1112 Pharmacology Jobs - Page 26

8810348617 @Well known Private Medical colleges - Call- 8810348617 Pharmacology - SR /AP/Associate professor/ professor Qualifications - MD/DNB Pharmacology Locations - Lucknow / Ghaziabad / Jaipur / Udaipur/ Mathura / Hapur /Bhopal /Lucknow /Maharashtra /Rajasthan /Muzaffarnagar / Bareilly Package- Negotiable If interested, please call / WhatsApp on 8810348617 Email- hr15@pathfindersglobal.com You can share your spouse CV if He/ She is doctor. (Kindly share references if any, also circulate in your groups for Better Reach) Thanks & Regards Roshni 8810348617

Urgent vacancies for SR, Assistant professor,Associate professor , with good experience in medical college at a medical college in Meerut, UP Salary as per industry Norms,

Vice Principal: Parul University is seeking candidates who will be responsible for driving academic and administrative excellence within the faculty. Key responsibilities include ensuring the efficient conduct of classes, examinations, and technical training programs, fostering innovation and research, strengthening industry partnerships, and promoting international collaborations and exchange programs. Eligibility criteria: PhD degree with Minimum 15 years experience in Teaching/industry/Research out of which 5 years must be at the level of Professor. Administrative experience is desirable

Job Description: Assistant Professor Pharmacy Position: Assistant Professor Pharmacy Department: Pharmaceutical Sciences Location: Rama University , Mandhana Job Type: Full-Time. Position Overview: Rama University ,Kanpur is seeking a dedicated, motivated, and passionate individual to join our faculty as an Assistant Professor in the Department of Pharmacy. The successful candidate will have a minimum of 3 years of teaching experience in pharmaceutical sciences or related fields. This position offers an opportunity to contribute to the academic, research, and clinical education of future pharmacists, while advancing the department's goals and fostering innovation in pharmaceutical education. Key Responsibilities: Teaching: Deliver undergraduate and/or graduate-level courses in the field of pharmacy (Pharmaceutical Sciences, Pharmacology, Pharmacokinetics, Pharmaceutical Chemistry, etc.). Develop course materials, including syllabi, assignments, and assessments. Foster a positive learning environment that promotes student engagement and success. Mentor and advise students on academic and career-related matters. Contribute to the development of new curriculum and educational programs. Research: Conduct and publish research in pharmaceutical sciences or related areas. Secure external funding for research projects through grants and other funding opportunities. Supervise and mentor graduate students in research. Service: Participate in departmental, university, and community service activities. Contribute to the development of academic policies and programs within the department. Serve on academic committees and engage in continuous professional development. Qualifications: Education: Ph.D. in Pharmacy, Pharmaceutical Sciences, Pharmacology, or a related field. Candidates with a Pharm.D. and additional research experience may also be considered. Experience: A minimum of 3 years of teaching experience at the university level, preferably in a pharmacy-related field. A demonstrated record of research and scholarly activity. Skills: Strong communication and interpersonal skills. Ability to engage and motivate students in a classroom setting. Proficiency in using modern teaching technologies and learning management systems. Ability to work collaboratively with colleagues, students, and external partners. Preferred Qualifications: Experience in curriculum development and course design. A track record of research publications in peer-reviewed journals. Experience with securing research funding.

About Company ASG Eye Hospitals is a chain of super specialty eye hospitals in India. It offers a comprehensive range of eye care services including treatment and surgeries of Retina, Cataract, Squint, Oculoplasty, Cornea, Lasik, ICL, Glaucoma, and Paediatric Ophthalmology. Currently, the group has 165+ Eye Hospitals across 83+ cities in India. Role - Executive - Pharmacist Location - Kolkata Job Responsibilities Provide advice about health issues, symptoms and medications in response to customer enquiries. Process prescriptions and dispense correct medication. Ordering, selling and controlling medicines and other stock. Manage inventory to ensure an adequate supply of medications. Managing budgets Keeping statistical and financial records Preparing publicity materials and displays Counsel patients on proper medication and side effects. Desired Candidate Profile D.Pharm / B.Pharm Must be a registered Pharmacist from the State Pharmacy Council. Good Communication Skills. Must have Basic computer knowledge. Perks and Benefits + Performance Based Incentives Interested candidates mail your resume along with below details to or WhatsApp the same on 8875022129 Total Experience - Current CTC - Expected CTC - Notice Period -

Job Summary: As part of the team, you'll be responsible for extracting and categorizing pharmacological data from a variety of journals and research papers. Roles and Responsibilities: • Reading and understanding research papers from leading pharmacology journals. • Extracting key datathings like drug names, mechanisms of action, side effects, and pharmacokinetic details. • Categorizing this data using a user-friendly tool, ensuring it’s structured and ready for use by the people who need it. Skills and Competencies: • Capable of understanding patents/articles related to different areas of chemistry (main focus: Pharmacology). • Ability to deal with the excerption / extraction of pharmacological data from articles and patents. • Serves as an educational resource to the team to assist with pharmacological assays. • Participates and plans activities as needed to maintain an awareness of the current and emerging quality issues of the organization. • Has an ability to explain and discuss why and how the error occurred during feedback and training discussions • Able to analyze an error and identify preventive measures • Has a high-level technical knowledge to edit according to specifications and main controlling areas • Ability to face quality issues with customer, internal and/or external, write and convey appropriately and independently, in order to improve and promote project.

