Job Description Designation: Subject Matter Expert (SME) – Pharmacy Employment: Full Time Location: Hyderabad, India Job Summary: We are looking for a dedicated and detail-oriented Subject Matter Expert (SME) in Pharmacy to join our academic content team in Hyderabad. The SME will be responsible for developing, reviewing, and ensuring the accuracy and quality of pharmacy-related academic content in alignment with current curriculum and industry standards. Key Responsibilities: · Develop and structure academic content for Diploma, B.Pharm courses, including study material, assessments, case studies, MCQs, and digital learning modules. · Ensure all content is scientifically accurate, pedagogically effective, and aligned with pharmacy regulatory bodies (e.g., PCI, AICTE, UGC). · Collaborate with instructional designers, editors, and multimedia teams to create engaging and interactive e-learning content. · Review and validate existing content created by internal teams or external contributors for accuracy, consistency, and curriculum alignment. · Research and incorporate the latest developments in the field of pharmacy, including pharmacology, pharmaceutics, pharmacognosy, and pharmaceutical chemistry. · Provide academic expertise in planning curriculum structures and designing learning outcomes. · Train and mentor junior writers, freelancers, or interns, if applicable. · Participate in academic audits, feedback implementation, and content improvement strategies. Required Qualifications & Skills: Master’s degree in Pharmacy (M.Pharm) from a recognized institution. Minimum 1+ years of experience in academia, clinical research, pharmaceutical industry, or content development. Strong foundational knowledge in core pharmacy subjects such as Pharmacology, Pharmaceutical Analysis, Pharmaceutics, and Medicinal Chemistry. Familiarity with academic frameworks like Bloom’s Taxonomy, outcome-based education (OBE), etc. Proficiency in MS Office Suite (Word, Excel, PowerPoint); experience with LMS or content tools (Articulate, Moodle) is a plus. Ability to work independently with attention to detail and accuracy. Job Types: Full-time, Permanent Pay: ₹28,000.00 - ₹35,000.00 per month Benefits: Commuter assistance Provident Fund Schedule: Day shift Work Location: In person

Work Schedule Standard (Mon-Fri) Environmental Conditions Office At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Discover Impactful Work: We are passionate about being data and technically agile and driving enhanced value for our clients and patients. Determined to improve patient health, we help PPD provide industry-leading statistical, programming and clinical pharmacology contributions through global delivery, consistent quality adherence and scientific insight. A day in the Life: Administers the daily financial management of simple or moderately complex studies, for the functional area's portion of a project budget, as assigned with minimal supervision. Performs review of contract and bidding assumptions. Performs analysis of budget to actual data on monthly or other specified basis. Works closely with project lead to update resource forecasts and unit grids, present and resolve pending issues with resource forecasts, unit grids and contract modifications. Close collaboration with other departments and project lead to coordinate financial aspects of functional area's portion of projects. Assists project team to identify risks, define reasons for unsupported hours, and attends risk meetings as needed. Prepares estimates for contract modifications. Keys to Success: Education Bachelor's degree in finance, accounting, mathematics or related field or equivalent and relevant formal academic / vocational qualification, and Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). The following education and experience is preferred: Experience 2+ years complex project management experience to include allocation of resources against budget, forecasting, and completion/coordination of related quantitative and analytical tasks Knowledge, Skills, Abilities Shown budgeting and forecasting skills Solid analytical skills and capable of handling data effectively Solid problem solving skills Good written and verbal communication skills Strong digital literacy (Microsoft Office, etc.) for analysis and presentation of data Good understanding of project management principles and application Capable of focusing on individual projects while covering similar aspects across multiple projects Capable of working independently Capable of providing mentorship and promoting partnership in a multi-disciplinary team setting Solid organizational skills with the ability to adapt and adjust to changing priorities Positive attitude Show more Show less

Bachelor’s degree in pharmacy or pharmacology is not mandatory Proven experience as a pharmacist or any medical shop Detailed understanding and knowledge of dosage requirements and administration, chemical compounds, and pharmaceutical brands. Working knowledge of Microsoft Office Suite and software applications, used by pharmacies, such as MEDITECH and Mediware. Great organizational skills. Excellent verbal and written communication skills. Job Types: Full-time, Permanent Pay: ₹10,000.00 - ₹14,000.00 per month Benefits: Cell phone reimbursement Paid sick time Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Application Question(s): Are you comfortable with Dunlop location? How many years do you have experience as a pharmacist? fresher is not applicable Work Location: In person

We are looking for an MSL- Oncology for a Global Pharmaceutical MNC Profile: Medical Science Liaison- Oncology Location: Delhi/ Kolkata/ Chennai (3 openings) Qualification: MD Pharmacology fresher or with minimum 6 months of experience MDS/ PhD with minimum 1yr of Oncology experience as MSL/RMA 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

