Pharmacy Jobs

Roles & Responsibilities • Lead product strategy and brand planning for domestic pharma brands • Develop and execute marketing campaigns and promotional strategies • Prepare product positioning, visual aids, and marketing collaterals • Coordinate with sales teams to drive product performance • Analyze market trends, customer insights, and competitor activity • Manage product lifecycle including launches and line extensions • Conduct training programs for field force and internal teams • Collaborate with cross-functional teams such as sales, medical, and supply chain Qualification • Graduate in Science or Pharmacy Experience • Minimum 4 years of experience in Product Management Team (PMT) • Proven experience in domestic pharmaceutical marketing Skills • Strong brand management and strategic planning skills • Market analysis and competitive intelligence • Excellent communication, presentation, and leadership abilities • Ability to manage multiple products and projects effectively About the Organisation IPCA Laboratories is a leading Indian pharmaceutical company with a strong presence in domestic and global markets. The organization is known for its quality-driven manufacturing, robust brand portfolio, and commitment to innovation in healthcare.

Roles & Responsibilities • Support product planning and execution for domestic pharma brands • Develop promotional strategies and marketing campaigns • Prepare product literature, visual aids, and training materials • Coordinate with sales teams for product launches and campaigns • Analyze market trends, competitor activities, and product performance • Assist in brand positioning and lifecycle management • Work closely with cross-functional teams including sales, medical, and supply chain Qualification • Graduate in Science or Pharmacy Experience • Minimum 2 years of experience in Product Management Team (PMT) • Experience in domestic pharmaceutical marketing required Skills • Strong understanding of pharma marketing and brand management • Market analysis and competitive intelligence skills • Good communication and presentation abilities • Ability to work cross-functionally and manage multiple projects About the Organisation IPCA Laboratories is a leading Indian pharmaceutical company with a strong domestic and international presence. The company is recognized for its quality-driven approach, robust brand portfolio, and consistent growth in the pharmaceutical market.

Roles & Responsibilities • Perform IPQA activities during manufacturing and packing operations • Ensure line clearance, in-process checks, and compliance with SOPs • Review batch manufacturing and packing records • Monitor adherence to cGMP, GDP, and quality standards • Support deviation handling, CAPA, and change control activities • Coordinate with production and QC teams to ensure quality compliance • Assist during internal audits and regulatory inspections Qualification • B.Pharm Experience • 3 to 4 years of relevant experience in IPQA • Experience in formulation manufacturing is mandatory Skills • Strong IPQA and shop-floor quality knowledge • Understanding of cGMP, SOPs, and regulatory requirements • Documentation review and compliance skills • Attention to detail and good coordination abilities About the Organisation IPCA Laboratories is a reputed Indian pharmaceutical company with a strong presence in domestic and international markets. The company is known for its quality-focused manufacturing, regulatory compliance, and wide portfolio of formulations and APIs.

Roles & Responsibilities • Dispense Ayurvedic medicines as per prescriptions • Maintain proper storage and inventory of Ayurvedic drugs • Ensure correct labeling, dosage, and patient guidance • Maintain pharmacy records and documentation • Support doctors in patient care and treatment management • Follow AYUSH and government healthcare guidelines Qualification • D.Pharm Age Limit • Minimum: 21 years • Maximum: 45 years • Age relaxation applicable as per organisation norms Important Date • Application Deadline: 27-01-2026Skills • Knowledge of Ayurvedic medicines and formulations • Inventory management and record keeping • Attention to detail and accuracy in dispensing • Basic patient counselling skills • Ability to follow government healthcare protocolsAddress: Rama Varma District Ayurveda Hospital Campus, Patturaikkal, Thrissur About the Organisation The National Ayush Mission (NAM) is a Government of India initiative aimed at promoting AYUSH systems of medicine including Ayurveda, Yoga, Unani, Siddha, and Homeopathy. NAM Kerala works to strengthen Ayurvedic healthcare services through quality treatment, medicine availability, and skilled professionals.Official Notification and Application FormClick Here

