Role & responsibilities • To receive and understand the technology from FnD dept. • To design optimisation for process parameters & participate in the trials at R&D. • To transfer the technology from R&D to receivers site for the respective product. • To monitor the TT demo / exhibit/scale up and optimization batches. • To review the technical information sheet, product detail, raw material/accessories/ equipment requirement for plant trial/SU/Exhibit batches. • To propose and fix the batch size i.e. of the Demo, Scale up, Exhibit and Commercial based on Equipment Capacity/Qualification, Scale Up factor calculations & annual requirements. • To get involved and observe in the TT demo batch with F&D. • To take scale up batch at manufacturing locations and prepare scale up batch protocol, Scale Up Reports, MFC, Sampling Protocol, Risk Assessment etc. • To take the exhibit batches at the manufacturing locations and take care for its trouble shooting. • To prepare the summary reports. • To perform investigation for Deviation/ OOS/ OOT observed during SU/EB at plant. To prepare agency query responses.

Key Result Areas: Portfolio performance ORG (Growth & market share) Strategy planning & innovation Strategy implementation & monitoring Market research & data analysis Training/conferences & SPMs handled Preferred Profile : Candidate must have done full time Master's Program (Post Graduation)

Roles and Responsibilities Develop and maintain relationships with vendors through vendor development initiatives. Conduct market research to identify potential suppliers and negotiate prices. Ensure compliance with regulatory requirements during purchase processes. Manage procurement activities for API regulated markets like USA, Europe & Brazil. Desired Candidate Profile 1-6 years of experience in procurement or related field (pharmaceutical industry preferred). Bachelor's degree in Any Specialization (B.Sc/B.Pharma). Strong understanding of APIs, sourcing strategies, strategic sourcing principles, vendor negotiation techniques. Proficiency in managing multiple priorities simultaneously while maintaining attention to detail.

Role & responsibilities *Feasibility assessment/ new product evaluation *Literature review and BA/BE study designing *BE Study Monitoring *Preparation of documents for regulatory submission (i.e BENOC, Import license application etc.) *Establishment and maintenance of study documents *Document preparation for dossier submission (i.e clinical overview, non-clinical overview, summery tables etc.) *Review of BE study documents i.e protocol, reports, ICF etc. *Preparation/review of medical write up *Coordination for serious adverse event reporting and safety update to Regulatory agency Preferred candidate profile M. Pharm (Pharmacology) with 2-6 Yrs of Relevant Experience Interested candidates can share their CVs on meghamaheshwari@torrentpharma.com / vilshashah@torrentpharma

Please find below job description for Executive Sales Admin role. Coordinating with internal and external customers, tracking customer order history. Assist with sales forecasting, sales lead generation, sales proposals and contract negotiation. Coordinate with the Manager to work on the internal & external team requirements Acquire data from primary or secondary data sources and maintain databases/data systems Analyze data to identify trends, patterns, and insights that can support the decision-making process. Generate reports, MIS. Preferred candidate profile Good in communication, Fluent in excel, knows MS office Perks and benefits Role & responsibilities Preferred candidate profile

Role & responsibilities Responsible for designing overall marketing & communication strategy for brands Conceptualization & creation of deliverables to aid brand promotion Sales & market data analysis, core customer feedback & competitor analysis to aid decision making Assisting in making annual marketing plans & promotional activities for the SBU Designing communication for field force to keep them enthuse about brand promotions Conducting quarterly briefing, product launch & product strategy orientation meetings for field force. Responding to scientific queries of field force Allocation & dispatch co-ordination of promotional inputs. Managing & conducting training program for field force Preferred candidate profile Basic: Graduation in Pharmacy/ Science Desirable: MBA (Marketing) Experience: 3 years atleast into product management team (PMT)

Analytical Development Laboratory Position: Executive Experience: 3-8 years Qualification: M.Sc. / M.Pharm. Job Responsibilities: HPLC/GC/IC method development, feasibility, verification, equivalency, validation of API for complex OSD products, oncology products, topical products having exposure to regulated, Semi Regulated & India markets Comparative evaluation of methods with alternative vendor methods versus existing primary vendor and regulatory impact analysis Dissolution development, comparative dissolution, multimedia dissolution and statistical evaluation and report preparation Good understanding and hands on experience of analytical instruments like HPLC, IC, GC etc. NI/GI & NDSRI' with LCMS/GCMS expertise, Solid state characterization and API sameness study Hands on experience on In-vitro Studies, E&L, Solid State characterization, IVPT/IVRT, Impurity characterization, sameness study Well versed with USP/EP/BP/JP and various current regulatory guidelines (ICH/EMEA/FDA) Perform maintenance and calibration of lab instruments / equipment. Formulation & Development Position: Executive Experience: 3-8 years Qualification: M.Pharm. Job Responsibilities: OSD, Oncology, Alternative vendor development, Exposure of Regulated, Semi Regulated & India Markets FnD Documents like Specifications, MFC,BMR, Stability protocol, CCF , Deviation etc. (For FnD doc cell), Knowledge of SAP, loading of Specification in SAP, BOM loading, Stock overview, PR generation etc.