Job Summary: As part of the team, you'll be responsible for extracting and categorizing pharmacological data from a variety of journals and research papers. Roles and Responsibilities: • Reading and understanding research papers from leading pharmacology journals. • Extracting key datathings like drug names, mechanisms of action, side effects, and pharmacokinetic details. • Categorizing this data using a user-friendly tool, ensuring it’s structured and ready for use by the people who need it. Skills and Competencies: • Capable of understanding patents/articles related to different areas of chemistry (main focus: Pharmacology). • Ability to deal with the excerption / extraction of pharmacological data from articles and patents. • Serves as an educational resource to the team to assist with pharmacological assays. • Participates and plans activities as needed to maintain an awareness of the current and emerging quality issues of the organization. • Has an ability to explain and discuss why and how the error occurred during feedback and training discussions • Able to analyze an error and identify preventive measures • Has a high-level technical knowledge to edit according to specifications and main controlling areas • Ability to face quality issues with customer, internal and/or external, write and convey appropriately and independently, in order to improve and promote project.

We are looking for an MSL- Oncology for a Global Pharmaceutical MNC Profile: Medical Science Liaison- Oncology Location: Delhi/ Kolkata (2 openings) Qualification: MD Pharmacology with minimum 6 months of experience in solid cancers MDS/ PhD with minimum 1yr of Oncology experience as MSL/RMA MD Pharmacology with clinical experience in Oncology can apply too Job Purpose: The Medical Science Liaison (MSL) will establish the company’s medical affairs presence with external stakeholders through scientific exchange and research support in oncology. The focus will be on licensed and non-licensed products for hard-to-treat cancers, including metastatic pancreatic cancer, cholangiocarcinoma, digestive cancers (such as stomach cancer, pancreatic cancer, and cholangiocarcinoma), glioma, brain tumors, hematologic cancers (acute myeloid leukemia, acute lymphoblastic leukemia, and lymphoma), and pediatric cancers. This role is field-based, covering the India region. The MSL will communicate balanced therapeutic area-related, product-related, and clinical information to external stakeholders (e.g., physicians, academic institutions, hospital formulary committees), respond to unsolicited requests for medical information, facilitate research discussions, and bring key insights from the medical and scientific community to internal stakeholders. The role also involves ensuring compliance with all company procedures, confidentiality standards, and contributing to business success with a focus on patient safety. Principal Accountabilities: 1. Exchange of Medical and Scientific Information: Responsible for communicating fair and balanced therapeutic area-related, product-related, and clinical information to external stakeholders. Execute the scientific engagement plan in alignment with the Therapy Medical Plan. Proactively develop long-term peer-to-peer relationships with opinion leaders and relevant stakeholders. Respond to unsolicited requests for medical information, including off-label data, related to marketed products and pipeline products. Provide clinical and medical presentations to external stakeholders as needed. Disseminate updates from scientific meetings and report information of strategic interest to cross-functional teams. 2. Supporting Clinical Research: Support ongoing and future Medical Affairs Company-Sponsored Studies, providing country-level review of proposed research site lists, attending site visits if necessary, and providing feedback to the line manager. Support unsolicited requests for investigator-initiated trials (IITs) proposals by offering appropriate investigator support as per company SOPs. Assist in the development and support of national disease registries and Real-World Evidence (RWE) projects as necessary. 3. Contributing to the Organization through Medical Expertise & Market Insights: Maintain up-to-date knowledge of scientific/medical developments in the relevant therapeutic area through literature searches, clinical papers, conferences, and other relevant events. Capture and share in-field insights to develop territorial Field Medical Plans and support medical and scientific strategies. Provide medical and scientific expertise to commercial partners within regulatory guidelines. Act as a field-based scientific and clinical reference for internal stakeholders (e.g., sales, market access) through training and ad-hoc support. 4. Cross-Functional Collaboration: Support the development of medical/scientific materials, ensuring content is reviewed and approved according to company policies. Contribute to the development and execution of the regional medical affairs strategy and action plan in collaboration with field departments such as Sales, Clinical Research, and Market Access. Keep medical representatives and their managers informed about the latest scientific developments. Support the market access strategy at a regional level, including hospital listings, in coordination with the market access manager. 5. Compliance with External Regulations and Company Policies: Maintain a high level of scientific, clinical, and environmental knowledge through courses, self-learning, and attendance at relevant meetings. Stay informed about regulations related to medical information services in the pharmaceutical industry. Ensure all activities comply with internal and external codes of conduct, prioritizing patient safety by following pharmacovigilance processes. Support the company’s reputation in the field by adhering to industry regulations. 6. Patient-In Activities: Support patient awareness initiatives, both physical and digital. Contribute to the Patient-In strategy, understanding the patient journey in coordination with therapeutic area experts, and set up Patient Support Programs (PSPs) to improve patient outcomes as per local regulations. General Administration: Complete all required administration within the specified timelines. Submit monthly reports and expenses by the second working day of each month. Ensure timely completion and submission of all required documentation to the Head Office as appropriate. Profile Requirements A] Minimum Requirements: Education: MBBS/MD Minimum 1-2 years of working experience in oncology. B] Indispensable Qualities: Strong ability to learn new subjects and environments comprehensively. Excellent written and spoken communication and presentation skills, with the ability to build and maintain collaborative relationships with opinion leaders, physicians, and other healthcare decision-makers. Substantial business acumen and autonomy in managing priorities and activities. Strong commitment to compliance with relevant rules and procedures, as well as scientific integrity and quality. Ability to manage cross-functional projects effectively. Leadership skills, emotional intelligence, active listening, and strength of conviction. Negotiation and problem-solving abilities. Proficiency in English is essential. Ability to innovate and execute strategies effectively. Relevant candidates can share their CV at pooja.j@domniclewis.com Show more Show less

