1112 Pharmacology Jobs - Page 23

Job Title: Dispensing & Billing Pharmacist (D/B Pharmacist) Organization: Ahad Mult speciality Hospital Location: Burdwan, West Bengal Department: Hospital Pharmacy Reporting to: Chief Pharmacist / Hospital Administrator Employment Type: Full-Time Job Summary: The D/B Pharmacist is responsible for accurately dispensing medications to patients as per prescriptions and generating proper billing. This role ensures safe medication practices, patient guidance, stock monitoring, and compliance with pharmacy and hospital standards. Key Responsibilities: ✅ Prescription Handling & Dispensing Review prescriptions for accuracy, legality, and interactions. Dispense medicines correctly and label them as per guidelines. Counsel patients on dosage, usage, side effects, and storage if required. ✅ Billing & Cash Handling Generate bills accurately using pharmacy or hospital billing software. Ensure all medicines issued are recorded and billed properly. Maintain cash register, reconcile collections, and submit reports to accounts. ✅ Inventory Management Monitor stock levels of medicines, injections, and consumables. Check for expired or near-expiry items regularly. Support in indenting and receiving stock from the main store. ✅ Documentation & Compliance Maintain patient dispensing logs and billing records. Ensure prescription and billing records are NABH-compliant. Follow legal norms for controlled drugs, including Schedule H/H1/Narcotics. ✅ Customer Service & Coordination Respond politely to patient queries regarding medicine availability or substitutes. Coordinate with doctors and nurses for medicine clarification or shortages. Handle return or exchange of medicines as per policy. Qualifications: D.Pharm or B.Pharm from a recognized institute Registered Pharmacist with the State Pharmacy Council 1–3 years of experience in hospital or retail pharmacy preferred Key Skills: Strong knowledge of medicines and pharmacology Accuracy in billing and data entry Familiarity with HIS/pharmacy billing software Good communication and customer service skills Responsible and ethical handling of medicines

Help us bring cutting-edge medical treatments to life! Become a key player in clinical research and accelerate advancements in healthcare. Opportunities We offer two paths into the exciting world of clinical research: Internship: Get a hands-on introduction to clinical trials through a time-bound internship program. Ideal for students or recent graduates eager to experience the field. Fresher-Level Position: Launch your career as a Clinical Research Coordinator! This position offers ongoing employment for those committed to this exciting field. Regardless of path, you'll get to: Manage the flow of clinical trials: Oversee study logistics, participant documentation, and ensure the study progresses smoothly. Be a meticulous record-keeper: Collect and safeguard essential research data with the highest industry standards. Champion safety and ethics: Protect patient rights and ensure all research practices are ethical and compliant. Work within a team of like-minded professionals: Collaborate with investigators, healthcare providers, and fellow research enthusiasts. Qualifications Internship: Enrolled in or a recent graduate of a degree program in life sciences, health sciences, nursing, or a related field. Fresher-Level Position: Recent graduate with a degree in life sciences, health sciences, nursing, or a related field. For both: Passion for research, detail-orientation, strong organizational skills, clear communication, and willingness to learn. What We Offer Hands-on experience: Jumpstart your career or get real-world training. Training and mentorship: Get guidance from experienced researchers in the field. Professional development: Access resources or company-sponsored coursework to enhance your potential. Competitive compensation: Interns receive a stipend; fresher-level position offers salary and benefits. A role at the forefront of medical innovation: Shape the future of healthcare.

We are seeking a highly motivated and detail-oriented recent graduate to join our Drug Safety team as an Entry-Level Drug Safety Associate. This is an excellent opportunity to launch your career in the pharmaceutical industry and contribute to the safety surveillance of our products. You will gain practical experience in various aspects of drug safety, including adverse event processing, data entry, and safety reporting. This role is perfect for individuals with a strong interest in drug safety and a desire to learn and grow in a fast-paced environment. Responsibilities: Adverse Event Case Processing: Receive, triage, and accurately enter adverse event reports into the drug safety database. Ensure timely and accurate data entry in compliance with company Standard Operating Procedures (SOPs) and regulatory guidelines. Assist in the follow-up of adverse event reports to obtain complete and accurate information. Perform quality control checks on case data to ensure accuracy and consistency. Data Management and Safety Reporting: Assist in the preparation of safety reports and data summaries. Maintain accurate and organized drug safety records. Assist in the tracking and monitoring of adverse event trends. Learn to identify and escalate potential safety signals. Regulatory Compliance: Develop a basic understanding of global drug safety regulations and guidelines (e.g., ICH guidelines). Adhere to company SOPs and regulatory requirements. Assist in the preparation of regulatory submissions. General Support: Assist in the maintenance of drug safety databases and systems. Participate in team meetings and training sessions. Support senior drug safety staff as needed. Perform other duties as assigned. Qualifications: Bachelor's degree in Pharmacy, Pharmacology, Life Sciences, Nursing, or a related healthcare field. Strong interest in drug safety and pharmacovigilance. Excellent attention to detail and accuracy. Strong organizational and time-management skills. Ability to work independently and collaboratively within a team. Good communication and interpersonal skills. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). Must be a recent graduate. Preferred Qualifications (but not required): Basic understanding of medical terminology. Familiarity with drug safety databases or systems. Coursework related to pharmacology or drug safety.