The candidate will undergo a self-financed job-oriented patent analyst training at the Indian Institute of Patent and Trademark. On successful completion of the training, they will be placed for full-time patent analysis in the pharmaceutical domain. Required Candidate profile Scientific and Analytical Thinking Eager to work in drugs and formulation Candidates must have sound knowledge about the subjects they study in Graduation

🔹 Job Title: Freelance Subject Matter Expert (SME) – Pharmacy Subjects 📍 Employment Type: Freelancer 🌐 Location: Work From Home 📢 Open Positions (Subject-wise): Pharmacology Pharmaceutical Chemistry Pharmacognosy Pharmaceutics Allied Subjects (Biochemistry, HAP, Biotechnology, etc.) 🎓 Qualification & Eligibility: Must hold or be in the final year of a B.Pharm degree. Strong command over the selected subject area. 🧠 Experience: 0 to 1 year of relevant experience. Freshers with good knowledge are welcome. 💼 Skill Set Requirements: Basic understanding of Google Suite (Docs, Sheets, Drive, etc.) Clear understanding of quality standards in academic question creation. Must have appeared for Pharmacy entrance/competitive exams like GPAT, NIPER, Drug Inspector, etc. 📌 Roles & Responsibilities: Create high-quality, original, and exam-relevant MCQs and questions for: GPAT NIPER Drug Inspector Exams Ensure academic accuracy, clarity, and relevance of content. Follow the prescribed format and quality benchmarks. 💻 Work Mode: Remote/Freelance – flexible working hours. If you are passionate about pharmacy education and want to contribute to helping aspirants succeed, apply now! Show more Show less

We Are Hiring - International Sales Specialist – Life Sciences Online Education Experience: Minimum 6 to 8 Years Industry: Education / E-Learning / EdTech Joining: Immediate Joiners Preferred Company: YesM Pharma Job Description: We are a US-based online education provider offering specialized courses in Life Sciences, including Pharmacology, Pharmacokinetics & Pharmacodynamics, Signal Detection, Clinevo database training, and Clinical Trial Management. We are looking for a results-driven International Sales Specialist to promote our courses to foreign medical doctors and healthcare professionals. The ideal candidate should have a solid background in international education or healthcare sales, with an understanding of life sciences or medical training. Key Responsibilities: Drive international sales for online Life Sciences training programs Generate leads, pitch services, and convert prospects across the USA, UK, and Middle East markets Conduct virtual presentations and follow-ups with individual Build and maintain long-term relationships with foreign medical professionals and clients Maintain CRM and sales reporting tools with updated pipeline and progress Coordinate with academic and marketing teams for campaign execution Desired Candidate Profile: 6–8 years of international sales experience (preferably in education, training, or healthcare industry) Strong exposure to USA, UK, and Middle East markets Excellent English communication skills (spoken and written) – must be able to engage fluently with foreign clients Background in Life Sciences, Pharmacy, or Medical domain is a strong advantage Familiar with CRM tools and remote sales practices Must be comfortable working USA shift hours Only candidates with relevant international B2B/B2C sales experience will be considered. Mail CV - pankaj@marketingpanthers.com Show more Show less

Pharmacist (Immediate Joiners) Walk-in Interview : Time : 12 pm Location:- Nashik / D. Vijay Pharma Pvt. Ltd. Old, Mumbai - Agra National Hwy, next to Samrat Hotel CBS, Nashik, Maharashtra 422001 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 a Jr. 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 Salary : 12000 to 20000 (per month) Job Types: Full-time, Permanent, Fresher Pay: ₹12,000.00 - ₹20,000.00 per month Benefits: Cell phone reimbursement Health insurance Leave encashment Life insurance Paid time off Provident Fund Schedule: Day shift Evening shift Morning shift Rotational shift Supplemental Pay: Overtime pay Performance bonus Shift allowance Yearly bonus Education: Diploma (Required) Experience: Total: 1 year (Required) License/Certification: Pharmacist License (Required) Location: Nashik, Maharashtra (Required) Shift availability: Day Shift (Required) Night Shift (Required) Overnight Shift (Preferred) Work Location: In person