About Eurofins: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and the environment safer, healthier and more sustainable. From the food you eat to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is a global leader in food, environmental, pharmaceutical and cosmetic product testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a network of over 1,000 independent companies in 54 countries, operating 900 laboratories. Performing over 450 million tests every year, Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. Eurofins is one of the fastest growing listed European companies with a listing on the French stock exchange since 1997. In FY 2021, Eurofins achieved a record revenue of over EUR 6.7 billion. Eurofins IT Solutions India Pvt Ltd (EITSI) is a fully owned subsidiary of Eurofins and functions as a Global Software Delivery Center exclusively catering to Eurofins Global IT business needs. The code shipped out of EITSI impacts the global network of Eurofins labs and services. The primary focus at EITSI is to develop the next generation LIMS (Lab Information Management system), Customer portals, e-commerce solutions, ERP/CRM system, Mobile Apps & other B2B platforms for various Eurofins Laboratories and businesses. Young and dynamic, we have a rich culture and we offer fulfilling careers. Job Description Position Overview: IT Application Monitoring and Observability team is global Eurofins team that provides knowledge on operation of IT Systems and IT Infrastructure. Over 61K+ Eurofins employees rely on the services that we are providing to conduct their daily operations. From basic application availability monitoring, through complex process analysis ending on advanced statical and ML/AI methods to proactively counteract any unexpected events that can negatively impact the business. Handling over 6TB of data daily our goals is to collect, process, and visualize data to provide knowledge in easy and understandable way to the end users. As a team member you will be responsible for handling operational activities and supporting other colleagues in maintaining our data pipelines. You will be also leading operational standups and manage ticket execution hence experience in people management would be an additional asset. Primary Skills (mandatory) Linux administration. Containerization concepts with Docker. Familiarity with Elastic stack (Elasticsearch, beats, Logstash). Secondary Skills (nice to have) Familiarity with Grafana tool is an advantage. Familiarity with data visualization and data story telling techniques is an advantage. People management and experience in ticket execution tracking. Additional experience with networking and security concepts would make your application to stand out. EXPERIENCE REQUIRED Minimum 4- 8 years of IT Professional Experience Personal profile Very good English communication skills (concise writing) Very good interpersonal relation skills. Able to engage and influence others to obtain enough follow up and attention. Drive continuous improvement efforts. Ability to work in a complex international environment. Eager to learn and continuously develop personal and technical capabilities. Consultant mindset. Qualifications Qualifications Bachelor’s degree in computer science, Information Technology, or a related field Languages: Fluent English Show more Show less

Company Description About Eurofins: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and the environment safer, healthier and more sustainable. From the food you eat to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is a global leader in food, environmental, pharmaceutical and cosmetic product testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a network of over 1,000 independent companies in 54 countries, operating 900 laboratories. Performing over 450 million tests every year, Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. Eurofins is one of the fastest growing listed European companies with a listing on the French stock exchange since 1997. In FY 2021, Eurofins achieved a record revenue of over EUR 6.7 billion. Eurofins IT Solutions India Pvt Ltd (EITSI) is a fully owned subsidiary of Eurofins and functions as a Global Software Delivery Center exclusively catering to Eurofins Global IT business needs. The code shipped out of EITSI impacts the global network of Eurofins labs and services. The primary focus at EITSI is to develop the next generation LIMS (Lab Information Management system), Customer portals, e-commerce solutions, ERP/CRM system, Mobile Apps & other B2B platforms for various Eurofins Laboratories and businesses. Young and dynamic, we have a rich culture and we offer fulfilling careers. Job Description Senior Software Engineer Eurofins IT Solutions, Bengaluru, Karnataka, India With 36 facilities worldwide, Eurofins BioPharma Product Testing (BPT) is the largest network of bio/pharmaceutical GMP product testing laboratories providing comprehensive laboratory services for the world's largest pharmaceutical, biopharmaceutical, and medical device companies. Behind the scenes, BPT is enabled by global engineering teams working on next-generation applications and Laboratory Information Management Systems(LIMS). These are sophisticated computer programs that will be used by our scientists, engineers, and technicians to document research, experiments, and procedures performed in our international network of laboratories. This role reports to a Manager. Required Experience and Skills Experience: 4 to 7 years of experience with developing end-to-end web applications using Microsoft stack of technologies. Strong working knowledge of Web application development using .NET, C#, Asp.net, MVC, WebAPI. Strong Working knowledge of Angular 2 or above, JavaScript, TypeScript, jQuery, HTML5 and CSS3. Good working knowledge of MSSQL – SQL etc. Experience with usage of TFS Familiar UI testing and Unit Testing (MS Test/ Jasmine/ MOQ/ NUnit/ Karma etc.) Good understanding of object-oriented programming (OOP) Strong working knowledge of SOLID principles and design patterns that includes Creational, Structural, Behavioral Strong experience in designing and working with n-tier architectures Able to provide technical recommendations and solve technical problems Should have working knowledge on Code review that includes, raising code review, resolve comment reviews, Closing code reviews. Should be aware of best practices in programming Should know how to troubleshoot performance-related issues, how to write efficient code and query, how to use SQL profiler Should have worked on at least one SOA (Service Oriented Architecture) project Should have worked in an AGILE practice methodology (preferably SCRUM) Additional Information Desirable Experience Strong orientation towards Performance tuning and optimization with Microsoft technologies Required Qualifications: Bachelors in Engineering, Computer Science or equivalent. Personal Skills: The successful candidate will have a self-motivated, get-it-done attitude; the ability to think critically; enjoy working with teams spread globally and across cultures; a desire to learn in new areas, working with uncertainties; and the discipline to pay attention to deadlines, details and quality. Good communication and interpersonal skills. Quick learner, strong troubleshooting skills PERFORMANCE APPRAISAL CRITERIA : Eurofins has a strong focus on Performance Management system. This includes quarterly calibrations, half-yearly reviews and annual reviews. The KPIs shall be set and may vary slightly between projects. These will be clearly communicated, documented during the first 30 days of your joining.

