Handling entire transaction relating to variety of corporate commercial agreements & other legal documentation from initiation, drafting, vetting, negotiation, finalization & execution for IRF business and other SBUs Creating standard template agreements & other legal documentation for internal business teams Advising on various marketing activities/ initiatives for IRF business Application of principles of law to transactions, holding discussions with business & cross functional teams, advising transaction structure and ensuring execution of appropriate legal documentation Tracking, monitoring and controlling the status of various transactions through the contract life-cycle management system and generating MIS/ reports Advice, support and guidance to business & cross functional teams on various transactions Such other work as may be assigned from time to time based on needs of the team and the business Competencies Customer Centricity Process Excellence Developing Talent Collaboration Strategic Agility Stakeholder Management Innovation & Creativity Result Orientation Education Graduation in Law Work Experience 6 plus years of experience, preferably pharma sector

Execution of production batches in the Upstream process area as per approved BPR and timely documentation of the same. Operating of Upstream equipment for process and CIP/SIP as per SOP e. g. 100 L fermenter, Centrifuge, High Pressure homogenizer, spectrophotometer, Autoclave, DHS, Cold room, Integrity Machine etc. Preparation of process and equipment related SOPs. Raising change control and deviations in the QA approved format and working with concern departments for closure of the same. Timely instructions to engineering team in case of facility or equipment breakdown. Coordination for PM/AMC of manufacturing equipment. To Assist in Technology transfer from R&D to Manufacturing To attend on Job, cGMP and Safety trainings To ensure safety at workplace

Long Description Responsible for submissions of Response to Deficiencies to Health Agencies of Europe, Australia, New Zealand and Canada market and Customers. Responsible for post approval submissions to Europe, Australia, New Zealand and Canada market. To provide Regulatory inputs during inspections by Regulatory authorities and Customer as and when required. To provide Regulatory inputs during product development, manufacturing and testing and to evaluate all types of change proposals during product life cycle Competencies Customer Centricity Developing Talent Collaboration Strategic Agility Process Excellence Stakeholder Management Innovation Creativity Result Orientation Education Masters in Pharmacy Work Experience 5 to 6 years in Europe, Australia, Canada markets

1 Coordination, Implementation, execution, and completion of projects in time within allocation budget. 2 Coordination with between different inter-departmental team, site project team, consultant, and vendors. 3 Project planning and preparing schedule and tacking work progress. 4 Check and track all long lead items for procurement of materials. 5 Preparation of techno commercial evaluation. 6 Ability to work multiple projects in various stages. 7 Hands of experience in handling Electrical, Instrumentation projects, Pharma Process equipment & utilities, Water system. Competencies Strategic Agility Innovation & Creativity Process Excellence Customer Centricity Collaboration Stakeholder Management Developing Talent Result Orientation Education B.Tech Graduation in Electrical Work Experience Year of Experience 5 to 6 Years in field of Pharma

Long Description - Preparation of dossiers for Europe, Australia, New Zealand, and Canada (EANC). - Responding to queries from regulatory agencies of EANC advanced markets and customers. - Liaising with R&D, manufacturing plants, clinical teams, and respective EANC offices/BD teams. - Assisting in the life cycle management of EANC-registered products by obtaining variation approvals. - Maintenance of departmental databases. - Regular study of regulatory guidelines and electronic Common Technical Document (eCTD). Competencies Customer Centricity Developing Talent Collaboration Strategic Agility Process Excellence Stakeholder Management Innovation & Creativity Result Orientation Education Masters in Biochemistry Work Experience 2 years experience in RA

