Pharmacy Jobs

Role & Responsibilities • Draft and revise Pharmacovigilance Agreements (PVAs) ensuring alignment with company requirements • Review PVAs for quality and consistency with global and local regulatory standards • Address comments from company and collaborating partners on PVAs • Manage dedicated PVA mailbox and respond to queries • Announce new or revised PVAs to all relevant client stakeholders • Maintain PVA tracker for all active global PVAs, including reconciliations and updates • Perform compliance monitoring of PVAs and prepare dashboards for management review • Assist Project Manager in managing project-related documents and trackers • Upload and maintain PVAs and associated documentation in company repository • Attend team meetings to provide status updates and report any issues with PVAs Qualification • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related field • Strong knowledge of global pharmacovigilance regulations (ICH, GVP)Experience • Minimum 2–3 years of experience in pharmacovigilance • Hands-on experience with global and local PVAs and contractual pharmacovigilanceSkills • Expertise in drafting, reviewing, and maintaining PVAs • Knowledge of global pharmacovigilance standards and compliance monitoring • Excellent written and verbal communication skills • Strong organizational and document management skills • Attention to detail and ability to manage multiple tasks concurrentlyAbout Company • Tata Consultancy Services (TCS) is a leading global IT and consulting services organization , Provides solutions across Life Sciences, Healthcare, and technology domains

Role & Responsibilities • Perform onsite monitoring visits in compliance with ICH-GCP and SOPs • Conduct interim monitoring visits as per study protocol and timelines • Ensure subject safety, data integrity, and protocol compliance • Review source documents, CRFs, and essential trial documents • Identify, document, and resolve site issues and deviations • Liaise with investigators, site staff, and study teams • Ensure timely follow-up and closure of monitoring findings • Maintain accurate monitoring reports and documentation Qualification • B.Pharm / M.Pharm / Pharm.D • BHMS / BAMS / BDSExperience • Minimum 2+ years of onsite clinical monitoring experience • Completion of at least 90+ onsite interim monitoring visits (mandatory)Skills • Strong knowledge of ICH-GCP and clinical trial regulations • Excellent documentation and report writing skills • Good communication and stakeholder management skills • Strong attention to detail and compliance mindset • Ability to work independently in a field-based roleAbout Company • IQVIA is a global leader in clinical research, healthcare intelligence, and data-driven innovation , Offers a diverse, inclusive, and growth-oriented work culture , Committed to improving patient outcomes through science and technology

Role & Responsibilities • Execute medicinal chemistry research for hit-to-lead optimization • Design, synthesize, and characterize adamantane–quinoxalone hybrid compounds • Perform multi-step organic synthesis and heterocyclic chemistry • Analyze compounds using spectroscopic and analytical techniques • Support drug discovery efforts for precision chemotherapy in AML • Maintain proper laboratory records and documentation • Assist in data analysis, report preparation, and research publications • Collaborate with project team and Principal Investigator • Ensure compliance with institutional and ICMR research guidelinesQualification • PhD in Organic / Medicinal / Pharmaceutical Chemistry • OR PG degree with relevant research experience • Strong background in organic synthesis, heterocycles, and drug discoveryExperience • Hands-on research experience in medicinal or organic chemistry • Experience in drug discovery projects preferred Skills • Expertise in organic synthesis and medicinal chemistry • Strong knowledge of heterocyclic chemistry • Experience with analytical and spectroscopic techniques • Scientific writing and data interpretation skills • Ability to work independently and in a research teamAbout Company • NIPER Ahmedabad is a premier national institute under the Government of India , Focused on advanced pharmaceutical education and researchProject Funding: ICMR Department: Medicinal Chemistry Positions: 02 Salary: ₹78,000 + HRA (Approx. ₹1.01 Lakh/month) Tenure: 1 Year (Extendable up to 3 Years) Last Date to Apply: 05 February 2026

