Pharmacy Jobs

Roles & Responsibilities: Quality Control: • Perform routine QC testing of raw materials, in-process samples, and finished products. • Conduct analytical testing as per approved specifications and SOPs. • Maintain accurate documentation, test records, and data integrity. • Support stability studies and sample management activities. • Follow GMP, GLP, and safety guidelines strictly. • Assist during audits, inspections, and compliance activities. Formulation Production: • Assist in formulation manufacturing operations as per Batch Manufacturing Records (BMR). • Support granulation, blending, compression, coating, and packing activities. • Ensure adherence to GMP guidelines and production SOPs. • Maintain production records, logbooks, and documentation accurately. • Follow safety procedures and work in shift-based operations. • Support equipment cleaning, area maintenance, and production readiness. Qualification: • Quality Control: M.Sc. (Analytical Chemistry) / B.Pharm / M.Pharm • Formulation Production: D.Pharm / ITI / Diploma (relevant discipline) Experience: • Fresher only (Pass-out candidates).Walk-in Interview Details: • Date: 31-01-2026 (Saturday) • Venue: Ahmedabad Management Association (AMA), ATIRA Campus, Dr. Vikram Sarabhai Marg, Near Panjrapol Cross Roads, Ahmedabad – 401506 • Candidates should carry updated CV, relevant education documents, Aadhaar card, and recent photographs. • Smart phone required for online registration and assessment.About the Organisation: Macleods Pharmaceuticals is one of India’s fastest-growing pharmaceutical companies with a strong presence across multiple therapeutic segments, ranked among the top pharma companies, and committed to excellence in quality, innovation, and manufacturing through its world-class facilities and Centre of Excellence training programs.

Roles & Responsibilities: • Manage day-to-day medical coding operations. • Assign accurate diagnosis and procedure codes to patient charts. • Maintain a minimum of 95% quality on production. • Adhere to internal and external coding compliance policies and client requirements. • Improve performance based on feedback from reporting managers. • Follow organizational policies related to information security, HIPAA, and HR compliance. Qualification: • Life Science or Paramedical graduate. • No backlogs with complete academic documentation. Skills: • Strong analytical and logical thinking skills. • High attention to detail and accuracy. • Average written and spoken English communication skills. • Ability to understand medical terminology and coding standards. Assessment / Interview Process: • HR Interview. • Online Assessment – Anatomy & Physiology. • Medical Transcription (MT) Training. • MT-cleared candidates will be onboarded into Medical Coding training batch. Compensation & Benefits: • Competitive remuneration. • Annual performance-based bonus. • Standard industry benefits. • Relocation package as per company policy (for candidates outside base city). About the Organisation: AGS Health is a global leader in healthcare revenue cycle management, combining AI-enabled technologies with expert services to support leading U.S. health systems, physician groups, and academic medical centers, with 12,000+ professionals serving 100+ clients worldwide.

Roles & Responsibilities: • Manage day-to-day medical coding operations. • Assign accurate diagnosis and procedure codes to patient charts. • Maintain a minimum of 95% quality on production. • Adhere to internal and external coding compliance policies and client requirements. • Improve performance based on feedback from reporting managers. • Follow organizational policies related to information security, HIPAA, and HR compliance. Qualification: • Life Science or Paramedical graduate. • No backlogs with complete academic documentation. Skills: • Strong analytical and logical thinking skills. • High attention to detail and accuracy. • Average written and spoken English communication skills. • Ability to understand medical terminology and coding standards. Assessment / Interview Process: • HR Interview. • Online Assessment – Anatomy & Physiology. • Medical Transcription (MT) Training. • MT-cleared candidates will be onboarded into Medical Coding training batch. Compensation & Benefits: • Competitive remuneration. • Annual performance-based bonus. • Standard industry benefits. • Relocation package as per company policy (for candidates outside base city). About the Organisation: AGS Health is a global leader in healthcare revenue cycle management, combining AI-enabled technologies with expert services to support leading U.S. health systems, physician groups, and academic medical centers, with 12,000+ professionals serving 100+ clients worldwide.

