years in the Indian pharmaceutical industry , including 3+ years specializing in Manufacturing Execution Systems (MES) and L2 integration. This role demands expertise in optimizing MES platforms (e.g., Werum-PASX , Siemens Opcenter, Rockwell PharmaSuite) and integrating Level 2 systems (SCADA, PLCs, historians) to enhance manufacturing efficiency, compliance, and digital transformation. The ideal candidate will ensure adherence to global regulations (FDA 21 CFR Part 11, EU GMP, GAMP5) while driving innovation in pharma manufacturing processes. Experience with implementing greenfield MES and/or being part of core team from inception will be a big plus. Key Responsibilities MES Leadership: Lead MES implementation, upgrades, and harmonization across sites Optimize workflows (e.g., batch records, electronic logbooks) to align with cGMP. Collaborate with IT/OT teams to ensure seamless MES-ERP (e.g., SAP) integration Cross-Functional Collaboration: Mentor teams on MES/L2 best practices and digital tools (IIoT, Industry 4.0) Work with QA teams during audits Work with QA, production, and supply chain to streamline processes Innovation: Identify opportunities for advanced analytics, AI/ML, and paperless manufacturing. Stay updated on emerging technologies and regulatory trends. Qualifications Education : Bachelor’s in Chemical/Pharma Engineering, Computer Science, or related field. Master’s preferred. Experience : 10+ years in pharma manufacturing/operations, with 3+ years in MES implementations; experience in doing L2 integrations and OT setup will be a big advantage. Hands-on experience with MES platforms (e.g., Werum PAS-X) ; preferred if also proficient on L2 systems (Ignition SCADA, OSIsoft PI etc. ). Strong grasp of ISA-95 standards, 21 CFR Part 11, and data integrity principles will be a plus Skills : Project management (Agile/Waterfall) and leadership. Technical troubleshooting and scripting (SQL, Python). Excellent communication for stakeholder alignment. Certifications (Preferred): PMP, Six Sigma, GAMP5. Preferred Skills Experience with ERP interfaces (SAP S4HANA) and L2 integration Experience on cloud-based MES and L4 integration a plus Knowledge of data analytics tools (Power BI, Tableau) and IIoT platforms.

Title: Key Account Manager- Ecommerce Date: Jun 9, 2025 Location: Sun House - Corporate Office Company: Sun Pharmaceutical Industries Ltd Job Title: Junior Ecommerce Key Account Manager (KAM) Location: Mumbai Job Description: Account Support: Assist in managing day-to-day relationships with key ecommerce clients, ensuring their needs are met and expectations exceeded. Sales Growth: Help execute strategies to boost product visibility, sales, and market share on platforms like Amazon etc. Data Analysis: Monitor sales performance, inventory levels, and customer reviews; generate reports to identify trends and opportunities. Listing Optimization: Collaborate with brand, category & digital to refine product listings (keywords, images, descriptions) for maximum conversion. Campaign Coordination: Support the implementation of promotional campaigns, including lightning deals, sponsored ads, and seasonal sales. Cross-Functional Collaboration: Work with supply chain, marketing, and customer service teams to ensure seamless operations Weekly Search Reviews – Drive weekly reviews with agency and category for Prohance, sharing insights and actionable for each Market Research: Track competitor activity and industry trends to recommend actionable insights. Lead newer portals with currently low base but with a high potential Qualification: Prior experience of working in e-commerce / online / internet retail company is mandatory Prior experience of working with e-commerce portals’ backend – Vendor Central, Seller Central, Vendor Hub etc. Excellent written and verbal communication skills – fluent in English 4-8 years of relevant experience

