Pharmacy Jobs

Roles & Responsibilities: • Perform Ayurvedic therapies such as Abhyanga, Shirodhara, Pizhichil, Podikizhi, Njavarakizhi, and other treatments as per protocols. • Conduct basic client consultations and intake assessments. • Explain treatment plans and after-care instructions to clients. • Maintain high standards of hygiene, treatment room setup, linens, and equipment. • Document therapy sessions and client notes as per clinic procedures. • Upsell responsibly by recommending packages and follow-up therapies aligned with client goals. • Support clinic operations during peak hours and special events when required. Qualification: • DHA License (Active) as Ayurveda Therapist OR DHA Eligibility Letter with ability to convert quickly. Experience: • Minimum 2+ years of relevant experience. • UAE experience preferred but not mandatory. Skills: • Professional communication and strong client-handling skills. • Ability to communicate in English (Hindi/Arabic is an advantage). • High standards of hygiene, punctuality, and service orientation. • Patient-focused mindset with attention to quality and care. What We Offer: • Competitive salary with incentives (based on experience). • Visa sponsorship. • Supportive work environment with steady client flow. • Career growth opportunities into Senior Therapist or Lead roles. About the Organisation: Ayurveda R Us is a well-established wellness clinic in Dubai, offering authentic Ayurvedic therapies with a strong emphasis on quality care, traditional practices, and an exceptional client experience.

Formulation development and stability testing for new drug products.

Formulation development and stability testing for new drug products.

Roles & Responsibilities: • Prepare and submit Drug Master Files (DMFs) for the USA and EU. • Ensure compliance with regulatory guidelines and filing procedures. • Maintain and update regulatory documentation for accreditation processes. • Coordinate with internal teams to gather required data for submissions. • Liaise with regulatory agencies to address queries and ensure timely approvals. • Monitor changes in global regulatory requirements and update documentation accordingly. • Support audits and inspections by regulatory authorities. Qualification: • M.Pharm in Regulatory Affairs. Experience: • 1-2 years in Regulatory Affairs. Skills: • Strong knowledge of DMFs and regulatory filing procedures. • Familiarity with global regulatory guidelines (FDA, EMA). • Excellent documentation, organizational, and problem-solving skills. • Ability to work collaboratively with cross-functional teams. • Strong communication skills. About the Organization: Infinium Pharmachem Limited, established in 2003, is a leading manufacturer of pharmaceutical intermediates and APIs serving clients worldwide. The company focuses on quality, compliance, and innovation, delivering high-standard products to meet global regulatory requirements and supporting the pharmaceutical industry with reliable and efficient solutions.

Roles & Responsibilities • Drive overall brand strategy and long-term product planning for key domestic brands • Lead product positioning, messaging, and lifecycle management • Develop and execute high-impact marketing and promotional campaigns • Prepare and approve visual aids, campaigns, and promotional materials • Conduct market research, competitor analysis, and performance tracking • Guide and mentor junior product managers and PMT members • Coordinate closely with sales, medical, regulatory, and supply chain teams • Plan and execute product launches, extensions, and rebranding activities • Organize and deliver training programs for the field force Qualification • Graduate in Science or Pharmacy Experience • Minimum 6 years of experience in Product Management Team (PMT) • Strong exposure to domestic pharmaceutical marketing Skills • Strategic brand management and leadership skills • Market analysis, forecasting, and portfolio management • Excellent communication, presentation, and decision-making abilities • Ability to manage multiple brands and cross-functional stakeholders About the Organisation IPCA Laboratories is a globally recognized pharmaceutical company with a strong domestic presence. Known for its quality-driven approach and wide therapeutic portfolio, IPCA offers a dynamic work environment and long-term career growth opportunities.

