1075 Pharmacology Jobs - Page 16

Location: Noida, Onsite Role Description This is a full-time on-site role for a Pharmacist/Medication Specialist at SayaCare's location in Noida. The Pharmacist/Medication Specialist will be responsible for transcribing prescriptions, suggesting appropriate substitutes, contributing to our large medicine database, providing pharmaceutical advice to customers, ensuring medication safety and efficacy, and promoting health and wellness education. Skills Pharmaceutical Dispensing and Medication Safety skills Pharmacology and Pharmacotherapy knowledge Medical Ethics and Legal Compliance knowledge Attention to Detail and Accuracy in Prescription Filling Good Communication and Interpersonal skills Ability to research online Basic knowledge of Excel Qualifications Bachelor's degree in Pharmacy (BPharm) or PharmD Previous experience in a retail or clinical, or e-pharmacy setting is a plus Company Description SayaCare is a healthcare initiative dedicated to making healthcare accessible and affordable for everyone in India. SayaCare provides tested medicines at significantly lower prices than the market rate to ensure quality healthcare is affordable. With a mission to make healthcare easy for every Indian, SayaCare educates people and raises awareness about health and pharma.

Job Summary We are looking for an experienced Medical Advisor to provide the scientific foundation for the Therapeutic Area (TA) medical strategy, including managing various medical activities and engaging key thought leaders. Oversee the execution of the medical affairs plan, facilitate the flow of medical developments to the sales and marketing team, and contribute to the development of the Medical Affairs strategic plan for identified Therapeutic Area (TA) and products. " Roles & Responsibilities Serve as a core scientific member of the cross-functional franchise team, providing the scientific foundation for the Therapeutic Area (TA) medical strategy. Conceptualize and manage a wide range of medical activities aligned with the TA Medical strategy, including research, publications, medical education, and patient support programs. Engage key thought leaders through medical affairs activities in line with the overall strategic plan. Ensure the optimal execution of the strategic medical affairs plan through Regional Medical Affairs, encompassing medical education, product education, and special projects. Act as a therapeutic area scientific expert, discussing scientific data with leading specialists and providing training on the latest medical developments to the sales and marketing team. " Qualifications Educational Qualification MBBS with M.D. Pharmacology/Medicine or full-time post-graduate qualification in any discipline of medicine Minimum Work Experience 2-4 years of experience in the pharmaceutical industry or research company in a Medical Advisor capacity Skills & Attributes Technical Skills Training in medical writing, clinical trial methodologies, research design, and ICH – GCP will be an added advantage. Must have a working knowledge of Indian regulations pertaining to Health care professional’s interactions (MCI code of ethics for doctors & UCPMP Code for Pharma) and Drugs and Cosmetic Act regulations pertaining to clinical trials and new drug approvals. Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data. Strategic mindset with scientific acumen and communication skills to be accepted by leading specialists in peer-to-peer relationships. Experience with complex business environments is preferred. Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards. Behavioral Skills Integrity-driven decision-making skills. Sound scientific knowledge. Collaboration and teaming with the ability to work in a matrix environment. Strategic thinking & sound analytical skills. Intellectual curiosity. Self-awareness and adaptability to work in a matrix environment. Result-oriented and performance-driven. Excellent interpersonal & communication skills to effectively interact with a broad range of audiences.

