Pharmacy Jobs

Total Vacancies: 23Roles & Responsibilities:• Provide medical, dental, nursing, and allied healthcare services as per assigned role• Diagnose, treat, and manage patients in accordance with ECHS healthcare protocols• Maintain accurate medical records and patient documentation• Assist senior medical professionals in delivering quality healthcare services• Ensure compliance with hygiene, safety, and government healthcare standards• Perform administrative and support duties related to healthcare operations• Carry out duties responsibly as per designation (Medical, Paramedical, Technical, or Support Staff)Qualification:• Medical Officer: MBBS• Dental Officer: BDS• Nursing Assistant: GNM / B.Sc Nursing• Other Posts: 8th / 12th (as per post)Experience / Age Limit:• Minimum Age: 21 Years• Maximum Age: 45 Years• Age relaxation applicable as per ECHS / Government normsSelection Process:• InterviewImportant Dates:• Application Start Date: 22-01-2026• Last Date to Apply: 12-02-2026About the Company:The Ex-Servicemen Contributory Health Scheme (ECHS) is a Government of India initiative established to provide comprehensive medical care to ex-servicemen and their dependents. ECHS operates through a wide network of polyclinics and empanelled hospitals across the country, ensuring accessible, affordable, and quality healthcare services. The organization plays a vital role in supporting the health and well-being of veterans by delivering reliable and structured medical assistance under government healthcare standards.Official NotificationClick Here

Roles & Responsibilities • Perform analytical development activities including method development, validation, and routine analysis (API/CDMO/Peptides) • Execute manufacturing operations in OSD/API production, formulation, and packing • Support process development, scale-up, and troubleshooting activities • Ensure compliance with GMP, safety, and quality standards • Maintain batch records, analytical documentation, and manufacturing logs • Support EHS activities and follow environmental, health, and safety guidelines • Collaborate with cross-functional teams for smooth production and development Qualification • Analytical Development: M.Sc / M.Pharm • Manufacturing (OSD/API): Diploma / B.Sc / B.Pharmacy Open Postion & Requirements • Analytical Development: 1–10 years • Manufacturing (OSD – Formulation, Production & Packing): 1–11 years • Relevant pharmaceutical industry experience mandatory Skills • Hands-on knowledge of pharmaceutical manufacturing or analytical techniques • Understanding of GMP, quality systems, and regulatory compliance • Strong documentation and data integrity practices • Ability to work in a fast-paced manufacturing/R&D environment • Good communication and teamwork skills Walk-In Interview Details • Venue: Hotel VR Ashoka Grand, 1-11/2/7/A, Alwyn X Road, Miyapur, Hyderabad – 500049 • Schedule: 30 January 2026 – Analytical Development & Process Development (10:00 AM – 4:00 PM)                       31 January 2026 – Manufacturing (API) (10:00 AM – 4:00 PM)                       1 February 2026 – Manufacturing (OSD) & EHS (10:00 AM – 4:00 PM) • Documents Required: • Updated resume (multiple copies) • Educational certificates • Experience letters • Recent passport-size photographs About the Organisation Laurus Labs is a leading pharmaceutical company with strong capabilities in API, CDMO, peptides, and formulations. Driven by the vision of “Chemistry for Better Living,” Laurus Labs serves global regulated markets with innovation, quality, and sustainable manufacturing practices.