Role & Responsibilities • Drive sales and promotion of Interventional Cardiology products within assigned territory • Achieve monthly, quarterly, and annual sales targets as per company goals • Develop new accounts and expand product usage in existing hospital accounts • Plan and execute territory sales strategies based on market, competition, and pricing analysis • Conduct regular sales calls with cardiologists, surgeons, and hospital stakeholders • Observe procedures in cath labs, EP labs, and operating rooms to support clinical usage • Build strong relationships with physicians, purchasing teams, and key decision-makers • Deliver product presentations, demonstrations, and clinical education programs • Address customer queries, complaints, and service issues with effective solutions • Coordinate with internal teams (clinical, marketing, pricing) for optimal account support • Ensure strict compliance with quality systems, patient safety, and company policies • Mentor and guide junior team members when requiredQualification • Graduate in Science / Pharmacy / Biomedical / Engineering or related discipline • MBA or relevant sales qualification preferredExperience • Mandatory experience in the medical device industry • Experience in Interventional Cardiology preferred • Exposure to Cardiology, Neurology, Endoscopy, Peripheral Intervention, Vascular Surgery, or CRM is an advantage Skills • Strong sales, negotiation, and relationship-building skills • Good understanding of interventional cardiology procedures and devices • Ability to analyze sales data and develop actionable plans • Excellent communication and presentation skills • Strong customer-centric and result-driven mindset • Ability to work independently in a field-based role • Sound judgment, problem-solving, and decision-making abilitiesAbout Company • Boston Scientific is a global leader in medical devices with 40+ years of innovation , Dedicated to advancing science for life and improving patient outcomes

Role & Responsibilities • Provide high-quality toxicological support for new and existing products • Perform literature and database searches to retrieve toxicological data • Review, analyze, and document safety data for ingredients, products, and technologies • Prepare ingredient monographs, toxicological assessments, safety statements, and product summaries • Summarize risk assessment data on various toxicological endpoints • Identify, analyze, and report project-relevant data from secondary sources and databases • Respond to consumer queries and regulatory agency questions with scientific accuracy • Ensure all reports contain latest, accurate, and relevant toxicological information • Work independently and collaboratively in project-specific teams • Actively participate in team discussions and knowledge-sharing activities Qualification • Master’s degree in Toxicology / Pharmacology / Life Sciences or related discipline Experience • 1–2 years of relevant experience in toxicology or safety assessment • Experience in on-demand research or regulatory support preferred Skills • Strong domain knowledge in Toxicology • Hands-on experience with toxicological and regulatory databases (ECHA, PCPC, EFSA, Toxplanet, Embase, PubMed, etc.) • Excellent scientific report writing and documentation skills • Strong written and verbal communication skills • Ability to work autonomously in a fast-paced environment • Proficiency in MS Office (PowerPoint, basic Excel) • Strong internet research and data screening skills About Company • A reputed, globally leading pharmaceutical organization • Focused on ensuring product safety through scientific excellence • Offers a performance-driven environment with strong learning and growth opportunities

Key Responsibilities Act as scientific liaison with healthcare professionals and KOLs Support medico-marketing activities, CMEs, and scientific content development Deliver clinical training and scientific presentations Collect and manage clinical/real-world data Support channel partner onboarding and post-sales medical supportQualifications Degree in Medical/Life Sciences (MBBS, BDS, BPharm, MPharm, MSc, Biomedical, etc.)Experience 2–3 years of experience in Medical Affairs/MSL or medical device industry (preferred)Skills Strong scientific communication and presentation skills KOL engagement and stakeholder management Clinical data interpretation and problem-solvingAbout Company Bioscan Research, based in Ahmedabad, is an innovative healthcare technology company focused on improving outcomes for traumatic brain injury patients.

Roles & Responsibilities • Prepare and submit regulatory dossiers in ACTD and CTD formats • Handle applications for Certificates of Pharmaceutical Product (CoPP) and Free Sale Certificates (FSC) • Manage item approvals and brand registrations with regulatory authorities • Draft, compile, and process No Objection Certificates (NOC) and related regulatory documentation • Coordinate with internal departments to ensure accurate and timely regulatory submissions • Track regulatory timelines, approvals, and compliance requirements • Ensure documentation complies with applicable regulatory guidelines and standards Qualification • B.Pharm / M.Pharm Experience • Proven experience in a Drug Regulatory Affairs (DRA) role is mandatory Skills • Strong expertise in ACTD/CTD dossier preparation and submission • Hands-on experience with CoPP, FSC, and NOC documentation • Good understanding of pharmaceutical regulatory requirements • Strong documentation, coordination, and follow-up skills • Ability to manage multiple regulatory activities simultaneously About the Company Sarthak Biotech Private Limited is a growing pharmaceutical company based in Karnal, Haryana, engaged in the development, registration, and marketing of quality pharmaceutical products. The company focuses on regulatory compliance, efficient market approvals, and delivering reliable healthcare solutions while maintaining high quality and ethical standards.

