Job Purpose: To operate and monitor granulation equipment and processes in compliance with cGMP, SOPs, and safety standards, ensuring consistent production of high-quality pharmaceutical granules for tablet or capsule formulation. Key Responsibilities Operate granulation equipment such as high-shear mixers, fluid bed dryers, oscillating mills, and blenders. Weigh, dispense, and mix raw materials as per batch manufacturing records (BMR). Monitor granulation parameters and adjust settings to maintain product quality. Perform in-process checks (e.g., moisture content, granule size) and document results accurately. Clean and maintain equipment and work areas as per SOPs. Execute machine changeovers and line clearance activities. Identify and report deviations or equipment malfunctions to the supervisor. Ensure compliance with cGMP, safety, and environmental regulations. Participate in continuous improvement and troubleshooting initiatives. Qualifications ITI / Diploma / B.Sc or equivalent; technical diploma preferred. 4–6 years of experience in pharmaceutical manufacturing, preferably in granulation. Familiarity with cGMP, USFDA guidelines, and pharmaceutical documentation practices. Ability to read and interpret batch records and SOPs. Basic computer skills and understanding of production documentation. Preferred Skills Attention to detail and strong documentation habits. Mechanical aptitude for operating and troubleshooting equipment. Team player with good communication skills. Forklift certification (if required for material handling).

Job Title Sr. Manager – Global Quality Lead Business Unit Global Quality & Compliance Job Grade G9B Location : Mumbai 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.” Position Summary Manage overall batch certification review of QC lab records, certificates of analysis/compliance and all related supporting documentation (i.e. documentation review, SOP compliance, laboratory application data reviews, instrument preventive maintenance/calibration/qualification/validation as per good manufacturing practices/good documentation requirements and ALCOA++ principles). This role will be an individual contributor with expert in manufacturing investigations from FDA approved facilities that make sterile and OSD products. The incumbent will assure individual compliance with all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, standard operating procedures, and Sun Pharma policies and procedures. Key Responsibilities Lead the review of all QC records related to Batch certification program. QA SME for manufacturing & packaging Investigations (Sterile & OSD) Batch Certification activities at Dadra and possibly other sites in India. Experience in manufacturing contract manufacturing organizations, inculding Batch records, investigations and product quality compliants. Experience in FDA and Health Canada inspections Review Deviations, CAPAs, OOS/OOT investigations. Ensure that all activities are compliant with Standard Operating Procedure, STP and GP etc. Review initiated CAPA records related to QC investigations for completeness and adequacy. Review and approval of qualification, analytical method transfer, validation protocol and reports for accuracy, completeness and traceability as well as adherence to the Protocol/procedures. Training of QC and QA teams. Work in partnership with Quality Control and Quality Assurance. Follow the EHS policy, laboratory procedures and maintain the compliance to cGMP requirements. Travel Estimate Job Requirements Educational Qualification B.Pharm / M.Pharm Experience Tenure : 15 to 17 Yrs 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).

Company Description Sun Pharma is the world's fourth-largest specialty generic pharmaceutical company and the leading pharmaceutical company in India. We produce high-quality, affordable medicines trusted by customers and patients across over 100 countries. With a strong global presence sustained by over 40 manufacturing facilities and cutting-edge R&D centers, Sun Pharma is powered by a diverse workforce from more than 50 nationalities. Committed to fostering innovation and growth, we support our teams with an inclusive environment and opportunities for continuous development. At Sun Pharma, our mission is to enable every individual to thrive, guided by our Employee Value Proposition—'Create Your Own Sunshine'—focused on constant improvement, empowerment, and teamwork. Role Description This is a full-time on-site role for a Sales Executive, located in Varanasi. The Sales Executive will be responsible for achieving sales targets, managing customer relationships, and identifying new business opportunities. The role involves building and maintaining a strong understanding of company products, conducting detailed market analysis, implementing sales strategies, coordinating with the marketing team, and delivering excellent service to clients. Qualifications Experience in sales, client acquisition, and account management Strong negotiation, communication, and interpersonal skills Knowledge of pharmaceutical products and industry trends Skills in analyzing market data and creating sales strategies Proficiency in using CRM and other sales-related tools Ability to work independently and efficiently while meeting sales targets Willingness to travel for client meetings and business development Bachelor’s degree in Business, Pharmacy, Life Sciences, or a related field Prior experience in the pharmaceutical sales industry is a plus