Roles & Responsibilities • Dispense medicines as per valid prescriptions • Maintain drug inventory, stock registers, and expiry records • Ensure proper storage and handling of pharmaceuticals • Follow hospital SOPs and regulatory guidelines • Assist in patient counselling and medication management • Maintain accurate documentation and recordsEligibility & Qualifications• Qualification: B.PharmAge Limit • Minimum: 18 years • Maximum: 45 years • Age relaxation applicable as per JKSSB norms Selection Process • Written Test • Document Verification • Interview Application Fee • SC / ST Candidates: ₹600 • All Other Candidates: ₹700Important Date• Application Deadline: 25-03-206Skills • Knowledge of pharmaceutical dispensing and inventory management • Understanding of drug storage and handling requirements • Basic knowledge of pharmacy laws and regulations • Good communication and record-keeping skills • Attention to detail and accuracy • Ability to work in a hospital or government healthcare setupAbout the Organisation Jammu & Kashmir Services Selection Board (JKSSB) is a government body responsible for recruiting qualified candidates for various departments in the Union Territory of Jammu & Kashmir. The board ensures transparent, merit-based selection to strengthen public healthcare and administrative services.Official NotificationClick Here

Roles & Responsibilities • Coordinate day-to-day clinical trial activities at the site • Support investigators during patient screening, enrollment, and follow-up • Maintain essential trial documents including ISF, CRFs, and study logs as per GCP • Ensure compliance with ICH-GCP, SOPs, and regulatory guidelines • Coordinate with sponsors, CROs, ethics committees, and study monitors • Support study initiation, monitoring visits, and close-out activities • Ensure accurate data collection and timely resolution of queries Qualification • B.Pharm or M.Pharm (Pharmacology) Experience • Freshers or candidates with prior clinical research experience Skills • Knowledge of clinical research processes and GCP principles • Strong documentation and communication skills • Proficiency in Gujarati, Hindi, and English • Willingness to work full-time at the Ahmedabad site About the Organisation Nirmit Clinical Research is a clinical research organization focused on conducting ethical, high-quality clinical trials while providing hands-on training and growth opportunities for aspiring clinical research professionals.

Roles & Responsibilities • Research global regulatory requirements for pharmaceuticals, medical devices, biologics, and nutraceuticals • Support preparation, review, and lifecycle management of CTD and eCTD dossiers • Assist with regulatory submissions, variations, renewals, and post-approval changes • Track global regulatory updates, approvals, guidelines, and policy changes • Maintain and update regulatory databases and regulatory intelligence tools • Support development of client presentations, regulatory reports, and internal knowledge content • Collaborate with senior regulatory consultants on active client projects • Assist in documentation review, data analysis, and compliance-related activities Qualification • Pursuing or recently completed B.Pharm, M.Pharm, MSc (Life Sciences), Biotechnology, or Regulatory Affairs Experience • Freshers or students with academic exposure to Regulatory Affairs are encouraged to apply • Prior internship, project work, or coursework in regulatory affairs is an advantage Skills • Strong interest in global regulatory frameworks including USFDA, EMA, CDSCO, and ICH • Good understanding of regulatory documentation and submission processes • Proficiency in MS Word, Excel, and PowerPoint • Strong research, analytical, and documentation skills • Detail-oriented with good written and verbal communication • Ability to work independently and adapt in a startup consulting environment About the Organisation ArtiXio is a fast-growing life sciences consulting startup delivering regulatory affairs, compliance, and regulatory intelligence solutions to global pharmaceutical, medical device, and biotech companies. With a strong focus on practical learning and real-world exposure, ArtiXio provides interns and professionals the opportunity to work on live regulatory projects while building industry-relevant skills in a dynamic consulting environment.