Long Description Department: Production Designation: Jr. Officer - Production (E0) Working Section: Granulation / Compression / Coating Comply with all cGMP, GxP and any other applicable regulatory requirement, including EHS requirements. Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task. Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to immediate supervisor/managers. Report any quality concern or suggestion for improvement to supervisors/ managers. Manufacturing / processing of batches of assigned products under supervision as per instructions given in the BMR. Handling and movement of raw material, bulk, semi-finished and finished goods. Operation, washing and cleaning of equipment s and accessories used in related production activities as per respective SOP. Up-keeping area and machines as per GMP requirements. To Support Quality Management Systems and to report any discrepancy, abnormity, non-conformance or any incidence observed to the Department Head and QA Head. Receipt of RM and PM from Warehouse and ensuring overall cleanliness of areas. Doing operations as per the SOPs and BMR with online recording in respective documents as applicable. To ensure self-hygiene before entering in the production area and follow all the other rules regulation set by HR department. Performing in-process checks as per respective BMR and recording of results of in respective documents as applicable. To fulfil the training need as per current needs with respect to cGMP, Job, safety, health Hygiene by attending the training programmes. Cost effectiveness in production operation by controlling overtime, revenue expenses and achieving standard yield. Critically monitoring of the environmental conditions with a view to meet the standards mentioned in BMR and SOP. Ensure calibration and preventive maintenance of manufacturing equipment and instruments as per approved schedule and the results of same meeting the standards. To perform line clearance activity during batch to batch and product to product change over and ensure the compliance as per SOP. Issuance, retrieval and destruction of dies and punches, product dedicated bags and sieves, silicon sleeves, pipes, hose pipes and screens. To ensure the audit compliance. Trouble-shooting: To attend the problems of machine and process as and when necessary. Any other assignment allocated by production Head. To attend required cGMP/ On Job /Functional training activities as per planner. Competencies Customer Centricity Developing Talent Collaboration Strategic Agility Process Excellence Stakeholder Management Innovation Creativity Result Orientation Education Work Experience

Role & responsibilities Round the clock monitoring of LBC facility in shifts.To maintain HK standards up to the mark in the old as well as new premises.To prepare MIS for all admin activities related to LBC facility. Should be ready to attend office in shifts. Labour compliance check. Labour recruitment through vendor. Material inventory.Pest control management. Cafeteria Management. Transport Management. Preferred candidate profile Knowledge of MS office & SAPExperience in hotel or facility management

Job Description Accountable for successfully delivering the assigned clinical trial(s) in compliance with Lupin SOP, ICH-GCP and applicable Ensure compliance with regulatory requirements within the assigned budget. Maintain and provide information regarding monthly study status, risks and mitigation strategies (including enrollment curves and timelines), and report this information to senior management. Lead the site selection process by identifying potential investigators for clinical trial(s). Accountable for the timely submission of applications/documents to the applicable regulatory authority and IRB/EC at startup and throughout the duration of clinical trial(s). Review study documents, such as the study protocol and ICF, and provide feedback. Ensure that clinical trial(s) are registered with the appropriate regulatory authorities. Prepare study and site-related manuals, plans, logs, and operational documents. Review protocol deviations and the escalation process to ensure that appropriate follow-up actions are taken. Oversee monitoring of the clinical trial, including reviewing visit reports and conducting co-monitoring visits with CRA(s) and/or sponsor oversight visits. Ensure that all aspects of GCP compliance and audit readiness are maintained throughout the conduct of the trial. Prepare reports and presentations on study progress for senior management. Lead CRA(s), CTA(s), and the project for assigned clinical trial(s). Provide significant input into the development of the Case Report Form to influence the final version. Manage clinical trial materials and assist in forecasting. Track and report on study expenditures. study spend Work Experience Minimum 6 years of clinical project management experience. Ability to manage delegated aspects of assigned clinical trial Ability to manage CRO and Clinical Study Vendor Robust understanding of ICH GCP and knowledge of Regulatory Requirement Proficiency in MS office including Word, Excel, Power point and other applications Strong clinical stud/project management skills Outstanding communication skills, both verbal and written Ability to work Independently and prioritize duting Understanding of EDC, CTMS, eTMF etc Education Masters in Life Science or Pharmacy Graduation in Dental Surgery or Ayurveda Competencies