Title: MES Team Member-Digital Transformation Date: Jun 9, 2025 Location: Sun House - Corporate Office Company: Sun Pharmaceutical Industries Ltd Job Summary We are looking for a seasoned professional with 10-15 years in the Indian pharmaceutical industry , including 3+ years specializing in Manufacturing Execution Systems (MES) and L2 integration. This role demands expertise in optimizing MES platforms (e.g., Werum-PASX , Siemens Opcenter, Rockwell PharmaSuite) and integrating Level 2 systems (SCADA, PLCs, historians) to enhance manufacturing efficiency, compliance, and digital transformation. The ideal candidate will ensure adherence to global regulations (FDA 21 CFR Part 11, EU GMP, GAMP5) while driving innovation in pharma manufacturing processes. Experience with implementing greenfield MES and/or being part of core team from inception will be a big plus. Key Responsibilities MES Leadership: Lead MES implementation, upgrades, and harmonization across sites Optimize workflows (e.g., batch records, electronic logbooks) to align with cGMP. Collaborate with IT/OT teams to ensure seamless MES-ERP (e.g., SAP) integration Cross-Functional Collaboration: Mentor teams on MES/L2 best practices and digital tools (IIoT, Industry 4.0) Work with QA teams during audits Work with QA, production, and supply chain to streamline processes Innovation: Identify opportunities for advanced analytics, AI/ML, and paperless manufacturing. Stay updated on emerging technologies and regulatory trends. Qualifications Education : Bachelor’s in Chemical/Pharma Engineering, Computer Science, or related field. Master’s preferred. Experience : 10+ years in pharma manufacturing/operations, with 3+ years in MES implementations; experience in doing L2 integrations and OT setup will be a big advantage. Hands-on experience with MES platforms (e.g., Werum PAS-X) ; preferred if also proficient on L2 systems (Ignition SCADA, OSIsoft PI etc. ). Strong grasp of ISA-95 standards, 21 CFR Part 11, and data integrity principles will be a plus Skills : Project management (Agile/Waterfall) and leadership. Technical troubleshooting and scripting (SQL, Python). Excellent communication for stakeholder alignment. Certifications (Preferred): PMP, Six Sigma, GAMP5. Preferred Skills Experience with ERP interfaces (SAP S4HANA) and L2 integration Experience on cloud-based MES and L4 integration a plus Knowledge of data analytics tools (Power BI, Tableau) and IIoT platforms.

Title: DGM - Operations (Sterile) Date: Jun 9, 2025 Location: Halol 1 - Operations Block I Company: Sun Pharmaceutical Industries Ltd Job Role : DGM Operations (Sterile) Education Qualification : B.Pharm, M.Pharm (Operations - Sterile) Experience: 20 to 22 Years Job Location : Halol Job Responsibilities : 1. Approving sign authority for: Commercial product/stability batches/ exhibit batches/ characterization Batches-Master Batch manufacturing record and Master Batch Packaging record Risk assessment, process validation protocol, incident and investigation report, action, compliance and closure. CAPA Plans and closure. Protocols & reports. Internal Quality Audit/Regulatory Quality Audit Compliance and closure. Change control, standard operating procedure, Planned modification. Other quality documents including amendments. 2. To assist the VP in batch manufacturing, packing and controlling the functions related of sterile manufacturing. To plan and execution of schedule as per work plan. 3. Provide leadership and expertise to ensure achievement of production with respect to Quality and commercial demands. 4. To ensuring that there are appropriate manufacturing and technical processes and procedures in place for the production. 5. To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality. The production records are evaluated and signed by a designated person. 6. In coordination with Quality head monitor the factor that may affect product quality compliance of GMP, retention of records. 7. To approve the instructions related to production operations, including the in-process controls, and to ensure their strict implementation. 8. To check the maintenance of the department, premises and equipment. 9. To ensure that the appropriate process validations and calibrations of control equipment are performed and recorded and the reports made available. 10. To ensure that the required initial and contuining training of production personnel for SOP, CGMP, and personal hygiene like men, materials and machines in manufacturing and packing area. 11. Optimization of the resources like men, materials and machines in manufacturing and packing area. 12. Ensure efficient collaboration and coordination between relevant departments like warehouse, engineering, PPIC, quality control, Quality assurance, procurement and management. 13. To coordinate with FDD/PDD(R&D) MSTG for execution of trail/exhibit/process validation batches and trouble shooting. 14. Responsible for destruction of the rejected products as per SOP. 15. Ensure implementation and adherence to Environment, health and safety procedures. 16. Procurement of new suitable equipment’s required for process as per CGMP requirements. 17. Identify and implement improvements to the production process, yield. 18. Preparation and adherence to approved budget and manage expenditure and head count budget over the fiscal year. 19. To ensure protection of the product from contamination. And monitor quality standards of products. 20. Shall delegate authority to deputed deputies with satisfactory level of qualification and experience. 21. Coach and develop direct and indirect reporters through on going, example based performance, feedback, annual performance reviews and provision of training and development opportunities. 22. Assure all time readiness department for regulatory agency inspections/internal audits and appropriate implementation of corrective actions regarding observations made by the agencies and internal audit teams. 23. Responsible for ensuring market complaints, failures deviations are investigated and corrective and preventive actions are implemented as per set timeline. 24. Performs all work in support of our corporate values of pride-humility, integrity, passion and with accountability and diligence. Perform all work in accordance with all established regulatory and compliance and EHS requirements.

