Role & responsibilities Investigation of market complaints, OOS/OOT result related to product. To ensure that the manufacturing and packing operation are carried out as per the instruction given in the batch production Record. To Handle (Initiation /Evaluation/Closure) Change control, Deviation/Incident management System. To verification and Check the dispensed raw material and packing material before batch processing and during dispensing. Preferred candidate profile Perks and benefits

Role & responsibilities To carry out investigations related to OOS, OOT, Incident and Extraneous Peaks to ensure their closure and implementation of CAPA. Responsible for execution of Regulatory Notification as per SOP. To ensure implementation of all proposed actions identified as a CAPA of investigations related to OOS, OOT, and incident. Review of investigation reports, hypothesis protocol and hypothesis reports related to OOS/OOT and Incidents. Co-ordination with R&D, Production, Central Cell, CQA and other responsible for investigations. To prepare and review Quality documents such as (but not limited to) protocols, reports, SOPs STPs Specification, Investigation. Preferred candidate profile Perks and benefits

Role & responsibilities We are looking for candidate on below criteria at our Nalagarh Plant Himachal Pradesh location. Candidate must have completed Pharma, M.Sc. or B.Sc. in Chemistry. Experience of regulatory industry would be preferred. Candidate should have 1-3 years of working experience Preferred candidate profile Responsible for Line clearance in Warehouse and Production area during dispensing, MFG, Filling and Packing & review of log books and status label of each equipments before start of activity. Responsible to carry out in-process checks as per respective Batch Production Record in Manufacturing, packing and warehouse. To ensure that the manufacturing and packing operations are carried out as per the instructions given in the Batch Production Record. Responsible for collection of in-process samples, FP sample, control samples, validation & stability samples. Responsible to make SAP entries, Release of inspection lot of SFG & FG, Physical sampling confirmation, Approval of Batch Production Records for printing and additional page issuance. Responsible for online review of Batch Production record and make entry of data required for trending in maintained excel sheet for preparation of APQR. Responsible for Line clearance in Warehouse and Production area during dispensing, MFG, Filling and Packing & review of log books and status label of each equipment’s before start of activity. Responsible to carry out in-process checks as per respective Batch Production Record in Manufacturing, packing and warehouse. To ensure that the manufacturing and packing operations are carried out as per the instructions given in the Batch Production Record. Responsible for collection of in-process samples, FP sample, control samples, validation & stability samples. Responsible to make SAP entries, Release of inspection lot of SFG & FG, Physical sampling confirmation, Approval of Batch Production Records for printing and additional page issuance. Responsible for online review of Batch Production record and make entry of data required for trending in maintained excel sheet for preparation of APQR. Perks and benefits

Role & responsibilities We are looking for candidate on below criteria at our Nalagarh Plant Himachal Pradesh location. Candidate must have completed B.Pharma, M.Sc. or B.Sc. in Chemistry. Candidate should have hands on experience in testing Experience of regulatory industry would be preferred. Candidate should have 1-5 years of working experience Preferred candidate profile Perks and benefits

Role & responsibilities Recruitment : To assist in the recruitment process, including job postings, resume screening, and coordinating interviews, release job offers. Operations : To manage and streamline the onboarding process for new hires and support the Exit Process including the exit formalities, fnf settlement and issuance of experience letters. Engagement : Support HRBP for an employee engagement activities. Administrative Task : Handle Employee files, preparation and maintain of employee data. Interested candidates share your profiles - neha.yadav@glenmarkpharma.com