Roles & Responsibilities • Act as the primary surgical point of contact for Roche’s Port Delivery System (PDS) within the Ophthalmology community • Provide operating room support during ophthalmic procedures, including hands-on device support, training, and ensuring safe and effective device use • Support ophthalmology clinical trials by assisting with site set-up, investigator and site staff training, and sharing key clinical data • Build and maintain strong relationships with ophthalmology stakeholders including Vitreo-Retinal surgeons, Medical Retinal specialists, General Ophthalmologists, Optometrists, ORDMs, and surgical theatre staff • Deliver high-quality medical education on surgical ophthalmology devices to healthcare professionals and patient organizations • Act as a connector between external clinical experts and Roche internal teams to support scientific exchange and collaboration • Gather expert insights, share best practices, and contribute to strategies that improve patient outcomes and inform lifecycle planning • Explore and support partnership opportunities such as joint working initiatives, patient safety programs, education, and data generation • Ensure full compliance with regulatory, quality, and industry standards in all activities • Travel within Canada up to 60% to support clinical, educational, and stakeholder engagement activities Qualification • Degree or certification in a scientific or related discipline • Postgraduate qualification (PhD, PharmD, MSc, MD, or MBA) preferred Experience • Minimum 7 years of experience in the pharmaceutical or healthcare sector • At least 2 years of experience in ophthalmology • Hands-on experience in ophthalmic surgery or surgical device support • Experience supporting clinical trials and engaging with medical experts Skills • Strong knowledge of clinical trials, regulatory requirements, and compliance standards including GCP, PV, and industry codes (e.g., IMC) • Excellent communication, presentation, and relationship-building skills • Strong project management and cross-functional collaboration abilities • Customer-focused mindset with demonstrated scientific credibility • Proficiency in both English and French is required • Ability to work independently in a field-based role and manage extensive travelRelocation benefits are not available for this posting. About the Organisation Roche is a global, research-driven healthcare company committed to advancing science to prevent, stop, and cure diseases while ensuring access to healthcare for all. Roche fosters a culture of inclusion, open dialogue, and respect, where every individual is encouraged to bring their authentic self to work. Through innovation in pharmaceuticals and diagnostics, Roche continues to shape the future of healthcare and improve patient lives across generations.

Roles & Responsibilities • Support clinical studies through coordination of study data and documentation • Assist in development, testing, and maintenance of case report forms (CRFs), databases, and study reports • Verify clinical study data, resolve discrepancies, and ensure timely completion of study forms • Process subject compensation and resolve related discrepancies • Create, organize, and maintain clinical study files in compliance with regulatory requirements • Support internal and external audits to ensure accuracy and completeness of study documentation • Communicate with internal teams and stakeholders to provide updates and clarifications • Provide guidance and support to new or entry-level team members as required Qualification • Bachelor’s degree in Life Sciences, Pharmacy, or a related discipline Experience • Minimum 2 years of experience in clinical research, clinical studies coordination, data coordination, or document management • Experience working with clinical study documentation and data verification processes Skills • Strong organizational, communication, and problem-solving skills • Ability to work under moderate supervision using established processes • Familiarity with clinical data management systems and regulatory documentation • Attention to detail and ability to manage multiple tasks effectively About the Organisation Medtronic is a global leader in healthcare technology, committed to alleviating pain, restoring health, and extending life. With a strong focus on innovation and patient-centered solutions, Medtronic supports clinical research that drives safe, effective, and transformative medical technologies worldwide.

Roles & Responsibilities • Dispense medicines accurately as per valid prescriptions • Ensure safe storage, handling, and distribution of medicines • Maintain pharmacy stock, batch records, and expiry monitoring • Follow FIFO / FEFO practices in medicine management • Provide basic medication guidance to beneficiaries when required • Maintain proper documentation and pharmacy records • Ensure compliance with ECHS guidelines and standard operating procedures • Support audits, inspections, and inventory verification activities Qualification • B. Pharm Age Limit • Minimum Age: 21 Years • Maximum Age: 45 Years • Age relaxation applicable as per organisation norms Important Date • Application Deadline: 12-02-2026 About the Organisation ECHS (Ex-Servicemen Contributory Health Scheme) is a Government of India healthcare scheme providing comprehensive medical care to ex-servicemen and their dependents through a network of polyclinics and empanelled hospitals across the country.

Roles & Responsibilities • Dispense medicines accurately as per prescriptions and ECHS guidelines • Maintain proper records of medicines, stock, batch numbers, and expiry dates • Ensure correct storage of medicines following FIFO/FEFO practices • Issue medicines to beneficiaries against authorized prescriptions • Monitor inventory levels and prevent stock shortages or expiries • Maintain cleanliness and hygiene of the pharmacy area • Support audits, inspections, and documentation as per organizational norms • Ensure compliance with pharmacy laws, safety standards, and ethical practices Qualification • Diploma in Pharmacy (D.Pharm) • Bachelor of Pharmacy (B.Pharm) Age Limit • Minimum Age: 18 Years • Maximum Age: 45 Years • Age relaxation applicable as per ECHS / Government norms No. of Vacancies: 19Important Date • Application Deadline: 10-02-2026 About the Organisation The Ex-Servicemen Contributory Health Scheme (ECHS) is a Government of India initiative under the Ministry of Defence, providing comprehensive medical care to ex-servicemen and their dependents through a wide network of polyclinics, empanelled hospitals, and diagnostic centers across the country.Official NotificationClick Here