Job Description You’re an important part of our future. Hopefully, we're also a part of your future! At B. Braun, we protect and improve the health of people worldwide. You support this vision, bringing expertise and sharing innovation, efficiency and sustainability as values. That’s why we would like to keep developing our company with you. Keeping your future in mind, we’re making a joint contribution to health care worldwide, with trust, transparency and appreciation. That's Sharing Expertise. Officer - Store Company: Ahlcon Parenterals IN Ltd Job Posting Location: IN-Bhiwadi Functional Area: Supply Chain Management Working Model: Onsite Requisition ID: 4929 Are you a Store Officer passionate about Physical verificationa, dispensing and documentation of Raw Material in Store? If so, this opportunity could be for you! Join us in Bhiwadi at Ahlcon Parenterals, a pioneer in medical devices, where your skills and experience will be recognized and celebrated. Take the next step in your career with us and help shape the future of healthcare! As a Store Officer at B. Braun Group you will play a vital role in efficient dispensing, physical verification, RM Store temperature monitoring as per SOP. Your key responsibilities: Dispensing of Raw Material as per BMR. Physical verification of Raw materials. Maintain clean record, temperature monitoring of RM Store and Dispensing area. Issuance of material as per FEFO and calculation of material. Maintaing dispensing and raw material store clean and presentable for audit. What you will bring to the team: Strong knowledge of receipt and dispensing of raw material in Store. Experience in inventory management, documentation, and Audit related to store activities. A Bachelor's degree in Pharmacy or a Bachelor of Science or a Master of Science in a relevant scientific discipline (e.g., Chemistry, Biology, Microbiology, Pharmacology) provides a strong foundation for the role. With 2-5 years of experience, you bring valuable hands-on knowledge of industry processes and best practices. What sets B. Braun apart? Ahlcon Parenterals (India) Limited is a B. Braun group company, located at Bhiwadi, Rajasthan. We are a major pharmaceutical formulation manufacturer of both Large and Small Volume Parenterals (LVP and SVP) for domestic and export markets. Our core values of Innovation, Efficiency, Sustainability, Trust, Accountability, and Diversity foster a performance-driven culture where we challenge each other constructively to grow personally and professionally. Recognized through awards such as 'Dream Companies to Work For' and 'Great Place to Work,' we invite you to join our team driven by a shared vision - to protect and improve the health of people around the world. What can we offer you? Convenient transport and subsidized canteen services. Mediclaim and Life Insurance. Learning programs and workshops to drive your development. Mental Wellness Support with counselling and mindfulness sessions. Paternity & Birthday Leave for life’s special moments. Fun activities and team building events. What’s next? Upon receiving your application, our dedicated Talent Acquisition team will review your application. If you stand out, you’ll be invited to engage in dynamic interviews, ranging from phone calls to video chats and in-person meetings. Throughout this process, we will keep you informed and inspired with regular updates and feedback. Finally, if you shine through and decide to join us, we will lead you into our seamless onboarding experience. Join us and be part of something extraordinary! We appreciate different perspectives, thoughts, experiences and backgrounds. By strengthening an appreciative, inclusive, respectful and equal working environment, we create a culture in which all our employees feel free to be who they are. To find out more about our commitment to diversity click here Check us out on social media! B. Braun Group LinkedIn B. Braun India Facebook B. Braun Group YouTube

Main responsibilities: Provide scientific expertise and build knowledge-based relationships with Key Opinion Leaders (KOLs) to advance medical practice and research for societal benefit, enhancing Pfizer’s image in the scientific community. Act as an interface with identified scientific leaders, building regional relationships to contribute to understanding diseases, research trends, clinical practice guidelines, and treatment patterns. Educate healthcare professionals about specific drugs or medical devices, answering their scientific questions and ensuring products are used effectively. Collect insights from KOLs regarding product usage, unmet needs, and potential areas for research, feeding this information back to internal teams (marketing, sales, clinical development). Stay informed of the latest scientific research and clinical developments in their therapeutic area. Collaborate with internal teams, including marketing, sales, clinical research, and medical information, to ensure consistent and accurate messaging. Implement the medical activities relevant to brand plan strategies for specific products and therapy areas. Participate in and provide medical inputs for KOL meetings, advisory boards, customer pre-launch and launch meetings (CLMs). Conduct/facilitate round table meetings/group discussions and CMEs as a speaker/moderator for assigned therapy areas/products. Support sales force training by providing medical expertise Skill set: Basic knowledge of the pharmaceutical industry, drug discovery, research & development, commercialization, promotion, and applicable policies, procedures, regulations, and guidelines Knowledge of “pharmaceutical medicine” including clinical pharmacology, medical and paramedical sciences, medicine and medical statistics, and relevant therapeutic areas/products Communication skills, both written and verbal (including medical writing and presentation skills) Analytical skills and reasoning, and sound medical judgment/decision making Interpersonal skills, internal & external networking, and the ability to impact and influence & present complex information clearly and concisely to diverse audiences Experience in neurology and gastrology therapy area are preferred. Managerial: N/A Certifications: N/A Education: Graduate/Post Graduate in Medicine or other medical sciences (e.g., MBBS, MD in Pharmacology or Community Medicine, PhD in allied sciences, MPH etc.) Work Location Assignment: Remote - Field Based Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Medical Show more Show less