Job ID R-229394 Date posted 06/17/2025 Job Title: Senior Data Engineer Career Level: D Introduction to role: Are you ready to make a significant impact on patient outcomes and improve lives? At AstraZeneca, we are on a mission to become an AI and data-led enterprise. We are seeking a Senior Data Engineer to join our Predictive AI & Data team. This pivotal role involves driving transformative change by converting complex data into life-changing insights. You'll collaborate with leading experts and contribute to innovative solutions. Are you prepared to shape the future of a dynamic business in the technology space? If so, this opportunity is for you! Accountabilities: In this position, you will deliver tailored solutions to our Clinical Pharmacology & Safety Science colleagues, utilizing enterprise infrastructure and technology in alignment with AstraZeneca's "Bold Ambition" initiative for 2030. Your responsibilities will include gathering requirements from stakeholders, prototyping solutions, leading delivery (including testing and release), and collaborating closely with R&D IT, AI, and Bioinformatics teams. You will work with colleagues globally, primarily in Sweden, the United Kingdom, and the United States. Essential Skills/Experience: Relevant graduate degree: Bioinformatics, Computer Science, or Engineering Great interpersonal skills and a collaborative approach to delivery Ability to communicate effectively with different audiences (written and spoken) in English Ability to understand business needs and translate them into a solution Experience delivering scalable and well-engineered solutions across key elements of the data and analytics domain Excellent problem-solving, analytical, and critical thinking skills, with a keen attention to detail Strong data analysis, data visualization, and data engineering skills Strong programming skills in Python and other similar languages Experience in Unix, SQL databases, cloud computing (AWS), and HPC (High Performance Computing) Experience in machine learning, AI, and statistical data analysis Experience in data modeling, data warehousing, and data integration Familiarity with professional software engineering practices and tools (version control, CI/CD, automated testing) Desirable Skills/Experience: Experience with GenAI and Agentic workflows Experience architecting data platforms and data-driven solutions Experience in data processing, analysis, and visualization related to drug development processes, particularly clinical and pre-clinical Experience in data processing and analysis of omics data and bioinformatics in general Experience in developing methods and algorithms in the data engineering and analytics domain When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, curiosity meets courage as we explore the possibilities of science to tackle some of the world's most complex diseases. Our inclusive environment fosters collaboration with academia and biotech partners, empowering us to push boundaries and accelerate progress. With open doors and diverse voices, we are committed to making a difference by integrating digital, data science, and AI into our scientific endeavors. Here, lifelong learning thrives alongside cutting-edge innovations. Ready to take the next step? Apply now to join our team! AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. Senior Data Engineer Posted date Jun. 17, 2025 Contract type Full time Job ID R-229394 APPLY NOW Why choose AstraZeneca India? Help push the boundaries of science to deliver life-changing medicines to patients. After 45 years in India, we’re continuing to secure a future where everyone can access affordable, sustainable, innovative healthcare. The part you play in our business will be challenging, yet rewarding, requiring you to use your resilient, collaborative and diplomatic skillsets to make connections. The majority of your work will be field based, and will require you to be highly-organised, planning your monthly schedule, attending meetings and calls, as well as writing up reports. Who do we look for? Calling all tech innovators, ownership takers, challenge seekers and proactive collaborators. At AstraZeneca, breakthroughs born in the lab become transformative medicine for the world's most complex diseases. We empower people like you to push the boundaries of science, challenge convention, and unleash your entrepreneurial spirit. You'll embrace differences and take bold actions to drive the change needed to meet global healthcare and sustainability challenges. Here, diverse minds and bold disruptors can meaningfully impact the future of healthcare using cutting-edge technology. Whether you join us in Bengaluru or Chennai, you can make a tangible impact within a global biopharmaceutical company that invests in your future. Join a talented global team that's powering AstraZeneca to better serve patients every day. Success Profile Ready to make an impact in your career? If you're passionate, growth-orientated and a true team player, we'll help you succeed. Here are some of the skills and capabilities we look for. 0% Tech innovators Make a greater impact through our digitally enabled enterprise. Use your skills in data and technology to transform and optimise our operations, helping us deliver meaningful work that changes lives. 0% Ownership takers If you're a self-aware self-starter who craves autonomy, AstraZeneca provides the perfect environment to take ownership and grow. Here, you'll feel empowered to lead and reach excellence at every level — with unrivalled support when you need it. 0% Challenge seekers Adapting and advancing our progress means constantly challenging the status quo. In this dynamic environment where everything we do has urgency and focus, you'll have the ability to show up, speak up and confidently take smart risks. 0% Proactive collaborators Your unique perspectives make our ambitions and capabilities possible. Our culture of sharing ideas, learning and improving together helps us consistently set the bar higher. As a proactive collaborator, you'll seek out ways to bring people together to achieve their best. Responsibilities Job ID R-229394 Date posted 06/17/2025 Job Title: Senior Data Engineer Career Level: D Introduction to role: Are you ready to make a significant impact on patient outcomes and improve lives? At AstraZeneca, we are on a mission to become an AI and data-led enterprise. We are seeking a Senior Data Engineer to join our Predictive AI & Data team. This pivotal role involves driving transformative change by converting complex data into life-changing insights. You'll collaborate with leading experts and contribute to innovative solutions. Are you prepared to shape the future of a dynamic business in the technology space? If so, this opportunity is for you! Accountabilities: In this position, you will deliver tailored solutions to our Clinical Pharmacology & Safety Science colleagues, utilizing enterprise infrastructure and technology in alignment with AstraZeneca's "Bold Ambition" initiative for 2030. Your responsibilities will include gathering requirements from stakeholders, prototyping solutions, leading delivery (including testing and release), and collaborating closely with R&D IT, AI, and Bioinformatics teams. You will work with colleagues globally, primarily in Sweden, the United Kingdom, and the United States. Essential Skills/Experience: Relevant graduate degree: Bioinformatics, Computer Science, or Engineering Great interpersonal skills and a collaborative approach to delivery Ability to communicate effectively with different audiences (written and spoken) in English Ability to understand business needs and translate them into a solution Experience delivering scalable and well-engineered solutions across key elements of the data and analytics domain Excellent problem-solving, analytical, and critical thinking skills, with a keen attention to detail Strong data analysis, data visualization, and data engineering skills Strong programming skills in Python and other similar languages Experience in Unix, SQL databases, cloud computing (AWS), and HPC (High Performance Computing) Experience in machine learning, AI, and statistical data analysis Experience in data modeling, data warehousing, and data integration Familiarity with professional software engineering practices and tools (version control, CI/CD, automated testing) Desirable Skills/Experience: Experience with GenAI and Agentic workflows Experience architecting data platforms and data-driven solutions Experience in data processing, analysis, and visualization related to drug development processes, particularly clinical and pre-clinical Experience in data processing and analysis of omics data and bioinformatics in general Experience in developing methods and algorithms in the data engineering and analytics domain When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, curiosity meets courage as we explore the possibilities of science to tackle some of the world's most complex diseases. Our inclusive environment fosters collaboration with academia and biotech partners, empowering us to push boundaries and accelerate progress. With open doors and diverse voices, we are committed to making a difference by integrating digital, data science, and AI into our scientific endeavors. Here, lifelong learning thrives alongside cutting-edge innovations. Ready to take the next step? Apply now to join our team! AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. APPLY NOW Explore the local area Take a look at the map to see what’s nearby. Reasons to Join Thomas Mathisen Sales Representative Oslo, Norway Christine Recchio Sales Representative California, United States Stephanie Ling Sales Representative Petaling Jaya, Malaysia What we offer We're driven by our shared values of serving people, society and the planet. Our people make this possible, which is why we prioritise diversity, safety, empowerment and collaboration. Discover what a career at AstraZeneca could mean for you. Lifelong learning Our development opportunities are second to none. You'll have the chance to grow your abilities, skills and knowledge constantly as you accelerate your career. From leadership projects and constructive coaching to overseas talent exchanges and global collaboration programmes, you'll never stand still. Autonomy and reward Experience the power of shaping your career how you want to. We are a high-performing learning organisation with autonomy over how we learn. Make big decisions, learn from your mistakes and continue growing — with performance-based rewards as part of the package. Health and wellbeing An energised work environment is only possible when our people have a healthy work-life balance and are supported for their individual needs. That's why we have a dedicated team to ensure your physical, financial and psychological wellbeing is a top priority. Inclusion and diversity Diversity and inclusion are embedded in everything we do. We're at our best and most creative when drawing on our different views, experiences and strengths. That's why we're committed to creating a workplace where everyone can thrive in a culture of respect, collaboration and innovation.