Knowledge of Energy monitoring system, Analysis Energy saving technique. Knowledge of Electrical project like Electrical load calculation, capacity calculation of Transformer, HT Panel, Bus bars, PCC, MCC APFC Panels. Knowledge of URS, IQ, OQ, PQ, Change control, Deviation, CAPA, QAMS, Qualification Documents, preparation of SOPs and preventive maintenance documents. Should be conversant with Knowledge of procedure to be followed in Good Manufacturing practices area. Knowledge of Operation Maintenance of HT, LT Substation, DG sets, UPS and Electrical PCC, MCC, Panels. Should have Knowledge and experience to handle modification and project activity. Should have electrical Knowledge of Process equipment of biotech plant. Should have Knowledge of Licensing work of MSEDCL, Electrical Safety Norms like Electrical work permit LOTO Knowledge of Motor, DOL, star delta starter, VFD, Door interlocking system, Pass box and equipment control drawing. Should have good knowledge of various document preparation tools like as MS word, MS power point, AutoCAD..

Job Description Supervise compliance to all cGMP, or any other regulatory requirements, including EHS requirements into Granulation section. Complete self-training and monitor training of team members on the relevant SOPs. Report any quality concerns or suggestions for improvements in granulation area to production head. To ensure the implementation of Current Good Manufacturing Practices. To improve instruction/documents related to production and ensure their strict implementation. Enforcement and maintenance of high degree morale, discipline and technical expertise of the team. To ensure the maintenance of the premises and equipment. To ensure that the required initial and continuous training is being carried out for all the employees. Carrying out self-inspections and review of self-inspection reports. Carrying out vendor audits/inspections as and when required. Execute and supervise all tasks and activities as per the applicable SOPs. To ensure that products are produced and stored according to the appropriate documentation in order to obtain the required quality. To approve the procedures relating to production operations and to ensure their strict implementation. Work Experience 14 to 18 years Education Masters in Pharmacy Graduation in Pharmacy Competencies Strategic Agility Innovation & Creativity Customer Centricity Developing Talent Result Orientation Process Excellence Collaboration Stakeholder Management

Long Description Department:Production Designation:Officer - Production Working Section:Vial Filling & PFS Filling Area. Comply with all GMP, GxP, and any other applicable regulatory requirements, including EH&S requirements. Complete training on relevant SOPs and perform tasks as per the applicable procedures, reporting any deviations or difficulties. Plan departmental activities as per delivery schedules, ensuring material availability and proper handling of raw materials, bulk, and finished goods. Coordinate with Engineering, QA, and other departments to ensure smooth production operations. Maintain hygiene, discipline, and current good manufacturing practices in all production areas. Optimize usage of manpower, machinery, and materials, manage inventory, and allocate jobs effectively. Perform troubleshooting for machinery and processes. Support quality management systems and report discrepancies, non-conformance, or incidents to department and QA heads. Any other assignment allocated by Manager. Competencies Strategic Agility Process Excellence Collaboration Innovation & Creativity Result Orientation Stakeholder Management Customer Centricity Developing Talent Education Diploma Graduation in Pharmacy Work Experience 2-5 Yrs.