Contact no. 9315768794 *Explore Exciting Opportunities in Clinical & Non-Clinical Medicine Across India!* We're hiring for various positions in *All Clinical and Non- Clinical Profiles* across multiple locations in India! 1. *Assistant Professor* 2. *Associate Professor* 3. *Professor* 4. *Senior Resident* *PAN India Locations:* Explore new horizons in your medical career across various cities in India! *How to Apply:* Call/WhatsApp: *9315768794* Email: hr22pathfinders@gmail.com *Dual Career Support:* Share your spouse's CV if they're a medical professional (clinical or non-clinical). References are also appreciated! *Help Us Spread the Word!* Circulate this announcement within your networks and help your peers discover these amazing opportunities. *Best Regards,* *HR. Kritya* *9315768794* Pathfinders Global (P) Ltd _Let's shape the future of healthcare together!_

Contact no. 8810527696 *Explore Exciting Opportunities in Clinical & Non-Clinical Medicine Across India!* We're hiring for various positions in *All Clinical and Non- Clinical Profiles* across multiple locations in India! 1. *Assistant Professor* 2. *Associate Professor* 3. *Professor* 4. *Senior Resident* *PAN India Locations:* Explore new horizons in your medical career across various cities in India! *How to Apply:* Call/WhatsApp: * 8810527696 * Email: hr8pathfinders@gmail.com *Dual Career Support:* Share your spouse's CV if they're a medical professional (clinical or non-clinical). References are also appreciated! *Help Us Spread the Word!* Circulate this announcement within your networks and help your peers discover these amazing opportunities. *Best Regards,* *HR. Jaishree* *8810527696* Pathfinders Global (P) Ltd _Let's shape the future of healthcare together!_