Roles & Responsibilities • Build, maintain, and automate dashboards and reports using Power BI, SQL, and MS Excel • Analyze Denial, Payment, and Open AR trends across payers and sites • Perform data-level root cause analysis (RCA) to improve operational performance • Customize operational and strategic reports based on business requirements • Identify opportunities for process automation through analytics • Share insights, reports, and status updates with internal stakeholders • Ensure adherence to Optum policies, compliance standards, and operational guidelines • Support analytics initiatives aligned with US healthcare operations Qualification • Any Graduate (Bachelor’s degree mandatory) Experience • Experience in Reporting, Data Analytics, or Business Analysis • Exposure to healthcare analytics preferred Skills • Strong hands-on experience in MS Excel • Working knowledge of SQL and Power BI • Good analytical, logical, and problem-solving abilities • Strong written and verbal communication skills • Ability to work independently and manage multiple deliverables • Willingness to work in US night shift (3:30 PM – 1:00 AM IST) • Comfortable with hybrid / office-based work About the Organisation Optum, part of UnitedHealth Group, is a global healthcare services and technology leader that uses data, analytics, and innovation to improve healthcare outcomes, streamline operations, and support healthcare systems worldwide.

Roles & Responsibilities • Listen to live physician–patient interactions and document encounters in EHR systems • Accurately record medical history, examinations, assessments, and treatment plans • Ensure documentation complies with U.S. healthcare standards and guidelines • Maintain strict confidentiality and data security of patient information • Coordinate with U.S.-based physicians and internal quality teams • Meet documentation accuracy, quality benchmarks, and turnaround timelines Qualification • Life Science background only- B.Sc / M.Sc (Biology, Biotechnology, Microbiology, Zoology) • B.Pharm / M.Pharm • Nursing or allied health sciences Experience • Freshers only • No prior medical scribing experience required (training provided) Skills • Excellent English communication skills (written & spoken) • Good typing speed and listening ability • Strong attention to detail and accuracy • Willingness to work night shifts (U.S. time zones) • Interest in U.S. healthcare documentation and clinical workflows About the Organisation OG Healthcare Pvt Ltd is a healthcare services company providing medical scribing and clinical documentation support to U.S.-based physicians, offering structured training and real-time exposure to U.S. healthcare operations for life science graduates.

Roles & Responsibilities • Implement and maintain ISO 13485:2016 Quality Management System • Support risk management activities as per ISO 14971 • Prepare and review regulatory submissions for CDSCO, US FDA, and EU MDR/IVDR • Develop and maintain Design & Development documents, DHF, DMR, and Technical Files • Manage IFU, labeling, SOPs, and regulatory documentation • Support internal audits, external audits, and regulatory inspections • Assist with software lifecycle documentation as per IEC 62304 • Support usability engineering activities per IEC 62366 • Coordinate with R&D, software, clinical, and operations teams • Ensure continuous regulatory compliance and quality improvement Qualification • Bachelor’s degree in Engineering, Life Sciences, Pharmacy, or Quality Management Experience • Experience in Medical Device Quality Assurance & Regulatory Affairs (QARA) • Hands-on exposure to CDSCO, US FDA, and EU MDR/IVDR submissions Skills • Strong knowledge of ISO 13485, ISO 14971, ISO 15223-1, ISO 20417 • Familiarity with IEC 62304 and IEC 62366 • Excellent regulatory writing and documentation skills • Strong analytical, organizational, and communication abilities About the Organisation Aytasense Technologies Pvt. Ltd. is a fast-growing medical device and digital health company developing SenseH, an advanced remote health monitoring solution that combines wearable sensors, AI-driven analytics, and real-time health insights, with a focus on global regulatory compliance and innovation.

Roles & Responsibilities • Create and maintain Safety Data Sheets (SDS) for global markets • Perform hazard classification as per GHS, CLP, OSHA regulations • Handle regulatory compliance workflows including labels, registrations, renewals • Review raw materials, formulations, and finished products for compliance • Maintain regulatory data accuracy in SDS authoring tools and ERP systems • Respond to regulatory queries from internal and external stakeholders • Ensure documentation and records meet regulatory standards and timelines Qualification • Bachelor’s or Master’s degree in Chemistry, Pharmacy, Chemical Engineering, or related field Experience • Experience in corporate regulatory affairs or chemical regulatory environment • Hands-on exposure to SDS and label authoring • Experience in product registration or regulatory compliance preferred Skills • Strong knowledge of global chemical regulations (GHS, CLP, OSHA) • SDS and label authoring experience • Good analytical, documentation, and communication skills • Ability to work independently and with cross-functional teams About the Organisation Diversey, a Solenis company, is a global leader in hygiene and cleaning solutions. Its Global Regulatory Affairs Service Center (GRASC) in Mumbai supports worldwide regulatory compliance across Diversey’s chemical product portfolio, offering strong global exposure and professional growth.