Title: DGM - Operations (Sterile) Date: Jun 9, 2025 Location: Halol 1 - Operations Block I Company: Sun Pharmaceutical Industries Ltd Job Role : DGM Operations (Sterile) Education Qualification : B.Pharm, M.Pharm (Operations - Sterile) Experience: 20 to 22 Years Job Location : Halol Job Responsibilities : 1. Approving sign authority for: Commercial product/stability batches/ exhibit batches/ characterization Batches-Master Batch manufacturing record and Master Batch Packaging record Risk assessment, process validation protocol, incident and investigation report, action, compliance and closure. CAPA Plans and closure. Protocols & reports. Internal Quality Audit/Regulatory Quality Audit Compliance and closure. Change control, standard operating procedure, Planned modification. Other quality documents including amendments. 2. To assist the VP in batch manufacturing, packing and controlling the functions related of sterile manufacturing. To plan and execution of schedule as per work plan. 3. Provide leadership and expertise to ensure achievement of production with respect to Quality and commercial demands. 4. To ensuring that there are appropriate manufacturing and technical processes and procedures in place for the production. 5. To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality. The production records are evaluated and signed by a designated person. 6. In coordination with Quality head monitor the factor that may affect product quality compliance of GMP, retention of records. 7. To approve the instructions related to production operations, including the in-process controls, and to ensure their strict implementation. 8. To check the maintenance of the department, premises and equipment. 9. To ensure that the appropriate process validations and calibrations of control equipment are performed and recorded and the reports made available. 10. To ensure that the required initial and contuining training of production personnel for SOP, CGMP, and personal hygiene like men, materials and machines in manufacturing and packing area. 11. Optimization of the resources like men, materials and machines in manufacturing and packing area. 12. Ensure efficient collaboration and coordination between relevant departments like warehouse, engineering, PPIC, quality control, Quality assurance, procurement and management. 13. To coordinate with FDD/PDD(R&D) MSTG for execution of trail/exhibit/process validation batches and trouble shooting. 14. Responsible for destruction of the rejected products as per SOP. 15. Ensure implementation and adherence to Environment, health and safety procedures. 16. Procurement of new suitable equipment’s required for process as per CGMP requirements. 17. Identify and implement improvements to the production process, yield. 18. Preparation and adherence to approved budget and manage expenditure and head count budget over the fiscal year. 19. To ensure protection of the product from contamination. And monitor quality standards of products. 20. Shall delegate authority to deputed deputies with satisfactory level of qualification and experience. 21. Coach and develop direct and indirect reporters through on going, example based performance, feedback, annual performance reviews and provision of training and development opportunities. 22. Assure all time readiness department for regulatory agency inspections/internal audits and appropriate implementation of corrective actions regarding observations made by the agencies and internal audit teams. 23. Responsible for ensuring market complaints, failures deviations are investigated and corrective and preventive actions are implemented as per set timeline. 24. Performs all work in support of our corporate values of pride-humility, integrity, passion and with accountability and diligence. Perform all work in accordance with all established regulatory and compliance and EHS requirements.

Title: General Manager - Engineering Date: Jun 9, 2025 Location: Halol 1 - Plant Company: Sun Pharmaceutical Industries Ltd Job Role : General Manager (Engineering) Education: BE Electrical & Electronics Experience : 22 to 24 Yrs (with expereince in Regulated markets and Sterile background) Responsibilities : 1. He is authorize to sign (as a doer / reviewer / verifier) A. Engineering GMP Documents B. Break Down / Preventive Maintenance Report C. Qualification Documents. D. QMS document review and closing. E. Any other documents related to QMS. Handling of Halol-1 (NOSD) Engineering Operation, HVAC, Electrical and Facility Management related activity. Preventive Maintenance approval, Instrument / Equipment inward approval, Qualification protocol and SOP review and approval. Improvements to reduce the Break down time of Production Equipments. To ensure all critical utilities as HVAC and Water systems are available round the clock as per requirement. Conceptualize and Implement Energy Conservation measures for Energy & water. Preparation of annual Revenue budget and ensure expenses are within budget. Propose annual Capital budget for finalization & implement the sanctioned Capex. Handling of Engineering & Facility modification related activity. Rolling out the Good Engineering Practices and standards in various functions of Engineering. To ensure availability of the spares and maintain inventory of critical spares having long delivery time. Standardization and Harmonization of documentation and procedure in engineering department. Ensure continuous improvement in engineering operating system in coordination with plant maintenance leaders & production team leaders to avoid breakdowns and repeated failures. Tracking of Capex and Modification related activity. Ensuring delivery of the activity in terms of safety, quality, timelines and budget. To ensure all engineering SOP, records and schedule are updated as per QMS. Participate in Technical Investigations. Participate in monthly Quality council meetings and update status of QMS documents. Ensure that QMS documents are closed as per time line. Compliance of internal and external observation points. To ensure timely completion of training related activity. Handling the Facility Management team operations for the site. To evaluate change control related to global IT division.