Role & Responsibilities Lead site monitoring activities across multiple clinical trials Ensure compliance with ICH-GCP, SOPs, and regulatory requirements Perform site initiation, monitoring, and close-out visits Review CRFs, source documents, and resolve data queries Mentor junior CRAs and CTAs Qualification Bachelor’s / Master’s in Life Sciences, Pharmacy, Nursing, or related fieldExperience 4–6 years of clinical monitoring experience in a CRO or pharmaceutical company Skills Strong knowledge of ICH-GCP and clinical trial regulations Excellent documentation and communication skills Leadership and problem-solving abilities About Company REV Clinical (formerly CBCC Global Research) is a rapidly growing CRO delivering high-quality clinical research services globally.

Roles & Responsibilities • Optimize medication therapy for complex patients to improve safety and clinical outcomes • Manage and monitor adverse drug events and conduct drug level monitoring when required • Provide patient counseling and medication-related guidance as part of multidisciplinary care • Educate healthcare professionals and patients on rational drug use and therapy optimization • Support development and implementation of hospital drug policies and treatment protocols • Contribute to antibiotic stewardship programs and formulary management guidelines • Monitor, document, and report medication errors and prescription-related issues • Perform pharmacovigilance activities, including monitoring long-term drug safety post-market • Assist in regulatory-related activities to ensure compliance with applicable standards and guidelines Qualification • Bachelor of Pharmacy / Master of Pharmacy / PharmD (as applicable) Experience • Minimum 1 year of hands-on experience in a hospital or clinical setting• Valid Pharmacy Council Registration (Mandatory) Skills • Strong knowledge of clinical pharmacology and medication management • Understanding of pharmacovigilance and medication safety processes • Ability to analyze prescriptions and identify drug-related problems • Good communication and teaching skills for interaction with patients and healthcare staff • Attention to detail and strong documentation skillsAbout the Company WMF’s Villoo Poonawalla Memorial Hospital is a leading multi-specialty healthcare institution in Pune, committed to delivering high-quality, patient-centered medical care. Backed by modern infrastructure, experienced clinicians, and strong clinical governance, the hospital focuses on excellence in treatment, safety, education, and continuous improvement across all healthcare services.

Roles & Responsibilities • Perform initial triage and validity assessment of adverse event reports and clinical trial safety data • Manage end-to-end case processing activities in line with pharmacovigilance requirements • Execute accurate medical coding using MedDRA and WHO-DD dictionaries • Conduct duplicate checks, reconciliation, and quality control (QC) to ensure audit-ready safety data • Ensure strict compliance with ICH-GCP guidelines, 21 CFR Part 11, and global PV regulations • Apply clinical judgment to audit and validate safety data within the digital platform • Collaborate with the technology team by providing subject matter expertise to maintain clinically accurate workflows • Support continuous process improvement aligned with evolving regulatory expectations Qualification • Doctor of Pharmacy (PharmD) Experience • Freshers to 4 years of experience in Pharmacovigilance or Drug Safety • Candidates without prior industry experience will be trained during the probationary period Skills • Strong theoretical knowledge of MedDRA coding, case validity assessment, and triage processes • Sound understanding of Pharmacovigilance fundamentals and ICH-GCP guidelines • High attention to detail and strong quality orientation • Good analytical and problem-solving skills • Proficiency in MS Excel and MS Word • Ability to work accurately in a compliance-driven environment About the Company CoReason.ai is a fast-growing HealthTech company operating at the intersection of life sciences and technology. The company develops advanced analytical platforms that enable pharmaceutical companies and healthcare organizations to make precise, data-driven decisions. With a strong focus on innovation, compliance, and patient safety, CoReason.ai is building next-generation solutions that transform how safety and clinical data are managed.