Roles & Responsibilities: • Manage day-to-day medical coding operations. • Assign accurate diagnosis and procedure codes to patient charts. • Maintain minimum 95% quality and productivity standards. • Ensure adherence to internal and client-specific coding compliance policies. • Implement feedback provided by reporting managers to improve performance. • Follow organizational policies related to information security, HIPAA, and HR compliance. Qualification: • Life Science or Paramedical graduate. • No backlogs with complete semester mark sheets. Experience: • Freshers only. • Passed out between 2022 and 2024. • Immediate joiners preferred. Skills: • Strong analytical and logical thinking skills. • High attention to detail and accuracy. • Average written and spoken English communication skills. • Ability to learn medical coding standards and healthcare workflows. Assessment / Interview Process: • HR Interview. • Online Assessment – Anatomy & Physiology. • Medical Transcription (MT) Training. • MT-cleared candidates will be onboarded into Medical Coding training batch. Compensation & Benefits: • Competitive remuneration. • Annual performance-based bonus. • Standard industry benefits. • Relocation package as per company policy (for outstation candidates). About the Organisation: AGS Health is a global leader in healthcare revenue cycle management, combining AI-enabled technologies with expert services to support leading U.S. health systems, physician groups, and academic medical centers, with a global workforce of 12,000+ professionals serving over 100 clients across diverse care settings.

Roles & Responsibilities: • Prepare and compile CTD dossiers for pharmaceutical product registration and renewals in the UAE. • Ensure full compliance with UAE MOH regulations and regulatory guidelines. • Monitor and stay updated on regulatory requirements for pharmaceutical products. • Coordinate with internal teams on documentation, labeling, and submission activities. • Support pharmacovigilance activities including adverse event reporting. • Liaise with UAE MOH and other regulatory authorities for approvals, queries, and follow-ups. • Assist during regulatory audits and inspections. • Maintain accurate records of submissions, approvals, and regulatory correspondence. Qualification: • B.Pharmacy or D.Pharmacy Experience: • Minimum 2 years of experience in the UAE pharmaceutical industry. • Hands-on experience in CTD dossier preparation and submissions. • Working knowledge of UAE MOH regulations and pharmacovigilance requirements. Skills: • Strong understanding of UAE regulatory frameworks and CTD documentation. • Good coordination and communication skills. • High attention to detail and compliance orientation. • Ability to manage multiple submissions and deadlines. • Proficiency in documentation and record management. About the Organisation: Microsynergy Pharmaceuticals is a pharmaceutical company focused on regulatory compliance, product registration, and lifecycle management, supporting the timely approval and safe marketing of pharmaceutical products within the UAE market.

Roles & Responsibilities: • Provide compliance and operational oversight of the CCDS and Global Labeling processes. • Support inspections and audits related to CCDS and labeling activities. • Monitor and manage labeling change control metrics with focus on safety-related changes. • Oversee labeling operations activities within internal systems (e.g., EAGLE, CCTA). • Support global RA Labeling and CCDS activities to ensure timely, high-quality, and compliant submissions. • Support global oversight of labeling submissions and approvals. • Ensure country-level compliance with global labeling procedures. • Maintain internal systems in line with company policies and procedures. • Ensure quality compliance of marketed products and timely labeling submissions. • Support review, development, and training on RA labeling tools, systems, practices, and policies. • Support GxP audits and inspections related to CCDS and labeling. • Conduct quality self-inspections and audits to ensure SOP compliance. • Drive process efficiency, optimization, and global technical alignment for labeling. • Coordinate training activities to ensure capability building and compliance. • Contribute to global RA collaboration and establishment of best practices. Qualification: • Master’s degree in Pharmacy or other Life Science discipline (or equivalent experience). Experience: • Minimum 8 years of experience in Regulatory Affairs within a global environment. • Experience managing projects and working in a matrixed organization. • Strong knowledge of regulatory landscape, systems, and procedures for CCDS and labeling. Skills: • Proficiency in English language. • Excellent communication, influencing, planning, and problem-solving skills. • Ability to build and manage strong stakeholder relationships. • Strong collaboration skills without direct reporting authority. • Leadership mindset with focus on shared accountability and quality culture. About the Organisation: Astellas is a global pharmaceutical company focused on turning innovative science into value for patients, delivering high-quality medicines across therapeutic areas through strong regulatory, quality, and compliance frameworks worldwide.