Main responsibilities: Provide scientific expertise and build knowledge-based relationships with Key Opinion Leaders (KOLs) to advance medical practice and research for societal benefit, enhancing Pfizer’s image in the scientific community. Act as an interface with identified scientific leaders, building regional relationships to contribute to understanding diseases, research trends, clinical practice guidelines, and treatment patterns. Educate healthcare professionals about specific drugs or medical devices, answering their scientific questions and ensuring products are used effectively. Collect insights from KOLs regarding product usage, unmet needs, and potential areas for research, feeding this information back to internal teams (marketing, sales, clinical development). Stay informed of the latest scientific research and clinical developments in their therapeutic area. Collaborate with internal teams, including marketing, sales, clinical research, and medical information, to ensure consistent and accurate messaging. Implement the medical activities relevant to brand plan strategies for specific products and therapy areas. Participate in and provide medical inputs for KOL meetings, advisory boards, customer pre-launch and launch meetings (CLMs). Conduct/facilitate round table meetings/group discussions and CMEs as a speaker/moderator for assigned therapy areas/products. Support sales force training by providing medical expertise Skill set: Basic knowledge of the pharmaceutical industry, drug discovery, research & development, commercialization, promotion, and applicable policies, procedures, regulations, and guidelines Knowledge of “pharmaceutical medicine” including clinical pharmacology, medical and paramedical sciences, medicine and medical statistics, and relevant therapeutic areas/products Communication skills, both written and verbal (including medical writing and presentation skills) Analytical skills and reasoning, and sound medical judgment/decision making Interpersonal skills, internal & external networking, and the ability to impact and influence & present complex information clearly and concisely to diverse audiences Experience in neurology and gastrology therapy area are preferred. Managerial: N/A Certifications: N/A Education: Graduate/Post Graduate in Medicine or other medical sciences (e.g., MBBS, MD in Pharmacology or Community Medicine, PhD in allied sciences, MPH etc.) Work Location Assignment: Remote - Field Based Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Medical Show more Show less

As a B.Pharm 3rd-year student, I assist in basic pharmaceutical tasks such as drug dispensing, inventory management, and research support. I have foundational knowledge in pharmacology and formulation, with a strong interest in healthcare, patient care, and medical research. Eager to apply my skills in a clinical or research setting to gain hands-on experience and contribute to the healthcare field. Show more Show less

Jubilant Biosys is hiring for Senior Research Associate - In Vivo Biology Experience : 5-8 Years Qualification : M. Pharmacy (Pharmacology) Responsibilties : Drug discovery in pre-clinical pharmacology, In-vivo pharmacology, Animal model development and Efficacy study and Pharmacological screening of Pharmaceutical drug molecules in the respective therapeutic areas such as CNS/ Metabolic disorder/ Autoimmune/Inflammatory diseases/ Pain/Oncology in Drug Discovery field. Evaluation of NCEs in target engagement and efficacy models. Responsible for writing of Protocols, uploading of the data, Lab note book record keeping. SOP writing Exploring scientific journals in order to find new ways/techniques to develop the animal models in a robust and reproducible manner. Follow the guidelines followed in the lab towards different safety aspects and help the lab head in designing the new guidelines. Follow ethical guidelines towards assay validation, data analysis and maintenance.

We are a start-up company offering B2B online marketplace platform connecting medical consumables & devices distributors and manufacturers with healthcare providers such as hospitals, clinics etc. Kogland is a subsidiary of Fingent Corporation and located inside Carnival Info park, Kochi. Skill Set Requirement: Should hold a B. Pharm / D Pharm degree. Should have experience in dispensing drugs for at least 5 years in an offline store. Thorough understanding of dosage administration and measurement, Integrity and compassion. Should have permanent address in Tamil Nadu(Chennai Preferred) as per address proof and currently based out of Kerala( or ready to move to Cochin), Roles and Responsibilities: Review and execute physician s prescriptions checking their appropriateness and legality Listen carefully to customers to interpret their needs and issues and offer information and advice Keep records of patient history and of all activities regarding heavy medication Support Drug Inspector with required documents and sample during inspection Comply with all applicable legal rules, regulations and procedures

Data Search & Analysis on the drug discovery and development Creating technology reports Kindly provide minimum two references with resume Required Candidate profile Keen interest in drug discovery, API Good Knowledge of organic chemistry Good Communication Skills

