About Sun Pharma: Sun Pharmaceutical Industries Ltd (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of US$ 5 4 billion Supported by 43 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe, Job Summary LIMS Testing & Documentation Specialist will be responsible for the thorough testing of LIMS application before deployment or patch deployment This role requires a deep understanding of laboratory workflows, strong technical & testing skills, and the ability to work closely with cross-functional teams to ensure the LIMS meets the needs of the organization Roles and Responsibilities Support testing of LIMS functionalities to ensure the functionality available, is working as per usersexpectation as well as it meets the approved user requirement specification, Develop testing strategy and execute it to meet the implementation timelines, Perform the impact assessment of newly added functions on the existing functionalities, Rigorously test the newly introduced functionalities based on its impact on the existing functionalities, Provide training and support to end-users, ensuring they are proficient in using the LIMS, Troubleshoot and resolve any issues related to LIMS performance, functionality, and integration with other systems/instruments, Maintain comprehensive documentation of the LIMS implementation process, including user guides and technical manuals, Shall be aware about documentation of LIMS application as per GMP Shall be able to create and manage documentation of LIMS application to ensure system is in compliance state, Qualifications and Preferences Qualifications: Bachelor's degree in Information Technology, or Computer Science or related field, Minimum of 4-5 years of experience in LIMS implementation & Instrument Integration activity, preferably in a pharmaceutical or biotech environment, Strong understanding of laboratory processes and workflows, Proficiency in LIMS software (Expertise on CaliberLIMS is preferred) Excellent testing skills, with the ability to manage multiple tasks and projects simultaneously, Strong analytical and problem-solving skills, Excellent communication and interpersonal skills, Experience with regulatory compliance requirements (e-g , FDA, GMP, GLP), Preferred Qualifications: Advanced degree in Life Sciences, Information Technology, or a related field, Familiarity with laboratory instruments and their integration with LIMS Experience with Caliber LIMS is preferred, Good documentation skills to create and manage GxP documents, Selection Process: Interested Candidates are mandatorily required to apply through the listing on Jigya Only applications received through Jigya will be evaluated further, Shortlisted candidates may need to appear in an Online Assessment and/or a Technical Screening interview administered by Jigya, on behalf on Sun Pharma Candidates selected after the screening rounds will be processed further by Sun Pharma

About Sun Pharma: Sun Pharmaceutical Industries Ltd (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of US$ 5 4 billion Supported by 43 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe, Job Summary sLIMS Implementation Specialist will be responsible for the successful deployment, configuration, and ongoing support of our Laboratory Information Management System (SLIMS) This role requires a deep understanding of laboratory workflows, strong technical skills, and the ability to work closely with cross-functional teams to ensure the SLIMS meets the needs of the organization, Roles and Responsibilities Support in implementation and configuration of the sLIMS, ensuring alignment with laboratory workflows and regulatory requirements, Execute the tasks defined in project plans, adhering to timelines, for successful implementation of sLIMS, Configure sLIMS software to meet the specific needs of the laboratory, configuring workflows, and setting up user roles and permissions, Provide training and support to end-users, ensuring they are proficient in using the sLIMS, Troubleshoot and resolve any issues related to sLIMS performance, functionality, and integration with other systems/instruments, Maintain comprehensive documentation of the sLIMS implementation process, including user guides and technical manuals, Shall be aware about documentation of sLIMS application as per GMP Shall be able to create and manage documentation of sLIMS application to ensure system is in compliance state, Qualifications and Preferences Qualifications: Bachelor's degree in Information Technology, or Computer Science or related field, Minimum of 4-5 years of experience in sLIMS implementation, preferably in a pharmaceutical or biotech environment, Strong understanding of laboratory processes and workflows, Proficiency in sLIMS software (Expertise on CaliberLIMS is preferred) Ability to manage multiple tasks simultaneously, Strong analytical and problem-solving skills, Excellent communication and interpersonal skills, Experience with regulatory compliance requirements (e-g , FDA, GMP, GLP), Preferred Qualifications: Advanced degree in Life Sciences, Information Technology, or a related field, Familiarity with laboratory instruments and their integration with SLIMS Experience with Caliber LIMS is preferred, Good documentation skills to create and manage GxP documents, Selection Process: Interested Candidates are mandatorily required to apply through the listing on Jigya Only applications received through Jigya will be evaluated further, Shortlisted candidates may need to appear in an Online Assessment and/or a Technical Screening interview administered by Jigya, on behalf on Sun Pharma Candidates selected after the screening rounds will be processed further by Sun Pharma