Title: Manager - 1 Date: Jun 9, 2025 Location: Gurgaon - R&D Company: Sun Pharmaceutical Industries Ltd Job Description Job Title: Operations Project Management (Data Management and Analytics). Purpose: Primarily responsible of consolidated portfolio management of Global Projects managed within RnD, Data and repository management, analytics helping management and leadership with Key decision making which is based on data, Budget Management, Support in Defining Shared Goals Targets and tracking the same, Capacity mapping, Review Management, Analytics on activities performed within RnD based on Historical data, Tracking overall project progress and RAG Reporting, Working with Dashboards like Tableau, Critical Chain Project Reports supporting Project Management Team and RnD Functional Heads on various Data driven inputs resulting to corrective actions where ever required. Roles and Responsibilities Role requires awareness on Project management methodologies and end to end project life cycle knowledge. Risk/Issue Management, Change Management, Re-prioritization, Optimization and Automating activities will be key requirement for the role Experience with working, managing and analysing huge data sets. RAG Reporting and escalate things on timely manner to avoid impact on deliverables. Prioritization, On Time Delivery, Excellent in Data Handling, Analysing and Summarization of the outcome. Automations, Dashboard and CCPM Tool report management, Budget and work plan management, global portfolio and project tracking, Review management, and MIS Readiness will be some of the key activities where in a person will be supporting Meeting Management, Stake holder’s management and understanding requirement and delivering outcome oriented analytics, which can help in decision making which is data driven. Key Skills Role will require excellent communication skills, good in co-ordinations, team player and will be required to work with all stake holders and departments within and outside R&D. Good with analytics, logical and lateral thinking, advance excel with key formulas, MS Office, MS Projects and power point knowledge, added advantage if aware of macros, SQL Queries and Dashboards. Innovative thinker, Flexible Approach, Go-getter with leadership skills as role requires interactions and getting work done with support of Peers, juniors, seniors and Leadership team. Qualification Bachelors or Masters in Any Field. PMP/Prince 2 Certified in Project Management Sun Pharmaceutical India Ltd JOB DESCRIPTION Position : Executive/Sr Executive Grade : G12B/G11 Experience : 5-7 years Job Location : Baroda/Gurgaon Education : Bachelors in any Stream/MBA/PMP or Prince 2 certified

Title: Senior Manager - Production (QMS) Date: Jun 9, 2025 Location: Paonta Sahib - Plant Company: Sun Pharmaceutical Industries Ltd Job Role : Sr.Manager - Production (QMS) Location : Paonta Sahib Qualification : B.Pharm / M.Pharm Experience : 15 to 18 Yrs Job Responsibilities: To ensure continuous improvement in achievement of productivity, manufacturing yields & quality norms; Launch of new products 100% in time. Quality: Demonstrate compliance to established Manufacturing Operations and Quality Standards. To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality. Strive for reduction in Out of Specification, Deviations, reduce Market complaints. Document Integrity: To support compliance of practices to established procedures and Good Manufacturing Practice standards. To approve the SOPs & format, batch records relating to production operations and to ensure their strict implementation. Cost: Overhead recovery, and manufacturing efficiency to be maintained. Cascading Sun Values and culture to the root level. People Development: Develop Talent pipelines for level II, III & IV key jobs. Monitoring and control of the manufacturing environment; Process validation and calibration of analytical apparatus; Designation and monitoring of storage conditions for materials and products; compliance with GMP requirements. To ensure the qualification and maintenance of department, premises and equipment. To ensure that the appropriate validations are done. Retention of records; Performance and evaluation of in-process controls; Training, including the application and principles of QA; To design and implement the policies, systems and procedures as required for the efficient management of the shop floor.