Job Title Plant HR & Admin Head Business Unit Global Human Resources Manager Title Cluster HR Head Function Human Resources Reportees 4-5 Direct (1-2 Indirect) Sub-Function Plant HR Grade G8 Location: Dadra Key Responsibilities Position Summary – To lead the HR and Administration functions at the manufacturing plant, ensuring effective people management, compliance and administration excellence in alignment with Sun’s culture, HR policies and business goals. Lead end-to-end HR management at the plant including manpower planning, recruitment, onboarding, performance management and employee engagement. Provide HR insights (data analytics) and recommendations to influence business decisions, ensuring alignment with overall company strategy Drive industrial relations, maintain harmonious relations with operator and handle disciplinary matters as per labour law Implement and monitor central Manufacturing Talent priorities along with corporate HR team e.g., Site Talent Health Scorecard, Succession Planning, Internal talent mobility programs, performance management cycle Partner with Plant leadership to support strategic business needs through talent management and productivity analysis Ensure compliance with statutory requirements under various regulatory guidelines e.g., cGMP, safety to ensure proactive audit preparation from HR perspective Facilitate training & development to instill multi-skilling along with Technical Training and Quality teams Oversee payroll inputs, attendance management and HRMS accuracy Conduct employee engagement, wellness interventions throughout the year Manage employee grievances, resolve conflict and partner with central investigation teams for code of conduct or POSH investigations if any. Co-create a plan to drive awareness programs Supervise general administration including security, transport, canteen, housekeeping, guest house and facility management Ensure infrastructure readiness support for audits and inspection (GMP, USFDA, MHRA) Lead emergency preparedness and safety-related administration protocols. Maintain vendor relationship for admin services and ensure cost effective operations Manage budgeting and cost controls for administrative support Travel Estimate Job Scope Internal Interactions (within the organization) Plant Head, Site Quality Head, Block and production Heads, EHS Head, Compliance & Audit Lead, Corporate HR team members, Finance & Supply Chain Heads External Interactions (outside the organization) Government and regulatory authorities, Labour Office, Contractors, Admin vendors Geographical Scope India Job Requirements Educational Qualification Masters in HR / Business Skills Behavioral skills: Strong knowledge of labour laws and HR best practices for a manufacturing site Excellent communication and interpersonal skills Strategic thinking with the ability to translate business goals into HR strategies Strong problem-solving skills and the ability to make data-driven decisions High emotional intelligence and the ability to manage crisis, conflict & change effectively Functional Skills In-depth knowledge of HR practices, policies, and regulations Experience with talent acquisition, workforce planning, and employee engagement strategies Proficiency in HR management systems (e.g., Workday, SAP SuccessFactors) Strong analytical skills with the ability to interpret HR data and metrics Experience in leading HR initiatives in a complex, matrixed environment Experience Tenure : 14+ years of experience

Job Purpose: To operate and monitor granulation equipment and processes in compliance with cGMP, SOPs, and safety standards, ensuring consistent production of high-quality pharmaceutical granules for tablet or capsule formulation. Key Responsibilities Operate granulation equipment such as high-shear mixers, fluid bed dryers, oscillating mills, and blenders. Weigh, dispense, and mix raw materials as per batch manufacturing records (BMR). Monitor granulation parameters and adjust settings to maintain product quality. Perform in-process checks (e.g., moisture content, granule size) and document results accurately. Clean and maintain equipment and work areas as per SOPs. Execute machine changeovers and line clearance activities. Identify and report deviations or equipment malfunctions to the supervisor. Ensure compliance with cGMP, safety, and environmental regulations. Participate in continuous improvement and troubleshooting initiatives. Qualifications ITI / Diploma / B.Sc or equivalent; technical diploma preferred. 4–6 years of experience in pharmaceutical manufacturing, preferably in granulation. Familiarity with cGMP, USFDA guidelines, and pharmaceutical documentation practices. Ability to read and interpret batch records and SOPs. Basic computer skills and understanding of production documentation. Preferred Skills Attention to detail and strong documentation habits. Mechanical aptitude for operating and troubleshooting equipment. Team player with good communication skills. Forklift certification (if required for material handling).