Role & responsibilities Review of Raw Material/Packaging Material /Stability/ Microbiology/ Cleaning Method Validation/ Validation/ Finished Product Analytical data, Certificate of Analysis & related documents. Review and approval of Exhibit Stability Protocols. Preparation and review of validation /pre-validation /commercial/annual addition batch/thermal excursion/additional study stability protocol. Approval of additional testing requests (if required). Review and approval of ln-Vitro/CU and dissolution sheets. Review and approval of Analytical Method Transfer documents. Participation in handling OOS, OOT, Investigation and deviations related to Quality Control. Review and approval of weekly and monthly software verification reports of Empower3. Periodic verification of application software on computer systems, associated with laboratory instruments with system administrator. Review of lab instruments calibration/preventive maintenance data. Review of Stability test results in NOVATEK software. Approval of Certificate of Analysis. Review and submission of analytical data to site regulatory affairs. To provide the response of regulatory affairs and Office of data reliability queries. Review and approval of change control request, specification, standard test procedure and SOP in Documentum Compliance Manager System. Preferred candidate profile Educational Qualification : B.Pharma/M.Pharma with 5 to 7 Yrs of working experience Mandatory USFDA Plant Exposure is required. Note - Sun Pharma does not seek payment of any kind from a prospective candidates for employment with Sun Pharma or authorise any agency or any individual to collect or charge any fees or charges for recruitment. Please be cautious while dealing with any recruitment agency or anyone asking you to pay money representing himself to be representing Sun Pharma.

Job Summary : Pharmaceutical experience is mandatory. Engineer designs, installs, and maintains systems like security, fire alarms, communication, and audio-visual systems, focusing on the technical aspects of these low-voltage electrical systems. Areas of Responsibility : Design and Planning: Develops and designs ELV systems for various projects, including commercial, residential, and institutional buildings Installation and Maintenance: Performs ongoing preventive maintenance and repair work on facility electrical and ELV systems. Project Management: Monitors work progress and site safety in compliance with contractual and statutory requirements. Technical Skills: Expertise in various ELV systems, including fire alarms, public address, security systems, and audio-visual systems. Knowledge of relevant codes, standards, and regulations. Ability to prepare drawings, documents, and statutory submissions. Familiarity with cable fault detection, insulation resistance tests, and preventive maintenance Assists project managers in overall project operations, coordination, and handover. Supervises junior technical staff and subcontractors to ensure smooth project execution. Knowledge of relevant codes, standards, and regulations Ability to prepare drawings, documents, and statutory submissions. Compliance and Regulations: Ensuring compliance with all relevant regulations and industry standards. Experience of Projects of Injectable / OSD block for Pharmaceuticals industries Job Location : Central India / South India (For Greenfield Project)

Role & responsibilities Responsibility of Upstream activities in bulk manufacturing facility. To ensure that upstream batches are carried out as per manufacturing instructions following relevant Process Development description document, MFR, SOPs, BMRs, Protocols etc. and to ensure appropriate documentation in order to maintain cGMP compliance Preferred candidate profile Preparation of process documents (PCS, MFR, BMR), SOPs, protocols, related documents for upstream activity. Hands on experience in operations of seed and production fermenters, continuous centrifuge, homogenizer and continuous involvement and support for commercial batches etc., Involving and supporting in Sun Pharma CQA audits, internal audits ,local DGCI audits CDSCO and any other third party/national &international regulatory agencies. Review of batch manufacturing records and related documents in upstream. To understand and follow the safety practices and usage of PPEs in Bulk Manufacturing facility and during process. Execution of Scale up of Development batches, commercial batches and other assigned tasks in Bulk manufacturing facility as per the assigned shift schedule (A,B,C Shift) hours. Ensure Facility monitoring, readiness & maintenance of BM facility. Coordination with engineering department on tracking and completion of preventive maintenance and calibration of Upstream process Equipment and instruments. Following good documentation practices such as online documentation like BMR, equipment log, record sheets, etc. in upstream process. Following up with Vendors on equipment and instrument related to upstream process. Support for creation of Process Order/material reservation related to SAP transactions and handling of QMS elements activities. Support and fulfill for any additional job work activities /other job responsibilities/tasks assigning by reporting manager.