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position Content Creation Subchapter Lead Roche India – Roche Services & Solutions Hyderabad A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. Roche is a leading biotechnology company renowned for its innovative approach, offering exceptional career paths and comprehensive benefits for both fresh graduates and professionals. As we continue to expand, we seek new talents to join our transformative Roche Services & Solutions Center. Our flexible working framework includes an average of two office days per week, accommodating diverse working styles and needs. The Global Digital Hub is a growing business line within the Roche Services & Solutions Center. Our primary goal is to enhance Roche's digital capabilities globally by supporting central initiatives in areas such as Social Media Management, Brand Support, Digital Publishing Services, Marketing Automation, Content Creation, and Creative Design. Your Opportunity The Content Creation Subchapter Lead is a pivotal people leader who inspires and engages subchapter members to collaborate across the network, significantly contributing to Roche’s Ten Year Ambitions. This role is accountable for driving the integration of the new operating model, exemplifying agile collaboration. The content creation chapter team consists of medical writers, content editors, project delivery coordinators, and medical copy quality assurance specialists. As the Content Creation Subchapter Lead, you will be responsible for supporting the strategic vision and direction of the chapter, continuously seeking opportunities for innovation and value creation. This critical position has a global scope, leading a diverse team across various regions. People Leadership: Lead, mentor, and develop team members, providing coaching and support to enable them to execute content creation projects successfully and continuously improve their skills. Create and implement personal development plans tailored to individual needs and aspirations Operational Leadership: Coordinate the operation of the Content Creation Subchapter, ensuring high effectiveness of assigned content creation activities. Manage content creation resources, monitor their utilization, and ensure customer satisfaction within the subchapter Recruitment: Find, attract, develop, and retain top talent, aligned with the evolving needs of the function and the business. Conduct interviews and facilitate the onboarding process Capability Building: Foster the development of the content creation team members, promoting a culture of continuous learning, innovation, and content excellence Agile Collaboration: Drive the embedding of the new operating model, serving as a role model for agile collaboration within the content creation subchapter Cross-Functional Leadership: Collaborate effectively with different chapters, subchapters, and other relevant teams to drive impactful content creation solutions and align with business and Global Digital Hub strategies Service Quality: Provide recommendations to enhance service quality, responsiveness, and content output to meet or exceed business partners' expectations Process Governance: Establish and maintain process governance principles, ensuring proper documentation and adherence to content creation best practices within the scope of the Content Creation Subchapter's responsibility Stakeholder Engagement: Professionally represent the Content Creation Subchapter with key stakeholders, promoting the value and impact of content creation within the organization OneRoche Mindset: Support the embedding of the OneRoche mindset within the content creation subchapter and across the Global Digital Hub, fostering a culture of innovation and collaboration Who You Are We are looking for a dynamic individual who is highly involved and passionate about medical copy and content services. As a Content Creation Subchapter Lead, you thrive in a team environment and excel in a fast-paced global setting. You are a proactive and innovative problem-solver, always seeking sustainable and scalable solutions. Keeping up with the latest digital updates and content trends is a natural part of your commitment to providing cutting-edge content capabilities to our partners You hold a Master’s degree or PhD in (Life Sciences), Medicine, Dentistry, Pharmacy/Pharmacology, Microbiology with 8+ years of experience with 4+ years of experience working in project management roles, preferably within large organizations, agencies, or startups 3+ years of experience in people development, coaching, and leadership, specifically within a content creation context A higher degree in life sciences is highly preferred, but candidates with other relevant experience will also be considered. Strong medical or science background High level proficiency in English, with excellent written and verbal communication skills Ability to work within a team and in different time zones Customer-service mentality & can-do attitude Experience with the standard IT applications, preferably including Google suite Continuous improvement and growth mindset Ability to work in a fast-paced and changing environment, ability to prioritize tasks Strong problem-solving skills, including analytical abilities, active listening, critical thinking, and a focus on sustainable and scalable content solutions Ability to thrive under pressure, manage complex challenges, and work independently while maintaining high content standards Quick learner with a passion for exploring new technologies, tools, and techniques Dynamic and flexible in adapting to different software and workflows Excellent interpersonal skills to foster collaboration within the team and effectively engage with senior leaders and stakeholders Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position Content Creation Subchapter Lead Roche India – Roche Services & Solutions Hyderabad A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. Roche is a leading biotechnology company renowned for its innovative approach, offering exceptional career paths and comprehensive benefits for both fresh graduates and professionals. As we continue to expand, we seek new talents to join our transformative Roche Services & Solutions Center. Our flexible working framework includes an average of two office days per week, accommodating diverse working styles and needs. The Global Digital Hub is a growing business line within the Roche Services & Solutions Center. Our primary goal is to enhance Roche's digital capabilities globally by supporting central initiatives in areas such as Social Media Management, Brand Support, Digital Publishing Services, Marketing Automation, Content Creation, and Creative Design. Your Opportunity The Content Creation Subchapter Lead is a pivotal people leader who inspires and engages subchapter members to collaborate across the network, significantly contributing to Roche’s Ten Year Ambitions. This role is accountable for driving the integration of the new operating model, exemplifying agile collaboration. The content creation chapter team consists of medical writers, content editors, project delivery coordinators, and medical copy quality assurance specialists. As the Content Creation Subchapter Lead, you will be responsible for supporting the strategic vision and direction of the chapter, continuously seeking opportunities for innovation and value creation. This critical position has a global scope, leading a diverse team across various regions. People Leadership: Lead, mentor, and develop team members, providing coaching and support to enable them to execute content creation projects successfully and continuously improve their skills. Create and implement personal development plans tailored to individual needs and aspirations Operational Leadership: Coordinate the operation of the Content Creation Subchapter, ensuring high effectiveness of assigned content creation activities. Manage content creation resources, monitor their utilization, and ensure customer satisfaction within the subchapter Recruitment: Find, attract, develop, and retain top talent, aligned with the evolving needs of the function and the business. Conduct interviews and facilitate the onboarding process Capability Building: Foster the development of the content creation team members, promoting a culture of continuous learning, innovation, and content excellence Agile Collaboration: Drive the embedding of the new operating model, serving as a role model for agile collaboration within the content creation subchapter Cross-Functional Leadership: Collaborate effectively with different chapters, subchapters, and other relevant teams to drive impactful content creation solutions and align with business and Global Digital Hub strategies Service Quality: Provide recommendations to enhance service quality, responsiveness, and content output to meet or exceed business partners' expectations Process Governance: Establish and maintain process governance principles, ensuring proper documentation and adherence to content creation best practices within the scope of the Content Creation Subchapter's responsibility Stakeholder Engagement: Professionally represent the Content Creation Subchapter with key stakeholders, promoting the value and impact of content creation within the organization OneRoche Mindset: Support the embedding of the OneRoche mindset within the content creation subchapter and across the Global Digital Hub, fostering a culture of innovation and collaboration Who You Are We are looking for a dynamic individual who is highly involved and passionate about medical copy and content services. As a Content Creation Subchapter Lead, you thrive in a team environment and excel in a fast-paced global setting. You are a proactive and innovative problem-solver, always seeking sustainable and scalable solutions. Keeping up with the latest digital updates and content trends is a natural part of your commitment to providing cutting-edge content capabilities to our partners You hold a Master’s degree or PhD in (Life Sciences), Medicine, Dentistry, Pharmacy/Pharmacology, Microbiology with 8+ years of experience with 4+ years of experience working in project management roles, preferably within large organizations, agencies, or startups 3+ years of experience in people development, coaching, and leadership, specifically within a content creation context A higher degree in life sciences is highly preferred, but candidates with other relevant experience will also be considered. Strong medical or science background High level proficiency in English, with excellent written and verbal communication skills Ability to work within a team and in different time zones Customer-service mentality & can-do attitude Experience with the standard IT applications, preferably including Google suite Continuous improvement and growth mindset Ability to work in a fast-paced and changing environment, ability to prioritize tasks Strong problem-solving skills, including analytical abilities, active listening, critical thinking, and a focus on sustainable and scalable content solutions Ability to thrive under pressure, manage complex challenges, and work independently while maintaining high content standards Quick learner with a passion for exploring new technologies, tools, and techniques Dynamic and flexible in adapting to different software and workflows Excellent interpersonal skills to foster collaboration within the team and effectively engage with senior leaders and stakeholders Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.

Hiring Alert : Professor and Associate Professor Chandigarh Group of Colleges Landran Campus ( Punjab) We are looking for enthusiastic and knowledge individuals to join our Pharmacy Department. Position: Professor and Associate Professor Pharmacology Pharma practices. Eligibility Criteria Qualification: Masters in Pharmacology and Pharma Practices. PhD Mandatory (Pharmacology and Pharma Practices ) Experience: 8 to 15 years of experience required. Job Type: Full-time Pay: ₹35,000.00 - ₹70,000.00 per month Schedule: Day shift Work Location: In person