Company Description Soundarapandian Bone and Joint Hospital, established in 1983 as a pioneer in orthopaedic care in Chennai, is dedicated to providing superior bone and joint care. With over 40 years of expertise, our team of orthopaedic surgeons and specialists collaborate to treat a wide range of conditions, all while prioritizing patient well-being and setting new benchmarks in orthopaedics. We integrate advanced medical technology with a compassionate, patient-first philosophy to ensure every patient feels cared for like family. Role Description This is a full-time on-site role for a Pharmacist based in Chennai at Soundarapandian Bone and Joint Hospital. The Pharmacist will be responsible for dispensing medications, providing drug information to patients and healthcare professionals, ensuring compliance with pharmacy laws and regulations, and collaborating with the healthcare team to optimize patient care. Qualifications Strong knowledge of pharmacology, medication management, and drug interactions Experience in dispensing medications and providing drug information Attention to detail and accuracy in pharmacy tasks Excellent communication and interpersonal skills Ability to work collaboratively in a healthcare team Pharmacist license in the state of Tamil Nadu Experience in a hospital or clinical setting is a plus Bachelor's degree in Pharmacy Show more Show less

Skills: Pharmaceutical Sciences, Pharmacology, Pharmaceutics, Pharmacy Practice, Pharm D, Pharmacognosy, Company Overview Cheran Group of Institutions, was established in 1991 by the Cheran Foundation Trust. The institution is dedicated to providing quality education through diverse educational entities. Job Overview We are seeking an Assistant Professor for our Pharmacy College in Coimbatore. This role requires a candidate with 1 to 3 years of experience in teaching at the college or university level. As an Assistant Professor, you will be responsible for delivering high-quality lectures, conducting research, and mentoring students in their academic pursuits. This is a full-time position in our prestigious institution. Roles And Responsibilities Deliver lectures and facilitate engaging discussions in the field of Pharmacy Design and develop curriculum and teaching materials that align with industry standards Conduct research and publish scholarly articles in reputable journals Provide mentorship and guidance to students in their academic pursuits Assess student performance and provide constructive feedback Participate in faculty meetings, committees, and other institutional activities Stay updated with the latest developments and trends in the field of Pharmacy Qualifications And Skills 1 to 3 years of experience in teaching at the college or university level M Pharm with/without Ph.D. in Pharmaceutics or Pharmacology or Pharmacy Analysis/Chemistry, Pharmacognosy or Practice. Strong communication and mentoring skills Proven ability to conduct research and publish scholarly articles Excellent organizational and collaborative skills Passionate about teaching and dedicated to student success Proactive and problem-solving mindset Show more Show less