Role Overview Supervise and oversee all compression operations in a US FDA‑approved Oral Solid Dosage (OSD) manufacturing plant. Ensure tablet compression lines meet cGMP, FDA standards, and production goals. Key Responsibilities Supervise daily tablet compression operations as per cGMP and FDA guidelines. Manage and allocate manpower across shifts for smooth production. Ensure compliance with SOPs, batch records, and regulatory requirements. Monitor in-process checks (weight, hardness, thickness, friability) and resolve deviations. Oversee equipment setup, cleaning, and preventive maintenance. Coordinate with QA/QC for line clearance and documentation accuracy. Handle changeovers and ensure timely completion of production schedules. Train and guide operators on equipment handling and safety protocols. Maintain housekeeping and safety standards in compression area. Prepare daily production reports and escalate issues to management. Qualifications Bachelor’s in Pharmacy or related field. 3–5 years experience in OSD compression; 1–2 years in supervisory role. Strong knowledge of cGMP, FDA 21 CFR Part 211, and data integrity principles. Leadership, problem-solving, and documentation skills.

Job Title Senior Officer / Executive – MSTG Orals Business Unit R&D1 Regulatory Affairs Job Grade G12B/G12A Location Dadra 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 Description To coordinate with different departments i.e. Formulation development (FDD), Analytical development (ADD), Packaging development (PDD), Production, Engineering, Quality control, Quality Assurance, Supply chain, Business development, Project management and any other department for timely execution of New projects To plan, monitor and support for execution of the trial batch, exhibit batch, scale up/characterization batch and process qualification batches To prepare and review new product documents like material requirement sheet, master formula card, bill of material, risk assessment reports, scale up protocol and reports, exhibit/ trial batch manufacturing record and exhibit protocols and reports etc To initiate the gate pass for sample transfer at various sites of Sun Pharmaceutical Industries Limited To prepare and review approve new launch documents i.e. material requisition sheet, product history, trial/ characterization protocol and report, batch manufacturing record, process qualification protocol and reports etc To share process knowledge to cross functional departments through presentation for smooth technology transfer To review and evaluate product history and process parameters for technical remediation and improvement of product robustness To prepare and review investigation report/Justification report, additional activity protocol, regulatory evaluation etc To prepare and review investigation report/Justification report, additional activity protocol, regulatory evaluation etc Travel Estimate NA Job Requirements Educational Qualification M.Pharm Experience Tenure : 2-5 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).

Job Title Executive Business Unit R&D1 Regulatory Affairs Job Grade G12A Location : Baroda 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 Description: - Responsible to work as per cGMP and maintain the compliance requirement Responsible to develop the method for Extractable and Leachable compounds Responsible to perform method validation & verification on different technique for E&L related work Responsible to perform extractable & leachable(s) study for different packaging materials by using different analytical techniques like GC/GC-MS, HPLC/LC-MS, ICP/ICP-MS, IR, UV and other relevant techniques Responsible to perform Identification, Investigation and troubleshooting task. Responsible to perform chemical analysis like, Extraction, Refluxing, Residue on ignition, Centrifuging & Evaporation etc Responsible to prepare the study template, extractable & leachable(s) reports, analytical method validation & verification reports & protocols. Travel Estimate NA Job Requirements Educational Qualification M.Pharm Experience Tenure : 2- 4 yrs 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).