Contact Mr Manoj Thenua WhatsApp 639865 2832 Company Overview Medico Hub is a leading healthcare organization in India, dedicated to providing exceptional medical services to our community. Our mission is to enhance patient health and well-being through high-quality, comprehensive medical care. We pride ourselves on fostering a culture of compassion, integrity, and excellence within our team. As we continue to grow, we are looking for passionate professionals who share our commitment to improving the quality of life for our patients. Role Responsibilities Conduct regular patient consultations in the outpatient department (OPD). Examine and diagnose patients based on their medical history and symptoms. Administer appropriate treatment plans and medications as per standard medical protocols. Maintain accurate patient records and documentation of all consultations. Provide effective communication to patients regarding their health and treatment options. Stay updated on medical advancements and participate in continuous education. Collaborate with nursing and support staff to ensure comprehensive patient care. Assist in conducting educational workshops for patients on preventive health measures. Respond to medical inquiries and provide healthcare guidance. Ensure adherence to safety and health regulations in the practice. Participate in staff meetings and contribute to policy changes and improvements. Work towards achieving departmental goals and maintaining a high standard of care. Support emergency procedures and manage critical situations efficiently. Engage in community health activities and outreach programs. Review and analyze lab results to contribute to diagnosing patient conditions. Qualifications MBBS degree from a recognized institution. Valid Medical License in India. Experience in a clinical setting, particularly in outpatient services. Strong understanding of medical terminology and pharmacology. Excellent interpersonal and communication skills. Ability to work effectively within a team. Good organizational and time-management skills. Proficient in electronic medical records (EMR) systems. Demonstrated empathy and patient-centered care approach. Strong problem-solving abilities and analytical skills. Commitment to continuous professional development and learning. Willingness to work flexible hours, including weekends if necessary. Ability to handle sensitive and confidential information responsibly. Team-oriented with a collaborative mindset. Proficiency in local languages is a plus. If you are a passionate and dedicated medical professional looking to make a difference in patient lives, we invite you to apply for the MBBS RMO position at Medico Hub. Join our team and contribute to our mission of delivering high-quality healthcare services! Skills: patient-centered care,interpersonal skills,patient consultations,empathy,treatment plans,valid medical license,time management,electronic medical records (emr) systems,medical terminology,decision making,diagnosis,collaboration,problem-solving abilities,medical license,communication,health,records,team collaboration,contribute,patient records maintenance,consultations,analytical skills,communication skills,problem-solving,electronic medical records (emr),time-management skills,adherence,organizational skills,healthcare,record keeping,pharmacology,hub,clinical experience,skills,mbbs

University: Helmholtz Centre for Infection Research (HZI) Country: Germany Deadline: 2025-07-30 Fields: Chemistry, Biochemistry, Pharmacology, Molecular Biology, Microbiology The Chemical Biology Department at the Helmholtz Centre for Infection Research (HZI), under the leadership of Prof. Brönstrup, is seeking applications for a PhD researcher in the field of Bioanalytical Chemistry / Metabolomics. HZI is a member of the Helmholtz Association of German Research Centres, the largest scientific organization in Germany, and is dedicated to advancing strategies for the prevention, diagnosis, and treatment of infectious diseases. Research at HZI focuses on both bacterial and viral pathogens, their interactions with the immune system, and the discovery of novel therapeutic compounds. The Chemical Biology Department is committed to the discovery and characterization of new anti-infective agents through screening, mode of action studies, and chemical synthesis. Requirements For Application – Cover letter outlining your motivation and suitability for the position – Curriculum vitae (resume) – Employment references and certificates – Work samples or reference projects (if available) – Please do not include a photograph Application Procedure Applicants should submit all required documents, quoting the reference number 076/2025, to the Human Resources Department, Helmholtz Centre for Infection Research GmbH, Inhoffenstr. 7, 38124 Braunschweig, Germany. Applications may also be submitted by email as a single PDF document to jobshzi@helmholtz-hzi.de. Further information about the position can be found at: https://www.helmholtz-hzi.de/en/career/job-portal/job/076-2025-phd-researcher-f-m-d-in-bioanalytical-chemistry-metabolomics/ Get the latest openings in your field and preferred country—straight to your email inbox. Sign up now for 14 days free: https://phdfinder.com/position-alert-service/ We’re an independent team helping students find opportunities. Found this opportunity helpful? Support us with a coffee!