Key Responsibilities: Serve as a technical liaison between engineering, sales, and medical clients to support biomedical product and pharmaceutical-related negotiations. Evaluate biomedical devices and solutions in relation to drug delivery, compatibility with pharmaceuticals, or combined device-drug systems. Participate in negotiations and product positioning with hospitals, procurement teams, and pharmaceutical partners. Provide scientific and technical input during product discussions, focusing on both device and medicine aspects. Collaborate with R&D, Quality, and Regulatory teams to ensure product compliance and relevance to clinical needs. Conduct market and competitor analysis on medical devices and pharmaceutical solutions to enhance negotiation outcomes. Support the customization of products to meet client needs in clinical, pharmaceutical, or hospital environments. Deliver technical presentations, training, and documentation related to products and drug-device integration. Requirements: Bachelor’s or Master’s degree in Biomedical Engineering , Pharmaceutical Sciences , or related field. 3–5 years of experience in medical devices, pharmaceuticals, or a healthcare-focused technical role. Proven experience in product negotiation or technical sales involving biomedical products and/or medicines. Solid understanding of pharmacology, drug-device combinations, and regulatory standards. Strong interpersonal and communication skills, with the ability to simplify complex information. Proficiency in CRM tools, Microsoft Office, and technical documentation software. Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Cell phone reimbursement Schedule: Day shift Work Location: In person

Associate Professor / Professor Department of Pharmaceutical Sciences at Rama University, Kanpur : Job Title: Associate Professor / Professor Department: Pharmaceutical Sciences Institution: Rama University, Kanpur Employment Type: Full-Time Experience Required: Associate Professor: Minimum 8 years of teaching/research/industry experience Professor: Minimum 10 years of teaching/research/industry experience with at least 5 years as Associate Professor Role Summary: We are seeking qualified and dynamic individuals for the post of Associate Professor / Professor in the Department of Pharmaceutical Sciences. The incumbent will contribute to teaching, research, academic mentoring, and curriculum development, and guide students at undergraduate, postgraduate, and doctoral levels. Key Responsibilities: Teaching & Academics: Deliver high-quality lectures and lab sessions in core pharmaceutical subjects (Pharmaceutics, Pharmacology, Pharmaceutical Chemistry, Pharmacognosy, etc.) Develop course materials, lesson plans, and assessment tools aligned with industry standards and PCI norms Supervise B.Pharm, M.Pharm, and Ph.D. research projects Engage in interdisciplinary teaching and contribute to curriculum development Research & Publications: Conduct independent and collaborative research in pharmaceutical sciences Publish in reputed national and international journals (SCI/Scopus-indexed) Apply for sponsored research grants (DST, ICMR, AICTE, DBT, etc.) Guide Ph.D. scholars and promote a culture of innovation and research Administration & Mentoring: Actively participate in departmental and university-level committees Assist in organizing seminars, workshops, and conferences Mentor junior faculty and students on academic and career goals Contribute to accreditation (NBA, NAAC) and compliance processes Eligibility Criteria: Educational Qualification: Ph.D. in Pharmaceutical Sciences or allied disciplines First class in B.Pharm and M.Pharm from a recognized university/institute Must meet UGC / PCI / AICTE norms for faculty recruitment Experience: Associate Professor: Minimum 8 years of total experience with proven academic and research credentials Professor: Minimum 10 years of total experience including at least 5 years as Associate Professor, with significant research contributions Desirable: Recognized research awards, patents, or funded projects Experience in pharmaceutical industry collaborations Strong publication record in high-impact journals Skills Required: Excellent communication and presentation skills Strong academic writing and analytical thinking Proficiency in modern teaching tools and LMS platforms Leadership abilities and team collaboration skills

TCS is hiring - Medical Writer Job Location – Mumbai, Pune, Bangalore Experience Range – 3 to 12 Years Responsibilities: Overall ~5 years of authoring/editing experience in medical writing domain across different therapeutic areas in clinical documents including clinical study protocol, pediatric investigation plan, informed consent document, clinical study report, investigator’s brochure, clinical summary of pharmacology, clinical overview (efficacy and safety), briefing package/pre-meeting package preferred. Experience in preparation of clinical documents necessary for national and international regulatory submissions to the US, European and other regulatory agencies Clear, concise and scientific style of writing, with attention to detail Strong analytical skills and expertise in writing and review of scientific/clinical documents Good knowledge of clinical research domain, ICH GCP principles, Common Technical Document (CTD) structure and regulatory requirements Effective coordination and presentation skills - good organization and time management skills Exceptional interpersonal, verbal and written communication skills Computer Literate: Knowledge of MS Word, PowerPoint, Adobe Acrobat, MS Excel, etc.

PMS College of Dental Sciences & Research is looking for Asst Proffesor - Pharmacology to join our dynamic team and embark on a rewarding career journey Develop and deliver high-quality lectures and instructional materials. Conduct research and publish findings in academic journals. Advise and mentor students on academic and career matters. Participate in academic committees and contribute to curriculum development. Stay current with developments in the field and incorporate them into teaching.