Title: SME Granulation Location: Mumbai/Mohali/ Open to other Sun Locations 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 DESCRIPTION: Job Summary Provide technical leadership for granulation processes and equipment ( wet, dry/roller compaction, and fluid-bed systems ), ensuring robust, compliant, and efficient operations across development, scale-up, and commercial manufacturing & operations at all sites of SGO. Area Of Responsibility Technical Expertise • Act as the primary expert for high-shear mixers/RMG, fluid-bed granulators/dryers (FBD), roller compactors, milling and blending systems , bin handling, and closed transfer systems. • Define and optimize critical process parameters (CPPs) and material attributes (CMAs) for consistent granule quality (PSD, LOD, porosity, flowability—Carr Index / Hausner Ratio). Troubleshooting & Support • Lead resolution of chronic issues: low yield, poor granule flow, inconsistent LOD, segregation, over/under granulation, capping/chipping in downstream compression. • Execute structured RCA (5-Why, Fishbone) and implement permanent corrective actions. Process Optimization/Benchmarking • Drive OEE improvement, cycle time reduction, and SMED for batch changeovers. • Implement PAT tools (e.g., NIR moisture, torque/power trend analysis) and digital logging to stabilize batches. Compliance & Validation • Ensure adherence to cGMP, cleaning validation, cross-contamination control, containment (OEB levels), ATEX/dust explosion safety. • Own equipment lifecycle: URS FAT/SAT IQ/OQ/PQ, change control, and periodic review; ensure 21 CFR Part 11 compliance for data integrity. Training & Capability Building • Ability to Train operators/maintenance on best practices: endpoint detection, sieving/milling, cleaning/line clearance, and safety protocols. Vendor/OEM Management/Emerging Technologies • Liaise with OEMs for upgrades, process audits, spares, retrofits (e.g., WIP/CIP, improved bowl designs, containment solutions). • Candidate should have a flair to remain update on latest Trends and technologies in the field Physical Requirements: Physically fit for extensive Travel Technical Knowledge • Granulation science: binder systems, torque/power curves, endpoint criteria, moisture profiles, PSD control, and downstream compressibility. • Equipment qualification and validation; data integrity; cleaning validation; containment and ATEX. • CI toolset: TPM, Lean, Six Sigma (Green/Black Belt preferred), SMED, Kaizen. • Digital & Analytics: Comfortable with OEE dashboards, trend analysis, PAT signals, and batch data review for CPV. • Soft Skills : Strong problem-solving, shop-floor presence, stakeholder influence, and vendor management. *Work experience with Equipment manufacturers will be an added advantage Travel Estimate Up to 40%-50% India and Globally Job Requirements Educational Qualification Bachelor’s or Master’s degree Experience 12–15 years in pharma granulation (OSD), with hands-on exposure to wet granulation, fluid-bed drying, and roller compaction. 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).

Job Title Executive Business Unit R&D1 Regulatory Affairs Job Grade G12A Location : Baroda 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 Description: - The candidate is expected to develop Surface Plasmon Resonance (SPR) based methods to measure the kinetic and equilibrium binding constants for protein and peptide products. Responsible for analytical method qualification for all pipeline products. Characterization of innovator product batches sourced from different geographical region and preparation of qualitytarget profile. Analytical similarity assessment of in-house products. Preparation of method development reports (MDR) and analytical test procedures (ATP). Responsible for operating and maintaining analytical laboratory in compliance with GLP regulations. The candidate is responsible for the operation and maintenance of the SPR instruments To manage chemicals,consumables & critical reagents inventory. Performs calibration of instruments and equipment. Troubleshoots instrument performance and equipment issue Travel Estimate NA Job Requirements Educational Qualification M.Sc. Experience Tenure : 2-4 yrs 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).