Ayurveda Physician (with MBBS Background) Location: Kochi, Kerala Employment Type: Full-Time Hospital: Upcoming Ayurveda Wellness Hospital Start Date: 01 August 2025 Position Overview: We are seeking a highly qualified and integrative-minded Ayurveda Doctor to join our upcoming Ayurveda and Wellness Hospital in Kochi . The ideal candidate must possess a Bachelor of Ayurvedic Medicine and Surgery (BAMS) and/or an MD in Ayurveda , alongside an MBBS degree , with at least one year of practical experience in modern medicine . This unique role is designed for physicians who, after gaining exposure to allopathic practice, have chosen to dedicate their future to Ayurveda-based preventive, promotive, and curative care . The position offers an exciting opportunity to bridge traditional Ayurvedic wisdom with scientific understanding of modern medicine , in a facility that emphasizes holistic healing and patient-centered wellness. Educational Qualifications: Mandatory : BAMS (Bachelor of Ayurvedic Medicine and Surgery) MBBS (Bachelor of Medicine, Bachelor of Surgery) Preferred : MD (Ayurveda) from a recognized institution Certification in integrative medicine, panchakarma, or functional medicine (optional but advantageous) Experience: At least 1 year of clinical practice in modern medicine (MBBS setting) 2–5 years of Ayurvedic clinical practice (may include internship) Experience in a hospital or wellness center setting is preferred Strong inclination towards holistic and integrative healthcare models Roles and Responsibilities: Clinical Duties: Conduct detailed Ayurvedic consultations, including prakriti analysis, disease diagnosis , and customized treatment planning. Utilize Ayurvedic therapies including herbal prescriptions, panchakarma , detoxification protocols, and lifestyle/diet counseling. Apply biomedical understanding when necessary to explain conditions, educate patients, and collaborate with other clinicians. Supervise Ayurvedic therapists and ensure proper execution of treatments. Interpret lab reports and imaging (from a modern medicine standpoint) if required to support holistic management. Hospital & Team Engagement: Work closely with other Ayurvedic physicians, therapists, dietitians, yoga consultants, and allopathic professionals (if part of integrated model). Participate in patient case reviews, interdisciplinary planning, and wellness program development. Maintain detailed patient records using both Ayurvedic and biomedical diagnostic frameworks. Patient Education: Guide patients on Ayurvedic nutrition, dinacharya (daily regimen), ritucharya (seasonal regimen), and mental wellness practices. Conduct public awareness sessions, webinars, or in-house wellness lectures when needed. Administrative & Research: Contribute to the creation of SOPs and treatment protocols. Assist in developing integrated care pathways or Ayurvedic health packages. Optional: participate in clinical research or documentation of treatment outcomes. Desired Skills & Attributes: Deep knowledge of Ayurvedic texts and their clinical application. Basic understanding of pharmacology and diagnostics from MBBS curriculum. Compassionate communication and patient-handling skills. Strong ethical grounding and passion for holistic healing. Openness to learning and adapting within an integrative team. Fluent in English and Malayalam (other languages an advantage). Salary & Benefits: Competitive salary based on experience and qualifications. Incentives for patient satisfaction and innovation in treatment delivery. Free or subsidized meals, accommodation (if required), and wellness treatments. Opportunities for professional development and training. How to Apply: Interested candidates may send their CV, a brief statement of interest (why they wish to practice Ayurveda full-time), and scanned copies of degrees to: Email: info@respublica.in Mobile: +91 974 522 25 51 Please mention “Ayurveda Physician – Kochi” in the subject line. Job Types: Full-time, Contractual / Temporary Schedule: Rotational shift Weekend availability Work Location: In person Expected Start Date: 01/08/2025

Knowledge Park Pvt Ltd is looking for Laboratory Technician (Pharmacy) to join our dynamic team and embark on a rewarding career journey. The Laboratory Technician performs laboratory tests and experiments, maintains laboratory equipment and supplies, and assists in the development of new laboratory techniques and procedures. 1. Collect and prepare laboratory samples for analysis. 2. Perform laboratory tests and experiments according to established protocols and procedures. 3. Analyze test results and prepare reports for interpretation by laboratory professionals. 4. Maintain laboratory equipment and supplies, including cleaning and sterilizing equipment and ordering supplies when needed.

R&D-IT Executive/Sr. Executive will be responsible for supporting IT applications, managing QMS across R&D Baroda functions. The person should have a strong understanding of CSV and QMS. The role requires a good understanding and experience in R&D/Lab policies and procedures to ensure applications/QMS are comply as per the applicable regulation. Job Description Role and Responsibilities Application support for Pharmacology, PKD, MPS and Biotechnology department Computer System Validation of scientific software and instrument software Managing and closure of assigned QMS within the timelines Application implementation support, testing and documentation of ongoing projects at R&D Baroda site Installation and Operation Qualification of NuGenesis and Empower clients Helping and providing IT support to business users during Performance Qualification phase Periodic review of Privilege and User Access Rights for assigned systems Monitor Periodic activities as per Global SOPs for R&D Baroda Perform miscellaneous job-related duties as assigned. Qualifications and Preference Qualifications Bachelors degree in Information Technology, or Computer Science or related field. Minimum of 3-5 years of experience in application support, preferably Pharma/ life sciences domain Strong understanding of CSV, IQ /OQ and testing Understanding of Lab Software functionality such as NuGenesis, Empower Preferred Qualifications CSV certification Familiarity with Laboratory instruments and software Experience in NuGenesis, Empower and any R&D pharma domain applications is preferred Good documentation skills to create and manage GxP documents