Roles & Responsibilities • Handle regulatory compliance workflows including SDS creation, labels, product registrations, notifications, and renewals • Author Safety Data Sheets (SDS) for multiple global geographies as per applicable regulations • Derive hazard classifications for substances and mixtures using GHS, CLP, OSHA, and other regulations • Perform raw material, formulation, and finished product compliance reviews • Maintain data accuracy and integrity in SDS authoring tools and ERP systems • Respond to regulatory queries from internal and external stakeholders within defined TATs • Coordinate with team leads and SMEs for resolution of complex or high-priority requests • Maintain regulatory records as per defined formats and standards • Support global regulatory compliance across Diversey’s product portfolios Qualification • Bachelor’s or Master’s degree in Chemistry, Chemical Engineering, Environmental Science, Pharmacy, or related discipline Experience • Experience working in a corporate regulatory affairs or chemical regulatory environment • Hands-on experience in SDS and label authoring • Exposure to product registration, regulatory compliance, or regulatory consulting • Proven interaction with competent authorities is preferred Skills • Strong knowledge of global chemical regulations and hazard communication (GHS, CLP, OSHA) • Experience with SDS authoring software and regulatory databases • Good analytical, documentation, and problem-solving skills • Ability to prioritize tasks and meet strict timelines • Excellent written and verbal communication skills in English • Ability to work independently and in cross-functional teams About the Organisation Diversey, a Solenis company, is a global leader in hygiene, cleaning, and sustainability solutions. Through its Global Regulatory Affairs Service Center (GRASC) in Mumbai, Diversey supports regulatory compliance across worldwide markets. Solenis values its people as its greatest asset, offering a collaborative, inclusive, and growth-oriented work environment with exposure to global regulatory operations.

Roles & Responsibilities • Assign accurate diagnosis and procedure codes to patient medical records • Ensure compliance with ICD-10-CM, CPT, and HCPCS coding guidelines • Review clinical documentation to extract relevant coding information • Maintain high accuracy and quality standards in coding deliverables • Coordinate with internal teams and medical staff for documentation clarification • Support revenue cycle processes through compliant medical coding Qualification • Bachelor’s degree in Pharmacy, Biotechnology, Nursing, Health Information Management, or related discipline Experience • Fresher / Entry-level candidates • Prior healthcare or medical coding exposure is an added advantage Skills • Strong attention to detail and analytical skills • Basic understanding of medical terminology • Good written and verbal communication skills • Willingness to learn US healthcare and RCM processes • Ability to work in a process-driven environment About the Organisation AGS Health is a global leader in Revenue Cycle Management (RCM), supporting over 150 healthcare clients and major U.S. hospitals with intelligent automation and expert-driven solutions. With a workforce of 14,000+ professionals worldwide, AGS Health focuses on compliance, accuracy, and sustainable revenue outcomes, offering strong long-term career growth in medical coding and healthcare analytics.