Job Title Senior Executive IT- Quality Informatics Job Grade (refer to JE) G12A/G11B Function Information Technology Sub-function Quality Informatics Location: Dadra Areas Of Responsibility 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 Summary The Job holder will be responsible to Lead the Quality Informatics Team and maintain software related data of Laboratory Instrument / Equipment’s as an Application Administrator and perform the activities of Laboratory instruments and also for Manufacturing System software’s like Archival / backup, restoration, validation & qualification etc. Responsibilities Manage and perform Quality Management System like Change Control/Deviation etc. To maintain software related data of Laboratory Instrument / Equipment’s as an Application & System Administrator. To perform activities like creation / modification /Disable / Re-activation of User Account(s) and assigning of privileges for application. To prepare, review configuration specification documents. To prepare and review standard operating procedures associated with the planning, development and operation of IT related systems. To maintain User Account Request / record of user(s) for Laboratory application. To perform the activities of Server software like: Project creation, template migrations, Archival / backup of soft data, Restore projects. To perform the activities of standalone Laboratory instruments software’s like Archival / backup, restoration etc. To prepare periodic review scheduler and execute periodic review of each instrument accordingly. To control and maintain the Password of Analytical Balances, pH meter and Stability chambers (HMI) used in the Quality Control Laboratory. To prepare validation / Review documents such user as requirement specifications, validation plans, test plans, summary test result and final validation reports. IT activity related to IQ/OQ/PQ and configuration policies for standalone Laboratory instrument software. To coordinate and verify that all validation activities and documents comply with applicable regulations and internal procedures at all locations. To follow and comply timeline adherence with the new IT project plan and CSV compliance. To monitor and maintain record of Quality Control IT compliance status. To support site IT for regulatory compliance. Accountable for designing/implementing and ensuring compliance to all quality related, Policies, Standards and IT systems at QC of the site. Facilitate internal and regulatory agency audits, ensuring that findings from site QC audits are understood, assessed and addressed site wise in a comprehensive manner. Travel Estimate Based on the need job holder can travel to other sites. Job Scope Internal Interactions (within the organization) QI and CSV Teams, Business Users, Corporate IT & Plant Management Teams External Interactions (outside the organization) Business Users, External Vendors Geographical Scope Provide onsite support to Dadra, other site whenever needed. Financial Accountability (cost/revenue with exclusive authority) Based on Approved Budgets for the sites – Both Opex & Capex Job Requirements Educational Qualification BE/B. Tech, MCA, BCA, MSc IT, BSc. IT, Graduation + PGDCA. Specific Certification NA Experience 3-9 year Skill (Functional & Behavioural): QI support, CSV Support, IT regulatory requirements, Validation & Qualification activities as per standards, backup related activities. 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 employees 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 the incumbent(s).

Job Title Executive – Regulatory & Business Continuity Business Unit R&D1 Regulatory Affairs Job Grade G12A Location Panoli 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 Description To evaluate and categories QMS related activities like Change Controls w.r.t. US/EDQM/Europe/UK/Australia/Japan/Korea/CADIFA/China/South Africa guidelines To Review, follow up and compilation of data for submission of USDMF, CEP, DCP, CP, MRP for New DMF submission and DMF-Amendment / Update based on the Planning To Review, follow up and compilation of data for submission of Japan, China, TGA, Canadian... for New DMF submission and DMF-Amendment / Update based on the Planning Compilation of raw data for Registration /re-registration and queries received from authorities for ROW market, such as China, Korea, Taiwan, Indonesia, South Africa...etc Travel Estimate NA Job Requirements Educational Qualification Graduate : M.Sc Experience Tenure : 2-5 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).