Roles & Responsibilities • Greet patients and guide them to appropriate departments • Handle patient inquiries via phone and coordinate call-backs with doctors and nurses • Manage appointments, confirmations, rescheduling, and no-shows • Register new patients and update existing patient records • Explain medical insurance coverage and collect payments or co-payments • Provide claim and reimbursement forms when required • Handle daily cash, card, and cheque collections as per finance protocols • Maintain working knowledge of Hospital Information Systems, clinic schedules, and doctor rosters • Respond to emails and patient queries in a timely manner • Ensure operations follow hospital policies, procedures, and duty rosters • Handle patient complaints professionally and confidentially • Maintain data accuracy, patient confidentiality, and compliance with privacy regulations • Generate, process, and explain patient bills and invoices • Ensure billing accuracy and compliance with insurance and legal requirements • Participate in hospital training, quality assurance, and continuous improvement initiatives Qualification • College Diploma in any discipline or related field Experience • 3 to 8 years of experience in hospital front office, patient services, or billing operations Skills • Strong patient handling and customer service skills • Knowledge of hospital operations, billing, and insurance processes • Excellent communication and interpersonal abilities • Attention to detail and data accuracy • Ability to handle cash, billing systems, and hospital information systems • Professional approach with strong confidentiality and compliance awareness About the Organisation NMC Hospital is a leading healthcare provider known for its patient-centric approach, high clinical standards, and commitment to quality and safety. The organization emphasizes continuous improvement, compliance with international healthcare standards, and delivering exceptional patient experiences.

Roles & Responsibilities • Assist in accurate and efficient dispensing of medications • Maintain proper inventory of medicines and pharmacy supplies • Counsel patients on correct medication usage and possible side effects • Address patient queries and ensure excellent customer service • Perform medication therapy management services • Coordinate with healthcare providers to optimize patient care Qualification • Bachelor’s degree in Pharmacy or related field • Registered or eligible for pharmacist registration with relevant authority Experience • 1 to 4 years of relevant pharmacy experience Skills • Strong knowledge of pharmaceuticals, drug interactions, and dosage forms • High attention to detail and accuracy in dispensing • Good communication and patient counselling skills • Customer-focused approach and teamwork ability About the Organisation Life Pharmacy is a trusted healthcare and pharmacy services provider focused on delivering quality medications, professional guidance, and patient-centric care across its pharmacy network.

Roles & Responsibilities • Accurately dispense prescription medications in compliance with legal and professional standards • Provide medication counselling on usage, side effects, and drug interactions • Collaborate with healthcare providers to develop and manage patient-specific treatment plans • Monitor patient outcomes and support therapy adjustments with medical teams • Conduct medication safety and wellness training for staff and patients • Manage pharmacy inventory, stock levels, and minimize wastage • Stay updated with new drugs, clinical guidelines, and pharmacy practices Qualification • Doctor of Pharmacy (Pharm.D.) from a recognized institution • Active and valid pharmacist license Experience • Minimum 3 years of experience in pharmacy practice preferred Skills • Strong knowledge of pharmacotherapy and clinical guidelines • Excellent communication and patient counselling skills • Team collaboration and coordination with healthcare professionals • Attention to detail and strong analytical abilities • Customer-focused mindset and problem-solving skills • Commitment to continuous learning and professional development About the Organisation Ninja is an innovative healthcare organization focused on transforming patient engagement and care delivery. By combining technology-driven solutions with personalized healthcare services, Ninja aims to improve treatment outcomes and enhance the overall patient experience.