Long Description Assign and coordinate with external vendors and execute the HVAC & Utilities validations as per planned schedule with coordination of user departments. Develop good rapport with external agencies to ensure validation of system is in place on time and ability to lead team of 5 to10 members. Develop and maintain accurate, efficient HVAC & Utilities operational and validation procedures. Keep abreast of the latest amendments as per ISO14644 and other regulatory standards. Implementation and review of departmental documentation & QMS activities. Shall have Hands-on experience on Change Control Management, Investigations & CAPA modules. Tracking allocated QMS task completion and closer within time. Lead continuous improvement initiatives in the HVAC & Utilities to increase process efficiency, energy conservation and capacity while maintaining a high level of quality. Should have hands on experience in HVAC / BMS / EMS / Air compressors / Air Dryers/ Heat Pumps /Brine chillers / Chillers / Cooling Towers etc. Analysis of breakdown notifications. Maintaining and procurement of critical spare parts. Preparing and renewal of annual maintenance contracts with external agencies. Maintaining UPS & electrical panels in safe and compliance condition. Ensure compliance to cGMP and quality system. Develop and train the HVAC & Utility staff on procedures and validations. Having exposure to face the regulatory auditors like USFDA, MHRA, ANVISA and TGA etc. Prepare the budget and capex for the engineering department and monitoring of yearly expenditure of engineering department. Legal compliance with respect to safety & environment, licensing with government authorities. Competencies 3. Customer Centricity 2. Innovation & Creativity 6. Process Excellence 8. Stakeholder Management 4. Developing Talent 7. Collaboration Education B. Tech Diploma in Mechanical Engineering or Electrical Work Experience 6 to 8 Years in Injectable HVAC & Utilities lead position

Lupin Pharmaceuticals Pvt Ltd is looking for Associate to join our dynamic team and embark on a rewarding career journey Processing requisition and other business forms, checking account balances, and approving purchases Advising other departments on best practices related to fiscal procedures Managing account records, issuing invoices, and handling payments Collaborating with internal departments to reconcile any accounting discrepancies Analyzing financial data and assisting with audits, reviews, and tax preparations Updating financial spreadsheets and reports with the latest available data Preparation of operating budgets, financial statements, and reports Reviewing existing financial policies and procedures to ensure regulatory compliance Providing assistance with payroll administration Keeping records and documenting financial processe

1. Responsible for overall engineering functions of OSD & Injectable plant. 2. Responsible for O&M of utility, HVAC, Water system & process maintenance. 3. Responsible for PM/Calibration/Facility maintenance and department safety function. 4. Responsible for regulatory / statutory audit compliance at site. 5. Responsible fo preparation of maintenance reports, budget & expense control. Work Experience 18 to 22 years Education B.Tech in Mechanical Engineering Competencies

Long Description Define productivity metrics and align operating definitions with QC teams. Simplify and digitize data for reporting QC productivity metrics. Publish monthly QC productivity metrics reports for all labs. Identify improvement levers for QC productivity and develop action plans to address them, reporting progress regularly. Manage projects and track the deployment of new technology in QC. Technical/Functional Skills: Hands-on experience in operations, with a strong understanding of Lean Manufacturing methodologies. Proficient in data analysis using Excel/Minitab. Proven track record of executing high-value projects. Competencies Developing Talent Innovation & Creativity Result Orientation Strategic Agility Process Excellence Customer Centricity Collaboration Stakeholder Management Education Masters in Business Administration Graduation in Biopharmaceutics 6 - 8 Years of Work Experience

1.Ensure smooth operation and maintenance of ETP & Zero liquid discharge plant (RO, MEE & ATFD). 2.Waste management (Hazardous, Biomedical waste, E-waste & Battery Waste etc.) and handling as per SPCB norms. 3. Knowledge about environmental & Safety regulations. 4.Prepare and follow all EHS Guideline & SOP. 5.Ensure compliance to all applicable EHS regulations. 6.Conducting the EHS Risk assessment and aspect impact, EHS audits, to complete all the related documents. 7. Planning and conducting the EHS training. 8.Manpower planning works allotment and follow up. 9.Implementation of ISO 45001 & ISO 14001 standards at site. 10.Training on EHS topics / modules / guidelines to increase awareness among the workforces. Ensure CEHS Guidelines compliance at site. Work Experience 2 - 4 year Education Graduation in Environment Science or Science Masters in Chemistry or Biology Competencies Customer Centricity Stakeholder Management Collaboration Process Excellence Result Orientation Developing Talent Strategic Agility Innovation & Creativity

