Pharmacy Jobs

Roles & Responsibilities • Review, dispense, and monitor medications as per physician prescriptions and hospital formulary • Ensure safe, rational, and cost-effective use of medicines • Provide clinical pharmacy support including medication therapy review and patient counseling • Monitor drug interactions, adverse drug reactions, and medication errors • Maintain accurate pharmacy records, inventory control, and narcotics management • Support multidisciplinary healthcare teams with drug information and therapeutic guidance • Ensure compliance with Saudi Health regulations, hospital policies, and accreditation standards Qualification • Pharmacist: Bachelor’s degree in Pharmacy (B.Pharm or equivalent) • Clinical Pharmacist: PharmD or Master’s degree in Clinical Pharmacy • Valid Saudi Commission for Health Specialties (SCFHS) classification (Mandatory) Experience • Hospital pharmacy experience preferred• Saudi Nationals preferred • Saudi Commission classification is mandatorySkills Required • Strong knowledge of pharmacology and clinical therapeutics • Attention to detail and high ethical standards • Good communication and patient counseling skills • Ability to work effectively in a hospital-based multidisciplinary team About the Company Saudi German Hospital is a leading healthcare group in the Middle East, known for delivering high-quality, patient-centered medical services through advanced infrastructure, skilled professionals, and internationally accredited standards.

Roles & Responsibilities • Dispense and compound prescriptions as per hospital formulary and doctors’ orders • Ensure availability of required medicines at the right time and affordable cost • Identify therapeutic incompatibilities and ensure patient safety • Place and receive orders for pharmaceutical supplies • Manage indents, storage, stock maintenance, and inventory control • Ensure compliance with antibiotics, narcotics, and controlled drug procedures • Maintain accurate records of medicines issued and received • Counsel patients, doctors, and nursing staff on drug usage, side effects, and interactions • Monitor drug utilization and support adverse drug reaction reporting • Inspect and supervise destruction of expired or unserviceable drugs • Handle FDA registrations, license updates, and renewals • Train newly joined pharmacy staff • Participate in Drug & Therapeutics Committee activities • Coordinate with other hospital departments Qualification • B.Pharm or any graduates Experience • Minimum 2+ years • Hospital experience preferred Skills Required • Knowledge of hospital pharmacy operations • Understanding of drug safety and regulatory compliance • Strong communication and patient counseling skills • Attention to detail and ability to work in a team About the Company A patient-focused healthcare organization committed to quality, safety, and regulatory-compliant medical services.

Role & Responsibilities • Perform analytical method development and validation for pulmonary dosage forms • Conduct routine and stability sample analysis as per regulatory guidelines • Support formulation development through analytical inputs • Prepare and review analytical reports, protocols and validation documents • Ensure compliance with GLP, GMP and regulatory standards • Handle analytical instruments related to pulmonary product analysis • Participate in technology transfer and regulatory submission activities Qualifications & Experience • M.Pharm with GPAT qualification • 2–6 years of experience in Analytical Development – Pulmonary products • Strong knowledge of analytical method development and validation • Experience in pulmonary dosage form analysis is mandatory About the Company • Zydus Lifesciences Ltd is a leading global pharmaceutical company with strong R&D capabilities in specialty and complex formulations

Roles & Responsibilities • Prepare, review, and submit high-quality regulatory filings (pre- and post-approval) for US FDA–regulated complex generic products including inhalation, ophthalmic, implant, and drug–device combinations • Manage original applications, amendments, deficiency responses (IRs, DRLs, CRLs), and post-approval supplements • Evaluate change controls and determine appropriate regulatory pathways (PAS, CBE-30, CBE-0, AR) in coordination with regulatory management • Compile and submit post-approval changes in compliance with FDA, ICH guidelines, and internal SOPs • Support early FDA engagement to align development strategies and reduce regulatory risks • Act as a regulatory point of contact for cross-functional teams (R&D, QA, Manufacturing, Packaging, DMF holders) as needed • Monitor regulatory timelines, identify documentation gaps, and ensure “Right-First-Time” submissions • Track regulatory intelligence and monitor FDA databases such as Drugs@FDA and Orange Book • Participate in audits, inspections, and continuous process improvement initiatives Qualifications • Master’s degree in Pharmacy with specialization in Regulatory Affairs / Quality Assurance preferred Experience • Minimum 4+ years of pharmaceutical industry experience • Hands-on experience with complex generics such as inhalation, ophthalmic, implant, or drug–device combination products preferred Skills • Strong knowledge of US FDA and ICH regulatory guidelines • Experience in regulatory submissions and post-approval change management • Excellent written and verbal communication skills • Strong organizational skills with attention to detail and multitasking ability • Analytical, critical, and logical thinking skills • Ability to work independently and collaboratively across cross-functional teams About the Company Teva Pharmaceuticals is a global leader in generic and specialty medicines, operating in nearly 60 countries. Driven by a mission to make healthcare more affordable and accessible, Teva supports over 200 million patients worldwide every day through high-quality medicines, innovation, and a strong commitment to diversity, inclusion, and ethical practices.