Roles & Responsibilities • Implement and maintain Quality Management Systems (QMS) as per GMP and regulatory guidelines • Execute process, equipment, and cleaning validation activities • Prepare, review, and approve validation protocols and reports • Handle deviations, change controls, CAPA, and quality investigations • Participate in internal audits, regulatory inspections, and compliance activities • Ensure proper documentation control and data integrity • Train personnel on SOPs, GMP practices, and quality procedures • Support continuous improvement and quality risk management initiatives Open Positions • Assistant Manager – QA • QMS Senior Officer • QMS Officer • Validation Executive • Validation Officer / Senior OfficerQualification • B.Pharm / M.Pharm • MSc (Microbiology / Biotechnology / Chemistry) or equivalent Experience • 2 to 10+ years of relevant experience in QA, QMS, or Validation • Experience level varies depending on the role applied for • Prior exposure to regulated pharma manufacturing preferred Skills • Strong knowledge of GMP, GLP, WHO, USFDA, EDQM guidelines • Hands-on experience in validation and quality systems • Documentation, data analysis, and audit-handling skills • Familiarity with QMS tools and regulatory inspections • Good communication, problem-solving, and attention to detail About the Organisation Ceph Lifesciences Pvt Ltd is a growing pharmaceutical company with manufacturing operations across India, including Himachal Pradesh, and a registered base in Telangana. The company focuses on delivering high-quality pharmaceutical products while maintaining strong compliance with global regulatory standards.

Roles & Responsibilities • Dispense medicines as per doctor’s prescriptions • Maintain proper storage, labeling, and handling of drugs • Manage pharmacy inventory, stock registers, and expiry tracking • Ensure compliance with government healthcare guidelines and SOPs • Maintain patient and prescription records accurately • Assist medical officers and healthcare staff in daily operations Qualification • B.Pharm / D.Pharm / M.Pharm Age Limit • Minimum Age: 18 years • Maximum Age: 45 years • Age relaxation as per organisation norms Important Date • Application Deadline: 02-02-2026 Skills • Knowledge of drug dispensing and inventory management • Familiarity with pharmacy laws and government healthcare systems • Good documentation and record-keeping skills • Attention to detail and accuracy • Basic computer knowledge and communication skills About the Organisation The District Medical & Health Office (DMHO), Guntur operates under the state health department and is responsible for implementing public health programs, managing healthcare facilities, and ensuring quality medical services to the population at the district level.Official Notification and Application FormClick Here

Roles & Responsibilities • Dispense medicines as per prescribed treatment • Maintain pharmacy stock, inventory, and expiry records • Ensure proper storage and handling of drugs and medical supplies • Maintain prescription records and pharmacy documentation • Support doctors and healthcare staff in patient care services • Follow ECHS guidelines, SOPs, and regulatory requirements Qualification • B.Pharm or D.Pharm Age Limit • Minimum Age: 21 years • Maximum Age: 45 years • Age relaxation as per organisation norms Important Date • Application Deadline: 08-02-2026Skills • Knowledge of drug dispensing and inventory management • Understanding of pharmacy regulations and storage standards • Good communication and record-keeping skills • Attention to detail and accuracy • Ability to work in a healthcare environment About the Organisation The Ex-Servicemen Contributory Health Scheme (ECHS) is a government healthcare initiative under the Ministry of Defence, providing comprehensive medical care to ex-servicemen and their dependents through a network of polyclinics and empanelled hospitals across India.Official NotificationClick Here

Roles & Responsibilities • Review and approval of MBR, APQR, and QA documentation • Handle deviations, change control, CAPA, complaints, and QMS activities • Execute and review media fill studies, process simulations, and equipment qualification • Ensure cGMP and regulatory compliance (USFDA, EU, CDSCO) • Coordinate with cross-functional teams for compliance and audit readiness • Use QA systems such as Trackwise, SAP, LIMS, DMS, and Minitab Available Positions • QA – Documentation (Team Leader / Manager) Qualification: B.Pharm / M.Pharm Experience: 10–13 years • QA – QMS (Executive / Sr. Executive) Qualification: B.Pharm / M.Pharm Experience: 3–7 years • QA – Media Fill / Validation (Asst. Manager) Qualification: B.Pharm / M.Pharm Experience: 8–10 years • QA – Media Fill / Validation (Executive / Sr. Executive) Qualification: B.Pharm / M.Pharm Experience: 3–7 yearsSkills • Sterile QA operations • QMS (Deviation, CAPA, Change Control) • Media fill & validation activities • Regulatory compliance • Documentation & audit handling About the Organization Micro Labs Limited is a reputed Indian pharmaceutical company with strong expertise in sterile manufacturing and global regulatory compliance, offering stable growth and exposure to advanced quality systems.