About The Role Grade Level (for internal use): 07 The Team The team is responsible for developing, maintaining, and enhancing drug database products, delivering strategic and financial insights to clients, and creating innovative, client-facing functionalities. The team values collaboration, precision, and a forward-thinking approach to driving impact in the healthcare data landscape. The Impact This role contributes directly to the creation and management of high-quality drug databases, supporting critical decision-making in the healthcare and biopharma sectors. By providing contextual information on drugs and ensuring the accuracy and usability of drug data, this position enhances the value delivered to clients and drives meaningful advancements in healthcare insights. What’s In It For You Opportunity to work on cutting-edge drug databases and contribute to impactful client-facing dashboards. Develop a deep understanding of pharmacology, drug life cycles, and healthcare industry processes. Build expertise in database management and interactive data visualization tailored to healthcare clients. Gain foundational understanding of Healthcare company financials Collaborate with a dynamic, innovative team within a global organization. Professional growth through structured learning and cross-functional teamwork. Responsibilities Support the development and enhancement of drug database products, including interactive dashboards and client-facing functionalities. Manage and update drug databases, focusing on key elements such as Mechanism of Action (MOA), indications, and drug development phases. Drive process improvements to enhance data accuracy, reliability, and usability. Conduct in-depth research using diverse sources, including healthcare databases, research articles, regulatory sites, and industry publications. Collaborate with clients to create tailored use cases and strategic dashboards, providing actionable insights. Key Qualifications What We’re Looking For Education - Bachelor’s degree in pharmacy (B. Pharma) is required. Experience – 2 years relevant experience in the healthcare industry. Proven experience in creating and maintaining healthcare databases. Expertise in working with regulatory websites. Primary shift – Day Shift Soft Skills A positive attitude with attention to detail. Strong problem-solving and troubleshooting abilities. Excellent analytical skills and aptitude for critical thinking. Ability to articulate effectively with stakeholders across the organization. Strong attention to detail and the capability to spot errors. About S&P Global Market Intelligence At S&P Global Market Intelligence, a division of S&P Global we understand the importance of accurate, deep and insightful information. Our team of experts delivers unrivaled insights and leading data and technology solutions, partnering with customers to expand their perspective, operate with confidence, and make decisions with conviction. For more information, visit www.spglobal.com/marketintelligence. What’s In It For You? Our Purpose Progress is not a self-starter. It requires a catalyst to be set in motion. Information, imagination, people, technology–the right combination can unlock possibility and change the world. Our world is in transition and getting more complex by the day. We push past expected observations and seek out new levels of understanding so that we can help companies, governments and individuals make an impact on tomorrow. At S&P Global we transform data into Essential Intelligence®, pinpointing risks and opening possibilities. We Accelerate Progress. Our People We're more than 35,000 strong worldwide—so we're able to understand nuances while having a broad perspective. Our team is driven by curiosity and a shared belief that Essential Intelligence can help build a more prosperous future for us all. From finding new ways to measure sustainability to analyzing energy transition across the supply chain to building workflow solutions that make it easy to tap into insight and apply it. We are changing the way people see things and empowering them to make an impact on the world we live in. We’re committed to a more equitable future and to helping our customers find new, sustainable ways of doing business. We’re constantly seeking new solutions that have progress in mind. Join us and help create the critical insights that truly make a difference. Our Values Integrity, Discovery, Partnership At S&P Global, we focus on Powering Global Markets. Throughout our history, the world's leading organizations have relied on us for the Essential Intelligence they need to make confident decisions about the road ahead. We start with a foundation of integrity in all we do, bring a spirit of discovery to our work, and collaborate in close partnership with each other and our customers to achieve shared goals. Benefits We take care of you, so you can take care of business. We care about our people. That’s why we provide everything you—and your career—need to thrive at S&P Global. Our Benefits Include Health & Wellness: Health care coverage designed for the mind and body. Flexible Downtime: Generous time off helps keep you energized for your time on. Continuous Learning: Access a wealth of resources to grow your career and learn valuable new skills. Invest in Your Future: Secure your financial future through competitive pay, retirement planning, a continuing education program with a company-matched student loan contribution, and financial wellness programs. Family Friendly Perks: It’s not just about you. S&P Global has perks for your partners and little ones, too, with some best-in class benefits for families. Beyond the Basics: From retail discounts to referral incentive awards—small perks can make a big difference. For more information on benefits by country visit: https://spgbenefits.com/benefit-summaries Global Hiring And Opportunity At S&P Global At S&P Global, we are committed to fostering a connected and engaged workplace where all individuals have access to opportunities based on their skills, experience, and contributions. Our hiring practices emphasize fairness, transparency, and merit, ensuring that we attract and retain top talent. By valuing different perspectives and promoting a culture of respect and collaboration, we drive innovation and power global markets. Equal Opportunity Employer S&P Global is an equal opportunity employer and all qualified candidates will receive consideration for employment without regard to race/ethnicity, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, marital status, military veteran status, unemployment status, or any other status protected by law. Only electronic job submissions will be considered for employment. If you need an accommodation during the application process due to a disability, please send an email to: EEO.Compliance@spglobal.com and your request will be forwarded to the appropriate person. US Candidates Only: The EEO is the Law Poster http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf describes discrimination protections under federal law. Pay Transparency Nondiscrimination Provision - https://www.dol.gov/sites/dolgov/files/ofccp/pdf/pay-transp_%20English_formattedESQA508c.pdf OPRTON203 - Entry Professional (EEO Job Group) Job ID: 311273 Posted On: 2025-05-27 Location: Noida, Uttar Pradesh, India Show more Show less