Roles & Responsibilities • Dispense medicines accurately as per prescriptions and institutional guidelines • Ensure proper storage, labeling, and inventory management of pharmaceutical products • Maintain records of drug receipt, issue, and stock levels • Ensure compliance with pharmacy laws, safety standards, and university regulations • Provide basic medication-related guidance to patients/staff when required • Monitor expiry dates and ensure timely replacement of medicines • Coordinate with procurement and administrative departments for smooth pharmacy operations Qualification • Diploma in Pharmacy (D. Pharm) from a recognized institution • Registration with the State Pharmacy Council is mandatory Age Limit • Minimum Age: 21 Years • Maximum Age: 45 Years • Age relaxation applicable as per organisation norms Important Date • Application Deadline: 30-01-2026Skills • Good knowledge of medicines, dosages, and dispensing practices • High attention to detail and accuracy • Basic computer skills for record keeping • Strong organizational and documentation abilities • Good communication and interpersonal skills About the Organisation Kerala Veterinary and Animal Sciences University (KVASU) is a reputed academic and research institution dedicated to veterinary education, animal healthcare, and scientific advancement in the livestock sector.Official Notification Click Here

Join a leading tertiary care hospital. Responsibilities include medication therapy management.

Role & Responsibilities • Dispense medications accurately, verifying prescriptions for dosage, interactions, and allergies • Counsel patients on proper medication usage, side effects, and storage • Oversee pharmacy operations: inventory management, ordering, and stock maintenance • Provide clinical pharmacy services including medication therapy management • Collaborate with healthcare professionals to ensure safe and effective medication use • Maintain accurate patient records and comply with regulatory standards • Stay updated on new medications, treatment guidelines, and pharmacy practices • Prepare and compound medications using sterile and non-sterile techniques • Ensure a clean, organized, and regulation-compliant pharmacy environmentQualification • Bachelor of Pharmacy (BPharm) / Master of Pharmacy (MPharm) / Doctor of Pharmacy (PharmD) / PhD • Valid UAE license to practice pharmacy (DHA or MOH registration)Vacancies: 50Experience • Minimum 2 years in hospital, retail, or clinical pharmacy settingSkills & Competencies • Strong knowledge of pharmaceutical calculations, drug interactions, and therapeutics • Proficient with pharmacy software and electronic health records • Excellent communication and interpersonal skills • Strong problem-solving and critical-thinking abilitiesAbout Company • Life Pharmacy is a leading pharmacy chain in the UAE providing patient-centered care and advanced pharmaceutical services • Committed to safe, effective, and high-quality medication management

Roles & Responsibilities • Handle medical and drug-related queries through Medical Information Contact Center (MICC) operations • Support pharmacovigilance and medical information documentation activities • Ensure accurate data collection, case intake, and safety information reporting • Adhere to SOPs, GxP, and applicable regulatory guidelines during all activities • Coordinate with internal medical, pharmacovigilance, and safety teams for query resolution • Maintain strict confidentiality and data integrity in line with compliance standards Qualification • B.Pharm / M.Pharm / Pharm.D Skills • Basic understanding of Pharmacovigilance and Medical Information processes • Good verbal and written communication skills • Willingness to work in night shifts • Strong attention to detail and documentation accuracy • Eagerness to learn and ability to work in a regulated environment About the Company Mitocon Biopharma is a growing pharmaceutical organization focused on delivering high-quality healthcare and safety solutions. The company offers structured training, real-world exposure, and strong career development opportunities in pharmacovigilance and medical information services. This paid internship provides a solid entry point into the drug safety and pharmaceutical industry, with potential for permanent employment based on performance.

