Pharmacy Jobs

Roles & Responsibilities • Perform wet chemistry sample extraction as per study protocols and SOPs • Handle centrifugation, evaporation, freezing, storage, and aliquoting of biological samples • Prepare reagents, solvents, mobile phases, calibration standards, and QC samples • Support method development and validation of drugs and metabolites using LC/MS/MS • Execute validation parameters including accuracy, precision, recovery, matrix effect, and stability studies • Carry out routine bioanalysis for bioequivalence and subject sample analysis • Operate and maintain LC/MS/MS, HPLC, and ICP-OES instruments • Perform system suitability checks, troubleshooting, and basic instrument maintenance • Complete analytical worksheets, QC sheets, raw data records, and logbooks accurately • Ensure compliance with GLP, SOPs, and regulated bioanalytical guidelines • Support audits, inspections, and mandatory training activities Qualification • M.Pharm / M.Sc / MS (Science) – Any Specialization Experience • Hands-on exposure to LC/MS/MS bioanalysis preferred • Experience with biological matrices such as plasma, serum, and urine is an advantage • Regulated bioanalytical lab exposure is desirable (not mandatory) Skills • LC/MS/MS operation and troubleshooting • Wet chemistry and bioanalytical workflows • Bioanalytical method development and validation • GLP compliance and documentation practices • Data integrity and basic MS Office skills About the Organisation Cliantha Research is a leading global Contract Research Organization (CRO) providing integrated clinical research, bioanalytical, and regulatory services. The organization is known for its strong compliance culture, advanced analytical capabilities, and commitment to quality-driven clinical research.

Roles & Responsibilities • Plan and conduct clinical trial audits in compliance with ICH-GCP, regulatory guidelines, and internal SOPs • Review and maintain Quality Management Systems (QMS) documentation and processes • Lead CSV validation and qualification activities related to clinical systems • Ensure audit and inspection readiness for sponsor, regulatory, and internal audits • Manage sponsor interactions and audit responses effectively • Identify compliance gaps and drive CAPA implementation • Lead and mentor QA audit teams to meet project timelines • Monitor audit timelines and ensure timely closure of audit findings • Support continuous quality improvement initiatives across clinical operations Qualification • M.Sc / B.Pharm / M.Pharm / Other relevant life science qualifications Experience • 10 – 15 years of experience in Clinical QA, auditing, and compliance Skills • Regulatory guidelines and compliance requirements • Clinical QMS and auditing practices • CSV validation and qualification • Audit and inspection readiness • Team leadership and timeline management • Sponsor handling and communication About the Organisation Cliantha Research is a globally recognized clinical research organization providing integrated clinical, bioanalytical, and regulatory services. The company is known for its strong quality culture, regulatory expertise, and commitment to delivering compliant and reliable clinical research solutions.

Roles & Responsibilities • Support project monitoring and coordination using project management tools • Prepare study safety documents including SAE reporting forms and guidelines • Develop training materials for investigator meetings and safety trainings • Generate progress reports, listings, and study-related outputs for PVSM and clients • Assist in SAE and ICSR processing as per protocols, SOPs, and regulatory guidelines • Maintain and update internal safety databases • Follow up with investigator sites for query resolution • Prepare high-quality case narratives for safety reporting • Distribute ICSRs to Ethics Committees, Investigators, and MAHs • Prepare and circulate 6-monthly SUSAR line listings • Support preparation and submission of DSURs to Competent Authorities and Ethics Committees • Assist with MedDRA coding in coordination with Data Management and Statistics teams • Support additional pharmacovigilance activities as per departmental requirements Qualification • Degree in Pharmacy, Life Sciences, or related discipline Experience • Relevant experience in Pharmacovigilance, Clinical Research, or Safety Operations Skills • Pharmacovigilance processes and SAE / ICSR reporting • Safety database handling and case processing • MedDRA coding knowledge • ICH, EMA, and FDA regulatory guidelines • Microsoft Office and database management tools • Strong documentation, coordination, and communication skills About the Organisation Veeda Clinical Research is a leading global CRO providing comprehensive clinical research, bioanalytical, and pharmacovigilance services. The organization is known for its regulatory expertise, quality-driven processes, and strong presence in domestic and international clinical research.

Roles & Responsibilities • Handle OOS, OOT, deviations, CAPA, and laboratory investigations • Review analytical data generated from HPLC, GC, UV, and IR instruments • Ensure compliance with Quality Management Systems (QMS) and SOPs • Perform documentation review and maintain data integrity in lab operations • Use Chromeleon Software 7.2 for chromatography data handling and review • Support internal, regulatory, and customer audits (FDA, USFDA, MHRA) • Ensure timely closure of lab incidents and implementation of corrective actions • Contribute to continuous improvement in laboratory quality systems Qualification • B.Pharm / M.Pharm / M.Sc (Chemistry or Analytical preferred) Experience • Relevant experience in Pharmaceutical Lab QA / QC environment Skills • OOS, OOT, CAPA, deviations handling • QMS and SOP compliance • HPLC, GC, UV, IR instrumentation • Chromeleon Software 7.2 • Regulatory audit exposure (FDA, USFDA, MHRA) • Documentation and data integrity About the Organisation IPCA Laboratories is one of India’s leading pharmaceutical companies with a strong global presence. The company is known for its commitment to quality, regulatory compliance, and excellence in manufacturing, offering professionals a stable and growth-oriented work environment.

Roles & Responsibilities • Lead and manage a portfolio of brands across key therapeutic segments • Define long-term brand vision, strategy, and growth roadmap • Oversee product managers and ensure alignment with business objectives • Drive product lifecycle management, including launches and extensions • Plan and execute integrated marketing campaigns and brand promotions • Conduct market research, competitor analysis, and performance reviews • Collaborate with sales, medical, regulatory, and supply chain teams • Develop and monitor marketing budgets and ROI metrics • Train, mentor, and motivate the PMT and field force teams Qualification • Graduate in Science or Pharmacy Experience • Minimum 8 years of experience in Product Management Team (PMT) • Proven track record in domestic pharmaceutical marketing Skills • Strong leadership and brand strategy expertise • Excellent analytical, communication, and presentation skills • Market insight, forecasting, and portfolio management • Ability to manage multiple brands and cross-functional teams About the Organisation IPCA Laboratories is a leading pharmaceutical company with a strong presence in domestic and international markets. The organization is known for its focus on quality, innovation, and sustained brand growth, offering professionals a dynamic environment and excellent career progression.

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.