Role & Responsibilities • Lead global medical review and device safety pharmacovigilance operations • Oversee in-line medical assessment of ICSRs for expectedness, causality and reportability • Ensure compliance with global PV, ICH, and medical device safety regulations • Act as SME for audits, inspections and regulatory interactions • Lead and manage in-house and outsourced PV medical review teams • Oversee first-line signal detection and escalation of safety risks • Maintain KPIs, quality metrics and compliance dashboards • Drive process automation and PV innovation initiatives • Support regulatory responses, inspections and CAPA management • Collaborate cross-functionally with Clinical Development, Research and Global Safety teams Qualifications & Experience • MD / DO / PhD or equivalent medical degree • Minimum 7 years pharmacovigilance / clinical industry experience • Minimum 5 years leadership and people management experience • Strong expertise in global PV regulations and ICSR lifecycle • Experience in medical device safety monitoring and vendor oversight • Cross-cultural global team collaboration experience Skills • Advanced medical review and safety assessment expertise • Regulatory compliance and audit readiness • Leadership, stakeholder management and decision-making • Metrics, KPIs and quality governance About the Company • Organon is a global $6.5B healthcare company focused on Women’s Health, biosimilars and established medicines

Roles & Responsibilities • Publish and dispatch regulatory submissions (eCTD/NeeS) for US, EU, and Canada markets • Handle post-approval and lifecycle management submissions with high quality and timeliness • Perform document-level publishing, QC checks, and troubleshoot submission issues • Collaborate with regulatory and scientific teams for planning and publishing activities • Ensure compliance with ICH guidelines and agency-specific publishing requirements • Maintain and update submissions using regulatory IT systems and tools Qualifications • Bachelor of Pharmacy (B.Pharm) • Master of Pharmacy (M.Pharm) • Master’s degree in Life Sciences Experience • 1-3 years of experience • Regulatory publishing exposure in US/EU markets preferred Skills • Knowledge of eCTD, NeeS, and regulatory submission standards • Hands-on experience with tools like Veeva Vault, Global Insight, ISI Toolbox, Adobe Acrobat, Lorenz Validator • Good understanding of regulatory IT systems • Strong written and spoken English communication • Ability to work in a global, culturally diverse environment About the Company Teva Pharmaceuticals is a global leader in generic medicines, operating in nearly 60 countries and providing affordable, accessible healthcare solutions. Every day, over 200 million people worldwide rely on Teva medicines, making a meaningful impact on global health through innovation, quality, and inclusivity.

Roles & Responsibilities: • Conduct market research on cell biology media and life sciences products • Analyze global pricing structures and pricing trends in biotech markets • Perform import–export data mining to assess demand, competition, and opportunities • Collect and interpret data on customers, competitors, and market conditions • Monitor sales and marketing trends to identify growth opportunities • Design research methodologies and analyze market and statistical data • Prepare analytical reports, presentations, and actionable insights for management • Develop dashboards using MS Excel and AI-based analytical tools • Support competitive intelligence and business strategy initiatives Qualification: • Bachelor’s or Master’s degree in Science / Biotechnology / Pharmacy / Life Sciences Experience: • 0-1 year • Freshers are encouraged to apply Skills: • Strong analytical and data interpretation skills • Proficiency in Microsoft Excel (analysis, dashboards, reporting) • Basic understanding of AI tools, market analytics, and data visualization • Interest in biotech, cell biology media, and life sciences markets • Good communication and presentation skills About the Company: HiMedia Laboratories Pvt. Ltd. is a globally recognized leader in life sciences, microbiology, molecular biology, and cell biology solutions. With a strong international presence and a focus on innovation and quality, HiMedia supports research, diagnostics, and industrial applications worldwide, offering excellent learning and growth opportunities for young professionals.