Associate Professor / Professor Department of Pharmaceutical Sciences at Rama University, Kanpur : 📌 Job Title: Associate Professor / Professor 📍 Department: Pharmaceutical Sciences 🏛 Institution: Rama University, Kanpur 📅 Employment Type: Full-Time 🧑‍🎓 Experience Required: Associate Professor: Minimum 8 years of teaching/research/industry experience Professor: Minimum 10 years of teaching/research/industry experience with at least 5 years as Associate Professor Role Summary: We are seeking qualified and dynamic individuals for the post of Associate Professor / Professor in the Department of Pharmaceutical Sciences. The incumbent will contribute to teaching, research, academic mentoring, and curriculum development, and guide students at undergraduate, postgraduate, and doctoral levels. Key Responsibilities: Teaching & Academics: Deliver high-quality lectures and lab sessions in core pharmaceutical subjects (Pharmaceutics, Pharmacology, Pharmaceutical Chemistry, Pharmacognosy, etc.) Develop course materials, lesson plans, and assessment tools aligned with industry standards and PCI norms Supervise B.Pharm, M.Pharm, and Ph.D. research projects Engage in interdisciplinary teaching and contribute to curriculum development Research & Publications: Conduct independent and collaborative research in pharmaceutical sciences Publish in reputed national and international journals (SCI/Scopus-indexed) Apply for sponsored research grants (DST, ICMR, AICTE, DBT, etc.) Guide Ph.D. scholars and promote a culture of innovation and research Administration & Mentoring: Actively participate in departmental and university-level committees Assist in organizing seminars, workshops, and conferences Mentor junior faculty and students on academic and career goals Contribute to accreditation (NBA, NAAC) and compliance processes Eligibility Criteria: Educational Qualification: Ph.D. in Pharmaceutical Sciences or allied disciplines First class in B.Pharm and M.Pharm from a recognized university/institute Must meet UGC / PCI / AICTE norms for faculty recruitment Experience: Associate Professor: Minimum 8 years of total experience with proven academic and research credentials Professor: Minimum 10 years of total experience including at least 5 years as Associate Professor, with significant research contributions Desirable: Recognized research awards, patents, or funded projects Experience in pharmaceutical industry collaborations Strong publication record in high-impact journals Skills Required: Excellent communication and presentation skills Strong academic writing and analytical thinking Proficiency in modern teaching tools and LMS platforms Leadership abilities and team collaboration skills

We require doctors for Medical Colleges & Hospitals Pan India Qualification : MD / MS / DNB (All Department ) 0-5 years of experience after MS/MD degree (any specialization) Position : Consultant , Senior Resident , Assistant Professor , Associate Professor , Professor Department : Clinical & Non Clinical Key-skills - Strong knowledge of Different Departments according to Qualification . Excellent communication skills for effective interaction with patients & colleagues. Ability to work efficiently under pressure during emergencies or critical situations Reema Call/Whatsapp : 9877677063 Email Id - weps.hrworld@gmail.com

Hiring Alert : Professor and Associate Professor Chandigarh Group of Colleges Landran Campus ( Punjab) We are looking for enthusiastic and knowledge individuals to join our Pharmacy Department. Position: Professor and Associate Professor Pharmacology Pharma practices. Eligibility Criteria Qualification: Masters in Pharmacology and Pharma Practices. PhD Mandatory (Pharmacology and Pharma Practices ) Experience: 8 to 15 years of experience required. Job Type: Full-time Pay: ₹35,000.00 - ₹70,000.00 per month Schedule: Day shift Work Location: In person

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services–from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)–in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology, in-vivo , in-vitro models and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology &In-vitroADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world’s leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com The Position Organization : - Jubilant Biosys Designation & Level: - Trainee research Associate/ A0 Location : - Greater Noida Department: - Synthesis Reporting Manager: - Group Leader Key Responsibilities Synthesis, purification and characterization of chemical intermediates. Deliver small to large quantities of novel chemical entities for drug discovery. Work collaboratively in a team to drive chemistry projects forward. Excellent knowledge of basic organic chemistry with mechanism. Good knowledge of Name Reactions & functional group transformation. Good knowledge of molarity, normality, equivalency. Practical experience in thin-layer chromatography, column purification and extraction. Good understanding of NMR, IR and mass spectrometry. Interest to adapt and knowledge of laboratory safety practices. Enthusiasm to work in a dynamic research environment. Good Soft & Scientific Communication skills. Person Profile Qualification: - M.Sc. in Chemistry/Organic Chemistry/Pharmaceutical Chemistry or related field or M. Pharma (Specialized in Organic Synthesis) with 0-1 years’ project experience. Experience: - 0-1 year of exp. Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services–from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)–in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology, in-vivo , in-vitro models and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology &In-vitroADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world’s leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com The Position Organization : - Jubilant Biosys Designation & Level: - Trainee Research Associate Location: - Greater Noida Department: - Analytical Key Responsibilities Learning the operations of Analytical Instruments under the guidance of mentor. Learning the new Analytical Techniques used in Analytical Research Department. Coordination with Synthesis and other cross-functional departments. To ensure Good Laboratory & safety practices in the lab. Participate in ARD SOP trainings and other departmental trainings (Quality Assurance & EHS, HRD etc.) as and when required. Basic knowledge of instrumental technique with its application. analytical chemistry (HPLC/LCMS/NMR or purification) Person Profile Qualification: - M. Sc (Analytical Chemistry) Experience: - 0 years Any kind of internship or course work done at some Industry or reputed institute Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.