Roles & Responsibilities • Perform hands-on wet analysis and instrumental analysis using GC, HPLC, and GC-MS • Carry out method development, routine analysis, and complete method validation • Ensure accurate documentation of all analytical activities • Maintain compliance with GMP and global regulatory requirements • Support analytical R&D activities for API development • Adhere to pharmacopoeial and regulatory standards across projects Qualification • M.Sc. (Chemistry) / M.Pharm or equivalent qualification Experience • Executive – AR&D: 2 to 4 years of API analytical R&D experience • Senior Executive – AR&D: 6 to 8 years of API analytical R&D experience • Mandatory experience in API pharmaceutical R&D Skills • Strong hands-on experience in Wet Analysis, GC, HPLC, GC-MS • Expertise in method development, validation, and routine analysis • Knowledge of USP, EP, IP, WHO, Brazil, and China pharmacopoeias • Sound understanding of GMP and regulatory compliance • Strong analytical, documentation, and problem-solving skills Walk-In Interview Details • Date: 24 January 2026 • Time: 09:00 AM – 01:00 PM • Venue: Optimus Drugs (P) Limited (API Unit), Plot No. 64, Survey No. 144/Part, EPIP, Pashamylaram (V), Near Isnapur, Sangareddy, Hyderabad, Telangana • Note: Candidates must bring multiple copies of their updated resume • Eligibility: Only candidates with prior API pharma experience should attend About the Organisation Optimus Drugs Pvt. Ltd., a Sekhmet Pharmaventures company, is a leading API manufacturer known for its strong analytical R&D capabilities and global regulatory approvals. The company focuses on high-quality API development and offers professionals a robust platform for growth in analytical research, regulatory compliance, and advanced pharmaceutical sciences.

Roles & Responsibilities • Perform hands-on wet analysis and instrumental analysis using GC, HPLC, and GC-MS • Carry out method development, routine analysis, and complete method validation • Ensure accurate documentation of all analytical activities • Maintain compliance with GMP and global regulatory requirements • Support analytical R&D activities for API development • Adhere to pharmacopoeial and regulatory standards across projects Qualification • M.Sc. (Chemistry) / M.Pharm or equivalent qualification Experience • Executive – AR&D: 2 to 4 years of API analytical R&D experience • Senior Executive – AR&D: 6 to 8 years of API analytical R&D experience • Mandatory experience in API pharmaceutical R&D Skills • Strong hands-on experience in Wet Analysis, GC, HPLC, GC-MS • Expertise in method development, validation, and routine analysis • Knowledge of USP, EP, IP, WHO, Brazil, and China pharmacopoeias • Sound understanding of GMP and regulatory compliance • Strong analytical, documentation, and problem-solving skills Walk-In Interview Details • Date: 24 January 2026 • Time: 09:00 AM – 01:00 PM • Venue: Optimus Drugs (P) Limited (API Unit), Plot No. 64, Survey No. 144/Part, EPIP, Pashamylaram (V), Near Isnapur, Sangareddy, Hyderabad, Telangana • Note: Candidates must bring multiple copies of their updated resume • Eligibility: Only candidates with prior API pharma experience should attend About the Organisation Optimus Drugs Pvt. Ltd., a Sekhmet Pharmaventures company, is a leading API manufacturer known for its strong analytical R&D capabilities and global regulatory approvals. The company focuses on high-quality API development and offers professionals a robust platform for growth in analytical research, regulatory compliance, and advanced pharmaceutical sciences.

Roles & Responsibilities • Perform routine calibration of laboratory instruments • Execute BABE laboratory activities as per approved SOPs • Maintain calibration logs, records, and related documentation • Support day-to-day laboratory operations ensuring quality and safety compliance • Assist senior analysts with routine laboratory and technical tasks • Follow GxP, QA guidelines, and internal compliance procedures Qualification • B.Pharm / M.Pharm / M.Sc (Life Sciences or related discipline) Skills • Basic knowledge of analytical instruments and laboratory practices • Understanding of SOPs and quality systems • Good documentation and record-keeping skills • Willingness to learn and adapt in a professional lab environment • Ability to work on-site and collaborate with team members About the Organisation Jeevan Scientific Technology Ltd (JSTL) is a reputed scientific services and laboratory solutions company providing high-quality testing, calibration, and research support across multiple industries. With a strong focus on compliance, accuracy, and technical excellence, JSTL offers fresh graduates an excellent platform to gain hands-on laboratory exposure and build a strong foundation in scientific and pharmaceutical operations.