Role & responsibilities Driving Business in assigned territory Preferred candidate profile Any graduate with minimum 3 yrs of experience in FMCG & OTC Interested candidate can share CV on shwetambarithakur@torrentpharma.com / ravirana@torrentpharma.com

Role & responsibilities In-Licensing Role : Lead Generation - To Explore new business development opportunities for In-licensing business for US Market. Evaluating business partner portfolio for partnering opportunity for different forum (DCAT, Europlex CPHI etc.) Market Analysis of IQVIA, IPD & Exim analysis to prepare market summary for Partner's portfolio Prepare business case of the potential partnership opportunity to check the profitability and propose a best fit plan to management Program Management for Due-diligence - Managing internal/external stake holder through regular meeting/discussion. Project discussion & tracking Prepare and evaluate CDA, commercial term sheet, commercial-supply agreement and technical quality agreement by working with legal/finance team & partner Periodically prepare BD deal presentation for IL products with BD Stake holders to review projections, competitive landscape and project strategy for prioritization & Re-prioritization CMO/CDMO Role : Identify CMO & CDMO for tech transfer of Torrent products & new development product pipeline. Program management: Co-ordinating with internal dept. including FTT/SCM/finance/regulatory/technical team/Quality for due-diligence & timely tech transfer Prepare and evaluate CDA, commercial term sheet, commercial-supply agreement and technical quality agreement by working with legal/finance team & partner

About the role: Responsible for designing overall marketing and communication strategy of brands Good at Sales & Market data analysis Must possess knowledge of product strategy, product launch Assist in making annual marketing plans & promotional activities for the SBU Handle scientific queries Conduct and plan training, conferences & quarterly meets Ready to undertake Field work in various HQs Should be able to work in Team and manage it for APM & Executive REQUIRED SKILLS: Good analytical skills, interpretation and communication skills, zeal to learn new things, good command over Microsoft Office, ready to relocate to Ahmedabad/Mumbai in the long run, look forward for a longer term association with good adaptation & capability to cope up with new challenges.

Role & responsibilities To develop and validate sensitive and rugged bioanalytical methods by using different extraction (i.e. SPE, LLE etc.) and quantitation (i.e. LCMS, HPLC) techniques for analysis of drug substance as per the instructions obtained from supervisor. To conduct study sample analysis by following pre-defined procedures with required accuracy. To operate, maintain and calibrate instruments adhering to written instrument operation procedures. To follow defined procedures and keep proper documentation of the performed procedures to maintain GLP compliance in the laboratory. To adhere to health and safety policy, and other requirements relating to care of instruments/equipment Preferred candidate profile M. Pharm /M.sc with 2-5 Yrs of relevant Experience. Interested candidates may share CV's on meghamaheshwari@torrentPharma.com; / Vilshashah@torrentpharma.com;

Role & responsibilities Audit planning and scheduling. Development of detailed audit scope, questioners and review checklist Conducting Internal Audits and preparing reports. Developing Standard Operating Procedure (SOP) documents. Ensuring adherence to DOA, SOPs, and organisation policies. Identifying risk exposure and creating risk control matrices with an emphasis on process improvement, optimization and risk mitigation. Evaluating internal controls, the reliability of financial reporting, compliance with applicable laws and regulations and the overall effectiveness and efficiency of operations. Demonstrating the ability to research, organize, and analyse data and execute selected tests of internal controls. Providing support to organizational and functional initiatives. Design & Development of IFC RCMs for various support and core areas Conducting IFC control testing. Coordination with external auditors, controllers and functional team across locations. Review of audit work and reports. Control Automations. Budget analysis, monitoring and controls. Preferred candidate profile Strong analytical and communication skills. Effective presentation skills Effective coordination with various process owners across multiple locations. Proficiency in Microsoft tools, especially PowerPoint, Excel, and Word. Ability to manage multiple assignments and work effectively to meet timelines. Proactive problem-solving abilities. SAP - Basic to Intermediate MS office - Advance Data Analytics - Moderate

Preferred candidate profile: Candidates who possess strong, core, and extensive experience specifically in EXIM operations. Should have thorough knowledge of export and import. Qualification: B.E. Total Experience: 10 to 20 Years

Role & responsibilities Providing secretarial service to the management such as attending phone calls, typing letters, writing and distributing emails, organising papers and managing files, etc. Preparing various reports, minutes of meetings, and other documents as required by the departments manager. Coordinating and facilitating Manager calendar to arrange meetings, appointments, and conferences. Receiving, greeting, screening and managing visitors and phone calls. Receiving, screening, assessing, distributing, and maintaining incoming correspondence. Making travel arrangements in coordinating with other dept., preparing itineraries, compiling, and maintaining travel records and vouchers. Organizing and maintaining files and records Performing various executive and administrative assistances to in a confidential manner. Coordinate with the finance departments maintaining relevant reports for tracking. Preferred candidate profile Minimum of 3-8 years of experience as an Executive Assistant or similar administrative role Experience supporting senior executives in a fast-paced environment Proven ability to manage complex calendars and coordinate logistics