Job Title Senior Officer / Executive – MSTG Orals Business Unit R&D1 Regulatory Affairs Job Grade G12A/G12B Location Dadra 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 Description To coordinate with different departments i.e. Formulation development (FDD), Analytical development (ADD), Packaging development (PDD), Production, Engineering, Quality control, Quality Assurance, Supply chain, Business development, Project management and any other department for timely execution of New projects. To plan, monitor and support for execution of the trial batch, exhibit batch, scale up/characterization batch and process qualification batches To prepare and review new product documents like material requirement sheet, master formula card, bill of material, risk assessment reports, scale up protocol and reports, exhibit/ trial batch manufacturing record and exhibit protocols and reports etc To provide the regulatory response and technical justification To initiate the gate pass for sample transfer at various sites of Sun Pharmaceutical Industries Limited To prepare and review approve new launch documents i.e. material requisition sheet, product history, trial/ characterization protocol and report, batch manufacturing record, process qualification protocol and reports etc To share process knowledge to cross functional departments through presentation for smooth technology transfer To review and evaluate product history and process parameters for technical remediation and improvement of product robustness To prepare and review investigation report/Justification report, additional activity protocol, regulatory evaluation etc Travel Estimate NA Job Requirements Educational Qualification Graduate : M.Pharm Experience Tenure : 2 – 5 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).

Job description Responsible for operation of Packing activities machine wise. Responsible for cGMP compliance in Packaging department Responsible to produce good quality product without complaint. Responsible for any other work to be performed as and when allotted by reporting authority. Responsible for fulfillment of production target monthly and daily basis. Interested candidate can send resume to akash.gogoi@sunpharma.com Job Location: Palasbari, Assam

Job description Responsible for operation of Granulation activities machine wise. Responsible for cGMP compliance in Granulation department Responsible to produce good quality product without complaint. Responsible for any other work to be performed as and when allotted by reporting authority. Responsible for fulfillment of production target monthly and daily basis. Interested candidate can send resume to akash.gogoi@sunpharma.com Job Location: Palasbari, Assam

Responsible for operation of compression activities machine wise. Responsible for operation of compression machines FETTE,SEJONG, CADMACH & BILAYER products Responsible for cGMP compliance in compression department Responsible to produce good quality product without complaint. Responsible for any other work to be performed as and when allotted by reporting authority. Responsible for fulfillment of production target monthly and daily basis. Interested candidate can send resume to akash.gogoi@sunpharma.com Job Location: Palasbari, Assam

Key responsibilities: To Ensure completion of all SOP as Training need matrix. To participate in the training programme and share the knowledge to the concern line members. To execute the Granulation activity as per the written procedure of SOP on line. To involve in the investigation pertaining to Supervised line for any Market compliant. To ensure Quality adherence during all stages of Granulation Operation To check Daily Verification and Monthly Calibration of checkweigher and balances. To control the rejection on line, with all the rejections bin are under lock and keys. To Follow Daily Plan and Execute the same. To Obtain the Line Clearance as per BPR, SOP and Checklist. To Monitor, Perform and record online inprocess Critical Process parametres, Such as Leak test, camera Checks, Pharma code challenges, Splice joint checking & verification, Forced rejection parametres ,rejection Handling and follow the same ,in case of any discrepancies same shall be reported to shift incharge. Responsible to fill all the log Books/BPR on line to maintain Data Integrity & GDP Compliance. To Follow up and organise the BPR, PM, Stereos from concerned responsible person to initiate the Granulation line operation. Responsible for generation of TRF, SAP posting for release. Ensure for improvement initiatives and Participate in PACE Activities. . To ensure for meeting of Line productivity as per the Plan and ensure that machines run as per Optimum validated speed. To Ensure & justify the utilization of resources to increase the Productivity/Person. Any other responsibility to be completed that may be assigned for time to time. Reconciliation of PM, rejection analysis and closing of BPR To Maintain work discipline and time management in area. Delegation of Responsibility : In the absence of job holder, delegation of responsibility shall be proceed as follows: a) Upward Delegation: - Strategic responsibilities upward to higher level. b) Downward Delegation: - Operational responsibilities downward to direct reporters or similar Job role. To provide at least four Kaizen in yearly basis. To identify safety related observation, report near miss and ensure for its online compliance. To Ensure that all the machine runs with proper Safety Guard, interlocks. To follow procedure, guidelines, polices, practices, requirement and carryout activities in safe manner. To take care of the equipment (Cleaning and Preventive maintenance) and document the same and if observation is there same to be communicated to shift incharge for intimation to Engg. Team. Interested candidates can send resume to akash.gogoi@sunpharma.com