Title: Officer Date: Jun 10, 2025 Location: Dewas API - Production Block 5 Company: Sun Pharmaceutical Industries Ltd Position- Officer API Production Qualification – B.Sc./ M.Sc. Exp- 3 to 8 Years of experience Job Description- Officer Production Penam Candidate from API regulatory plant will be preferred Job Responsibilities :- Carrying out the batch operations with safety, cGMP and SOP. BPR filling & on-line documentation and maintain the adequacy & accuracy with respect to data integrity. Maintain SOP compliance records with accuracy. Charging of batches & batch processing as per BPR & SOP. Handling and operation of the equipments as per SOP. Cleaning and sterilization of equipments and integrity testing of sterile grade filters. Planning the work of technician and follow up. To maintain housekeeping of owned area such that efficacy, purity and safety of product is ensured & ensure the cleanliness of equipment and its surroundings. Effective communication to superiors as well as subordinates in order to carry out work and its follow up according to instructions. Ensure good housekeeping in surrounding working area and personal hygiene. Sterilized articles unloading from sterilizer and transferring to respective place and aseptic connection. Execution of process simulation, validation / revalidation, qualification, requalification of equipments and system as per protocol. Coordination with IPQA, QC and Micro for PCO, Campaign changeover cleaning and In process sampling. Environmental monitoring of controlled and critical area. Review of Calibration reports, FMS trends and alarms. Calibration of sensors (Steam sterilizer, DHS and Kaye Validator). Checking of Raw material and Packing material, labeling and packing of FP. Verification of all critical routine operations. To perform & verify the cleaning & sanitization of articles, equipments & area as per respective SOP. To Complete all assigned training on time. To Maintain shop floor discipline and ensure harmonious relationship among employees Execution of Protocol based activities To be on their dedicated workstation & proper hand over the charge to another employee (who is well trained to perform the task) and inform his superior prior leaving the workplace. To do the entries of records as per their respective SOP’s (equipment log book, cleaning records etc.) To Check the entries recorded by doer as per respective SOP’s (equipment log book, cleaning records etc.)

Title: Officer Date: Jun 10, 2025 Location: Dewas API - Production Block 5 Company: Sun Pharmaceutical Industries Ltd Position- Officer API Production Qualification – B.Sc./ M.Sc. Exp- 3 to 8 Years of experience Job Description- Officer Production Penam Candidate from API regulatory plant will be preferred Job Responsibilities :- Carrying out the batch operations with safety, cGMP and SOP. BPR filling & on-line documentation and maintain the adequacy & accuracy with respect to data integrity. Maintain SOP compliance records with accuracy. Charging of batches & batch processing as per BPR & SOP. Handling and operation of the equipments as per SOP. Cleaning and sterilization of equipments and integrity testing of sterile grade filters. Planning the work of technician and follow up. To maintain housekeeping of owned area such that efficacy, purity and safety of product is ensured & ensure the cleanliness of equipment and its surroundings. Effective communication to superiors as well as subordinates in order to carry out work and its follow up according to instructions. Ensure good housekeeping in surrounding working area and personal hygiene. Sterilized articles unloading from sterilizer and transferring to respective place and aseptic connection. Execution of process simulation, validation / revalidation, qualification, requalification of equipments and system as per protocol. Coordination with IPQA, QC and Micro for PCO, Campaign changeover cleaning and In process sampling. Environmental monitoring of controlled and critical area. Review of Calibration reports, FMS trends and alarms. Calibration of sensors (Steam sterilizer, DHS and Kaye Validator). Checking of Raw material and Packing material, labeling and packing of FP. Verification of all critical routine operations. To perform & verify the cleaning & sanitization of articles, equipments & area as per respective SOP. To Complete all assigned training on time. To Maintain shop floor discipline and ensure harmonious relationship among employees Execution of Protocol based activities To be on their dedicated workstation & proper hand over the charge to another employee (who is well trained to perform the task) and inform his superior prior leaving the workplace. To do the entries of records as per their respective SOP’s (equipment log book, cleaning records etc.) To Check the entries recorded by doer as per respective SOP’s (equipment log book, cleaning records etc.)

Title: Senior Executive Date: Jun 11, 2025 Location: Gurgaon - R&D Company: Sun Pharmaceutical Industries Ltd Position : Executive / Sr Executive Grade : G11A/ G11B Job Location : Gurgaon (preferable)/Baroda/Mumbai Education : M.Pharm Department : Regulatory & Business Continuity - Branded Candidate shall be responsible for assuming the role for the assigned specialty programs (NCE/BLA) who shall be responsible for regulatory operations activities including but not limited to CTA applications(in EU, LATAM , USA, Canada, ROW) , CTIS management, submission management, eCTD publishing of all modules, document management etc. Must understand and be updated with current Global Regulatory filing requirements and eCTD /CTIS structure. Collaborate with Strategists (Leads) and coordinators for submission strategy and timelines. Prepare Regulatory Management Plan, Submission content plan for CTA Manage lifecycle of CTA for all in-house and outsourced activities Be the critical technical coordinator for Clinical Trial Application submission and notification/ Request for Information/Information request ensuring accurate and timely input of data Archival of necessary submissions and/or documents Assist with definition, development and implementation of processes to meet the evolving CTIS need Track, generate metrics as requested by the Functional Head from time to time Implement best practices, participate in process improvements / enhancement To support other Regulatory operations activities including, but not limited to, Clinical Trial Disclosure, eCTD publishing