About Walter: Walter® Healthcare is one of India’s most agile and fast-scaling Contract Development & Manufacturing Organizations (CDMO/CMO) — trusted by pharma brands, healthcare startups, and global exporters for high-quality, end-to-end pharmaceutical manufacturing. With state-of-the-art WHO-GMP certified facilities and an in-house GLP-compliant laboratory, Walter® operates across oral solids, liquids, injectables, nutraceuticals, and cosmeceuticals — bringing together regulatory rigour, speed, and executional excellence under one roof. But we’re not just building a pharma company. We’re building the backbone of India’s next wave of pharma and wellness brands — powered by quality systems, radical transparency, and a culture of ownership. Joining Walter® means being part of a high-performance team where accountability isn’t layered, speed isn’t optional, and ideas aren’t just heard — they’re implemented. Whether you’re in operations, QA, sales, R&D, or supply chain — you’ll get hands-on experience, cross-functional exposure, and direct impact from day one. With us, you'll get the support, guidance, and opportunities that you need to take your career to the next level. So, if you're ready to embark on the journey of your next challenge, we're ready to be your engine! ● Profile: Business Development (Sr. Executive / Assistant Manager / Deputy Manager) ● Division: Contract Manufacturing ● Experience: 0-2 years ● Location: Mohali, H.O. (Bestech Business Towers) ● CTC: 5 LPA - 10 LPA (Fixed 70% + Variable 30%) We are seeking a dynamic Business Development Manager to join our ‘Contract Manufacturing’ Vertical. Reporting directly to the Business Development Head, the successful candidate will play a key role in driving business growth. Your responsibilities will include identifying new business opportunities, promoting our third-party manufacturing services, and working towards individual and team targets for GMV (Gross Merchandise Value) & ER (Earned Revenue). You will work closely with a team of Business Development Executives and collaborate with the Business Development Head to implement strategies that expand our customer base and optimise market performance. Requirements: Drive business growth and expansion strategies for the Contract Manufacturing Vertical. Promote our third-party manufacturing services to potential clients. Manage monthly portfolio targets of Gross Merchandise Value and Earned Revenue. Develop and nurture relationships with key clients and industry stakeholders via Emails, LinkedIn, Exhibitions, Conferences, Cold-Calling. Identify and capitalise on new business opportunities in line with the company's strategic goals. Foster a culture of excellence and continuous improvement within the team. Support business growth and expansion strategies for the Contract Manufacturing Vertical. Identify new business opportunities in line with the company's strategic goals and report them to the Business Development Head. Skills Required: MBA required & academically strong, but not mandatory. Excellent communication and presentation skills. Excellent communication and presentation skills. Knowledge of Pharmacology, Pharmaceuticals, Physiology, Industrial Pharmacy would be an advantage. Strong Emotional Intelligence (EQ), empathy, self-actualization, self-awareness, and consciousness. Strong leadership, negotiation, and decision-making skills. Walter® Healthcare is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

About Eurofins – the global leader in bio-analysis Eurofins is Testing for Life. The Eurofins network of companies believes that it is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. With over 62,000 staff across a decentralized and entrepreneurial network of ca. 900 laboratories in 61 countries, Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of a wide range of products, as well as providing innovative clinical diagnostic testing services and in-vitro diagnostic products. Eurofins companies’ broad range of services are important for the health and safety of people and our planet. The ongoing investment to become fully digital and maintain the best network of state-of-the-art laboratories and equipment supports our objective to provide our customers with high-quality services, innovative solutions and accurate results in the best possible turnaround time (TAT). Eurofins companies are well positioned to support clients’ increasingly stringent quality and safety standards and the increasing demands of regulatory authorities as well as the evolving requirements of healthcare practitioners around the world. Eurofins has grown very strongly since its inception and its strategy is to continue expanding its technology portfolio and its geographic reach. Through R&D and acquisitions, the Group draws on the latest developments in the field of biotechnology and analytical chemistry to offer its clients unique analytical solutions. Shares in Eurofins Scientific are listed on the Euronext Paris Stock Exchange (ISIN FR0014000MR3, Reuters EUFI.PA, Bloomberg ERF FP). Job Description POSITION TITLE: Site Leader REPORTING TO: Regional IT Director, AMEA and Global IT Delivery Centre Director WORKING LOCATION: Indore or Coimbatore We are currently hiring a Site Leader who will be responsible for setting up and managing the daily operations of IT Delivery Centre in Indore or Coimbatore, overseeing the growth of this new facility in alignment with regional & group leadership, company goals, policies, and culture. This role requires a strategic thinker and strong people manager who can lead cross-functional teams, drive operational excellence, and foster a high-performance environment. Key Responsibilities: IT Delivery Centre Leadership. Setup an IT Delivery centre, primarily catering to s/w development, maintenance and IT support operations in accordance with group IT Delivery centre guidance Serve as the senior-most representative at the site, fostering a positive culture aligned with company values. Collaborate with regional and global leadership in a matrix organization to implement corporate initiatives and ensure timely compliances with group expectations. Drive operational efficiencies through process improvements, effective resource management, implementation of relevant & specific site policies in alignment with group leadership and local regulations. Oversee site performance metrics, including SLAs, KPIs, Hiring pipelines, attritions, and employee engagement etc. Serve as the highest point of contact for any site level decisions, and escalations related to financials, operations, technology, and people. Build and maintain relationships with local vendors, partners, and community organizations for the growth of site (i.e. local IT Delivery centre). Plan, forecast, present annual budgets related to site operations, managing and implementing the annual operating plan as per the approved site budget and in coordination with group IT Controlling teams. Ensure data privacy and site compliances in accordance with local laws, safety regulations, and group IT security policies. Operational Leadership Define, structure, lead and take operational accountability of service offerings. Oversee daily operations of delivery functions, including resource planning, service delivery, and client satisfaction. Ensure effective governance, SLA/KPI adherence, and continuous improvement in delivery processes. Foster a high-performance culture driven by innovation, agility, accountability, and excellence. Pro-active in cost optimizations to ensure the maximum value for a pre-agreed service level. Develop, Implement and manage internal service contracts, service availabilities and related results. Enable and implement relevant reporting systems to publish relevant KPIs & updates to the customers and stakeholders. Qualifications: Bachelor’s degree in information technology, Business Administration, or related field; master’s degree preferred. Minimum of 15 to 20 years of experience in IT Delivery centre operations, facilities management, or people leadership. Hands on experience in setting up and managing IT Delivery centre in Indore or Coimbatore in the last 5 years. Proven leadership experience managing cross-functional teams and large-scale technology initiatives. Excellent interpersonal, communication, and conflict resolution skills. Strong analytical and problem-solving abilities. Knowledge of IT s/w development, maintenance & support operations, IT Infrastructure and IT security practices. Experience in managing multi-cultural and geographically distributed teams is a plus. Preferred Skills: Someone with hands on experience in setting up and managing operations of IT Delivery centre in Tier-II locations (i.e., Indore and/or Coimbatore in particular). An analytical mindset who identifies new improvement opportunity in his/her ongoing scope and responsibilities. Project Management skills and preferably with PMP or Prince2 certifications Sound knowledge of ITIL framework Experienced in leading Agile or Lean environments Proficiency in collaboration tools (e.g., Microsoft 0365 suite, MS Teams, Slack, Jira, Confluence etc.) Hands on experience in Annual budget planning and delivering within the agreed budget Travel: Occasional domestic/international travel required