Applications are invited for the faculty positions Senior Resident, Assistant Professor, Associate Professor, and Professor. JOB LOCATION -TAMIL NADU 1. Anatomy – Senior Resident /Assistant professor /Associate professor/Professor 2. Physiology – Senior Resident /Assistant professor /Associate professor/Professor 3. BioChemistry – Senior Resident /Assistant professor /Associate professor/Professor 4. Pathology – Assistant professor /Associate professor/Professor 5. Microbiology – Senior Resident /Assistant professor /Associate professor 6. Pharmacology – Senior Resident /Assistant professor /Associate professor/Prof 7. Forensic Medicine– Senior Resident /Assistant professor /Associate professor/Professor 8. Community Medicine– Senior Resident /Assistant professor /Associate professor/Professor 9. General Medicine – Senior Resident /Assistant professor /Associate professor/Professor 10. Paediatrics – Senior Resident /Assistant professor /Associate professor/Professor 11. Dermatology –Associate professor/Professor 12. Psychiatry –Senior Resident/Associate professor/Professor 13. Respiratory-medicine– Senior Resident /Assistant professor /Professor 14. General Surgery– Senior Resident /Assistant professor /Associate professor/Professor 15. Orthopaedics –Senior Resident /Assistant professor /Associate professor//Professor 16. Ophthalmology– Senior Resident /Assistant professor /Professor 17. Obstertics & Gynaecology –SR/Assistant professor /Associate professor/Professor 18. Anaesthesiology –SR /Assistant professor /Associate professor/Professor 19. Radiology– Senior Resident /Assistant professor /Associate professor/Professor 20. Emergency-Medicine –Assistant professor /Associate professor/Professor 21.ENT-Associate professor/Professor Eligibility: As per NMC Norms. Remuneration: As per qualification & Experience JOB LOCATION -TAMIL NADU Job Type: Full-time Pay: ₹90,000.00 - ₹250,000.00 per month

Greetings From Sri Sai Medicode Certified Freshers For IPDRG Any Certification/ Non Certified Also Life Science Graduates Only Training After Placement WhatsApp - 63057 88230 SRI SAI MEDICODE - KPHB HYDERABAD https://ssmedicode.com/

The role of a hospital pharmacist is crucial in ensuring the safe and effective use of medications within a healthcare setting. Zen Hospital requires a honest and dedicated one with required (eligible) qualification. Following are duties of pharmacist> Medication Management: Hospital pharmacists play a key role in managing and dispensing medications to patients. They collaborate with doctors and nursing staff to ensure accurate prescriptions, dosage, and administration of drugs. Patient Safety: Pharmacists are responsible for verifying medication orders, checking for potential drug interactions, and ensuring that patients receive the right medications. Their attention to detail and knowledge of drug properties contribute to patient safety. Drug Information Resource: Hospital pharmacists serve as a valuable resource for healthcare professionals, providing up-to-date information on medications, including side effects, contraindications, and dosage recommendations. They may also educate patients on the proper use of medications. Clinical Pharmacy Services: Pharmacists are involved in clinical activities, participating in patient rounds, providing drug therapy recommendations, and collaborating with other healthcare professionals to optimize patient outcomes. Drug Procurement and Inventory Management: Hospital pharmacists are responsible for procuring medications, managing drug inventories, and ensuring that the hospital has an adequate supply of necessary drugs. They may also be involved in cost-effective drug utilization. Quality Assurance: Pharmacists contribute to the quality assurance programs within hospitals, ensuring compliance with regulatory standards, monitoring medication errors, and implementing measures to enhance the overall quality of pharmaceutical care. Compounding and Specialized Services: Pharmacists may be involved in preparing specialized medications, such as intravenous (IV) medications or compounded formulations. They ensure the accuracy and sterility of these preparations. Adherence Counseling: Pharmacists may counsel patients on medication adherence, potential side effects, and the importance of following prescribed regimens. This helps improve patient understanding and compliance with medication plans. Collaboration with Healthcare Teams: Hospital pharmacists work closely with physicians, nurses, and other healthcare professionals to develop comprehensive and individualized treatment plans. Effective communication and collaboration are essential for optimal patient care. Continuing Education: Staying updated on the latest developments in pharmacology, healthcare regulations, and emerging therapies is crucial for hospital pharmacists. They engage in continuous learning to provide the best possible care for patients. In summary, the desired role of a hospital pharmacist involves a combination of medication management, patient safety, clinical collaboration, and a commitment to ongoing education to ensure the highest standards of pharmaceutical care at ZEN HOSPITAL,KPHB 5,HYDERABAD. Job Type: Full-time Pay: ₹8,260.52 - ₹26,166.87 per month Schedule: Day shift Fixed shift Morning shift Rotational shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person Expected Start Date: 07/11/2025