Follows the Good Laboratory Practices, Safety measures and good documentation practices while working. Follow the Standard Operating Procedures and Standard Test Procedures while working. Ensure timely completion of SOP training as per SABA allocation. Regular participation in internal and external training programs. Usage and maintenance of instrument like HPLC, Dissolution Test apparatus, UV Spectrophotometer etc. Ensuring data integrity policy, GDP and its effectiveness up to compliance. Maintain QAMS, DMS tracker up to date and track the activities accordingly proactively. Sending of the instruments for the outside calibration / validation / AMC / preventive maintenance and their follow up as per the SOP. Monitoring and reporting of GLP practices in day to day working & Procurement of Chemicals/Glassware of QC. Record maintenance and handling of impurity solutions. Ensure the availability and procurement of reference standards, impurity standards, working standards, other revenue items, their record maintenance and stock updation. To comply current EHS Management Systems of Site. To comply all EHS Rules, Procedures, Guidelines, Policy, Practices, Requirements & Applicable Legal Compliances. Ensure controls effectively on High Risk Activities / Significant Environmental Aspect & Impact. To carry out all assigned jobs in Safe Manner. Ensure continual improvement on EHS performance Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs. Master in Science Others Competencies

To attend the mechanical related problems in process area. To execute the Preventive maintenance of all equipment s as per schedule. To comply current EHS Management Systems of Site. Responsible to report in shift duties & remain present till reliever reports. Should have good knowledge of Granulation compression, coating and packing machine. Work Experience 3 to 6 years Education Vocational in Mechanical Engineering Competencies

1. Basic knowledge about GDP & Data Integrity. 2. Online monitoring & recording of batch manufacturing data. 3. Optimum Utilization of equipment & materials during operation. 4. Setting & Operation of Granulation machine such as Sifter, RMG, FBE/FBD, Co mill, Conta and Octa Blender. 5. Co-ordination with engineering for PM of machine & inline equipment. 6. To intimate requirement of spare parts/change parts of equipment. Work Experience 3-6 Yrs. Education Diploma in Mechanical Engineering

The person follows Good Laboratory Practices, Safety measures and good documentation and to ensure compliance with all the existing SOPs in the routine work. The person follows Standard Operating Procedures and Standard Test Procedures while working. The person ensures charging and withdrawal of stability samples as per approved stability protocols. The person responsible for analysis of Stability / Finished product samples, and compile the report as per ALCOA procedure, other miscellaneous samples, and compile their report. Having experience in the operation of QC instruments like Dissolution Test apparatus, UV Spectrophotometer, Balance, PH meter, HPLC, GC and Sonicator etc. Ensuring data integrity policy, GDP, and its effectiveness up to compliance. The person is responsible for preparation of Stability protocol and summary reports, maintains the stability sample record and its analytical planning as per the pullout schedule. The person has an awareness of EHS Rules, Procedures, Guidelines, Policy, Practices, Requirements & Applicable Legal Compliances. Work Experience 5 to 7 years experience in QC. Education Post Graduation in Chemistry Graduation in Pharmacy Competencies Innovation & Creativity Result Orientation Collaboration Customer Centricity Developing Talent Stakeholder Management Strategic Agility Process Excellence

Prepare and maintain MIS reports Maintain files, documents, and records Manage the calendar, prepare letters, and draft emails and other correspondence Coordinate with other departments and locations to collect data and prepare reports Liaise with government offices to schedule appointments. Handling of Transport Handling of Company Accommodation & Guest House; Guest Relation Contractual Workers Management; Apprentice recruitment and compliance Liaison with Govt. official; Political person and other influential person of the village. Preparation, follow and Training of Admin related SOPs. MIS preparation; Handling of Admin related bills Handling Security operations; House keeping, Pest Control of the plant Managing Event and other function of the plant Work Experience 5 - 15 years of experience