Roles & Responsibilities: • Perform local safety case receipt, processing, data entry, QC tracking, and ICSR follow-up in line with agreed timelines. • Manage generic and client-specific safety email inboxes. • Register, triage, assign, and coordinate processing of vigilance cases. • Perform follow-up with local reporters for missing or additional information. • Respond to queries from clients and reporters. • Conduct periodic reconciliations to ensure complete and compliant handling of safety reports. • Support local pharmacovigilance activities as required. • Participate in audits, inspections, and implementation of corrective action plans. Qualification: • Bachelor’s or Master’s degree in Medicine, Pharmacy, Nursing, or a science-related field (or equivalent experience). Experience: • 2+ years of experience in Pharmacovigilance within a service provider environment. • Hands-on experience in safety case data entry and QC. • Experience working to strict timelines and managing client communications. • Knowledge of UK and EU PV regulations. • Strong pharmaceutical background with understanding of GVP, GCP, FDA, and drug safety regulations. • In-depth knowledge of PV principles, adverse event reporting, and causality assessment. Skills: • Excellent organizational and interpersonal skills. • Strong team-working capability. • Effective time management and prioritization skills. • High level of accountability and autonomy. • Process-oriented with strong attention to detail. • Clear written and verbal communication skills to explain complex concepts. • Flexible and adaptable in a dynamic work environment. • Ability to work under pressure and meet deadlines. • Safety database experience preferred. About the Organisation: ProductLife Group is a global life sciences consulting and services company delivering end-to-end solutions across pharmacovigilance, regulatory affairs, quality, and compliance, supporting pharmaceutical, biotechnology, and medical device companies worldwide throughout the full product lifecycle.

Roles & Responsibilities: • Perform quality control of vigilance cases. • Conduct medical evaluation of safety reports. • Data entry of vigilance cases into agreed databases/formats. • Follow-up of vigilance cases via phone and email. • Pre-analysis of complex cases prior to data entry. • Medical evaluation of files including coding, causality assessment, expectedness, and seriousness of events. • Identify submission requirements for each case. • Validate documents prepared by Data Managers/Vigilance Associates. • Close vigilance case files in compliance with regulations. • Define and implement ICSR/MLM filters and applicable changes. • Analyze inclusion/exclusion of EV/MHRA cases. • Provide medical information support and handle safety-related calls. • Review medical information queries and quality complaints to identify safety information. • Act as key contact for specific clients and prepare quality documents as required. Qualification: • Doctor of Pharmacy / Pharmacist Experience: • 1–3 years of experience in a similar Pharmacovigilance role • Knowledge of Pharmacovigilance is an advantage Skills: • Experience with safety databases preferred • Knowledge of current PV regulations • Process-oriented, detail-focused, and team player • Proficient in Microsoft Office tools • Strong multitasking and flexibility • Excellent communication skills in French and English About the Organisation: ProductLife Group is a global life sciences consulting and services company providing integrated solutions across pharmacovigilance, regulatory affairs, quality, and compliance, supporting pharmaceutical, biotechnology, and medical device companies worldwide throughout the entire product lifecycle.

Roles & Responsibilities: • Conduct experimental research and development in assigned project areas. • Design and execute research protocols and experiments. • Maintain accurate records of laboratory data and reports. • Collaborate with multidisciplinary teams to achieve project objectives. • Support publication and presentation of research findings. Qualification: • M.E / M.Tech / M.Pharm Skills: • Strong experimental and analytical skills. • Proficiency in laboratory techniques related to agri-food biotechnology. • Good documentation and reporting skills. • Ability to work collaboratively in a research environment. Age Limit: • Minimum: 21 years • Maximum: 40 years Walk-in Details: • Walk-in Interview: 03-02-2026 • Venue: NABI, Knowledge City, Sector-81, Mohali, Punjab – 140306 About the Organisation: National Agri-Food Biotechnology Institute (NABI) is a premier research institute focused on agri-food biotechnology. And it works on innovative solutions for agriculture and food security. It promotes cutting-edge research, technology development, and translational science.Application formClick HereOfficial NotificationClick Here