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 Pharmaceuticals Pharma practices. Eligibility Criteria Qualification: Masters in Pharmacology , Pharmaceuticals and Pharma Practices. PhD Mandatory (Pharmacology,Pharmaceutics and Pharma Practices ) Experience: 8 to 15 years of experience required. Job Type: Full-time Pay: ₹35,000.00 - ₹60,000.00 per month Schedule: Day shift Work Location: In person

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. The Medical Information Specialist (MIS) position is part of the ProPharma Medical Information Contact Center and follows all corresponding regulations, industry standards, and client/internal policies regarding medical information and the collection and documentation of adverse events, special situation events, and product complaints. Essential Functions Include:Medical Information service delivery Responds to unsolicited consumer, health care professional and other external customer requests for medical and safety information received via telephone, website/e-mail, letter, fax, and scientific meetings on behalf of ProPharma’ s pharmaceutical clients. Provides labeled and unlabeled medical/safety information responses in accordance with regulatory requirements, industry standards and client and ProPharma internal policies and practices. Accurately identifies, documents and reports adverse events, pregnancy reports, special situation events and product complaints in a clear and concise manner per government regulations, ProPharma Standard Operating Procedures (SOPs) and client Working Practices (WPs). Ensures tasks are completed within the deadlines documented in the agreed ProPharma SOPs and WPs. Formulates and provides accurate responses utilizing approved labeling and company standard responses, published literature and other data. Assists with writing custom medical information responses utilizing this data. Logging all enquiries handled in an accurate, comprehensive, and timely fashion into Inquiry Handling Systems. Quality Assurance Maintains quality in all areas of the job, including performing quality checks on Adverse Events, Product Quality Complaints, correspondence, and enquiries logged into the Inquiry Handling Systems General Provides after-hours coverage on a rotated basis subject to business requirements. Adheres to company and country-specific privacy policies, ensuring any confidential information or personal data related to ProPharma and its clients is managed in accordance with Data Privacy regulations described in ProPharma SOPs and the Confidentiality Statement within the Contract of Employment. Complies with the Company’s health and safety policies. Other activities as assigned as delegated by the Manager. Qualified Candidates Must Have Life science degree OR Nursing degree (RN/BS/BA/MS) OR Pharmacy degree Excellent verbal and written communication skills, including proofreading, professional telephone etiquette and empathetic customer service skills. Ability to write in a fluent and grammatically correct manner in the target language for the role English language proficiency. Japan-based roles only: TOEIC 800= Working knowledge of medical terminology, pathophysiology, pharmacology, regulations and industry standards. Strong cognitive abilities, including verbal reasoning, critical thinking and analytical ability. Ability to multitask with attention to detail within restrictive timeframes, including sound planning, prioritizing and organizational skills. Proactive with demonstrative ability to independently identify problems and suggest effective solutions. Ability to learn, take instruction and apply to daily operations/tasks. Receptive to constructive feedback and able to take responsibility for work allocated. Self-motivating. Ability to demonstrate initiative and internal drive. Willingness to seek out additional workload projects. Effectively work independently and as part of a team. Highly proficient in computer applications, including Microsoft Office software platforms and Adobe Acrobat, and experience using a document management system. Aptitude to learn other computer systems including inquiry handling database. We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*** Show more Show less