Pharmacovigilance Internship with Stipend For Pharmacy Life Sciences Medical & Paramedical Should have Pharmacovigilance Certification Good knowledge in Clinical Research Pharmacovigilance and MedDRA Required Candidate profile B.Pharm M.Pharm and Pharm D who are passionate to learn hands on Experience on Softwares and For Job Seekers ready to relocate can be Applicable for this Internship program

Domnic Lewis has been mandated to hire a Regional Medical Advisor – Oncology (Breast Cancer) for a leading Pharmaceutical company Regional Medical Advisor- Oncology ( Breast Cancer ) MEDICAL AFFAIRS Be part of redefining our future by thinking and acting differently. Be part of delivering our vision to be the leader in Cardiovascular, Renal, Metabolism, Respiratory and Immunology by 2025. We need to build on our heritage and think and act differently to evolve with the healthcare landscape. From becoming a digitally-enabled enterprise to accelerating launches. It means we are forward looking, challenge the status quo, reflect on insights, spot opportunities and act on smart risks. What you//'ll do As a Regional Medical Advisor, you will be responsible to engage medical / scientific experts in in-depth medical / scientific product or disease area discussions, and deliver presentations in a non-promotional scientific context as determined by global / local Medical Affairs plans (and in line with the TA and brand strategy). You also act as an educational resource to internal stakeholders, providing medical / scientific knowledge, training, and support to internal stakeholders on CLIENT//'s marketed products and compounds in development. Key Duties and Accountabilities :- Develop a strong local KOL network Jointly develop the market/local KOL engagement plan with other MSLs, identify and segment KOLs according to their scientific interest and related affiliations and build the KOL network pre- and post-launch. Engage with KOLs using deep scientific expertise and knowledge of CLIENT//'s marketed products and compounds in development. Support clinical trials and investigator engagement Provide support to the Global Medicines Development (GMD) team on clinical site identification and patient recruitment for Phase I, II & III studies. Create opportunities to complement existing flow of clinical data for CLIENT//'s products in line with stakeholder needs, i.e., by identifying pre-clinical, clinical and post-marketing study investigators in alignment with the Development Plan, and engaging in discussions on the ISS Program with potential investigators. Provides support to the internal Global Medicines Development (GMD) team on clinical site identification Engage in scientific exchange Engage with the medical / scientific community in a highly credible, balanced/objective way, representing CLIENT//'s dedication to and excellence in science Prepare and give relevant high level medical science presentations at congresses, symposia and scientific meetings Provide support for content development, agreeing agendas and delivery of effective clinical presentations e.g., advisory boards Help to develop medical science literature, i.e., write, edit and publish scientific articles and papers Build capability of other internal and external stakeholders Act as a subject matter expert for external clinical / scientific stakeholders Help to build stakeholders//' understanding about potential solutions to their needs, e.g., extended access programs, approaches to diagnostic testing, etc. Respond to unsolicited stakeholder inquiries and provide focused, balanced and objective clinical / scientific information that supports the safe and appropriate use of currently available products, including questions regarding off-label uses, and products under development, when appropriate to do so Act as an educational resource to internal stakeholders Support the sales force and other departments with medical science information (e.g., disease and treatment) and training Effectively gather, analyze, synthesize and forward relevant new knowledge and meaningful insights about the external scientific / medical / regulatory environment to internal colleagues Provide internal stakeholders with actionable items related to brand strategy and GMD based on stakeholders//' perspectives Review promotional and scientific documents for content accuracy and compliance Be compliant Successfully complete all training requirements, including product examinations and certifications Comply with all external regulations and internal policies Ensure understanding of the CLIENT Global MSL Guide, CLIENT Code of Ethics, External Interactions Policy and Standards, and Publications Policy along with relevant local industry codes of conduct. Essential for the role MBBS/MD-Pharmacology Sound knowledge of basic research, drug discovery, drug development, clinical environment Experience in pharmaceutical industry, health care or research environment Proven ability to understand, assimilate and communicate scientific information Proven track record to engage and develop lasting relationships with key thought leaders in complex clinical environments Existing network within the TA ecosystem, with proven ability to influence decision making processes in an ecosystem with multiple influential stakeholders Proven demonstration of successful working in complex cross functional teams Good Planning and Organizational Skills Excellent Scientific knowledge Problem solving and Decision making skills Ability to develop Strategic Partnerships Demonstrate CLIENT Values consistently Desirable for the role Relevant 1-2 years of experience in Pharma industry preferably in Oncology. Open to look at MD-Pharmacology freshers