Title Corporate Quality Projects- sLIMS Business Unit Corporate Quality IT Job Grade Sr. Executive Location : Vadodara 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. Position Summary To support Business owner for the timely execution and completion of qualification activities. To identify the actionable and accomplish the project milestone. To ensure preparation and review of qualification script, perform dry run and ensure updating of script as per the observations. To perform PQ activities as per approved script, raise TPR for any discrepancies and share to respective team for resolution. To ensure support to business during execution, qualification as well as Post Go-Live of all application and resolve their issues, if any. To review and approve documents related to project. To support for database creation, preparation and designing of execution sheet of each project. To perform functional testing with positive and negative challenge with logical program, as and when required. To ensure technical training/ support for each site, whenever required. To prepare and review of SOP/protocol related to project. Support to Site SME's and business owner for Stabilization of projects at all sites. To conceptualize and frame a consolidated approach for new identified requirements. To ensure support vendor for technical discussion for finalization of application functionalities. To ensure review of application functionalities as per current procedure through virtual testing. To coordinate operational change management /test activities to ensure ongoing compliance with business and regulatory requirements. To perform the activities as per the project plan for newly identified projects. To perform activities related to harmonization of SOP's and to ensure implementation Harmonized SOP's for calibration across sun sites. To perform activities related to harmonization of SOP's and to ensure implementation Harmonized SOP's across sun sites To implement GSOP/GQS for harmonized procedure. To support any other project initiated for simplification and productivity enhancement. To work in collaboration with IT, API, SGO, Site Quality and different teams for identification of the right solution /tool/Vendor, to resolve the Specific problem statement and have correct solution for the organization. To ensure successful handover of the projects to their respective business owner, upon completion. Support sites during the regulatory audits and internal/external audit observations. The above list is not exhaustive and may be assign additionally responsibility from time to time. In the case of absenteeism, Job responsibilities shall be delegated to his/her designee. Travel Estimate Medium-High Job Requirements Educational Qualification Master in Science/ B. Pharm Experience 8-10 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).

Job Title Officer Business Unit Sun Global Operations Job Grade G12C Location : Ranipool 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. Key Responsibilities Supervision of compression activities machine wise. Responsible for cGMP compliance in compression department Responsible for proper manpower utilization in department Responsible for BMR review Responsible for DPR preparation Responsible for follow the SOPs for every activity. Responsible to produce good quality product without complaint. Responsible for any other work to be performed as and when allotted by reporting authority. Responsible for fulfillment of production target monthly and daily basis. Responsible for maintaining of Punch Utilization and Tool Room record. Responsible for SAP and EDMS related activities Responsible for operation and cleaning of Punch Polishing Machine. Responsible for closing the BMR in compression stage on SAP in daily basis Responsible for taking line clearance from QA. Co-ordination with QA/QC/Store/Engg./Granulation/coating/packing department for smooth functioning of compression activities. Responsible for operation, cleaning and calibration of Friability Apparatus. Responsible for operation, cleaning and calibration of Auto tester 4 Responsible for operation, cleaning and calibration of Disintegration Apparatus. Travel Estimate Job Requirements Educational Qualification B.Pharma Experience Tenure : 2 to 4 Yrs 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).

Job Title Executive Business Unit R&D1 Regulatory Affairs Job Grade G12A Location : Baroda 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 Description Impurity Synthesis to avoid external procurement Literature search with respect to assigned project and its documentation Experimentation (Process development, optimization and validation) Analysis, interpretation (HPLC, IR, NMR, Mass and CHN) and documentation of data General Laboratory Management etc. Require to Plan and carry out Chemistry related experiments, recording the observation in Protocol Computer literacy etc. Travel Estimate NA Job Requirements Educational Qualification M.Sc. Experience Tenure : 2- 4 yrs. 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).