Skills: Pharmaceutical Sciences, Pharmacology, Pharmaceutics, Pharmacy Practice, Pharm D, Pharmacognosy, Company Overview Cheran Group of Institutions, was established in 1991 by the Cheran Foundation Trust. The institution is dedicated to providing quality education through diverse educational entities. Job Overview We are seeking an Assistant Professor for our Pharmacy College in Coimbatore. This role requires a candidate with 1 to 3 years of experience in teaching at the college or university level. As an Assistant Professor, you will be responsible for delivering high-quality lectures, conducting research, and mentoring students in their academic pursuits. This is a full-time position in our prestigious institution. Roles And Responsibilities Deliver lectures and facilitate engaging discussions in the field of Pharmacy Design and develop curriculum and teaching materials that align with industry standards Conduct research and publish scholarly articles in reputable journals Provide mentorship and guidance to students in their academic pursuits Assess student performance and provide constructive feedback Participate in faculty meetings, committees, and other institutional activities Stay updated with the latest developments and trends in the field of Pharmacy Qualifications And Skills 1 to 3 years of experience in teaching at the college or university level M Pharm with/without Ph.D. in Pharmaceutics or Pharmacology or Pharmacy Analysis/Chemistry, Pharmacognosy or Practice. Strong communication and mentoring skills Proven ability to conduct research and publish scholarly articles Excellent organizational and collaborative skills Passionate about teaching and dedicated to student success Proactive and problem-solving mindset Show more Show less

Overview Cactus Life Sciences is a remote-first organization, and we embrace an accelerate from anywhere culture. You may be required to travel to our Mumbai office based on business requirements or for company/team events. If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you. Responsibilities Use scientific expertise to develop (write, proofread, and data-check) high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client needs with excellent attention to detail under the guidance of the scientific leads. Liaise and build trusting and professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders including authors, reviewers and key opinion leaders across therapeutic areas - learning to anticipate their needs. Effectively and proactively communicate with team members, authors/faculty, clients and vendors. Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives. Attend client and other external meetings and supporting senior team members as needed. Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans. You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date. Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines. Share best practices and client preferences, thereby contributing to skill development within the medical communications team. Qualifications And Prerequisites 1-3 years of experience in relevant fields of scientific writing. PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD OR MPharm/M.Sc with a good understanding of clinical research and medical communication. Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills. Ability to adapt writing style to different materials and target audiences. Basic knowledge of biostatistics. Literature reviewing and evaluation capabilities. Very good working knowledge of MS Office. Application Process Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds. For this role, the process starts with a Technical Interview with the Hiring Managers, followed by a Technical Assessment, where candidates will have agreed upon timeline to complete the task. The final round will be the HR Interview. All interactions will be conducted virtually via MS Teams. Equal Opportunity Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic. Accelerating from Anywhere As a remote-first organization, these are essential attributes we look for in all our candidates. Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently. Documenting work that brings everyone on the same page. Maturity to choose between synchronous and asynchronous collaboration. Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status. About CACTUS At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do. Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide. Show more Show less

Designs and delivers lectures and laboratory sessions on pharmacology topics, assesses student performance, develops and updates course materials, and engages in research and scholarly activities

Job description: Cactus Life Sciences is a remote-first organization, and we embrace an accelerate from anywhere culture. You may be required to travel to our Mumbai office based on business requirements or for company/team events. If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you. Job responsibilities: Use scientific expertise to develop (write, proofread, and data-check) high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client needs with excellent attention to detail under the guidance of the scientific leads. Liaise and build trusting and professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders including authors, reviewers and key opinion leaders across therapeutic areas - learning to anticipate their needs. Effectively and proactively communicate with team members, authors/faculty, clients and vendors. Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives. Attend client and other external meetings and supporting senior team members as needed. Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans. You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date. Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines. Share best practices and client preferences, thereby contributing to skill development within the medical communications team. #LI-Remote Qualifications and prerequisites: 1-3 years of experience in relevant fields of scientific writing. PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD OR MPharm/M.Sc with a good understanding of clinical research and medical communication. Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills. Ability to adapt writing style to different materials and target audiences. Basic knowledge of biostatistics. Literature reviewing and evaluation capabilities. Very good working knowledge of MS Office. Application process: Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds. For this role, the process starts with a Technical Interview with the Hiring Managers, followed by a Technical Assessment, where candidates will have agreed upon timeline to complete the task. The final round will be the HR Interview. All interactions will be conducted virtually via MS Teams. Equal Opportunity Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic. Accelerating from Anywhere As a remote-first organization, these are essential attributes we look for in all our candidates. Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently. Documenting work that brings everyone on the same page. Maturity to choose between synchronous and asynchronous collaboration. Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status. About Us: At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do. Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.