Roles & Responsibilities • Act as CMC regulatory lead or deputy for assigned projects and products, with guidance on complex issues • Develop and execute CMC regulatory strategies aligned with global regulatory requirements • Plan, prepare, review, and submit CMC sections for INDs, CTAs, NDAs, MAAs, amendments, and supplements • Manage preparation, review, version control, and submission of technical CMC documents • Assess CMC development data and manufacturing changes for potential regulatory impact • Respond to Health Authority queries, action letters, and deficiency responses • Ensure CMC dossier management, documentation accuracy, and compliance with internal SOPs • Ensure timely compilation and submission of regulatory packages within defined schedules • Monitor and facilitate resolution of CMC issues that may impact regulatory approvals • Advise internal teams on Health Authority and ICH regulatory requirements • Stay updated on regulatory changes and share regulatory intelligence and learnings internally • Collaborate with cross-functional and global teams, including manufacturing, quality, and regulatory stakeholders Qualification • Bachelor’s degree in a scientific or related discipline • Advanced degree (MS, PhD, or PharmD) preferred Experience • Minimum 6 years of pharmaceutical industry experience • At least 3 years of experience in Regulatory Affairs (CMC focus preferred) • Experience in pharmaceutical drug development and product lifecycle management • Exposure to regulatory submissions for NCEs, NBEs, or combination products (preferred) Skills • Strong knowledge of CMC principles and pharmaceutical development • In-depth understanding of Health Authority and ICH regulations and guidelines • Excellent regulatory writing and document management skills • Strong project management, prioritization, and multitasking abilities • High attention to detail with strong analytical and problem-solving skills • Effective written and verbal communication skills • Ability to work independently and influence cross-functional teams • High integrity and ability to maintain confidentiality • Strong computer literacy and familiarity with regulatory systems About the Company Astellas is a global pharmaceutical company dedicated to turning innovative science into value for patients. Through its Global Capability Centers (GCCs) located in India, Poland, and Mexico, Astellas strengthens operational efficiency, resilience, and innovation across the value chain. The Bengaluru GCC plays a key role in supporting global regulatory, scientific, and operational excellence while fostering collaboration, integrity, and sustainable growth.

Role & Responsibilities • Dispense prescription and OTC medicines accurately in compliance with Oman pharmacy regulations. • Provide appropriate medication counselling to patients, including dosage, usage, and precautions. • Ensure proper storage, handling, and inventory control of medicines. • Maintain accurate pharmacy records and documentation. • Coordinate with physicians and healthcare professionals for prescription clarification when required. • Ensure compliance with licensing requirements, ethical standards, and pharmacy laws. • Deliver professional, patient-focused pharmacy services during duty hours. Qualification • Bachelor of Pharmacy / Diploma in Pharmacy from a recognised institution. • Valid Pharmacist Licence (Oman or eligible) – Mandatory.Experience • Prior experience as a retail or community pharmacist is preferred. • Overseas/Gulf experience will be an added advantage.Skills • Proficiency in Hindi or Urdu (Mandatory). • Good communication and interpersonal skills. • Strong knowledge of medicines and dispensing practices. • Attention to detail with a focus on accuracy and patient safety. • Ability to work split shifts and extended evening hours.About Company • Thashkeel Business Consultancy India is a recruitment process outsourcing (RPO) organisation supporting overseas healthcare and professional staffing requirements, connecting qualified candidates with reputed employers in the Gulf region, including Oman.

Role & Responsibilities • Assist in dispensing medications accurately under the supervision of a licensed pharmacist. • Support daily pharmacy operations including inventory management, stock checking, and expiry control. • Provide basic medication information and customer support as per pharmacy guidelines. • Maintain proper documentation and comply with pharmacy regulations and standards. • Ensure cleanliness, organisation, and smooth workflow within the pharmacy. • Follow MOH/DHA guidelines and ethical pharmacy practices.Qualification • Assistant Pharmacist: MOH/DHA license mandatory. • Trainee Pharmacist: Pharmacy qualification (Diploma / B.Pharm / Pharm.D). • Freshers are welcome to apply for Trainee Pharmacist role. Experience • Minimum 6 months UAE experience required for Assistant Pharmacist. • No experience required for Trainee Pharmacist (freshers can apply).Skills • Basic knowledge of pharmacy practice and medicines. • Good communication and interpersonal skills. • Ability to work in shifts (evening shift readiness preferred). • Attention to detail and accuracy in dispensing. • Team-oriented, responsible, and patient-focused approach.About Company • Thashkeel Consultancy organisation in the UAE focused on delivering safe, ethical, and patient-centred pharmaceutical services while complying with MOH/DHA regulations.