Respected Sir/Mam, We are Hiring Senior Resident Medicine Surgeon Gynecology Physiology Pathology Microbiology ENT Pharmacology Anatomy Ophthalmology for Medical College in Pondicherry Qualification: MBBS & MD/MS Vaibhav Singh whatsapp-8423159700

Job Title: Director – Clinical Research Location: Greater Noida Experience Required: 5–10 Years in Clinical Research Educational Qualification: Ph.D., MD, or MPH (or equivalent) in a relevant scientific discipline (e.g., Biology, Medicine, Pharmacy) Budgeted CTC: Upto ₹36 LPA Employment Type: Full-Time | Onsite About the University: Our Client is a NAAC A+ accredited, multidisciplinary university in Greater Noida that fosters global learning, cutting-edge research, and innovation. With over 20,000 students from 85+ countries, the university is one of India’s leading education providers with a focus on holistic and interdisciplinary education. Position Overview: We are seeking a highly qualified and experienced Director – Clinical Research to lead and oversee clinical trials and research initiatives within our organization. The ideal candidate will have strong expertise in clinical research, particularly in oncology , and possess a deep understanding of global clinical trial regulations, study design, and execution. This role requires strategic thinking, team leadership, and the ability to manage multiple concurrent research projects in a fast-paced environment. Key Responsibilities: Leadership & Strategy: Lead and oversee all clinical research activities, ensuring alignment with organizational goals and regulatory requirements. Develop and implement clinical trial strategies, including protocol design, study planning, and risk mitigation. Provide mentorship and guidance to clinical research teams and collaborators. Clinical Trial Management: Oversee the planning, initiation, execution, and close-out of clinical trials. Ensure compliance with FDA regulations, ICH GCP guidelines, and applicable local regulations. Coordinate with CROs, investigators, and site staff for study implementation and monitoring. Regulatory & Compliance: Prepare and review clinical protocols, Investigator Brochures (IBs), informed consent forms, and regulatory submissions. Ensure ethical and regulatory compliance throughout all research activities. Data Analysis & Reporting: Collaborate with biostatisticians and data managers to analyze clinical data. Interpret study results and oversee preparation of study reports, publications, and regulatory documentation. Stakeholder Engagement: Liaise with cross-functional departments including medical affairs, pharmacovigilance, and R&D. Represent the organization in scientific meetings, regulatory discussions, and industry forums. Desired Candidate Profile: Educational Background: Ph.D., MD, or MPH in a relevant scientific field such as biology, medicine, pharmacology, pharmacy, or public health. Experience: Minimum 5–10 years of progressive experience in clinical research, with a strong track record in managing trials from concept to completion. Prior experience in oncology research is highly preferred. Experience working with global clinical trial regulations, particularly FDA and ICH GCP. Skills & Knowledge: Excellent knowledge of clinical trial design, regulatory pathways, and protocol development. Proficiency in statistical software (e.g., SAS, SPSS, R), data management tools (e.g., Medidata, Oracle Clinical), and relevant e-clinical systems. Strong communication, leadership, and problem-solving skills. Ability to work collaboratively in a cross-functional environment. Key Competencies: Strategic thinking and project leadership Clinical compliance and operational excellence Scientific acumen and data interpretation Team mentoring and stakeholder management Attention to ethical and quality standards Application Process: Interested candidates may send their updated CV and a brief statement of clinical leadership experience to: [connect@coral-ridge.com] | Subject Line: Application for Director – Clinical Research Shortlisted candidates will be contacted for an in-depth discussion and final round of interaction. Job Types: Full-time, Permanent Pay: ₹3,000,000.00 - ₹4,000,000.00 per year

Establish product presence with stakeholders through scientific information exchange in oncology drugs in hard-to-treat cancers in metastatic pancreatic cancer, digestive cancers, brain tumors, hematologic cancers,leukemia, pediatric cancers etc. Required Candidate profile Pharm D/MD (Pharmacology)/ Pharm D industry medical affairs experience in oncology with exposure to Radio Onco/Medical Onco/Solid tumors/Neuro surgery.Industry Field working essential in Pharma.