Roles & Responsibilities • Review and approval of batch manufacturing records and batch packing records • Ensure compliance with cGMP, SOPs, and regulatory requirements • Handle deviations, change controls, CAPA, and OOS/OOT investigations • Support internal, external, and regulatory audits • Review validation, qualification, and stability documents • Ensure data integrity and documentation accuracy for injectable products • Coordinate with Production, QC, and Engineering teams Qualification • Graduate in Pharmacy Experience • 4 – 8 years in DQA (Injectables) Skills • Documentation review (BMR/BPR) • Deviation, CAPA & change control handling • cGMP & regulatory compliance • Injectable QA operations • Audit handling & data integrity About the Organization Aspiro Pharma is a USFDA-approved pharmaceutical company specializing in injectable formulations. The company focuses on quality-driven manufacturing and offers growth opportunities in regulated environments.

Roles & Responsibilities • Supervise shop floor activities in injectable manufacturing • Oversee filtration, filling, sealing, and stoppering operations • Handle ophthalmic, suspension, and lyophilized injectable products • Ensure adherence to GMP, SOPs, and quality standards • Support training of operators and technicians • Implement and maintain Quality Management Systems (QMS) • Coordinate with QA and Engineering teams for smooth operations Qualification • B.Pharm / M.Pharm / M.Sc Experience • 2 - 6 years in injectable production operations Skills • Injectable manufacturing & aseptic operations • Filtration, filling, sealing & stoppering • Ophthalmic, suspension & lyophilized products • GMP, SOP & QMS compliance • Team supervision & documentation Walk-in Interview Details Dates: 24 January 2026 & 25 January 2026 (Saturday & Sunday) Time: 09:00 AM – 03:00 PM Venue: Aspiro Pharma Ltd, Plot No. 23, Survey No. 321, Biotech Park Phase-III, Karkapatla (V), Markook (M), Siddipet (Dist), Telangana Documents Required: Updated CV, educational certificates, experience letters & passport-size photographs About the Organization Aspiro Pharma Limited is a USFDA-approved pharmaceutical company specializing in high-quality injectable formulations. With a strong focus on compliance, innovation, and operational excellence, Aspiro offers professionals an opportunity to grow in a regulated manufacturing environment with global exposure.

Roles & Responsibilities QA (IPQA) • Perform line clearance activities for aseptic and injectable operations • Monitor washing, filling, sealing, and visual inspection processes • Conduct environmental monitoring in Grade A, B, C & D cleanrooms • Ensure compliance with GMP, SOPs, and regulatory requirements • Support batch documentation, deviations, and investigations • Coordinate with production and quality teams to maintain compliance Production (Injectables) • Monitor aseptic area operations for injectable manufacturing • Perform and support environmental monitoring and media fill activities • Handle infusion and solution preparation processes • Operate and monitor lyophilization, BFS, and injectable bag filling • Ensure adherence to GMP, safety standards, and SOPs • Maintain batch records and support process improvements Qualification • QA (IPQA): B.Pharm / M.Pharm • Production: B.Pharm Experience • QA (IPQA): 1 – 3 years • Production: 2 – 9 years Skills • Aseptic operations & injectable manufacturing • Cleanroom practices & environmental monitoring • Lyophilizer, BFS, infusion & solution preparation • GMP, SOP, and regulatory compliance • Good documentation and teamwork skills Walk-in Interview Details Date: Sunday, 25th January 2026 Time: 10:00 AM – 3:00 PM Venue: Aurobindo Pharma Ltd, Unit-III, Bhachupally, Hyderabad, Telangana (Selected candidates will be deployed at Eugia Pharma Specialities Ltd., Unit-III, Pashamylaram, Patancheru, Sangareddy, Telangana) About the Organization Eugia Pharma Specialities Limited, a part of the Aurobindo Pharma Group, is a leading pharmaceutical company focused on injectable formulations and specialty generics. The company is known for its strong presence in regulated markets, advanced aseptic manufacturing capabilities, and commitment to quality, compliance, and innovation. Eugia continues to expand its global footprint while delivering high-quality parenteral products to meet critical healthcare needs worldwide.