Role & responsibilities: To receive instructions from AM / Manager / GM. To plan the work as per instructions from department head. To track the daily exhibit / site shift product's trail, engineering, Exhibit & Validation (not limited to) batches manufacturing and monitor it's progress constantly. To organize, supervise and control the activities of Technology Transfer department. To co-ordinate and co-operate with various departments like Raw material store, Engineering, Quality Assurance, Administration, Information Technology, Operational Project, Quality Control, Production etc. for smooth functioning of Technology Transfer department. To check and update various documents and records, ensure production records filled online during batch manufacturing. To check and maintain housekeeping of the department. To enforce latest developments in GMP, SOP's etc. To observe and report to the seniors of Product / Material / Machine for their abnormal identified behaviour during production process. To counter check Raw Materials Dispensing and to recheck the material prior to their use in production processes. To ensure that the Quality, Health, Safety, Environment policy and procedures are followed. To prepare documents of New Product (ANDA) and site shift products (which includes CCF, MFC, BMR, QFR, ISP, PPQP, QRM, ESR TT Protocol, TT Report & PPQR (not limited to). To prepare documents for MES activity. To check, (i) Sampling request to Quality Assurance Department (ii) Material requirements requisitions (iii) Received batch from RM department To check / verify, (i) Daily Work in progress status. To achieve required production targets as per the budgetary norms. Handling of change parts. To ensure proper follow of company's rules and regulations. To ensure that all documents are complete in all respect prior to next stage of processing. To write requisition slips of Auxiliary Materials / Stationary materials etc. of daily use. To procure and control the utilization of such materials. To maintain optimum stock level of such materials for smooth functioning of department. To carry out any additional responsibility entrusted from time to time. Monitoring of Production process at each stage. To understand and follow all written procedure and manufacturing instructions mentioned in the respective batch record or any other quality document before starting production activity. To monitor constantly the CAPA of deviations, OOT and OOS to complete within time frame. To perform the investigation within timeframe related to quality system i.e. deviation, OOT and OOS. To be in communication with TRC and it's cross functional team for coordination and knowledge sharing of new site transfer products. To ensure that all SOP trainings are fulfilled on periodic basis. To coordinate activities like visit, document transfer and monitoring (but not limited to) related to manufacturing of products at CMO site. Preferred candidate profile: Candidates should have experience in Pharmaceutical background. Qualification: M. PHARM. Experience: 3 to 8 Years

Role & responsibilities: Candidates will have to work on Apprenticeship Training for one year. If your performance is excellent we will consider you for permanent job role opportunity. Department: Formulation Technology Transfer Preferred candidate profile: Candidates should have the below mentioned % criteria: In 10th & 12th Candidate should have 60% aggregate or above of both the classes. Candidates should not have any kind of ATKT/Backlog throughout M. Pharm degree. Location: Dahej, Gujarat Stipend: Rs. 12,000 per month (Fixed) Interested candidates please share your updated CV's on hrdahej@torrentpharma.com.

Role & responsibilities To perform the microbial limit test & validation of samples as per GLP and other different types of samples. To perform Sterility test, BET test & Preservative Efficacy testing of different samples & to perform their validation activity. To monitor the environment of the Microbiology lab. To perform the sterilization of glassware's by autoclave and dry heat sterilizer. To prepare the microbiological media and chemical reagent as and when required and perform the necessary microbial tests. Preparation of disinfectant solution Daily, quarterly and yearly calibration of the balance, pH meter and other instruments as per the master schedule. To check the performance of all instruments as per the master schedule. To review the microbiological documents. To approve the microbiological test related TRF. Documentation and writing journals related to the microbiological test and there validation. To represent the Microbiological lab during audits . Preferred candidate profile M.Sc (Micro) with 02-07 Yrs of relent experience. Interested Candidate may share their Cvs on vilshashah@torrentpharma.com

Position: Executive (Microbiology) Qualification: M.Sc (Microbiology) Experience: 3-8 Years Location: Torrent R&D Centre, Gandhinagar, Gujarat Requirement: Strong knowledge in planning and execution of microbial activities like BET/Endotoxin/Lysate sensitivity test , sterility , GPT, PET, MLT /Bioburden/ specified microorganisms method development and validation for finish product, raw material, in-process samples etc. Expertise in operation and validation/calibration of microbiology lab related instruments. Knowledge of handling of Trackwise and QMS activities. Able to develop and validate the method for antibiotic assays for different dosage forms . Strong knowledge in microbial pathways and probiotic characterization (from sample preparation to data analysis to results interpretations).

Role & responsibilities Driving Business in assigned territory Preferred candidate profile Any graduate with minimum 3 yrs of experience in FMCG & OTC Interested candidate can share CV on ravirana@torrentpharma.com

Role & responsibilities Driving Business in assigned territory Preferred candidate profile Any graduate with minimum 3 yrs of experience in FMCG & OTC Interested candidate can share CV on ravirana@torrentpharma.com