Roles & Responsibilities • Dispense prescription medications accurately in compliance with Qatar Ministry of Public Health (MoPH) regulations • Review prescriptions for appropriateness, dosage accuracy, potential drug interactions, and patient allergies • Counsel patients on correct medication usage, side effects, storage, and adherence to therapy • Ensure patient safety and provide high standards of pharmaceutical care • Maintain accurate medication records and documentation as per regulatory and organizational requirements • Collaborate with physicians and other healthcare professionals to optimize patient treatment outcomes • Ensure compliance with pharmacy laws, ethical standards, and internal SOPs • Stay updated with new drugs, treatment guidelines, and professional best practices Qualification • Bachelor’s Degree in Pharmacy (BPharm or PharmD) Experience • Minimum 4-8 years of relevant experience as a Pharmacist (preferred) Skills • Strong knowledge of pharmacology and medication safety • Good communication and patient counseling skills • Attention to detail and accuracy in dispensing • Ability to work independently and as part of a healthcare team • Familiarity with MoPH regulations and healthcare compliance standards About the Company Al Dibel is a reputable healthcare organization in Qatar committed to delivering high-quality medical and pharmaceutical services. The company focuses on patient safety, regulatory compliance, and professional excellence, offering a supportive environment for experienced healthcare professionals to contribute to quality patient care.

Roles & Responsibilities • Accurately enter medicines, prescriptions, and inventory data into the pharmacy system • Update and maintain medication records, pricing, and supplier details • Ensure correctness of drug names, strengths, dosages, dosage forms, and product codes • Support inventory tracking, stock reconciliation, and data verification processes • Coordinate with pharmacists to identify and resolve data discrepancies • Maintain confidentiality of pharmacy and patient data • Ensure compliance with pharmacy regulations, SOPs, and internal policies Qualification • Diploma or Bachelor’s degree in Pharmacy, Science, or a related field (preferred) Experience • Prior experience working in a pharmacy environment is mandatory • Experience with pharmacy ERP, POS, or inventory management systems is preferred Skills • Strong knowledge of medicines and pharmaceutical products • High attention to detail with excellent data accuracy and speed • Good computer proficiency and familiarity with pharmacy software systems • Ability to work under pressure and meet deadlines • Strong coordination and communication skills About the Company Hossam Pharmacies is a well-established pharmacy chain dedicated to delivering high-quality pharmaceutical services and healthcare products. The company emphasizes accuracy, compliance, and patient safety while providing a supportive environment for professionals to grow within organized pharmacy operations.

Role & Responsibilities • Collect, compile, and document toxicological, physical, environmental, and regulatory data required for authoring Safety Data Sheets (SDSs) for BMS materials. • Interpret chemical and toxicological data to classify hazards in accordance with GHS and other regional regulatory frameworks (e.g., EU CLP). • Ensure SDS compliance with global regulations including OSHA Hazard Communication, EU CLP, and REACH requirements. • Perform Dangerous Goods (DG) classifications in line with applicable regulations (DOT, IATA, IMDG). • Collaborate with cross-functional teams to manage formulation changes, regulatory updates, and new hazard information. • Participate in quality control and peer review processes to ensure accuracy, consistency, and completeness of SDS content. • Maintain and update internal databases and repositories for chemical hazard and regulatory information. • Design, improve, and streamline internal chemical stewardship and SDS authoring workflows to reduce turnaround time and minimize business risk. • Support the development of internal training materials and guidance documents related to SDS requirements and hazard communication. • Contribute to process improvement initiatives, including automation, AI-driven solutions, and continuous improvement efforts.Qualification • Bachelor’s degree in Chemistry, Toxicology, Product Stewardship, Industrial Hygiene, or a related scientific discipline. • Advanced degree is preferred but not mandatory. Experience • Minimum of 3 years’ experience in SDS authoring and/or regulatory compliance within chemical, pharmaceutical, or manufacturing industries. • Hands-on experience with SDS authoring software such as SAP EHS, WERCS, 3E, or equivalent platforms. • Exposure to project management and cross-functional collaboration is beneficial.Skills • Strong knowledge of global chemical regulations including GHS, OSHA HazCom, EU CLP, and REACH. • Proficiency in hazard classification, toxicological data interpretation, and regulatory documentation. • Certification in Dangerous Goods regulations (DOT, IATA, IMDG) is desirable. • Excellent attention to detail with strong organisational and documentation skills. • Strong communication and interpersonal skills with the ability to work effectively in cross-functional teams. • Ability to innovate, adapt to change, and enhance performance through process improvement and automation initiatives. • High level of integrity, accountability, and commitment to quality and compliance.About the Company • Bristol Myers Squibb (BMS) is a global biopharmaceutical company committed to transforming patients’ lives through science. • BMS delivers innovative medicines in areas such as oncology, immunology, cardiovascular disease, and cell therapy.