Roles & Responsibilities • Analyse large and complex datasets to identify trends and generate actionable insights • Support business and operations teams with data-driven decision-making • Troubleshoot data issues and resolve data quality problems • Automate recurring reports and streamline data workflows • Collaborate with cross-functional business and technical stakeholders • Capture and translate business requirements into analytics solutions • Improve reporting accuracy, efficiency, and data governance standards • Prepare dashboards, presentations, and insight summaries for leadership • Contribute to process optimization and performance improvement initiatives Qualification • Bachelor’s or Master’s degree in Computer Science, Engineering, Information Systems, or related fields • Pharmaceutical or Life Sciences background is an added advantage Experience • Minimum 1+ year experience in Data Analysis or Business Analytics Skills • Strong expertise in SQL and Advanced Excel • Hands-on experience with Python or PySpark • Working knowledge of data visualization tools (Power BI, Tableau, etc.) • Experience with ETL tools, data integration, and relational databases • Automation experience using Excel macros, Google Apps Script, or similar tools • Excellent communication and stakeholder management skillsAbout the Organization Roche is a global leader in pharmaceuticals and diagnostics, committed to advancing science to improve people’s lives. With a strong focus on innovation, data, and personalized healthcare, Roche leverages advanced analytics and digital solutions to drive better patient outcomes and smarter business decisions. Roche Services & Solutions India supports global Roche operations through high-impact analytics, automation, and technology-driven insights.

Roles & Responsibilities • Analyse drug development information from clinical trials, regulatory agencies, and scientific sources • Track new drugs, pipeline updates, development phases, indications, and sponsors • Perform primary and secondary research on global drug development activities • Summarize, edit, and validate scientific and pharmaceutical content with high accuracy • Conduct comprehensive online searches for drug and clinical intelligence • Maintain assigned production volumes, quality standards, and KPIs • Collaborate with global teams across regions and business units • Follow SOPs and contribute to process improvement initiatives • Adapt to workflow changes in a fast-paced research environment Qualification • M.Pharm / B.Pharm / D.Pharm Experience • Freshers or up to 6 months of relevant experience Skills • Strong understanding of drug development and clinical research concepts • Excellent written and verbal communication skills • Good content analysis, summarization, and editing abilities • Proficiency in MS Word, Excel, and PowerPoint • Strong attention to detail and time management skills • Exposure to AI tools for research or content analysis • Basic knowledge of SQL or Python • Interest in pharmaceutical analytics, clinical intelligence, and drug pipelines About the Team Clarivate’s Drug Development (CDDI) team delivers high-quality intelligence on clinical trials, regulatory pipelines, and drug research, covering MoA, development milestones, regulatory pathways, and disease focus to support global pharmaceutical decision-making.