We are seeking life science graduates interested in building a long-term career in the Clinical Research domain. This opportunity is part of our industry-integrated Clinical Research Training Program designed to prepare candidates for roles such as CRA, CRC, and Drug Safety Associate . Role Responsibilities (Post-Training Readiness) Understand and support clinical trial processes, site coordination, and documentation Learn Good Clinical Practices (GCP), ICH guidelines, and regulatory frameworks Monitor data collection and compliance Collaborate with CROs, hospitals, and research organizations (Post-placement) Eligibility Criteria Education: B.Sc, B.Pharm, M.Sc, BDS, BPT, BHMS, BAMS, Nursing, MBBS Background: Life Sciences or Healthcare domain Experience: 02 years Location: Open to all Indian cities (program delivered online & offline) Must have interest in Clinical Trials, Research, Pharmacovigilance, or Regulatory Affairs

Alvotech is looking to hire a Senior Principal Scientist to lead and innovate within our clinical pharmacology team . This role offers the opportunity to make a significant impact on our clinical programs and contribute to the development of groundbreaking therapies. We seek a highly experienced scientist with a deep understanding of clinical pharmacology, PKPD analysis, and population modelling. Your expertise will be crucial in designing and planning clinical trials, developing regulatory documents, and ensuring compliance with global standards. At Alvotech, you will play a key role in our mission to improve global access to affordable medicines. You will be part of a dynamic team dedicated to scientific excellence and innovation, enjoying a collaborative work environment, opportunities for professional growth, and the chance to contribute to transformative therapies. Please note that international travel may be required to support departmental activities. Scope & Responsibilities: Lead clinical pharmacology activities for assigned clinical programs/trials. Develop and revise relevant sections of regulatory documents and deliverables. Develop the clinical pharmacology strategy, briefing book, study design, and protocol development. Collaborate with biostatisticians on Statistical Analysis Plans (SAPs) and review mock-up displays for tables, listings, and figures. Provide statistical consultation to clinical teams and support decision-making processes. Ensure GCP compliance and high-quality standards for Alvotech's sponsored clinical trials. Support internal and external resources in assay development and validation. Work independently and as part of a multifunctional team to achieve project deliverables. Job Requirements: Master's Degree in a related discipline (PhD in Clinical Pharmacology or related discipline with relevant experience is desirable). Minimum 10 years of experience in clinical trials or clinical pharmacology. Expertise in PKPD analysis, population modelling, and simulation. Experience with large molecules and biosimilars is desired. Excellent written and verbal communication skills. Proficiency in technical software such as Phoenix, WinNonlin, SAS, R, Monolix, and NONMEM. Strong organizational and management skills. Deep knowledge of ICH-GCP and regulatory guidelines. Proven ability to collaborate effectively within cross-functional teams. Strong interpersonal skills, including the ability to build team spirit and communicate openly. What we offer: An inspiring challenge to work with great co-workers on ambitious projects that change people's lives. The chance to be part of a global and fast-growing company. An international work culture that encourages diversity, collaboration, and inclusion. Positive, flexible, and innovative work environment. A clear and developed organizational structure. Training and global opportunities to advance. A good work-life balance. Home internet and home office equipment. Why Alvotech At Alvotech, we are passionate about improving lives by increasing access to affordable biologics. We’re purpose-driven and committed to fostering an inclusive and diverse working environment that encourages curiosity, ingenuity and simplicity. We want our employees to feel inspired in their careers, challenged by interesting and meaningful work and empowered to succeed in an agile environment. True to our Icelandic roots, we also believe that integrity, gender equality, and fairness are foundational. We strive to bring together the brightest minds regardless of backgrounds and beliefs, to deliver to our partners and patients around the world. Let’s create a healthier world together, through affordable biologic medicines.

Pharmacist (Immediate Joiners) Designation: Pharmacist Gender: Male Work Experience: 0-4 Years in Retail / Hospital Attached Medical Store Job Description: Dispensing prescribed drugs as per physicians instructions / hospital’s indent. As Pharmacist attend to patients, manage high volume of prescriptions & get involved in operational activities. Check prescriptions to ensure that there are no errors & that they are appropriate & safe for the individual/ patient as per their need. Contacting referring physicians with the questions regarding prescription. Handle customer complaints/ queries & counselling/ resolving patient’s issues, whenever needed. Comply with all applicable rules and regulations of D&C Act and SOPs of the organization. Participate in daily / weekly / monthly stock checking processes & separate expired medicines on a periodic basis. Oversee & maintain a safe & clean working environment. Contributing to team effort by accomplishing related results as needed. Completing pharmacy operational requirements by organizing & directing workflow. Verifying bill entries, charges, discounts, inspections & tally with the cash inflow of each day. Requirements: 1. D. Pharm/ B. Pharm/ M. Pharm. From an accredited university. 2. Pharmacist License Critical Skills: 1. Analyzing information & stock time to time 2. Administering medication 3. Verbal communication 4. Pharmacology 5. Managing Process 6. Quality service 7. Attention to detail 8. Team work 9. Coordination 10. Professional Ethics Job Types: Full-time, Permanent, Fresher Pay: From ₹350,000.00 per year Benefits: Cell phone reimbursement Health insurance Leave encashment Life insurance Paid time off Provident Fund Schedule: Day shift Evening shift Morning shift Night shift Rotational shift Supplemental Pay: Overtime pay Performance bonus Shift allowance Yearly bonus Work Location: In person