Title: Senior Executive Date: Jun 13, 2025 Location: Dewas API - Process Engineering Company: Sun Pharmaceutical Industries Ltd Internal Job Posting Position: Officer Process Engineering Grade: Senior Executive No. of Position: 1 No. Job Location: Dewas API Qualification: B.E Chemical Experience: 7 years’ experience in Process Engineering (Yield improvement/Scale up batch etc) in API manufacturing plant Candidate from Regulatory API Plant will be preferred Job Description :- Review of current methods of production for cost efficiency, environmental friendliness, maximum output and product quality. Preparation of reports, feasibility studies and cost analysis of processes. Problem shouting and Technical support in production issues by co-ordinate the team of production manager, shift incharge, chemists and operators. Planning to install new equipments like Distillation column, Reactors, Filters, Dryers and Cooling towers in the plant with design and justification. Calculation of line size required for utilities and process lines Detailed product costing and power consumption calculations. Material and energy balances, Heat load calculations. Production capacity enhancement by optimizing the process parameters. Improvements in percentage of Solvent Recovery for established systems and utility consumption calculation in recovery process. Compliances to Safety procedures, cGMP & SOP’s Scale-up calculations from Lab scale/Pilot scale for new product development. Product and utility cost reduction. Preparation of PFD (Process flow diagram) for new and existing process. Critical process monitoring, data analysis & reduction of Batch cycle time (Wherever possible & applicable). To take part to minimize energy use, minimize waste production, including finding ways to turn the waste into valuable materials that can be re-used. To take part in the strategic activities those are executed at plant level. Planning and conducting PDL (process development lab) experiments for process optimization to improve yield and quality, whenever required. Planning and conducting PDL (process development lab) experiments for cycling and recovery improvement of solvents, wherever required.

Title: Manager 2 Date: Jun 12, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Experience from major pharma industries in Non-oral Products: Topical product and transdermal product. Experience in end-to-end topical product development activities for generic product development ANDA (Cream, ointment, gel, solution, lotion, foam, patch etc.) as well as NDA 505(b)(2), 505(b)(1). Experience in execution of lab scale manufacturing, reverse engineering, analytical know-how, plant level manufacturing activities; scale-up and exhibit batches based on quality principles QbD, QTPP, CQA, CMA, CPP, RA, FMEA. Experienced scientist to perform experiments for development of optimum prototypes (generic, non-infringing composition and robust manufacturing process) with diverse class of drugs & prodrugs (sensitive to pH, acid, base, temperature, oxygen, humidity). Experience in regulatory documentation CMC, MF, BMR, PDR, controlled correspondence for CMC, Biowaiver & Dossier preparation for US-FDA, EU-EMA, AU-TGA & DCGI through successful filing. Experience in working with cross-functional teams (ADD, MSTG, production, QC, QA, RA, IPC, PMO, BD, Microbiology, Pharmacology etc.) to achieve project goals - Filings and subsequent approvals. Knowledge and develop continuous understanding on competitive intelligence, due diligence, US-FDA quality concepts, statistics and global pharma trend analysis to support new product evaluation & introduction. Job Responsibilities: To design, conduct and verify/review experiments to develop a robust formulation. To do literature search, patent search, prepare summary report and review. To prepare product development reports and protocols. To do product scale-up, exhibit batches and prepare reports for product filing and regulatory queries including post filling and post approval market queries. To prepare documents (i.e. PDR, CPD etc.) for regulatory submission Group work co-ordination. Project status report preparation. Experimental result review, interpretation and conclusion. To prepare technology transfer documents. To procure raw materials (API / excipients), packaging materials, innovator samples in consultation with packaging/purchase department. To do product validation, site transfer/change activities of products. To write Laboratory Notebook to enter details related to drug product manufacturing. To prepare test request for analysis of raw materials (API/Excipients) and Drug product.