Job Description :SAS Programmer ABOUT GLENMARK Glenmark Pharmaceuticals Ltd. is an innovation-driven global pharmaceutical company with a presence across Specialty, Generics and OTC businesses. It focuses on the key therapeutic areas of respiratory, dermatology and oncology. The company has 11 world-class manufacturing facilities, 4 research and development centers, spread across 5 continents and operations in over 80 countries. Glenmark is ranked among the world's top 100 biopharmaceutical companies (Top 100 Companies Ranked by Pharmaceutical R&D and Sales, 2022, by In Vivo/Scrip 100) and among the world's top 50 companies in the Generics and Biosimilars (Top 50 Generics and Biosimilars Companies ranked by Sales, 2022, by Generics Bulletin/In Vivo). The company was listed on the Dow Jones Sustainability Index (DJSI), one of the world's most respected and widely accepted sustainability benchmarks, under the category of emerging markets (2021) for the fourth consecutive year. For more information, visit www.glenmarkpharma.com POSITION DETAILS: Business Unit: Research & Development Function: SAS Programming Location: Mahape, Navi Mumbai Reporting to: Sanjay Jankar, Sr. General Manager, Biometrics ROLE OVERVIEW/ PURPOSE Perform all Bio-statistical and SAS programming activities. OVERALL JOB RESPONSIBILITIES Develop CDISC related documentation ex aCRF, mapping specs. Be the lead programmers for the outsourced studies Develop Analysis Datasets and TLG for the internal studies Update project related documentation regularly. Provide support to data management /Clinical in developing listings or ad hoc reports as required. Other SAS programming related tasks assigned by line management. KEY RELATIONSHIPS/STAKEHOLDERS External Vendors Internal (other than Direct Reports) Data Management Team CRA DB Programmer Medical team DESIRED EXPERIENCE AND KNOWLEDGE Educational Qualifications Bachelor or Master Degree required, any statistics/biostatistics degree preferred Experience: 10-14 year's clinical trials in pharma or CRO. In depth SAS programming knowledge. Hands-on experience on multiple CDISC projects (10 or more studies) and Written Reviewers Guide with CDISC package. Working knowledge with SDTM/ADaM/XML Familiarity with statistical methods used for biomedical/pharmaceutical research required; Experience with clinical trials or pharmaceutical industry experience required Knowledge of current industry and regulatory submission practices, protocol designs, and terminology. Knowledge and Skills (Functional / Technical) Excellent SAS programming (Base SAS + Advance SAS + SAS STAT + SAS Graph) Proficiency in English language Good Interpersonal Skills Time Management Training and Mentoring Presentation Skills Adaptability Strategic Thinking Decision Making Comfort with Computer system usage Behavioral Attributes Team Player Other Requirements (License / Certification & Specialized Training) ICH-GCP

Managing multiple divisions anda sales force of around 600 + employees Partnering with the DivisionalHead in driving all people related Initiatives Recruitment of Field Staff(FSO, DSM, ZSM & SM) - Partnering with the business to identify talent -internally and externally for field sales force across levels. To maintain 100%manning within TAT Positively impacting the Costby ensuring right check and balances while hiring Attrition Control -Establishing touch points with Field Sales Force and implementing EmployeeEngagement Activities Driving central project onProductivity, Positivity and Progression for the assigned divisions Retention of Key Talent -Identifying the Key Talent & creating development plans for them Performance Management -Driving Performance Appraisal and Management through constant feedback Handling IR issues &grievances Employee Life Cycle Management - Resolution of day today operational queries Master s degree in Human Resources 6 to 8 years of experience in HR Skill and Competency: Influence and align stakeholders Problem Solving and Analytical Skills Planning and organizing Ability to plan andallocate resources, prioritize tasks

Role & responsibilities Handling Manufacturing/Packing section in rotational shifts. Ensuring execution of production plan. Ensuring cGMP compliance during rotational shifts. Handling manpower during shift. Preferred candidate profile Candidate must have Bachelor Degree in Pharmacy. Candidate must have good communication skills.

Key Responsibilities: Analyse pharma market to identify gaps and opportunities, especially in the innovative space Prepare market performance overview for Glenmark’s competition for all dosage forms Generate ideas of high value for proprietary products for Glenmark for global markets Evaluate new unique opportunities using multiple databases and recommend potential additions to the portfolio Conduct risk assessments of the existing portfolio with suitable mitigation strategies. Prepare business cases using standard forecasting tools for investments in product or portfolio acquisition with inputs from business and Product Development teams for in-house and in-licensed assets Support the regional portfolio leads in preparing product grids for next five years with high potential peak Sale factoring in complexity of various stakeholders like R&D, RA, Manufacturing, Clinical and IP. Ensure the selected grid remains relevant and in good standing through regular reviews. Knowledge and Skills Forecasting for NCE, generic, differentiated generic products Ability to incorporate qualitative inputs into quantitative models Understanding of market access, reimbursement, competitive environment in major markets Portfolio experience & Strong medical knowledge in various therapy areas specially in Dermatology, Respiratory and Oncology Strong communication, negotiation and influencing skills. Strong in business analytics and planning for short and medium term Good understanding of business operations management Identification of new innovative/specialty/505(b)2 opportunities Optional : Understanding of current regulatory processes for relevant markets Understanding of IP issues in pharmaceuticals including Hatch-Waxmann Strong CMC knowledge for various dosage form including oral solids, injectable, dermatology. Interested candidates can apply by sending their resume and application form to Sagar.Goswami@glenmarkpharma.com with subject line as “Application for Head – Analytics & Competitive Intelligence ” latest by 14th February 2025 Show more Show less