Roles & Responsibilities • Support and independently execute research activities under ongoing projects at NABI. • Design, plan, and conduct experiments related to life sciences, biotechnology, or pharmaceutical research. • Analyze experimental data and prepare technical reports, presentations, and documentation. • Maintain laboratory records, project documentation, and ensure data integrity. • Assist in coordination of project activities, timelines, and deliverables. • Ensure compliance with laboratory safety guidelines, SOPs, and institutional policies. • Support procurement, inventory management, and maintenance of laboratory equipment. • Mentor junior research staff and provide technical guidance when required. • Participate in meetings, reviews, and scientific discussions related to project progress. Qualification • MD / MS, M.V.Sc, B.Pharm, MDS (from a recognized university / institution) Experience • Relevant research or project experience in life sciences, biotechnology, pharmaceutical sciences, or allied fields is preferred. • Experience in handling laboratory techniques, data analysis, and research documentation is desirable. Skills • Strong understanding of research methodologies and experimental design. • Good analytical, documentation, and reporting skills. • Ability to work independently and in a multidisciplinary team environment. • Proficiency in MS Office and basic research data tools. • Effective communication and coordination skills. Age Limit • Minimum Age: 21 Years • Maximum Age: 40 Years • Age relaxation as per NABI / Government of India norms. Walk-in Interview Details • Date: 03-02-2026 • Venue: National Agri-Food Biotechnology Institute (NABI), Knowledge City, Sector-81, Mohali, Punjab – 140306 About the Organisation National Agri-Food Biotechnology Institute (NABI) is an autonomous institute under the Department of Biotechnology, Government of India, dedicated to translational research in agri-food biotechnology to improve human nutrition, food security, and agricultural sustainability.Application formClick HereOfficial NotificationClick Here

Role & Responsibilities • Dispense medicines as per prescriptions issued by authorised medical officers • Maintain proper storage, handling, and inventory of drugs and medical supplies • Ensure compliance with drug safety, expiry checks, and quality standards • Maintain pharmacy records, registers, and documentation • Assist in procurement, receipt, and stock verification of medicines • Support healthcare services provided within the institute • Follow institutional rules, SOPs, and government regulations Qualification • Degree or Diploma in Pharmacy from a recognised institution • Registration with State Pharmacy CouncilPay Level: Level 5 (7th CPC) Vacancies: 1 (UR) Experience • Relevant experience in hospital, institutional, or clinical pharmacy preferred • Government or autonomous institute experience desirable Skills • Knowledge of drug storage, dispensing, and inventory management • Attention to detail and record-keeping accuracy • Understanding of pharmacy laws and regulations • Ability to work independently and in coordination with healthcare staff • Basic computer skills for documentation and reporting About the Organisation • Indian Statistical Institute (ISI) is an Institute of National Importance, Funded by the Ministry of Statistics & Programme Implementation, Government of India

Role & Responsibilities • Perform quality control (QC) of pharmacovigilance cases • Conduct medical evaluation of adverse event reports • Enter vigilance case data into agreed databases and formats • Perform follow-up of cases via phone and email • Pre-analyse complex cases prior to data entry • Evaluate cases for medical coding as per applicable dictionaries • Assess causality between suspect product and reported events • Determine seriousness and expectedness of events • Identify regulatory submission requirements for each case • Validate documents prepared by Vigilance Associates or Data Managers • Close vigilance case files in compliance with timelines • Support setup and review of ICSR / MLM filters • Analyse inclusion or exclusion of EV / MHRA cases • Provide medical input to the Medical Information division • Support client-specific pharmacovigilance activities within the business unit Qualification • Doctor (MBBS or equivalent) or Pharmacist by training Experience • Minimum 3 years’ experience with service providers in pharmacovigilance • Hands-on experience in QC of safety cases • Experience with SafetyEasy database (mandatory) Skills • Strong knowledge of global pharmacovigilance regulations • Experience working with safety databases • Process-oriented and detail-focused approach • Ability to multitask and manage multiple priorities • Proficiency in Microsoft Office tools • Excellent written and verbal communication skills in English • Strong teamwork and collaboration skills • Flexible and adaptable in a dynamic environment About the Company • ProductLife Group is a global life sciences consulting and services company , Supports pharmaceutical, biotech, and medical device companies across the product lifecycle.