1. Basic knowledge about GDP & Data Integrity. 2. Online monitoring & recording of batch. 3.Optimum Utilization of equipment & material. 4.Operation of Granulation equipment such as RMG, FBE, Co mill, Sifter, Octagonal and Conta Blender. 5. Co-ordination with engineering for PM of machine & inline equipment. 6. To intimate requirement of spare parts/change parts of equipment. Work Experience 3 to 6 Yrs Education Diploma in Mechanical Engineering Vocational in Electrical Competencies Innovation & Creativity Result Orientation Collaboration Customer Centricity Developing Talent Stakeholder Management Strategic Agility Process Excellence

The person follows Good Laboratory Practices, Safety measures and good documentation and to ensure compliance with all the existing SOPs in the routine work. Person Having good knowledge of Handling of CCP / CCT / DEVIATION / LIR / OOS in QAMS system. Person Having skill of preparation of SOP, Standard testing procedure, Specification and test data sheet through eDMS software. Person Having skill of preparation of eTDS & CDS in SAP i.e. Linkage, creation of inspection points. Person Having skill to perform risk assessment as per QRM SOP. Ensure compliance with the laboratory with respect to environment, health and safety procedures. Having depth knowledge about QC operation with respect to reviewing the analytical data in documents. Work Experience 5 to 7 years experience in QC department. Education Post Graduation in Chemistry Graduation in Pharmacy Competencies Innovation & Creativity Result Orientation Collaboration Customer Centricity Developing Talent Stakeholder Management Strategic Agility Process Excellence

Long Description 1. Good accounting understanding in respect of Sales collection, Debtors MIS Reporting.2. Good understanding of Bank Operations, especially related to various modes of collections3. SAP Working Background is a must.4. Good computer skills (Microsoft Office, Word, Basic Analytics etc.).5. Good communication skills /Co-ordination with Internal Customers, Statutory Auditors.6. Candidate having previous experience of working in FSSC set-up (O2C/R2R Area) . Competencies Stakeholder Management Collaboration Strategic Agility Developing Talent Customer Centricity Result Orientation Innovation Creativity Process Excellence Education Post Graduation Graduation in Commerce Work Experience 6 to 8 years

Work Experience 12 to 15 years of experience in Pharma Vendor Audit Management 1. To perform and track the Vendor Qualification Compliance and review for all vendors & AVDs. 2. To review, approve, and extend the Q info for new alternate vendors. 3. To execute vendor Audits, CAPA tracking, and qualification documentation 4. To schedule and monitor the Vendor Audits 5. To work on VQ special projects in coordination with Project IT team 6. To track the project till its implementation and Go Live across all sites Technical , behavioral & managerial 1. Strategic Agility 2. Innovation & Creativity 4. Developing Talent 5. Result Orientation 3. Customer Centricity Education Masters in Pharmacy Post Graduation in Science or Chemistry

Long Description 1. To perform and track the Vendor Qualification Compliance and review for all vendors & AVDs. 2. To review, approve, and extend the Q info for new alternate vendors. 3. To execute vendor Audits, CAPA tracking, and qualification documentation 4. To schedule and monitor the Vendor Audits 5. To work on VQ special projects in coordination with Project IT team 6. To track the project till its implementation and Go Live across all sites Competencies Education Post Graduation in Organic Chemistry or Chemistry Masters in Pharmacy Work Experience 13-15 years of experience

Long Description Arranging the process accessories and consumables in process area before batch execution. Coordination for dispensing of raw material required for the production processes. Preparation of process, area and equipment qualification/ validation protocols. Preparation and execution of various reports like process, equipment, area qualification and validation. Preparation and execution of study protocols, URS as and when required. Handling of SAP related activities like process and maintenance. Operating downstream equipment s for process and CIP/SIP. e. g. TFF system, buffer and refolding vessels, AKTA Pilot system, k-prime system, pH Conductivity meter, Autoclave, DHS etc. Execution of production batches in the downstream process area as per approved BPR and submission of the same to QA. Coordination with engineering team for AMC, preventive maintenance and calibration of the equipment s / instruments. Reporting of deviation to superiors/QA. Competencies Education Post Graduation B.Tech in Biotechnology Work Experience Two to Four years of experience in Biotech Industry.