Key Responsibilities: Manages projects for products in different stages of lifecycle thus requiring frequent interaction and collaboration with Medical affairs, Regulatory, Finance, Clinical, Alliance management as well as Glenmark’s affiliates and partners. Analyses external and internal customer data using database queries, spreadsheet models, web analytics tools, statistical analysis tools, and campaign management software tools Research and analyse the latest marketing trends, customer behaviour, and competitors’ products and strategies to identify the best marketing practices Development of forecast, business cases, Pricing strategy, launch sequence in evaluating commercial opportunities as well as building launch strategies Produce meaningful KPI dashboards and delivering monthly, cross-channel performance reports with actionable insights. Create and manage Gantt charts for various projects and utilize analytical tools and compile relevant data into easy-to-understand reports Work closely with markets/affiliates for launch readiness, in close collaboration with different cross functional teams, aligned with the brand and portfolio launch strategies in accordance with Long Range Planning. Manage and implement various marketing materials, including website copy, promotional emails and newsletters, paid ads, landing pages, and case studies across multiple marketing Provides actionable overall market and customer insights to address key strategic questions. Responsible for tracking, reporting, and analysing the performance of marketing activities, ad-hoc analytic requests, and development/automation of regular reports Key Skills Comfortable multitasking, excellent organizational skills and good at prioritizing under minimum supervision; experience with managing cross functional teams A firm grasp of mathematical and statistical concepts. Knowledge of data structures, analytics techniques, and management applications is preferred. Strong strategic and analytical capabilities, with demonstrated experience in analysing complex datasets, collecting data, effectively synthesizing the analytics/data to form a complete, cohesive picture. Excellent written, communication, and analytical skills; tech-savvy, detail-oriented, and an effective communicator A good understanding of the pharmaceutical industry and the phases of drug development; previous experience required Deep understanding of datasets and platforms like IQVIA, Drug Pricing Intelligence (POLI), IRP (International Reference Pricing and Sequencing) etc. Proficiency in Microsoft Office suite (Word, PowerPoint, Excel, Outlook), Digital Interested candidates can apply by sending their resume and application form to Sagar.Goswami@glenmarkpharma.com with subject line as “Application for Lead – Global Marketing & Analytics” latest by 14th February 2025 Show more Show less

We are seeking a seasoned professional with 8+ years of expirence in the pharmaceutical industry, preferably in Marketing, Analytics or Portfolio Management, with a strong understanding of the industry, drug development and regulatory processes, as well as proficiency in data analysis and platforms like IQVIA, POLI & IRP Overall Responsibilities Market Analysis Analyses external and internal customer data using database queries, spreadsheet models, web analytics tools, statistical analysis tools, and campaign management software tools Research and analyze the latest marketing trends, customer behavior, and competitors’ products and strategies to inform decision making process. Development of forecast models, business cases, pricing strategy, launch sequence in evaluating commercial opportunities as well as building launch strategies Provides actionable overall market and customer insights to address key strategic questions Portfolio Planning Generate ideas of high value for branded products for Glenmark Evaluate new unique opportunities and recommend potential additions to the portfolio Perform risk assessment of the existing portfolio with suitable mitigation strategies. Prepare business cases for investments in product or portfolio acquisition working in collaboration with the Business and Product Development teams Managing Brand Performance Produce meaningful KPI dashboards and delivering monthly, cross-channel performance reports with actionable insights Create and manage Gantt charts for various projects and utilize analytical tools and compile relevant data into easy-to-understand reports Responsible for tracking, reporting, and analyzing the performance of marketing activities, ad-hoc analytic requests, and development/automation of regular reports Stakeholder Management Initiate, build and maintain deep relationships internally across business units and functions. Work closely with markets/affiliates for launch readiness, in close collaboration with different cross functional teams, aligned with the brand and portfolio launch strategies in accordance with Long Range Planning. Demonstrates close collaboration between stakeholders at every stage of the launch planning and execution. If Interested, please share your resume at Sagar.Goswami@glenmarkpharma.com – Subject line “Lead – Portfolio & Analytics, Global Oncology” Show more Show less

Job Description Accountable for all the compliance regarding activities for production block (OSD). Handling change controls and performing investigations for Deviation, OOS/OOT, Market complaints regarding soft floor. Handling Track wise activities. Performing Risk assessments Preparation of documents like SOP, URS, Protocols, BMR/BPR. Co-ordinating with cross functional departments for validation, qualification studies and Effectiveness check for CAPA. Training to sub-ordinates. Show more Show less