HIRING!! Raisoni Group of Institutions is hiring for teaching faculty. Need Associate / Assistant Professor for Pharmacy The applicant must fulfill the requirements mentioned below: Qualification Requirement: Applicant must have a Ph.D and M.Pharma. Specializations: 1. Pharmacology 2. Pharmaceutical Chemistry 3. Pharmacognosy JOB RESPONSIBILITY: Academic teaching at UG/PG level. Programme and curriculum design and development. Academic Administration Quality assurance and academic research. Any other work assigned by higher authority. Job Location: Saikheda (Chhindwara) Madhya Pradesh Interested and eligible candidates can mail their Cvs at samiksha.landge@raisoni.net Job Type: Full-time Schedule: Day shift Work Location: In person

On papers/Ghost faculty- All Non Clinical Subjects SR/AP/Associate/Professor @Medical college- Call- 7827524074 For ON PAPERS Qualifications-DNB/Md Locations- Lucknow/ Bhopal If interested, please call / WhatsApp on 7827524074 Email- hr21pathfinders@gmail.com You can share your spouse CV if He/ She is doctor. (Kindly share references if any, also circulate in your groups for Better Reach) Thanks & Regards Kirti

About Alkem: Alkem Laboratories Limited is an Indian multinational pharmaceutical company headquartered in Mumbai, that manufactures and sells pharmaceutical generics, formulations and nutraceuticals in India and globally over 50 countries. We have consistently been ranked amongst the five pharmaceutical companies in India. Our portfolio includes illustrious brands like Clavam, Pan, Pan-D, and Taxim-O, which feature amongst the top 50 pharmaceutical brands in India. Job Purpose: To actively contribute to the organization/division by taking responsibility for the scientific, technical and ethical soundness of all policies, statements and endeavors. To support the division medically in all activities related to the portfolio and provide high quality and timely service to internal and external stake holders. Responsibilities: To actively support development of promotion of allocated portfolio under supervision from the Line manager or the mentor, provide strategic inputs and support towards creation of marketing/brand plans/medical development plans, and towards design and execution of medical-marketing programs/clinical programs, including initiatives to enhance access to medicines Under supervision from the Line manager or mentor, create/review promotional, training, and Continuing Medical Education (CME) material in compliance with relevant industry codes and medical correctness In consultation with the Line manager or mentor, participate/facilitate/conduct customized promotional/educational interactions with Key Opinion Leaders (KOLs). These interactions include, but are not limited to, customer launch meetings, advisory boards, CME programs, scientific symposia, institutional presentations, medical projects and studies In consultation with concerned stakeholders plan research projects and develop / review / approve protocol synopsis/final protocols/supporting documents per need Provide useful, timely, accurate, and balanced medical information to internal (sales staff) and external (HCPs) customers, in adherence to relevant SOPs/policies Impart medical training to new sales staff on basic sciences/ TAs/assigned products. Provide refresher training to sales staff through ongoing training initiatives. Provide pre-launch and launch training to sales staff for new products Support New Product Evaluation (NPE), Marketing, and Business Development colleagues with medical evaluation and recommendations on commercial opportunities with new products. Support organization efforts at developing local formulations/line extensions through literature search/recommendations Support regulatory team by means of writing/revising/reviewing labeling documents for products as per relevant SOPs Support Pharmacovigilance activities by documentation and reporting of Adverse Events in a timely manner. Qualification : MBBS & MD Pharmacology (Mandatory) Experience : 1 to 3 years of experience in medico marketing Show more Show less

Position: Pharmacy Executive Company Website: https://onehealthassist.com/ Company LinkedIn: https://in.linkedin.com/company/one-health-assist Working time: Monday-Saturday between 10AM-7PM-(Onsite) Location:- Andheri West, Mumbai, Maharashtra 400102 About Company - One Health Assist is a Consumer Tech Platform in Health & Wellness. OHA is committed to redefining Health & Wellness by placing individuals at the forefront. Our platform is expertly crafted to meet specific needs, offering a seamless and integrated health & wellness experience that emphasizes personalized care and comprehensive support. Position Summary: We are seeking a Pharmacist to join our growing Health and Wellness company. This role goes beyond traditional dispensing and focuses on empowering clients to lead healthier lives through education, medication management, and integrative wellness support. You will collaborate with other health professionals to deliver personalized care and promote overall well-being. Key Responsibilities: Medication Management: Dispense prescription medications accurately, counsel clients on usage, side effects, and interactions, and ensure compliance with all regulations. Wellness Consultations: Provide guidance on over the counter (OTC) health products, supplements, and lifestyle choices to support holistic wellness. Client Education: Deliver clear, empathetic education on chronic disease management, medication adherence, nutrition, and general health. Collaborative Care: Work with healthcare providers, nutritionists, and wellness coaches to support comprehensive care plans. Health Screenings: Administer or assist with services such as blood pressure checks, immunizations, and health risk assessments (as applicable). Qualifications: Doctor of Pharmacy (Pharm.D.) degree from an accredited institution. Active state pharmacist license in good standing. Strong knowledge of pharmacology, integrative medicine, and OTC products. Passion for preventive care and a holistic approach to health. Excellent communication and interpersonal skills. Experience in retail, clinical, or wellness settings preferred Thanks & Regards Amisha Shelar Contact: 885-057-2613 Email: amisha@onehealthassist.com Job Type: Full-time Benefits: Provident Fund Schedule: Day shift Application Question(s): What is your Current CTC? What is your official notice period? What is your work experience? Do you have a license for the pharmacist? Are you comfortable to work in a night shift? Have you worked on Eco green software? Work Location: In person