Roles & Responsibilities: • Enter, update, and maintain accurate data in the Pharma CRM system • Support CRM operations for pharmaceutical and clinical research projects • Coordinate with internal teams to ensure timely and accurate data availability • Perform routine data validation, verification, and quality checks • Assist in preparation of basic CRM, MIS, and operational reports • Adhere to SOPs, data confidentiality norms, and compliance guidelines Qualification: • Any Graduate Experience: • Freshers / 0-1 year of experience Skills: • Minimum typing speed of 20 WPM • Basic knowledge of MS Word and MS Excel • Good attention to detail and data accuracy • Willingness to learn Pharma CRM and shared services processes • Clear written and verbal communication skills • Ability to work in a team-oriented, process-driven environment About the Company: Vimta Labs Limited is a leading contract research and testing organization in India, providing services across pharmaceuticals, clinical research, food, environment, and healthcare. Known for its strong regulatory compliance and quality-driven approach, Vimta offers an excellent platform for fresh graduates to gain hands-on exposure to regulated pharma operations and build long-term careers in the life sciences industry.

Roles & Responsibilities: • Provide scientific inputs for new product development and evaluate product claims • Review, validate, and approve product claims and medico-marketing materials • Plan and conduct claim substantiation studies and scientific training for marketing teams • Coordinate with third-party manufacturers for timely licenses and maintain license archival • Respond to medical, regulatory, and consumer queries with accurate scientific information • Monitor Adverse Events (AEs) and ensure pharmacovigilance and materiovigilance compliance • Ensure quality, integrity, and regulatory compliance of all information shared with stakeholders • Collaborate with internal teams including Marketing, QA, R&D, Supply Chain, and Business Development • Liaise with external stakeholders such as KOLs, legal teams, consultants, and manufacturing partners • Support business growth through regulatory strategy and compliance adherence Qualification: • M.Pharm or M.Sc in Pharmaceutical Sciences Experience:• 5-8 years of experience in Regulatory Affairs • Prior experience in OTC drugs preferred • Practical exposure to Pharmacovigilance and Materiovigilance processes Skills: • Strong knowledge of Indian regulations: D&C Act, DMR Act, UCPMP, ASCI Codes • Ability to critically review scientific and regulatory documents • Good analytical, communication, and presentation skills • Strong coordination and stakeholder management abilities About the Company: Piramal Pharma Ltd., part of the diversified Piramal Group, is a leading global healthcare organization with a strong presence in consumer healthcare, pharmaceuticals, and life sciences. Guided by the values of Knowledge, Action, Care, and Impact, the company focuses on ethical practices, innovation, and inclusive growth. Through its Consumer Healthcare division, Piramal touches millions of lives across India with trusted OTC brands and a robust distribution network, while fostering a people-centric and high-growth work culture.

Roles & Responsibilities: • Lead regulatory surveillance for South Asia (India, Pakistan, Bangladesh, Bhutan, Nepal, Sri Lanka) and monitor regulatory changes • Ensure compliance of Capsules & Health Ingredients (CHI) product portfolio with regional regulations • Act as primary regulatory interface with Indian food and drug authorities • Manage facility and product registrations, licenses, and regulatory submissions • Support new licenses, approvals, and importation activities including NOCs • Prepare, maintain, and update Drug Master Files (DMFs) with global authorities (US FDA, Health Canada, China, etc.) • Collaborate with Quality, R&D, Commercial, and Global teams on regulatory matters • Support regulatory audits and inspections, including preparation and remediation • Assess regulatory impact of changes, deviations, and control strategies • Provide regulatory guidance to customers and support business growth initiatives • Participate in industry associations and regulatory forums to maintain regulatory intelligence Qualification: • Master’s degree (or equivalent) in Pharmacy, Chemistry, Biotechnology, Bioengineering, Food Technology, or related scientific discipline Experience: • 5-10 years of experience in Regulatory Affairs, Quality, or Compliance • Experience within pharmaceutical, healthcare, nutrition, or food industries preferred Skills: • Strong knowledge of Indian and South Asian regulatory frameworks • Sound understanding of GMP, quality systems, and compliance processes • Experience dealing with regulatory authorities and certification bodies • Strong analytical, problem-solving, and organizational skills • Excellent written and verbal communication skills in English • Ability to work independently and collaborate with global cross-functional teams About the Company:Lonza is a global leader in life sciences, operating across five continents. The company partners with the pharmaceutical, biotech, and nutrition industries to deliver innovative solutions that improve health and quality of life. Lonza is committed to ethical practices, sustainability, and empowering its people to build impactful careers while making a meaningful difference worldwide.