Roles & Responsibilities • Provide technical support for ongoing research projects under the assigned department. • Assist in laboratory operations, sample preparation, and experimental procedures. • Maintain laboratory equipment, instruments, and ensure proper functioning. • Record, compile, and manage technical and experimental data accurately. • Support inventory management, including procurement and maintenance of laboratory supplies. • Ensure adherence to laboratory safety standards, SOPs, and institutional guidelines. • Assist in preparation of reports, documentation, and project-related records. • Perform additional technical duties as assigned by the Project Investigator or Department Head. Qualification • B.Pharm from a recognized university / institution. Skills • Basic knowledge of laboratory techniques and pharmaceutical sciences. • Good documentation and record-keeping skills. • Ability to handle laboratory instruments and equipment. • Proficiency in MS Office and basic data management tools. • Strong teamwork, communication, and organizational skills. Age Limit • Minimum Age: 21 Years • Maximum Age: 45 Years • Age relaxation as per DHSGSU / Government of India norms. Important Date• Application Deadline: 24-02-2026About the Organisation Dr. Harisingh Gour Vishwavidyalaya (DHSGSU) is a Central University committed to high-quality education and research, promoting scientific innovation and supporting national development through excellence in pharmaceutical and life sciences research.Official NotificationClick Here

Roles & Responsibilities • Conduct research activities as per the approved project objectives and study protocol. • Assist in planning, execution, and monitoring of research experiments and studies. • Collect, analyze, and interpret experimental and research data. • Maintain accurate laboratory records, research documentation, and reports. • Support preparation of technical reports, publications, and presentations. • Ensure compliance with institutional guidelines, ethical standards, and project timelines. • Coordinate with project team members, investigators, and supporting staff. • Perform any other research-related duties assigned by the Principal Investigator. Qualification • M.Pharm from a recognized university / institution. Experience • Research experience in a relevant pharmaceutical or life sciences field is desirable. • Freshers meeting the eligibility criteria may also apply. Skills • Strong understanding of research methodology and pharmaceutical sciences. • Ability to analyze experimental data and prepare scientific reports. • Good documentation and technical writing skills. • Proficiency in MS Office and basic research software/tools. • Ability to work independently as well as in a team environment. Age Limit • Minimum Age: 21 Years • Maximum Age: 45 Years • Age relaxation as per DHSGSU / Government of India norms. Walk-in Address • Prof. Asmita Gajbhiye, Department of Pharmaceutical Sciences, Dr. Harisingh Gour Vishwavidyalaya, Sagar – 470003, Madhya Pradesh Important Date• Application Deadline: 24-02-2026About the Organisation Dr. Harisingh Gour Vishwavidyalaya (DHSGSU) is a renowned Central University dedicated to excellence in education and research, fostering innovation in pharmaceutical sciences and contributing to national scientific development.Official NotificationClick Here

Roles & Responsibilities • Dispense medicines accurately in compliance with MOH regulations. • Review and validate prescriptions for dosage, safety, and legality. • Counsel patients on correct medication usage, dosage, and possible side effects. • Ensure proper storage, handling, and labeling of pharmaceutical products. • Manage inventory, monitor stock levels, and remove expired medicines. • Maintain accurate records of prescriptions, sales, and controlled drugs. • Ensure pharmacy operations follow MOH laws, guidelines, and SOPs. • Deliver excellent customer service and maintain a safe pharmacy environment. Qualification • Bachelor of Pharmacy (B.Pharm) or Diploma in Pharmacy (D.Pharm). • Valid MOH Pharmacist license or MOH eligibility letter (mandatory). Experience • UAE pharmacy experience preferred. • Freshers with valid MOH eligibility can also apply. Skills • Strong knowledge of medicines and dispensing standards. • Excellent communication and patient counseling skills. • High attention to detail and accuracy. • Ethical, responsible, and customer-focused approach. • Ability to work independently and as part of a team. About the Organisation The pharmacy is a trusted healthcare provider in Fujairah, focused on delivering safe, compliant, and patient-centered pharmaceutical services while adhering strictly to MOH regulations and quality standards. Interested candidates only share their CV: 📞 Contact: 971557499817