Role Overview TheSr. Executive/Assistant Manager/Deputy Manager - Medical Affairs will support scientific communication, ensure compliant medical review of materials, assist in KOL engagement, and contribute to training and clinical initiatives. Key Responsibilities Provide accurate, evidence-based responses to medical queries from internal and external stakeholders Review and approve promotional and scientific content in line with regulatory and ethical standards Support development and execution of training programs for internal teams Coordinate scientific engagements with healthcare professionals, including CMEs and advisory boards Contribute to clinical support activities such as literature reviews, IITs, and data generation projects Monitor therapy area trends, competitor insights, and scientific advancements Key Skills Strong foundation in pharmacology and therapeutic areas Strong academic background. Excellent written and verbal communication skills Attention to detail and high scientific accuracy Ability to work cross-functionally in a fast-paced environment Apply Now arya@talentleap.in +91 9998568056 Talent Leap Private Limited This job is provided by Shine.com Show more Show less

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent thats bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com Looking to jump-start your career? We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast-track career where you can grow along with Indegenes high-speed growth. We are purpose-driven. We enable healthcare organizations to be future ready and our customer obsession is our driving force. We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work. Job Responsibilities Act as SME for safety business and track industry trends relevant to safety Work in collaboration with the Sales and the Solutioning teams to improve win ratio and opportunity conversions Responsible for improving capability presentations and identifying service areas and solutions and work with the operational leadership to build capabilities Participate in the analysis and definition of efficient, cost-effective and creative solutions that deliver competitive value propositions to the industry Build partnerships with senior leadership across the industry in Safety and PV Represent the company in trade conferences, speaker sessions, etc. Identify and build potentially synergistic partnerships to expand client and service footprints Be part of safety consulting engagements as well as provide oversight and expertise on operations as needed Must Have MBBS/MD with a minimum of 8-10 years of experience in drug safety or a related field; Master/Diploma in Management degree is an added advantage Experience in the pharmaceutical industry, preferably in drug safety, pharmacovigilance, or clinical development Knowledge of pharmacology, toxicology, and clinical trial methodology Understanding of FDA and international regulatory requirements related to drug safety and pharmacovigilance Strong analytical and problem-solving skills Excellent communication and interpersonal skills, with the ability to work effectively in cross-functional teams Demonstrated ability to prioritize tasks and manage multiple projects simultaneously Proficiency in data analysis tools (e.g., Excel, SAS) and safety databases (e.g., Argus, ARISg) Good communication skills and relationship building skills Good to Have Equal Opportunity Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, the candidates merit, and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics. Locations Bangalore, KA, IN Show more Show less

HIRING!! Raisoni Group of Institutions is hiring for teaching faculty. Need Associate / Assistant Professor for Pharmacy The applicant must fulfill the requirements mentioned below: Qualification Requirement: Applicant must have a Ph.D and M.Pharma. Specializations: 1. Pharmacology 2. Pharmaceutical Chemistry 3. Pharmacognosy JOB RESPONSIBILITY: Academic teaching at UG/PG level. Programme and curriculum design and development. Academic Administration Quality assurance and academic research. Any other work assigned by higher authority. Job Location: Saikheda (Chhindwara) Madhya Pradesh Interested and eligible candidates can mail their Cvs at samiksha.landge@raisoni.net Job Type: Full-time Schedule: Day shift Work Location: In person

Job Title: Associate - OT Pharmacy Company Name: Manipal Hospitals Job Description: Manipal Hospitals is seeking a dedicated and detail-oriented Associate for our OT Pharmacy team. The ideal candidate will be responsible for managing pharmaceutical services in the operating theater environment, ensuring safe and effective medication management. Key Responsibilities: - Assist in the preparation and dispensing of medications for surgical procedures. - Collaborate with the surgical team to optimize pharmacological therapy. - Maintain accurate inventory of medications and supplies in the OT pharmacy. - Support the implementation of safety protocols and procedures in medication handling. - Provide guidance and information to healthcare staff regarding medication use and interactions. - Participate in continuous education and training to stay updated on pharmaceutical practices. - Ensure compliance with regulatory requirements and hospital policies. Qualifications: - Bachelor's degree in Pharmacy or a related field. - Valid pharmacy license. - Experience in a hospital pharmacy setting, particularly in an operating theater, is preferred. - Strong communication and organizational skills. - Ability to work efficiently in a fast-paced environment. Join Manipal Hospitals and become part of a team committed to delivering exceptional healthcare services. If you are passionate about pharmacy and patient care, we encourage you to apply for this exciting opportunity. Roles and Responsibilities Job Title: Associate - OT Pharmacy Company Name: Manipal Hospitals Roles and Responsibilities: 1. Assist in the management and organization of the outpatient pharmacy operations, ensuring the efficient flow of medication distribution. 2. Prepare, dispense, and label medications according to prescriptions and established safety standards. 3. Collaborate with healthcare professionals to provide optimal pharmaceutical care and support patient safety initiatives. 4. Maintain accurate patient medication records and ensure compliance with regulatory requirements. 5. Conduct medication inventory management, including ordering, receiving, and conducting regular audits to prevent stock discrepancies. 6. Provide medication counseling to patients and their families, addressing any questions or concerns regarding prescriptions and dosages. 7. Support the continuous improvement of pharmacy practices by participating in training programs and staying updated on industry trends and best practices. 8. Engage in quality assurance activities to monitor the effectiveness of pharmacy services and implement necessary improvements. 9. Assist in the preparation and maintenance of pharmacy policies and procedures to align with hospital standards. 10. Contribute to team meetings and collaborate effectively with colleagues to enhance overall pharmacy operations and patient care.