Job Description Ensure scientific assessmentinto the “Manufacturability” of the product for a robust process developmentduring new product introductions, product site transfers and processvalidation. Technical Support during process optimization activities related to ProductTransfer & ProcessValidations. Technical input andknowledge sharing with team and Cross functional team (CFT). Root Cause Analysis, Statistical evaluationsand Trouble Shooting of existing commercial as well as site transfer products. Improving process capabilities, yields androbustness. Prepare, Review and Approval of technical documents like MFR, PORM, BMR,BPR, Risk assessment , protocols and reports for Trial batch, Hold timestudy, Stability study, Process validation, Exhibit or submission batchdocumentation, alternate vendor development and side transfer project. Support documentation teamin order to deliver end to end documents from development batches (exhibit) tocommercial lifecycle management. Show more Show less

Job Description Ø Responsible forpacking activities in the Packing area. Ø To ensure thatproducts are packaged and stored according to appropriate documentation. Ø To ensure thatpackaging records are evaluated and signed by authorized person before they aresent to Quality Assurance Department. Ø To ensure that thepackaging operations are carried out as per cGMPregulations. Ø To ensure thatcalibrations and preventive maintenance are done at regular intervals. Ø Knowledge of Change control and Deviation. Ø Track and Trace system with Serializationand Aggregation. Ø Knowledge of SAP. Ø SOP's preparation. Show more Show less

Job Description Maintainthe compression area as per the procedure mentioned in SOP. Checkand ensure all the balances are in operational condition and calibrate as perthe schedule frequency mentioned in SOP. Record the details in logbook. Checkand ensure appropriate status labels are maintained in respective equipment/instrument accessories and change as when required. Ensure protection forall concerns from exposure to any substance or activity which may be hazardousto health through regular risk assessment and safety parameters. Responsible fortraining peers in particular areas so that work can be allocated to them incase of absence of the individual. Maintain the Granulation, Unit Operation area, Dispensed Material Store, Quarantine I & III as per the procedure mentioned in SOP. Check and ensure all the balances are in operational condition and calibrate as per the schedule frequency mentioned in SOP. Record the details in logbook. Check and ensure appropriate status labels are maintained in respective equipment/ instrument accessories and change as when required. Responsible for cleaning, lubrication, inspection & tightening of granulation equipment's. Responsible for cleaning of machineries of granulation & unit operation area as per respective SOP. Responsible for checking status of preventive maintenance of the equipment's of granulation & unit operation area. Check and ensure that the temperature, relative humidity and Differential pressure in the area is within the limit as mentioned in BPR. Check the fumigation status and perform as per respective SOP. Responsible for carrying out granulation & blending activity according to BPR. Responsible for In-process parameters checks and ensure it should be done according to scheduled frequency mentioned in the BPR of respective product. Record the in-process parameters online in the BPR of respective product. Responsible for updating logbook online. Handling & Cleaning of dies and punches/Change part/DEX bag. Responsible for improving productivity & yield: Check the present scenario of compression area as well as equipment/instrument. Counter check the planning of next product with your supervisor and ensure working as per deadline. Check the status of upcoming batch of respective product which should be taken for compression activity and report to your shift supervisor if it’s not ready for compression. Responsible for all the process related to Coating of compressed tablets: Co-ordinate with Engineering & QA for smooth implementation of the cGMP system & compliance related to compression. Show more Show less

We are seeking a seasoned professionalwith 8+ years of expirence in the pharmaceutical industry, preferably inMarketing, Analytics or Portfolio Management, with a strong understanding ofthe industry, drug development and regulatory processes, as well as proficiencyin data analysis and platforms like IQVIA, POLI & IRP Overall Responsibilities : Market Analysis Analyses external and internalcustomer data using database queries, spreadsheet models, web analytics tools,statistical analysis tools, and campaign management software tools Research and analyze the latestmarketing trends, customer behavior, and competitors products and strategiesto inform decision making process. Development of forecast models,business cases, pricing strategy, launch sequence in evaluating commercialopportunities as well as building launch strategies Provides actionable overall market andcustomer insights to address key strategic questions Generate ideas of high value forbranded products for Glenmark Evaluate new unique opportunities andrecommend potential additions to the portfolio Perform risk assessment of theexisting portfolio with suitable mitigation strategies. Prepare business cases for investmentsin product or portfolio acquisition working in collaboration with the Businessand Product Development teams Produce meaningful KPI dashboards anddelivering monthly, cross-channel performance reports with actionable insights Create and manage Gantt charts forvarious projects and utilize analytical tools and compile relevant data intoeasy-to-understand reports Responsible for tracking, reporting,and analyzing the performance of marketing activities, ad-hoc analyticrequests, and development/automation of regular reports Initiate, build and maintain deeprelationships internally across business units and functions. Work closely with markets/affiliatesfor launch readiness, in close collaboration with different cross functionalteams, aligned with the brand and portfolio launch strategies in accordancewith Long Range Planning. Lead Portfolio &Analytics, Global Oncology