Roles & Responsibilities • Perform plant troubleshooting and process optimization in coordination with Production teams • Investigate and close OOS/OOT cases; execute DOE and implement CAPA • Develop and implement salvage processes for non-conforming batches • Prepare and submit PDRs and technical reports to QA • Participate in Plant CFT meetings and provide technical inputs • Conduct laboratory trials to resolve plant issues and share technical data • Ensure documentation compliance with GLP, GMP, and cGMP guidelines • Participate in continuous training, safety programs, and technical skill development Qualification • M.Sc in Chemistry / Pharmaceutical Sciences or related discipline Experience • 1–3 years of experience in Process Technology / Manufacturing / Technical Services • Exposure to pharmaceutical plant operations preferred Skills • Strong knowledge of GMP, cGMP, and GLP requirements • Hands-on experience with OOS/OOT investigations, DOE, and CAPA • Good documentation and report-writing skills • Strong analytical and problem-solving abilities • Effective communication and cross-functional coordination skills About the Organisation Cadila Pharmaceuticals is one of India’s leading pharmaceutical manufacturers with a strong presence across domestic and international markets. Known for its focus on quality, innovation, and patient-centric solutions, Cadila offers robust opportunities for professionals to grow in pharmaceutical manufacturing, process technology, and GMP-driven operations through hands-on exposure and cross-functional collaboration.

Roles & Responsibilities • Conduct onsite monitoring visits in compliance with ICH-GCP guidelines • Ensure subject safety, data integrity, and protocol adherence • Review and verify source documents, CRFs, and eCRFs • Perform site initiation, routine monitoring, and close-out visits • Identify, document, and report protocol deviations • Coordinate with investigators, site staff, and internal study teams • Support regulatory documentation and audit/inspection readiness • Ensure timely resolution of data queries and follow-up actions Qualification • B.Pharm / M.Pharm • OR Diploma in Clinical Research Experience • 1–2 years of onsite clinical trial monitoring experience preferred • Exposure to site monitoring activities in clinical trials Skills • Strong understanding of ICH-GCP, GVP, and clinical trial processes • Excellent documentation and communication skills • Ability to coordinate effectively with sites and cross-functional teams • Willingness to travel for site monitoring visits • Detail-oriented with strong compliance mindset About the Organisation Innovate Research Pvt. Ltd. is a rapidly growing global Clinical Research Organization with operations across India, USA, UAE, UK, and Hungary. Known for its innovation-driven and quality-focused approach, Innovate Research delivers end-to-end clinical research services while maintaining the highest standards of regulatory compliance and patient safety. The organization offers professionals strong exposure to international clinical trials and long-term career growth in the clinical research domain.

Roles & Responsibilities • Manage end-to-end product lifecycle for US and Canada markets from launch to commercialization • Drive sales growth, profitability, and P&L ownership for assigned international markets • Coordinate with Regulatory Affairs, Manufacturing, Supply Chain, Planning, and Operations teams • Liaise with international customers to ensure optimal inventory planning and supply continuity • Analyze IQVIA and export data to prepare sales forecasts, demand plans, and profitability analysis • Prepare and circulate monthly MIS reports to track KRAs and business performance • Support alliance management and partner coordination in regulated markets • Monitor market trends, competition, and product performance to support strategic decision-making Qualification • Bachelor’s degree in Pharmacy or related science discipline (mandatory) • MBA or equivalent postgraduate qualification preferred Experience • 2–6 years of experience in International Business Development or Pharma Sales & Marketing • Hands-on exposure to regulated markets such as US and Canada • Experience managing finished formulations portfolios Skills • Strong analytical and data-driven decision-making skills • Proactive, result-oriented mindset with ownership attitude • Excellent verbal and written communication skills • Working knowledge of SAP or similar ERP systems • Proficiency in MS Excel, PowerPoint, and Word • Ability to manage risk, resolve conflicts, and coordinate cross-functional teams About the Organisation Umedica Laboratories Private Limited is a globally reputed pharmaceutical manufacturer with a strong presence in regulated markets, particularly the United States. With multiple USFDA-approved products already commercialized and a robust ANDA pipeline under development, Umedica continues to expand its footprint in the global generics space. The organization offers professionals strong exposure to international business strategy, product lifecycle management, alliance partnerships, and long-term career growth in a regulated market environment.