Title: Manager - 1 Date: Jun 13, 2025 Location: Acme Plaza - Office Company: Sun Pharmaceutical Industries Ltd Job Details Function Procurement Designation Manager-1 Job Description / Responsibility: Responsible for PM Procurement for 31 Loan License locations & 5 Own Locations Along with One R&D Location. Cost Savings projects - Identifying Alternate vendors. Sharing consolidated requirement with identified vendor and requesting quotes from them. Following up for prices from alternate vendor along with other terms and condition. (Detailed working is insisted) New vendor’s prices are incorporated and scrutinized as per company’s practice Sharing and seeking comments on cost comparison from reporting manager and acting according to the comments Re-negotiating with vendor in-case quote received is not in line with desired target savings. On receipt of signoff from reporting manager, sharing approved Purchase Order. Arranging for samples required for machine trial, agreements, vendor documents Following up with vendor for delivery, tracking of shipment until delivered at site. To ensure with site on agreed ratio of business with alternate vendor so as to achieve targeted savings. Identifying Cost Saving projects & Implementing the same with help of PDD & Plant. Purchase Order Preparation, Verification & Clearance Preparation of Purchase Order for SPIL Baddi & LL Sites (listed above) as per the Indents received from the planning team (Yearly 5500 transactions & monthly on an average 350 PO’s are made Annual Purchase Value is 110 Cr.). Allocation of A/w in AMS & Goose to respective approved Vendors. Submitting the proof in AMS for approval. Ensuring approved purchase orders are sent to Vendors. Verification of Purchase order in the Portal. Preparation of Excel work sheet for the list of order which ever are not linked with portal Scrutiny of Purchase price with Budget price / latest approved Price Lists and earlier purchase price. Verifying the PO Price & Order qty. with vendors offers to evaluate the slab rate benefit. Coordination with plant for clubbing the order quantity to meet the slab rate benefit. Checking of Incoterms, Payment Terms & Delivery Schedules. Clearance of Purchase order to next level for approval. Servicing & Material Availability. Regular follow up with vendors for timely supplies of Packaging materials Ordered for Above mentioned plants (Average 350 deliveries done on monthly basis) Coordination with plant team for arranging SFS products packing material to ensure there is zero sales loss Ensure timely production and dispatches of materials by the vendors. Sharing Dispatch details with necessary set of Documents with planning In case of anticipated delay by supplier (due to unavoidable reasons), communicate to Plant team & planner for appropriate action to avoid Production loss. Attending quality issues and providing investigation report and action plan (CAPA) to site in coordination with vendor. Coordination with Cross functional teams such as Logistics, PDD, Quality & Finance Follow up with vendor for dispatches details & B/L details. In case of quality issue’s in in-house location: Communicate between Site and vendor on the quality complaint and arranging for the samples from the Site for vendor’s reference and Investigation purpose followed by satisfactory CAPA for closure of complaints. Coordination with plant & vendor for replacement of materials. Providing the Artwork / Specification & Specimen Sample from PDD / Site QA for developing the New job. Co-ordinate with QA/PDD for Proof / Shade card approvals. Arranging timely payments to suppliers, by coordinating with Finance team against the material supplied by the supplier. Arranging pick up from various vendors, forwarding the pick up request to logistics teams & follow up for pick up n delivery. Monitoring dispatches of Imported material & filling documents in Go-Comed Portal for clearance of material from Customs. MIS Sharing monthly MIS & OTIF report. Keeping Track of Commodity price trend & deciding Procurement strategy based on Price trend. . Audit : Arranging vendor audit as desired by VQ Team for SPIL Baddi & LL Sites. Aligning itinerary as per auditor’s schedule Arranging documents from vendor before and after audit Coordinating with VQ team for audit report and providing compliance from vendor Assisting VQ team for vendor de-registration as and when required. Attending quality issues and providing investigation report and action plan to site in coordination with vendor.

Title: Executive/Senior Executive Date: Jun 13, 2025 Location: Gurgaon - Office Company: Sun Pharmaceutical Industries Ltd JOB DESCRIPTION (JD) Designation Executive/Senior Executive Location Gurugram Department Name R&D Quality-CMC QA List of Responsibilities / Job Functions: Review of R&D documents such as stability data, Analytical reports, Method Qualification reports, Method verification reports, Method validation protocols & reports, Working Standard / Impurity Standard profile, analytical data of pilot bio batches and Method transfers protocol & report. Review of Lab event/Deviations/Change control/CAPA and associated investigation reports prior to Technology Transfer. Support and participate in failure investigations and resolution of root causes for issues related to systems and products developed within Sun Pharmaceutical Industries Limited R&D sites. Visiting the AD Labs / Areas for verification of GDP & GMP compliance. Audit of Analytical Development department. Ensure the periodic activities as per the quality procedures are performed in a timely manner. Work in partnership with the site cross functions and corporate functions for “Audit readiness”. Lead the assessment, tracking of remediation and monitoring of identified actions as part of various corporate initiatives. Perform other duties as assigned by Functional Head time to time. Review and approve the periodic activities as per the quality procedures. Support operations team during corporate audit/ external audits Lead the assessment, tracking of remediation and monitoring of identified actions as part of various corporate initiatives. Review of Product development data and specification.