Roles & Responsibilities • Assist in preparation, formatting, and compilation of clinical trial documents such as Protocols, Investigator Brochures (IB), Informed Consent Forms (ICF), and Clinical Study Reports (CSR) • Support senior medical writers and medical leads in reviewing documents for accuracy, clarity, and regulatory compliance • Ensure documents align with ICH-GCP guidelines, ethical standards, and medical writing best practices under supervision • Coordinate document review cycles and track comments from Clinical Operations, Data Management, and Regulatory teams • Assist in compiling documentation for regulatory submissions including INDs and NDAs • Support ongoing clinical trials with documentation related to safety data, protocol amendments, and medical queries • Conduct literature searches and summarize scientific and clinical information • Maintain version control and document management records as per quality standards • Assist in preparing presentations, reports, and client-facing materials • Adhere to patient safety, data confidentiality, and ethical research practices at all times Qualification • Educational background in Pharmacy, Life Sciences, Biotechnology, Clinical Research, or related disciplines Skills • Basic understanding of clinical trials and medical writing concepts • Familiarity with ICH-GCP guidelines (preferred but not mandatory) • Strong written communication skills and attention to detail • Willingness to learn regulatory and clinical documentation standards • Good coordination and time management skills • Availability for immediate joining in Bengaluru About the Company Samahitha is a growing organization in the clinical research and healthcare domain, focused on delivering high-quality clinical and regulatory documentation services. The company provides hands-on learning opportunities, professional mentorship, and real-world exposure to clinical trials and medical writing, making it an ideal place for fresh graduates to begin a career in medical writing and clinical research.

Roles & Responsibilities • Generate and convert leads from pharmaceutical, nutraceutical, MedTech, and healthcare organizations • Promote market access services, pricing intelligence, product launch support, and healthcare research solutions • Build and maintain strong client relationships by understanding customer needs and business objectives • Prepare business proposals, presentations, and conduct follow-ups to close deals • Maintain and monitor the sales pipeline to achieve assigned business development targets • Coordinate with internal consulting, research, and delivery teams to ensure smooth project execution • Track market trends and identify new business opportunities in healthcare and life sciences Qualification • Graduate or Postgraduate in Pharmacy, Life Sciences, Healthcare, or Business Management Experience • 1–3 years of experience in business development, healthcare sales, or consulting services Skills • Basic understanding of pharmaceutical drugs, nutraceutical products, and healthcare markets • Strong communication, negotiation, and client relationship management skills • Ability to work in a target-driven, client-facing environment • Good presentation and proposal development skills • Self-motivated with a proactive approach to business growth About the Company Mark8Access is a leading healthcare intelligence and market access consulting firm that partners with pharmaceutical, nutraceutical, MedTech, and healthcare organizations. The company supports clients across pricing intelligence, market access strategy, product launch planning, scientific content services, and healthcare research, helping them make informed decisions and achieve successful market entry and growth.

Roles & Responsibilities • Collaborate with the Clinical Supplies Manager, Regulatory, and Clinical Operations teams to manage labeling, packaging, re-labeling, and shipment activities • Develop and execute drug distribution strategies aligned with recruitment trends, supply forecasts, and study timelines • Initiate and manage IMP and non-IMP packaging and sourcing activities with external vendors • Prepare, review, and maintain accurate clinical supply forecasts • Support IMP plans, including temperature excursion management to ensure product integrity • Coordinate with vendors for sourcing, labeling, packaging, and shipment in compliance with GMP and quality standards • Monitor vendor deliverables and resolve issues related to timelines, specifications, or quality • Initiate, track, and manage Import License (IL) processes, including submissions, renewals, and follow-ups • Ensure compliance with Quality Management Systems (QMS), Information Security Management Systems (ISMS), and global regulatory requirements • Maintain adherence to GMP, GCP, data protection laws, and applicable national and international regulations Qualification • Any Graduate • Life Sciences, Pharmacy, or related discipline preferred Experience • 3–5 years of relevant experience in clinical supplies, IMP/IP logistics, or clinical trial operations Skills • Strong knowledge of GMP and clinical supply chain processes • Hands-on experience in label generation, packaging, and shipment activities • Understanding of drug distribution strategies and supply forecasting • Experience working with CROs, sponsors, and third-party vendors • Familiarity with regulatory documentation and import licensing procedures • Strong coordination, documentation, and communication skillsAbout the CompanyVeeda Clinical Research (Veeda CR) is a leading global Contract Research Organization (CRO) headquartered in Ahmedabad, Gujarat, delivering end-to-end clinical research services across bioavailability/bioequivalence (BA/BE), clinical trials, clinical supplies, and regulatory solutions. Known for its strong quality culture, regulatory compliance, and global footprint, Veeda supports pharmaceutical and biotech companies in advancing safe and effective therapies worldwide.