Roles & Responsibilities • Dispense medicines accurately in compliance with DHA regulations. • Review prescriptions to ensure correct dosage, safety, and legality. • Counsel patients on proper medication use, dosage, and side effects. • Support day-to-day pharmacy operations and customer service. • Maintain proper storage, labeling, and handling of medicines. • Assist in inventory management, stock control, and expiry monitoring. • Ensure cleanliness, safety, and regulatory compliance within the pharmacy. • Maintain accurate records of prescriptions and sales. Qualification • Bachelor of Pharmacy (B.Pharm) or Diploma in Pharmacy (D.Pharm). • Valid DHA Pharmacist license or DHA eligibility letter (mandatory). • DHA Assistant Pharmacist license/eligibility for assistant role. Experience • Prior UAE pharmacy experience preferred. • Freshers with valid DHA eligibility can also apply. Skills • Sound knowledge of medicines and dispensing practices. • Strong communication and patient-handling skills. • Attention to detail and accuracy. • Customer-focused and ethical professional approach. • Ability to work independently and in a team. About the Organisation The pharmacy is a customer-centric healthcare provider in Dubai, committed to safe dispensing practices, quality patient care, and compliance with UAE healthcare regulations. The organization offers a professional work environment with growth opportunities for both pharmacists and assistant pharmacists. Urgently required – Interested candidates only: 📞 Send CV / WhatsApp: 971502534847

Role & Responsibilities • Promote company pharmaceutical products to doctors and healthcare professionals • Generate prescriptions and achieve sales targets in assigned territory • Conduct regular field visits and product detailing • Build and maintain strong relationships with doctors, chemists, and stockists • Ensure product availability at retail and stockist level • Organize doctor meetings, camps, and promotional activities • Monitor competitor activities and provide market feedback • Maintain daily call reports and sales records Qualification • B.Sc (Biology) / B.Pharm Experience • Minimum 1–2 years experience as a Medical Representative Skills • Strong communication and presentation skills • Good convincing and selling ability • Territory management skills • Relationship-building capability • Self-motivated and target-oriented Salary • Best in Industry About Company Apple Therapeutics Pvt. Ltd. is a growing pharmaceutical company focused on delivering high-quality medicines and building ethical, long-term relationships with healthcare professionals.

Roles & Responsibilities • Dispense prescribed medicines accurately in accordance with MOH regulations. • Review and verify prescriptions for correctness, dosage, and safety. • Provide proper patient counseling on medication usage, dosage, storage, and possible side effects. • Ensure correct storage, labeling, and handling of pharmaceutical products. • Maintain accurate records of prescriptions, sales, and inventory. • Monitor stock levels, manage expiry dates, and support inventory control. • Comply with all UAE pharmacy laws, SOPs, and quality standards. • Deliver excellent customer service and professional patient care. Qualification • Bachelor of Pharmacy (B.Pharm) or equivalent qualification. • Valid MOH Pharmacist license or eligibility letter (mandatory). Experience • Experienced pharmacists preferred. • Freshers with MOH eligibility are welcome to apply. Skills • Strong knowledge of medications and pharmaceutical practices. • Good communication and patient counseling skills. • Attention to detail and high accuracy in dispensing. • Customer-focused and ethical approach to pharmacy practice. • Ability to work independently and as part of a team. About the Organisation The organization is a growing healthcare provider in Sharjah, committed to delivering safe, reliable, and patient-focused pharmacy services. It offers a supportive work environment with opportunities for professional development and hands-on experience in retail pharmacy operations. Interested candidates only: 📧 Please share your CV at hrmedz@gmail.com

Role & Responsibilities • Promote pharmaceutical products to doctors, clinics, and hospitals • Achieve monthly and quarterly sales targets • Conduct regular doctor visits and product detailing • Build and maintain strong relationships with healthcare professionals • Ensure product availability at pharmacies and stockists • Organize CMEs, doctor meetings, and promotional activities • Collect market feedback and monitor competitor activities • Maintain daily call reports and sales records Qualification • B.Sc (Biology) / B.Pharm Experience • Minimum 1–2 years of experience as a Medical Representative Skills • Strong communication and convincing ability • Good product detailing skills • Relationship-building with doctors • Target-oriented mindset • Basic reporting and territory management skills Salary • Best in Industry About Company A Maximon Pharma Private Limited rapidly growing pharmaceutical company with a strong presence in the Delhi market, focused on quality products, ethical promotion, and expanding its field force across key territories.