Roles & Responsibilities • Accurately enter medicines, prescriptions, and inventory data into the pharmacy system • Update and maintain medication records, pricing details, and supplier information • Ensure accuracy of drug names, dosages, strengths, dosage forms, and product codes • Support inventory tracking, stock reconciliation, and data validation activities • Coordinate closely with pharmacists to identify and resolve data discrepancies • Maintain confidentiality of patient and pharmacy data at all times • Ensure compliance with pharmacy regulations, SOPs, and internal data standards Qualification • Diploma or Bachelor’s degree in Pharmacy, Science, or a related field (preferred) Experience • Previous experience working in a pharmacy environment is mandatory • Experience with pharmacy ERP, POS, or inventory systems is preferred Skills • Strong knowledge of medicines and pharmaceutical products • High attention to detail with excellent data accuracy and speed • Good computer skills and familiarity with pharmacy software systems • Ability to work under pressure and meet tight deadlines • Strong coordination and communication skills What We Offer • Stable and professional working environment • Competitive salary based on experience, including commission and bonus • Opportunities for career growth within a well-established pharmacy chain About the Company Hossam Pharmacies is a trusted pharmacy chain committed to delivering high-quality pharmaceutical services and healthcare products. With a strong focus on accuracy, patient safety, and professional standards, the company continues to grow as a reliable healthcare partner through efficient operations and experienced pharmacy teams.

Roles & Responsibilities • Manage and monitor pharmacy inventory to ensure optimal stock levels and prevent shortages or expiries • Coordinate ordering, receiving, storage, and distribution of pharmaceutical products • Ensure compliance with pharmaceutical regulations, safety standards, and hospital policies • Maintain accurate inventory records, stock registers, and documentation • Conduct regular stock audits, reconciliation, and expiry tracking • Collaborate with pharmacists, procurement, and supply chain teams for efficient inventory planning • Identify inventory discrepancies and implement corrective actions • Support pharmacy operations by ensuring timely availability of medicines and medical supplies Qualification • Bachelor’s Degree in Pharmacy or related field Experience • Previous experience in pharmacy inventory management is preferred Skills • Knowledge of pharmaceutical regulations and safety standards • Strong organizational, communication, and coordination skills • High attention to detail with strong problem-solving abilities • Ability to manage inventory systems and documentation accurately About the Company Gargash Hospital is a leading multi-specialty healthcare provider committed to delivering high-quality medical services through advanced infrastructure, experienced healthcare professionals, and patient-centered care. The hospital emphasizes safety, regulatory compliance, and operational excellence across all clinical and support services.

Roles & Responsibilities • Prepare professional presentations to introduce company products to doctors and other healthcare providers • Conduct frequent field visits to doctors through cold calls or pre-arranged appointments • Follow up with doctors and healthcare providers regarding product availability, stock consumption, and feedback • Plan and forecast monthly sales targets and execute action plans to achieve them • Liaise with and persuade targeted doctors to prescribe company products using effective selling techniques • Make telephone calls and in-person visits to existing and prospective customers across assigned medical centers • Coordinate closely with sales and collection teams to ensure smooth operations • Research and identify potential customers and assess their business potential • Develop clear and effective written proposals and quotations for current and prospective customers • Create and manage customer value plans highlighting profile, share, and growth opportunities to achieve monthly, quarterly, and annual targets • Continuously update product knowledge and stay informed about the latest medical and market developments • Plan and organize personal sales strategies to maximize return on time investment within the assigned territory • Monitor competitor activities and provide competitive insights to customers • Submit regular oral and written reports to management on customer needs, market trends, competitive activities, and new business opportunities Qualification • Bachelor’s Degree in Pharmacy Experience • 1–3 years of experience in a similar pharmaceutical sales role Skills • Strong communication, presentation, and persuasion skills • Ability to build and maintain relationships with healthcare professionals • Good planning, forecasting, and territory management skills • Self-motivated with a target-driven approach About the Company Tabuk Pharmaceuticals Manufacturing Co. is a leading pharmaceutical company in the Middle East, dedicated to improving patient lives through the development, manufacturing, and marketing of high-quality branded and generic medicines. With a strong commitment to innovation, compliance, and healthcare excellence, Tabuk Pharmaceuticals continues to expand its footprint across regional and international markets.