One of our Client who is a leading Ayurvedic Healthcare and Pharmaceutical Company is hiring for following role 🌿 Leader – Clinical Research (Ayurveda) 📍 Location: Thrissur, Kerala 💼 Compensation: Based on experience We are hiring a visionary leader to head our Ayurveda Clinical Research initiatives. This role is key to advancing the scientific credibility of Ayurveda and translating traditional knowledge into evidence-based, globally accepted solutions. ⸻ 🔍 Responsibilities: ✅ Lead clinical studies to validate Ayurvedic principles using modern research methods ✅ Publish in peer-reviewed journals and present findings to global healthcare communities ✅ Identify and secure funding from national/international bodies for R&D ✅ Build partnerships with universities, research institutes, and hospitals ✅ Represent the organization at conferences and technical forums ✅ Oversee R&D, clinical trials, product development, and regulatory compliance ✅ Manage projects and optimize resources across the research portfolio ✅ Promote Ayurveda as a solution for public health and wellness ⸻ 👤 Ideal Candidate: 🎓 MD or Ph.D. in Ayurveda, Life Sciences, or related field (preferred) 🧠 Strong track record in publishing high-impact clinical research 🌱 Expertise in Ayurveda, pharmacology, or integrative medicine 🤝 Excellent leadership, project management, and collaboration skills 🌍 Proven ability to work with research institutions, funding agencies, and stakeholders ⸻ 🎯 Key Outcomes: 📈 Launch groundbreaking clinical research programs 📰 Publish studies that enhance Ayurveda’s global reputation 🧪 Drive innovation in Ayurvedic product development 💡 Secure funding and foster long-term academic collaborations ⸻ Join us in shaping the future of Ayurveda by merging tradition with science. If you’re passionate about creating a global impact through Ayurvedic research, we’d love to hear from you! ⸻ 📩 Apply now or tag someone who fits this profile! 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 Cloud 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. BPT is enabled by global engineering teams working on next-generation applications and Laboratory Information Management Systems (LIMS). As Site Reliability Engineer, you will be a key part of our cloud strategy, ensuring our IT systems operate effectively on the Azure cloud. As a technology leader, BPT wants to give you the opportunity not just to accept new challenges and opportunities, but to impress with your ingenuity, focus, attention to details and collaboration with a global team of professionals. This role reports to a SRE Manager. Primary Responsibilities : We are looking for a skilled Site Reliability Engineer (SRE) to join our Cloud Engineering and Operations team. The ideal candidate will be responsible for ensuring high availability, performance, and reliability of our cloud-hosted systems, particularly in Microsoft Azure environments. This role combines software engineering practices with operational excellence to build scalable, automated, and resilient infrastructure. You’ll work closely with developers, security teams, and platform engineers to implement best practices, reduce toil, and proactively manage incidents and risks across production environments. Key Responsibilities Infrastructure as Code (IaC) Automate deployment and configuration of resources using Bicep, PowerShell, and Azure CLI. Build repeatable, version-controlled infrastructure aligned with Azure Well-Architected Framework. Cloud Operations & Monitoring Manage and monitor Azure cloud resources including VMs, App Services, AKS clusters, and storage solutions. Ensure platform health using tools such as Azure Monitor, Log Analytics, and custom alerting frameworks. Optimize system performance, plan capacity, and proactively identify reliability risks. Access & Identity Lifecycle Management Administer access controls and identity provisioning using Azure Active Directory. Implement RBAC policies and maintain secure access patterns across the environment. Incident Response & Troubleshooting Respond to incidents and performance alerts, ensuring rapid resolution with minimal impact. Collaborate with engineering teams to analyze root causes and implement preventive solutions. Security & Compliance Enforce best practices for cloud security including encryption, key management via Azure Key Vault, and access control. Align infrastructure with compliance standards such as GDPR, HIPAA, or internal policies. Cost Optimization & Resource Management Monitor and manage cloud spending using Azure Cost Management tools. Recommend and implement strategies for efficient resource usage and scaling. Disaster Recovery & Availability Planning Design and maintain robust backup and DR plans across Azure regions. Ensure recovery objectives are met and tested regularly. Collaboration & Documentation Work closely with DevOps, Security, and Architecture teams to align goals. Maintain clear documentation on infrastructure design, operations, and procedures. Specific Deliverables Daily operations support for Azure-hosted workloads. Timely provisioning and access management for end users. Effective triaging and closure of cloud incidents. Secure and scalable infrastructure design and automation. Support and drive adoption of SRE practices, including monitoring, incident postmortems, and continuous improvement. Skills required: Strong knowledge of Azure services (Compute, Networking, Storage, Identity). Hands-on experience with IaC tools (Bicep), scripting (PowerShell, Python), and deployment automation. Solid foundation in networking concepts and cloud-native security. Experience with cloud observability and logging tools. Proficiency in managing access control using Azure AD and RBAC. Preferred Qualities Strong analytical and problem-solving mindset. A passion for automation and eliminating manual work. Documentation-oriented—writes things down to scale learning and onboarding. Proactive attitude toward identifying and fixing reliability gaps. Collaborative, self-driven, and adaptable to changing priorities. Stack: Cloud: Microsoft Azure Languages: PowerShell, Python, YAML Tools: Azure DevOps, Azure Monitor, Bicep Practices: Infrastructure as Code, CI/CD, RBAC, Zero Trust Security, Postmortems Qualifications Preferred Qualifications: Bachelors in Engineering, Computer Science or equivalent. At least 2 years of professional experience in Azure cloud in a multiple region environment