03 - 06 years experience of external preparations, Ointment and OSD IPQA activities Job Responsibilities - - Totrack batches for process validation, packing validation and hold time study. Certificationof Appropriate and timely Line-Clearance for Manufacturing, Packing, Dispensing Tocarry out the online checks& to take on line SAP entries. - ToWithdraw & Submit the Samples (Analysis SFG and FG & Control samples,Validation, Regulatory, R&D, Hold time study & Micro samples) toConcern Dept. as & when required. - Toensure the cGMP on the shop floor and to highlightthe on line Problems / Non Conformances with the respect to Procedures,Specifications, SOPs, cGMP etc. on day to day basis Numbers ofcritical/major nonconformance noticed. OnlineBPR, Logbooks completion & Review of documents like Preventive calibrationrecords, daily/weekly quarantineregister etc. in the Concerned dept. - Issuanceof Batch Manufacturing Records and Batch Packing Records to productiondepartment. - Reviewof Executed Batch Manufacturing Records and Batch Packing Records Toverify online finished goods before transfer to BSR.

Accountable for all the compliance regarding activities for production block (OSD). Handling change controls and performing investigations for Deviation, OOS/OOT, Market complaints regarding soft floor. Handling Track wise activities. Performing Risk assessments Preparation of documents like SOP, URS, Protocols, BMR/BPR. Co-ordinating with cross functional departments for validation, qualification studies and Effectiveness check for CAPA. Q

Responsible forpacking activities in the Packing area. To ensure thatproducts are packaged and stored according to appropriate documentation. To ensure thatpackaging records are evaluated and signed by authorized person before they aresent to Quality Assurance Department. To ensure that thepackaging operations are carried out as per cGMP regulations. To ensure thatcalibrations and preventive maintenance are done at regular intervals. Knowledge of Change control and Deviation. Track and Trace system with Serializationand Aggregation. Q

Maintainthe compression area as per the procedure mentioned in SOP. Checkand ensure all the balances are in operational condition and calibrate as perthe schedule frequency mentioned in SOP. Record the details in logbook. Checkand ensure appropriate status labels are maintained in respective equipment/instrument accessories and change as when required. Ensure protection forall concerns from exposure to any substance or activity which may be hazardousto health through regular risk assessment and safety parameters. Responsible fortraining peers in particular areas so that work can be allocated to them incase of absence of the individual. Maintain the Granulation, Unit Operation area, Dispensed Material Store, Quarantine I III as per the procedure mentioned in SOP. Check and ensure all the balances are in operational condition and calibrate as per the schedule frequency mentioned in SOP. Record the details in logbook. Check and ensure appropriate status labels are maintained in respective equipment/ instrument accessories and change as when required. Responsible for cleaning, lubrication, inspection tightening of granulation equipments. Responsible for cleaning of machineries of granulation unit operation area as per respective SOP. Responsible for checking status of preventive maintenance of the equipments of granulation unit operation area. Check and ensure that the temperature, relative humidity and Differential pressure in the area is within the limit as mentioned in BPR. Check the fumigation status and perform as per respective SOP. Responsible for carrying out granulation blending activity according to BPR. Responsible for In-process parameters checks and ensure it should be done according to scheduled frequency mentioned in the BPR of respective product. Record the in-process parameters online in the BPR of respective product. Responsible for updating logbook online. Handling Cleaning of dies and punches/Change part/DEX bag. Responsible for improving productivity yield: Check the present scenario of compression area as well as equipment/instrument. Counter check the planning of next product with your supervisor and ensure working as per deadline. Check the status of upcoming batch of respective product which should be taken for compression activity and report to your shift supervisor if it s not ready for compression. Responsible for all the process related to Coating of compressed tablets: Co-ordinate with Engineering QA for smooth implementation of the cGMP system compliance related to compression.