Title: R&D IT Executive Date: Jun 30, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Job Title: Executive/Sr. Executive- R&D IT Job Category: Permanent Department/Group: R&D IT/Project Job Code/ Req#: NA Location: Baroda Travel Required: No Level/Salary Range: G11 Position Type: FTE Contact: NA Date Posted: June-25 Will Train Applicant(s): NA Posting Expires: NA External Posting URL: NA Internal Posting URL: NA Job Summary R&D-IT Executive/Sr. Executive will be responsible for supporting IT applications, managing QMS across R&D Baroda functions. The person should have a strong understanding of CSV and QMS. The role requires a good understanding and experience in R&D/Lab policies and procedures to ensure applications/QMS are comply as per the applicable regulation. Job Description Role and Responsibilities Application support for Pharmacology, PKD, MPS and Biotechnology department Computer System Validation of scientific software and instrument software Managing and closure of assigned QMS within the timelines Application implementation support, testing and documentation of ongoing projects at R&D Baroda site Installation and Operation Qualification of NuGenesis and Empower clients Helping and providing IT support to business users during Performance Qualification phase Periodic review of Privilege and User Access Rights for assigned systems Monitor Periodic activities as per Global SOPs for R&D Baroda Perform miscellaneous job-related duties as assigned. Qualifications and Preference Qualifications Bachelor's degree in Information Technology, or Computer Science or related field. Minimum of 3-5 years of experience in application support, preferably Pharma/ life sciences domain Strong understanding of CSV, IQ /OQ and testing Understanding of Lab Software functionality such as NuGenesis, Empower Preferred Qualifications CSV certification Familiarity with Laboratory instruments and software Experience in NuGenesis, Empower and any R&D pharma domain applications is preferred Good documentation skills to create and manage GxP documents Reviewed By: Date: Approved By: Date: Last Updated By: Date/Time:

Key Responsibilities: Liaising with doctors, nurses, and other healthcare professionals to ensure the safe, effective, and economical delivery of drug treatments. Participating in dispensary work, including clinical checks and accuracy checking of prescriptions and dispensed medicines. Ensuring all work complies with Medicines Ethics and Practice, local policies and procedures, risk management, and health and safety protocols. Dispensing and supplying medicines. Receiving, storing, and supplying controlled drugs in accordance with hospital policy. Creating purchase orders (P.O.) and preparing GRNs for the same. Processing purchase returns of medicines due to expiry. Handling narcotics and maintaining proper records. Arranging non-available medicines from nearby chemists. Handing over cash to the cashier. Conducting quarterly stocktaking.

Data Architect, Regulatory Strategy (Pharmacology) Start: ASAP Duration: long term, full-time REMOTE job The company’s Innovative Medicine Division is seeking an experienced Data Architect to support our Regulatory Strategy portfolio of products. NJ/PA preferred but will consider remote contractors available to work US East core business hours. Strong English and communication skills. Roles and Responsibilities: • Partner with Regulatory subject matter experts, development partners product technical owners and engineers, J&J Technology Services and other architects to design scalable, extensible and supportable data architectures that drive business value in support of Regulatory Strategy and Intelligence • Develop data architecture artifacts in collaboration with key stakeholders using JJ standard tooling: Data Flow Diagrams, Entity Relationship Diagrams, Data Integration Artifacts, etc. • Responsible for architecture alignment to Regulatory, R&D, J&J Innovative Medicine and J&J Enterprise data and data platform strategies, patterns and standards. • Regularly engage with key business leaders and technical teams to create and maintain a data dictionary of master data elements, reference data elements, critical data elements and associated attributes, and non-critical elements and attributes. • Develop and maintain conceptual, logical and physical data models associated with Regulatory Strategy solutions. • Assist in development of a data governance framework that includes policies for the creation, maintenance and stewardship of master data, reference data and critical data elements. • Identify data that will need to be integrated across Regulatory solutions and its authoritative source. • Define master and reference data relationships • Collaborate with business stakeholders to gather and translate their data needs into functional and technical specifications. • Advocate for data-driven decision-making by providing insights and recommendations based on data analysis and architecture principles. • Address and resolve conflicts arising from diverse business unit requirements, ensuring smooth integration of stakeholder needs • Serve as a coach to business and IT product team partners to shape strategy through sharing expertise in data governance, data quality, and data integration practices. • Proactively identify opportunities for leveraging data as an asset to enhance business capabilities and drive competitive advantage. Education: • BA/BS degree in a technical, engineering or scientific field • AWS Data Engineer Certification (or Azure/GCP equivalent) • Experience with Snowflake and Denodo preferred • AWS Well-Architected Framework certification preferred • AWS Certified Machine Learning Specialty certification preferred