Roles & Responsibilities: • Conduct effective field work to achieve and exceed assigned sales targets through prescription generation from HCPs • Perform RCPA activities accurately and update data in the system with proper pre-call planning • Promote and demonstrate products to doctors and pharmacists as per company guidelines • Build and maintain strong relationships with HCPs to ensure regular customer conversion and zero prescriber loss • Ensure adequate product availability at chemists to honor prescriptions and achieve POB targets • Prepare and update doctor and chemist lists as per division norms • Execute strategies for successful new product launches • Coordinate with stockists and manage distribution channel activities Qualifications: • B.Sc / Bachelor of Pharmacy (B.Pharm) / Diploma in Pharmacy (D.Pharm)Experience: • 0 to 4 yearsSkills & Requirement:  • Basic scientific knowledge • Good communication and interpersonal skills • Willingness to travel and relocate across India • Mandatory two-wheeler with valid driving license About the Company: Alembic Pharmaceuticals Ltd is a leading Indian pharmaceutical company with a strong presence in branded generics, committed to delivering high-quality healthcare solutions across domestic and international markets.

Role & Responsibilities • Perform medical review and clinical assessment of ICSRs in safety databases • Verify adverse event selection, seriousness, MedDRA coding, causality, labeling, narratives and company clinical comments • Handle medical queries, literature screening and safety database follow-ups • Ensure compliance with ICH, EMA, GVP and GCP guidelines • Mentor and train PV associates on safety conventions and event capturing • Support literature surveillance, signal detection and risk management activities • Review and prepare PSURs, PBRERs and Risk Management Plans (RMPs) • Participate in audits, inspections and global pharmacovigilance collaboration Qualifications & Experience • MBBS (PG degree preferred) • Minimum 3 years of Pharmacovigilance / Drug Safety experience Skills • Strong knowledge of global PV regulations (ICH, EMA, GVP, GCP) • Excellent communication and documentation skills • Ability to manage complex safety cases and work in regulated environments • Experience with safety databases and literature surveillance About the Company • Cencora is a global healthcare services organization dedicated to creating healthier futures worldwide. • The company supports pharmaceutical and life sciences organizations with end-to-end drug safety, regulatory, and clinical solutions.

Role & Responsibilities • Perform medical review of Individual Case Safety Reports (ICSRs) for seriousness, causality, labeling and MedDRA coding • Ensure accurate and timely safety case processing in line with global regulatory timelines and client SOPs • Review source documents and narratives for medical accuracy and database consistency • Write company causality comments and route cases through workflows as per SOPs • Validate E2B reporting and perform self-quality checks before case finalization • Lead internal and cross-functional trainings and mentor team members • Handle medical assessment queries, case follow-ups and regulatory clarifications • Support PV compliance, audits, inspections, documentation archiving and process transitions Qualifications & Experience • MBBS / MD • 7–11 years of experience in Pharmacovigilance / Drug Safety medical review Skills • Strong medical writing and safety narrative skills • Expertise in MedDRA, WHO-Drug, ICSR processing and global PV regulations • Proficiency in safety databases and MS Office • Excellent English communication skillsAbout the Company • Accenture is a leading global professional services company specializing in strategy, consulting, digital, technology, and operations.

Role & Responsibilities • Lead and implement HEOR strategies to support market access for Diabetes and Obesity brands • Drive evidence generation including economic models, cost-effectiveness, QoL and outcomes studies • Develop payer value stories and contribute to global reimbursement dossiers • Support affiliates for reimbursement and HTA submissions • Lead publication strategies for abstracts, posters, and peer-reviewed journals • Build and manage global stakeholder networks across healthcare, pharma, and academia • Deliver internal and external HEOR training and scientific presentations • Collaborate on retrospective and prospective real-world and clinical research studies Qualifications & Experience • Master’s degree in Health Economics, Outcomes Research, Epidemiology, Biostatistics, or related field • Minimum 6 years of HEOR experience (pharma/consulting preferred) • Proven publication track record Skills • Strong strategic planning and market access knowledge • HE modeling, HTA, and payer evidence generation expertise • Excellent communication and stakeholder management skills About the Company • Novo Nordisk is a global healthcare leader in Diabetes and Obesity care, driving long-term health impact through innovationHow to Apply • Apply online before 22-01-2026

Roles & Responsibilities: • Execute day-to-day ophthalmic (sterile) production activities as per SOPs and GMP • Operate, monitor, and document manufacturing processes for ophthalmic formulations • Ensure adherence to aseptic techniques and contamination control practices • Prepare, review, and maintain Batch Manufacturing Records (BMRs) • Perform line clearance, equipment cleaning, and changeover activities • Monitor critical process parameters and report deviations or abnormalities • Coordinate with QA, QC, Engineering, and Warehouse teams for smooth operations • Ensure compliance with GMP, safety standards, and regulatory guidelines Qualification: • B.Pharm / M.Pharm Experience: • 3-5 Years of experience in ophthalmic / sterile production Key Skills: • Strong knowledge of sterile manufacturing and ophthalmic processes • Good understanding of GMP and documentation practices • Hands-on experience in production equipment and cleanroom operations • Ability to work in a regulated pharmaceutical manufacturing environment About the Company: Ajanta Pharma Ltd is a leading pharmaceutical company with a strong global footprint, specializing in quality-driven formulations including ophthalmic products, and committed to international regulatory and GMP standards.