Title: Flow Chemistry - Senior Executive/Manager Date: Jun 13, 2025 Location: Gurgaon - Office Company: Sun Pharmaceutical Industries Ltd Position: Senior Executive/Manager - Flow Chemistry Job Grade: G11B/G11A Function: Process Engineering Sub-function: Research & Development Manager’s Job Title: Sr. Manager Skip Level Manager’s Title: Sr. GM Function Head Title: VP Location: Gurgaon Job Summary The position is responsible for tasks related to flow chemistry, design flow chemistry setups, transfer of technology to plant for commercial production , trouble shooting of existing tech etc. Areas of Responsibility 2-8 years of Experience in flow chemistry. Have worked on Corning, VapourTech, Chemtrix, Coflore, Fixed Bed, Plug flow reactor etc. Design flow chemistry setups. Carryout the experiments in micro reactor. Convert existing batch chemistry to flow chemistry. Basic knowledge of chemical characterization, regulatory, quality guidelines and documentation. Literature search using Scifinder, Reaxys and other tools and preparing product dossiers. Transfer technology to plant for commercial scale-up. Trouble-shooting of running technologies in plant. To prepare technology transfer documents and get audited. To support in addressing regulatory queries. To ensure the compliance by following GDP and GLP in lab. Generation of intellectual properties by publishing patent/papers. To work in Team Energetic Innovative thinking Willingness to take responsibilities Travel Estimate Travel to the plants on need basis (1-3 month / year) Job Scope Geographical Scope Across API sites (domestic) Job Requirements Educational Qualification B.Tech or M.Tech in Chemical Engineering / Ph.D. Organic Chemistry Skills Knowledge of organic chemistry and flow chemistry. Experience having 2-5 year of experience in Flow Chemistry / Continuous Synthesis Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Title: Executive - Corporate Quality Compliance (Compliants) Date: Jun 17, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Position: Executive Job Title: Executive Job Grade: Function: Corporate Quality Compliance Sub-function: Complaints Manager’s Job Title: Senior Manager-1 Skip Level Manager’s Title: Function Head Title: Head of Global Quality Systems Complaints Location: Vadodara No. of Direct Reports (if any) Nil Job Summary Logging of Product Quality Complaints (PQC) in the database (TrackWise). Acknowledge the complaints to the complainants. Providing the response letter to the complainant. Reconciliation of received market complaints. Review of Product Quality Complaint Investigation Reports (India Market). Coordinate with other stakeholders involved in the complaint handling process. Areas of Responsibility Product Quality Complaints Management Travel Estimate Approximately 5% Job Scope Internal Interactions (within the organization) Yes External Interactions (outside the organization) Nil Geographical Scope India Financial Accountability (cost/revenue with exclusive authority) Nil Job Requirements Educational Qualification M.Sc (Life Sciences) / B.Pharm Specific Certification Nil Skills Good Technical & Communication Skills, minimum 1 year experience in complaints handling process, candidate should have worked in USFDA work environment. Experience 4-6 years Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Title: Executive - Corporate Quality Compliance (Compliants) Date: Jun 17, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Position: Executive Job Title: Executive Job Grade: Function: Corporate Quality Compliance Sub-function: Complaints Manager’s Job Title: Senior Manager-1 Skip Level Manager’s Title: Function Head Title: Head of Global Quality Systems Complaints Location: Vadodara No. of Direct Reports (if any) Nil Job Summary Logging of Product Quality Complaints (PQC) in the database (TrackWise). Acknowledge the complaints to the complainants. Providing the response letter to the complainant. Reconciliation of received market complaints. Review of Product Quality Complaint Investigation Reports (India Market). Coordinate with other stakeholders involved in the complaint handling process. Areas of Responsibility Product Quality Complaints Management Travel Estimate Approximately 5% Job Scope Internal Interactions (within the organization) Yes External Interactions (outside the organization) Nil Geographical Scope India Financial Accountability (cost/revenue with exclusive authority) Nil Job Requirements Educational Qualification M.Sc (Life Sciences) / B.Pharm Specific Certification Nil Skills Good Technical & Communication Skills, minimum 1 year experience in complaints handling process, candidate should have worked in USFDA work environment. Experience 4-6 years Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).