Roles & Responsibilities Quality Assurance (Injectable / API) • Perform IPQA activities for injectable manufacturing • Review batch manufacturing and batch packing records • Ensure compliance with cGMP, SOPs, and regulatory guidelines • Support deviation handling, CAPA, and documentation • Assist in audits and regulatory inspections Production (Injectable) • Operate injectable manufacturing processes as per SOPs • Support activities related to filling, lyophilization, and packaging • Maintain production documentation and comply with safety guidelines • Follow cGMP and quality standards during manufacturing operations Qualification • M.Pharm / B.Pharm / M.Sc Experience • Freshers only Skills • Basic knowledge of injectable manufacturing processes • Understanding of cGMP, SOPs, and quality systems • Good documentation and compliance orientation • Willingness to work in shift-based manufacturing environments Walk-In Interview Details • Date: 24 January 2026 (Saturday) • Time: 10:00 AM to 04:00 PM • Venue: Gufic Biosciences Ltd, N.H. 48, Near GEB Grid, Kabilpore, Navsari, Gujarat – 396445 • Contact: +91 63599 21281 • Email for CV submission: binal.kapadia@guficbio.com • Documents to carry: Original degree certificate (provisional not accepted), updated resume, ID proof About the Organisation Gufic Biosciences Ltd is a leading pharmaceutical company specializing in lyophilized injectables and APIs, with multiple global regulatory accreditations including WHO GMP, EU GMP, and approvals across several international markets. The Navsari facility offers strong learning opportunities for freshers seeking careers in injectable manufacturing and quality assurance.

Roles & Responsibilities • Develop and validate bioanalytical methods using LC-MS/MS and HPLC • Perform sample analysis for Bioavailability/Bioequivalence (BA/BE) studies • Apply extraction techniques such as SPE and LLE for accurate quantitation • Operate, maintain, and calibrate laboratory instruments as per SOPs • Ensure compliance with GLP, GDP, and regulatory requirements • Perform quality control checks for method validation and BA/BE studies • Handle compliance observations, CAPA, and QA/RA review responses • Maintain calibration records, inventory, temperature logs, and lab documentation Qualification • M.Pharm or M.Sc Experience • 3 to 8 years of experience in bioanalytical or pharma R&D roles Skills • Hands-on expertise in LC-MS/MS and HPLC • Strong knowledge of bioanalytical method development and validation • Experience with BA/BE studies and regulatory guidelines (DCGI, USFDA) • Good documentation practices and compliance mindset • Attention to detail and strong analytical skills About the Organisation Torrent Pharmaceuticals Ltd is a leading Indian pharmaceutical company with strong R&D capabilities and a focus on innovation, quality, and regulatory excellence. Its Gandhinagar R&D Centre plays a key role in advancing bioanalytical research and supporting the company’s global product pipeline.

Roles & Responsibilities • Provide scientific and medical support for the GSM portfolio across Gulf countries • Ensure continuous scientific updates and medical input for cross-functional teams • Communicate scientific data on approved products and pipeline to scientific leaders • Support Policy & Access teams for formulary inclusion and reimbursement activities • Plan and execute scientific education programs to engage the GSM medical community • Conduct input-seeking activities to understand local epidemiology and treatment patterns • Deliver medical training to Commercial, Market Access, Sales, and Regulatory teams • Ensure all promotional and non-promotional activities comply with company SOPs, codes, and local/international regulations Clinical Research & Pharmacovigilance • Support global, regional, and local clinical research and data generation activities • Identify and support appropriate clinical trial sites and investigators • Ensure timely adverse event reporting and support pharmacovigilance activities Qualification • Physician or Pharmacist educational background Experience • 1 to 2 years of experience in Medical Affairs within a multinational pharmaceutical company • Immunology therapeutic area experience preferred Skills • Strong medical and scientific knowledge • Experience in medical communications and medical affairs strategy • Excellent communication and stakeholder engagement skills • Strategic thinking and project management abilities • Proficiency in Microsoft Word, PowerPoint, and Excel • Fluency in Arabic and English Additional Information • Relocation: Not available • VISA Sponsorship: Yes • Travel Requirements: None • Flexible Work Arrangements: As per company policy About the Organisation MSD (Merck Sharp & Dohme) is a global, research-driven biopharmaceutical company committed to using leading-edge science to save and improve lives worldwide. Through its General & Specialty Medicine portfolio, MSD continues to advance medical practice and address high unmet medical needs, striving to be the most trusted, science-driven Medical Affairs organization in the industry.