Roles & Responsibilities • Search and retrieve toxicological data from scientific literature and regulatory databases to support safety assessment of new and existing products • Review and document safety data for ingredients, products, and technologies used in consumer healthcare products • Prepare toxicology sections of Ingredient Monographs, safety statements, and product summaries • Summarize and interpret risk assessment data for key toxicological endpoints • Identify, analyze, and report project-relevant data from secondary sources and available databases • Respond to safety-related queries from consumers and regulatory authorities • Ensure accuracy, relevance, and up-to-date toxicological information in all deliverables • Work independently as well as collaboratively within project-specific teams Qualification • Master’s degree in Toxicology, Life Sciences, Pharmacy, or a related scientific discipline Experience • 1–2 years of experience in toxicological research, safety assessment, or scientific documentation Skills • Strong domain knowledge in Toxicology • Experience with regulatory and scientific databases (ECHA, PCPC, EFSA, ToxPlanet, Embase, PubMed, etc.) • Excellent scientific writing and report preparation skills • Strong analytical and data interpretation abilities • Proficiency in MS Office (PowerPoint, basic Excel) and internet research tools • Good written and verbal communication skills • Ability to work independently in a fast-paced environment About the OrganisationThe organization is a globally reputed pharmaceutical company committed to ensuring the safety of its products through robust toxicological evaluation and scientific excellence. It offers a dynamic, performance-driven environment with opportunities for learning, professional growth, and exposure to global product safety operations. 

Roles & Responsibilities • Access, review, and process safety cases in the Argus Safety database • Perform end-to-end ICSR case processing within global timelines • Code adverse events, indications, and medications using standard dictionaries • Ensure compliance with GVP, SOPs, and regulatory requirements • Manage follow-ups with reporters and relevant stakeholders • Support patient safety objectives and PV process improvements • Maintain high data quality, accuracy, and adherence to TATs • Collaborate effectively within cross-functional PV teams Qualifications • B.Pharm / M.Pharm • B.Sc / M.Sc (Life Sciences) • BAMS / BDS Experience • 2–5 years of experience in Pharmacovigilance / Drug Safety Skills • Strong knowledge of ICSR lifecycle and case processing • Hands-on experience with Argus Safety • Understanding of ICH-GCP and GVP guidelines • Excellent written and verbal communication skills • Strong analytical, time management, and teamwork abilities About the OrganisationTCS is one of India’s most trusted global organizations, delivering technology and life sciences solutions across industries. With a strong focus on employee growth, process excellence, and long-term stability, TCS offers a rewarding career path in pharmacovigilance and clinical safety operations.

Roles & Responsibilities Literature Review & Evidence Generation • Conduct systematic and targeted literature searches (PubMed, Embase, Cochrane, open sources) • Analyze clinical and scientific data to generate meaningful insights • Stay updated on therapeutic, regulatory, and guideline developments Medical & Scientific Writing • Create, review, and edit scientific content across OTC and Rx domains • Develop manuscripts, abstracts, posters, slide decks, guideline summaries, and white papers • Ensure compliance with publication and ethical standards (ICMJE, CONSORT) Content Review & Quality Control • Review medical, promotional, and scientific materials as per SOPs and guidelines • Validate references, ensure plagiarism-free content, and maintain formatting standards • Ensure clarity, accuracy, and consistency in all deliverables Project Execution & Collaboration • Understand client objectives and timelines and deliver high-quality outputs • Manage multiple projects simultaneously and respond to ad-hoc requests • Collaborate with cross-functional teams including medical writers, graphics, and clients Qualification • MBBS / BDS / PhD / Master’s in Pharmacy or related fieldSkills • Strong scientific writing, editing, and literature analysis skills • Excellent knowledge of clinical study designs and evidence synthesis • Proficiency in MS Word, PowerPoint, Excel, and online research tools • Strong attention to detail, time management, and independent working ability • Excellent written and verbal communication skills Good to Have • Exposure to US/EU regulatory documentation • Experience with reference management tools (EndNote, Zotero, Mendeley) • Familiarity with statistical or visualization tools (SPSS, RevMan, GraphPad, R) About the Organisation A global scientific communications organization supporting pharmaceutical, OTC, and consumer healthcare clients with high-quality medical writing, evidence synthesis, and compliant scientific content across therapeutic areas.

