Title: Executive - Quality Control - Investigator Date: May 19, 2025 Location: Dadra - Quality Control Company: Sun Pharmaceutical Industries Ltd Job Summary: We are seeking an experienced and detail-oriented QC Investigator to join our Quality Control team. The role involves leading and supporting laboratory investigations including OOS (Out of Specification), OOT (Out of Trend), and other lab-related events, ensuring timely identification of root causes, and implementation of effective CAPAs. The ideal candidate will bring in-depth technical expertise, investigative acumen, and strong documentation and communication skills. Key Responsibilities: Lead and conduct thorough investigations of OOS, OOT, and laboratory events in compliance with cGMP and regulatory standards. Perform root cause analysis (RCA), develop hypotheses, and ensure correctness and scientific soundness of the investigations. Define and implement Corrective and Preventive Actions (CAPAs), verify their implementation, and evaluate effectiveness. Draft high-quality investigation reports with clear, concise, and scientifically justified conclusions. Trend and analyze OOS/OOT/lab event data to identify recurring issues and opportunities for process improvement. Actively participate in troubleshooting laboratory instruments and equipment. Maintain proficiency in operation and troubleshooting of a wide range of laboratory instruments (e.g., HPLC, GC, UV, IR, etc.). Review and enhance existing QC systems and practices to drive continuous improvement and ensure regulatory compliance. Collaborate cross-functionally with QA, production, and other departments during investigation and resolution processes. Participate in audits and regulatory inspections as a subject matter expert for laboratory investigations. Desired Candidate Profile: Education: M.Sc. / B.Pharm / M.Pharm or equivalent in a relevant scientific discipline. Experience: 7–10 years of experience in pharmaceutical QC, with strong exposure to laboratory investigations. Solid understanding of cGMP, ICH guidelines, and regulatory expectations. Strong technical writing and communication skills. Proficiency in data analysis and trending of lab events. Hands-on experience with QC instruments and troubleshooting.

Title: Officer - Quality Control Date: May 19, 2025 Location: Paonta Sahib - Plant Company: Sun Pharmaceutical Industries Ltd 1. Analysis of RM/FG/PM validation samples allotted for testing using analytical instruments like IR, Dissolution, UV and other instrument as per STP and approved protocol. 2. Documentation of analytical data and calculation of results. 3. Responsible for samples receiving and perform the sample description test. 4. Ensure compliance to cGMP requirements and laboratory procedures. 5. Ensure integrity, accuracy and adequacy of the analysis performed.

Title: Senior Executive-Corporate Relation Date: May 24, 2025 Location: Dewas SGO - Corporate Affairs Company: Sun Pharmaceutical Industries Ltd Designation:Executive/ Sr Executive - Corporate Relation Grade: G12A/G11B Location: Dewas Responsibilities: 1. Liaison and follow-up with officers of following Government Departments for getting statutory permissions/ license/ approvals: Dy. Drugs Controller (I), CDSCO-WZ, Indore MP-Food & Drugs Administration (MP-FDA), Bhopal, Indore, Malanpur (Bhind) and Dewas MP-Pollution Control Board (MP-PCB), Bhopal, Ujjain, Malanpur (Bhind) and Dewas Narcotics Control Bureau (NCB), Indore Petroleum & Explosives Safety Organization (PESO), Bhopal State Excise, Gwalior, Ujjain & Dewas. Industrial Health and Safety, Indore, Dewas and Malanpur (Bhind) MP State Secretariat, Bhopal Collectorate & Revenue Department , Dewas and Bhind Dist. Trade & Industries Centre (DTIC), Dewas and Bhind Municipal Corporation, Dewas and Malanpur MP-Police, Police Station-Incharge, Dewas, Indore & Malanpur (Bhind) Madhya Pradesh Industrial Development Corporation Ltd, Ujjain, Bhopal and Gwalior Central Pollution Control Board (CPCB), Bhopal Madhya Pradesh Paschim Kshetra Vidyut Vitaran Company Limited (MPPKVVCL), Dewas & Ujjain Directorate of Boilers, Indore and Bhopal 2. Working with Association of Industries, Dewas . 3. Liaison with Advocate for certain court cases, Dewas Education Qualifications: B.Pharm Total Work Experience : 5 to 10 Years

Title: Senior Manager - Corporate Quality Projects Date: Jul 11, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Title: Seniorr Manager-II - Corporate Quality Projects Business Unit: Quality Job Grade G9B : Senior Manager Location : Baroda, Gujarat Key Responsibilities At Sun Pharma, we commit to helping you “ Create your own sunshine ”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Job Profile: Project Lead is responsible for To have good experience & exposure of LIMS System implementations (Project developments support, validation, enhancements & implementations) across various site To ensure the dynamics of computerized systems w.r.t regulatory standards (21 CFR part 11, EU Annexure 11, & GAMP 5). To have good experience & exposure of SAP-HANA system, well aware of SAP system functionality. To have very good experience & expertise of Quality Control Systems & process (Functional expertise on sample management & Stability programme) To have very good experience & expertise of Quality Assurance process. Specially knowledge of APQR preparation & Handle control sample management. To have knowledge of Quality control instruments handlings like HPLC, GC & UV for Sample Managements (Testing), Test Calculations (as per pharmacopeia general chapters & Monographs) & good understanding of Test different-different scenarios (like Dissolution & CU) for fate value check (Pass/fail). To provide guidance/Support sites for all the major regulatory audits by Remotely & Onsite visit Evaluation, assessments of different business requirements received, it’s impact assessments and decision for its consideration for digitization, simplification & automations. To identify the roadblocks and ensure the smooth execution of assigned projects. Responsible to ensure smooth functioning of the team operations and routine activities. Encouraged and developed the subordinates to explore their capabilities and take challenge to grow further. To identify the actionable and accomplish the project milestone. To prepare and review CSAP, qualifications scripts and ensure execution of qualification. To prepare, ensure and support for the preparation of database and design as per compliance requirements and functional needs. To ensure technical training / support for each site, whenever required. To ensure successful handover of projects to Site/Sites & support site SME’s for Stabilization of projects at sites. To conceptualize and frame a consolidated approach for new identified technique. To ensure vendor support for technical discussion on finalize of projects. To perform the activities as per the project plan / assigned scheduler. To execute, support other Quality project initiated for simplification, harmonization and productivity enhancement. To work in collaboration with IT, API, SGO, vendor, Site Quality and different teams for identification of the right solution /tool/Vendor, to resolve the “Specific problem” and have correct solution for the organization. Basic Expectation: Candidate should Have a balance of technical knowledge & managerial skills - Be able to prioritize & multi -task Be able to work independently with limited supervision Manage stakeholders & get work done Be able to create project plans/Charters which is efficient from a time, cost & effort perspective, while understanding at the long term impact of decisions Analytical & Report Creation Skills - Proficiency in Excel, Word & PowerPoint. Basic understanding of MySQL & Oracle database Travel Estimate Low Job Requirements Educational Qualification M.Sc / B.Pharma / M.Pharma Experience 17-22+ years Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! 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).