Company Description We suggest you enter details here. Role Description This is a full-time on-site role for a Pharmacist located in Kerala, India. The Pharmacist will be responsible for dispensing medications, counseling patients on the proper use of prescriptions, ensuring the accuracy of dosage and storage of medications, and managing patient health and wellness. Additionally, the Pharmacist will work closely with healthcare professionals to optimize treatment plans and contribute to the overall efficiency of the pharmacy operations. Qualifications Experience in dispensing medications and managing prescriptions Strong knowledge in pharmacology and drug interactions Excellent counseling and patient communication skills Ability to work collaboratively with healthcare professionals Attention to detail and accuracy in medication management Proficiency in pharmacy management software and tools Bachelor’s or Doctor of Pharmacy degree, and a valid license to practice as a Pharmacist in India Experience in a hospital or clinical setting is a plus Strong organizational and multitasking skills

Job Title: Pharmacist Department: Pharmacy Location: Raphael Life Care Hospital Reporting To: Pharmacy In-charge Job Type: Full-Time Shift: Rotational (including weekends and holidays) Job Summary:The Pharmacist is responsible for ensuring the safe, effective, and efficient distribution and use of medications for patients in accordance with hospital protocols and regulatory standards. The role involves dispensing prescriptions, managing inventory, providing drug information, and supporting healthcare professionals with pharmaceutical expertise. Key Responsibilities: Dispensing & Verification: Review and interpret physician prescriptions for accuracy and appropriateness. Dispense medications precisely as per prescription, checking dosage, interactions, and potential side effects. Ensure proper labeling and packaging of medications. Patient Counseling & Communication: Educate patients on medication usage, dosages, side effects, and storage instructions. Address patient queries and concerns regarding medications. Inventory Management: Maintain appropriate stock levels and check for expired or near-expiry drugs. Assist in procurement and record-keeping of medicines. Ensure proper storage conditions for all pharmaceuticals. Compliance & Safety: Adhere to all hospital policies, standard operating procedures (SOPs), and drug regulatory laws. Maintain cleanliness and hygiene in the pharmacy area. Participate in internal audits and ensure all records are up-to-date. Collaboration: Work closely with doctors, nurses, and other healthcare professionals to support patient treatment plans. Alert physicians about any potential drug interactions or contraindications. Documentation & Reporting: Maintain dispensing logs, billing, and patient records. Report adverse drug reactions (ADRs) and medication errors as per hospital policy. Qualifications: B.Pharm from a recognized institution. Registered with the Pharmacy Council of India. Minimum 1 year of hospital pharmacy experience preferred (freshers may also apply). Strong knowledge of pharmacology and hospital formulary systems. Excellent communication and interpersonal skills. Basic computer knowledge for pharmacy billing and stock systems. Work Environment:Fast-paced hospital environment. Must be able to work in shifts, including nights, weekends, and holidays. Requires attention to detail, precision, and ethical responsibility.

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: R&D IT Executive Date: Jun 30, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Job Title: Executive/Sr. Executive- R&D IT Job Category: Permanent Department/Group: R&D IT/Project Job Code/ Req#: NA Location: Baroda Travel Required: No Level/Salary Range: G11 Position Type: FTE Contact: NA Date Posted: June-25 Will Train Applicant(s): NA Posting Expires: NA External Posting URL: NA Internal Posting URL: NA Job Summary R&D-IT Executive/Sr. Executive will be responsible for supporting IT applications, managing QMS across R&D Baroda functions. The person should have a strong understanding of CSV and QMS. The role requires a good understanding and experience in R&D/Lab policies and procedures to ensure applications/QMS are comply as per the applicable regulation. Job Description Role and Responsibilities Application support for Pharmacology, PKD, MPS and Biotechnology department Computer System Validation of scientific software and instrument software Managing and closure of assigned QMS within the timelines Application implementation support, testing and documentation of ongoing projects at R&D Baroda site Installation and Operation Qualification of NuGenesis and Empower clients Helping and providing IT support to business users during Performance Qualification phase Periodic review of Privilege and User Access Rights for assigned systems Monitor Periodic activities as per Global SOPs for R&D Baroda Perform miscellaneous job-related duties as assigned. Qualifications Qualifications and Preference Bachelor's degree in Information Technology, or Computer Science or related field. Minimum of 3-5 years of experience in application support, preferably Pharma/ life sciences domain Strong understanding of CSV, IQ /OQ and testing Understanding of Lab Software functionality such as NuGenesis, Empower Preferred Qualifications CSV certification Familiarity with Laboratory instruments and software Experience in NuGenesis, Empower and any R&D pharma domain applications is preferred Good documentation skills to create and manage GxP documents Date: Reviewed By: Approved By: Last Updated By: Date/Time: Apply Now » Apply Now Start applying with LinkedIn Please wait...

Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Validation Engineer I What You Will Do Let’s do this. Let’s change the world. In this vital role you will join a collaborative team implementing and supporting the integrated case management systems on existing & future technologies. In this role, you will wear different hats including writing test scripts, implementing, analyze and resolve issues with case intake and data transfer across integrated systems. Collaborating closely with various teams, you will develop insights and implement solutions to improve system performance, ensuring reliable and efficient processing of data. Roles & Responsibilities: Monitor, test, and resolve issues related to case intake and case processing across multiple systems. Work closely with internal teams, external vendors, and business partners to address dependencies and resolve bottlenecks for critical issues Ownership in the development of test plans, scenarios to ensure robust validation of system updates, patches and new features Create test scripts, perform regression & functional testing to verify the changes do not negatively impact existing system functionality What We Expect Of You We are all different, yet we all use our unique contributions to serve patients. Master's degree / Bachelor's degree and 5 to 9 years of Life Science/Biotechnology/Pharmacology/Information Systems experience Preferred Qualifications: Functional Skills (Must Have) Experience in user requirements and acceptance criteria in agile project management systems such as JIRA and identification and execution of scripts. Experience in management of test plan, test protocols, defect management, and requirements traceability matrix Hands-on experience with the ITIL framework and methodologies like (Scrum). Hands on experience in HP ALM, JIRA, Visio, document management systems (e.g: Veeva) and Service Now. Good to Have Experience of DevOps, Continuous Integration, and Continuous Delivery methodology, and CRM systems Excellent communication skills and the ability to collaborate with Product Managers and business collaborators to define scope and value for new developments Soft Skills: Excellent analytical and solving skills Strong verbal and written communication skills Ability to work effectively with global, virtual teams High degree of initiative and self-motivation Team-oriented, with a focus on achieving team goals Shift Information: This position requires you to work a later shift and may be assigned a second or third shift schedule. Candidates must be willing and able to work during evening or night shifts, as required based on business requirements. What You Can Expect Of Us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Validation Engineer 1 What You Will Do Let’s do this. Let’s change the world. In this vital role you will join a collaborative team implementing and supporting the integrated case management systems on existing & future technologies. In this role, you will wear multiple hats including writing test scripts, implementing, analyze and resolve issues with case intake and data transfer across integrated systems. Collaborating closely with various teams, you will develop insights and implement solutions to improve system performance, ensuring reliable and efficient processing of data. Roles & Responsibilities: Monitor, test, and resolve issues related to case intake and case processing across multiple systems. Work closely with internal teams, external vendors, and business partners to address dependencies and resolve bottlenecks for critical issues Ownership in the development of test plans, scenarios to ensure robust validation of system updates, patches and new features Create test scripts, perform regression & functional testing to verify the changes do not negatively impact existing system functionality What We Expect Of You We are all different, yet we all use our unique contributions to serve patients. Master's degree / Bachelor's degree and 5 to 9 years of Life Science/Biotechnology/Pharmacology/Information Systems experience Preferred Qualifications: Functional Skills (Must Have) Experience in user requirements and acceptance criteria in agile project management systems such as JIRA and identification and execution of scripts. Experience in management of test plan, test protocols, defect management, and requirements traceability matrix Hands-on experience with the ITIL framework and methodologies like (Scrum). Hands on experience in HP ALM, JIRA, Visio, document management systems (e.g: Veeva) and Service Now. Good to Have Experience of DevOps, Continuous Integration, and Continuous Delivery methodology, and CRM systems Excellent communication skills and the ability to collaborate with Product Managers and business collaborators to define scope and value for new developments Soft Skills: Excellent analytical and troubleshooting skills Strong verbal and written communication skills Ability to work effectively with global, virtual teams High degree of initiative and self-motivation Team-oriented, with a focus on achieving team goals Shift Information: This position requires you to work a later shift and may be assigned a second or third shift schedule. Candidates must be willing and able to work during evening or night shifts, as required based on business requirements. What You Can Expect Of Us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

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