Roles & Responsibilities • Prepare and review CTD and ACTD dossiers for OSD products • Compile and maintain Process Validation (PV) documentation • Prepare and review stability study documentation • Develop Product Development Reports (PDR) • Perform artwork checking and regulatory compliance review • Prepare SmPC, package inserts, and leaflets • Ensure AMV and CDP matching and regulatory accuracy • Prepare and review specifications, COA, and MOA documents • Handle finished product specifications and DMF documentation support • Draft and submit product permissions, COPP, and FSC dossiers • Independently prepare, review, and manage regulatory documentation Qualification • B.Pharm / M.Pharm / M.Sc (Pharmacy background preferred) Experience • 1–4 years of experience in Pharmaceutical Regulatory Affairs • Hands-on exposure to OSD regulatory submissions • Strong knowledge of CTD and ACTD formats • Familiarity with Indian and export regulatory requirements Skills • Strong regulatory documentation and dossier compilation skills • High attention to detail and compliance accuracy • Good written and verbal communication skills • Ability to work independently and manage multiple submissions • Strong understanding of pharmaceutical lifecycle management About the Organisation Noronic Pharmaceutical Private Limited is a growing Indian pharmaceutical company focused on delivering high-quality pharmaceutical products across domestic and international markets. The organization offers a stable work environment, hands-on regulatory exposure, and long-term career growth opportunities for Regulatory Affairs professionals.

Roles & Responsibilities • Develop and maintain pharmaceutical forecasting models across multiple therapeutic areas • Support portfolio strategy and valuation decisions in collaboration with BD Analytics HOCT team • Apply statistical forecasting, time-series analysis, and predictive modeling techniques • Perform scenario analysis related to pricing, market access, and regulatory outcomes • Analyze large datasets including sales forecasts, epidemiology, and competitive intelligence • Build advanced Excel-based forecasting and financial models, including dashboards • Prepare insight-driven reports and PowerPoint presentations for senior leadership • Collaborate with cross-functional and IT teams to automate data collection and reporting • Monitor market trends, competitor activity, and pipeline developments Qualification • Bachelor’s or Master’s degree in Biology, Biotechnology, Finance, Economics, Business, or related field • MBA preferred but not mandatory Experience • 1–3 years of experience in pharmaceutical forecasting, portfolio analytics, or commercial analytics • Prior exposure to Oncology, Hematology, or Cell Therapy is an added advantage Skills • Strong proficiency in Advanced Excel and VBA • Experience handling pharma datasets (sales, epidemiology, competitive intelligence) • Knowledge of forecasting methodologies and analytical modeling • Exposure to BI tools, forecasting software, or Python is a plus • Strong analytical, problem-solving, and critical-thinking skills • Excellent communication and stakeholder management abilities • Ability to work independently and collaborate across teams About the Organisation Bristol Myers Squibb (BMS) is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines for patients with serious diseases. With a strong presence in Oncology, Hematology, and Cell Therapy, BMS leverages advanced analytics and data-driven decision-making to shape portfolio strategy and drive impactful business outcomes worldwide.