Roles & Responsibilities: • Execute day-to-day production activities as per approved SOPs and batch records • Operate and monitor manufacturing equipment to ensure smooth production operations • Ensure compliance with GMP, safety, and quality standards during manufacturing • Complete Batch Manufacturing Records (BMR) accurately and in a timely manner • Handle line clearance, equipment cleaning, and changeover activities • Report deviations, incidents, and abnormalities to seniors and support investigations • Coordinate with QA, QC, Engineering, and Warehouse teams for production support • Ensure adherence to production targets, timelines, and efficiency norms Qualification: • Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm) Experience: • 2 to 8 Years of relevant experience in pharmaceutical production Skills: • Good knowledge of GMP and pharmaceutical manufacturing processes • Hands-on experience in production operations and documentation • Ability to follow SOPs and regulatory guidelines strictly • Teamwork, discipline, and strong operational focus About the Company: Ajanta Pharma Ltd is a leading Indian pharmaceutical company with a strong presence in domestic and international markets, known for its quality-focused manufacturing practices and diversified product portfolio across multiple therapeutic segments.

Roles & Responsibilities: • Support Quality Assurance activities in formulation manufacturing operations • Review and maintain Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) • Assist in GMP documentation, SOP compliance, and record verification • Participate in in-process quality checks and line clearance activities • Support audits, deviations, CAPA documentation, and quality investigations • Ensure compliance with WHO-GMP, Schedule M, and internal quality standards Qualification: • Bachelor of Pharmacy (B.Pharm) Experience: • Freshers / Newly graduated candidates Skills: • Basic understanding of Quality Assurance and GMP concepts • Knowledge of pharmaceutical documentation and regulatory guidelines • Attention to detail and compliance-oriented mindset • Willingness to work in a formulation manufacturing plant environment About the Company: Akums Group is one of India’s leading pharmaceutical contract manufacturing organizations, operating GMP-compliant formulation manufacturing facilities and serving top domestic and global pharmaceutical companies with high-quality healthcare products.

Roles & Responsibilities: • Handle preparation, review, and submission of API Drug Master Files (DMFs) • Ensure compliance with ICH guidelines and global regulatory requirements • Manage regulatory submissions for US FDA and other international markets • Coordinate with cross-functional teams for data collection and documentation • Support responses to regulatory queries, deficiencies, and post-submission activities • Maintain regulatory documentation and ensure timely lifecycle management • Monitor changes in global regulatory guidelines and implement updates Qualification: • Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm) Experience: • 2-3 years of experience • Hands-on experience in API regulatory affairs with US FDA exposure preferred Skills: • Strong knowledge of API DMF preparation and submission • Good understanding of ICH and global regulatory guidelines • Experience in US FDA regulatory requirements • Excellent documentation and coordination skills • Ability to work in a fast-paced regulatory environment About the Company: Senores Pharmaceuticals Limited is a fast-growing Indian pharmaceutical company focused on the development and manufacturing of complex generics for regulated and emerging markets, including the US, EU, and ROW, with a strong commitment to global quality and compliance.

Roles & Responsibilities: • Prepare summary reports for medical devices • Perform trend analysis on customer complaints and product performance • Conduct monthly and ad-hoc data analysis from complaints, sales, and trending databases • Carry out literature searches and review clinical, scientific, and medical references • Identify, interpret, and evaluate data from medical literature, clinical studies, and post-market sources • Compile and submit clinical and post-market surveillance (PMS) documents • Support international regulatory submissions in line with global medical device regulations • Contribute to PMS plans and safety reports for assigned device portfolios Qualification: • Relevant degree in Life Sciences, Biomedical Engineering, Pharmacy (B.Pharm, D.Pharm, M.Pharm) , or related discipline Experience: • 3-6 years of experience in Medical Devices domain • Hands-on experience in medical review and post-market surveillance Skills: • Strong knowledge of medical device regulations and PMS requirements • Experience in complaint trending and safety data analysis • Expertise in literature search and regulatory documentation • Excellent analytical, documentation, and communication skills • Ability to work in a fast-paced, office-based environment • Immediate joiners preferred About the Company: ANRI Solutions is a leading recruitment partner connecting skilled professionals with top pharmaceutical, medical device, and healthcare organizations across India and globally.