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 Associate Software Engineer: Eurofins IT Solutions, Bengaluru, Karnataka, India With 54 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 like Eurofins Quality Management System(eQMS). eQMS is sophisticated web application that will be used by our scientists, engineers, and technicians to manage several quality and compliance management processes. This role reports to Engineering Manager. Required Experience and Skills Eligibility Criteria: 2024 /2025 pass out B.E./ B. Tech (CS, IS, EC,) / BSc (CS, IT) 0-12 months of IT Industry experience 60% aggregate in highest qualification (no backlogs) Technical Skills: 0 to 1 year of experience or strong foundational knowledge in .NET Core , C# , Angular , and Web API development. Familiar with database systems such as SQL Server , Cosmos DB , and MongoDB . Able to write code in at least one of the following languages like C# Basic understanding of Azure fundamentals including services like App Services , Azure Functions , Azure SQL , and Cosmos DB . Exposure to scripting with C# and PowerShell is a plus. Familiar with version control using Git and repositories hosted on Azure Repos . Experience with development tools like Visual Studio , Postman , and Swagger for API testing and documentation is an advantage. Knowledge of ElasticSearch and Azure Service Bus is beneficial. Soft Skills: Good communication and interpersonal relation skills in an international environment Good Attitude towards learning new things. Good Knowledge on logical reasoning and problem-solving skills. Ability to coordinate the work with different individuals / teams Continuous Improvement: Staying updated with technologies, improving processes. Preferred Qualifications: Certifications in Azure (e.g., AZ-900, AZ 204). Elasticsearch Engineer Certification. Understanding of cloud database management with Azure Cosmos DB . Familiarity with modern web development practices and RESTful APIs. Technology Stack: Backend Development: .NET Core, C#, Web API Frontend Development: Angular, TypeScript Databases: SQL Server, Cosmos DB, MongoDB Cloud & Azure: Azure App Services, Azure Functions, Azure SQL, Azure Repos Scripting & Tools: PowerShell (basic), C# scripting, Visual Studio, Git, Postman, Swagger Additional Technologies: ElasticSearch, Azure Service Bus, Redis Cache Qualifications Bachelors in Engineering, Computer Science or equivalent.

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 Associate Software Engineer: Eurofins IT Solutions, Bengaluru, Karnataka, India With 54 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. BPT is enabled by global engineering teams working on suite of next-generation applications including Laboratory Information Management Systems (LIMS), Electronic Notebook (ELN), LabAccess etc. As Associate Software Engineer, you will be a crucial part of our delivery team, ensuring the Eurofins Electronic Notebook product’s continuous integration and continuous deployment (environments maintenance, build, deployment etc. with quick turnaround time there by reducing the impact on Business) for a suite of applications in collaboration with other stake holders. 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. As a technology leader, BPT wants to give you the opportunity not just to accept new challenges and opportunities but to impress with your ingenuity, focus, attention to detail and collaboration with a global team of professionals. This role reports to a Deputy Manager. Required Experience and Skills Eligibility Criteria: 2024 /2025 pass out B.E./ B. Tech (CS, IS, EC,) / BSc (CS, IT) 0-12 months of IT Industry experience 60% aggregate in highest qualification (no backlogs) Technical Skills: 0 to 1 year experience OR Knowledge on, .Net, Angular, data base (SQL Server, Mongo DB, COSMOS DB) is good to have Must be able to write programs in one of the following programming languages: TypeScript, C++, C#, or Java. Knowledge on Azure Technologies (Azure Pipelines), PowerShell and C# Scripting, Azure artifacts & Azure Git Repos are added advantage Knowledge on tools like Azure DevOps, are added advantage. Knowledge on any programming language is added advantage. Note: The candidate must be willing to work in DevOps area and prepared to be challenged on any required capabilities in this regard during interviews. Soft Skills: Good communication and interpersonal relation skills in an international environment Good Attitude towards learning new things. Good Knowledge on logical reasoning and problem-solving skills. Ability to coordinate the work with different individuals / teams Continuous Improvement: Staying updated with technologies, improving processes. Preferred Qualifications: Certifications in Azure (e.g., AZ-900, AZ-400, AZ-104). Elasticsearch Engineer Certification. Experience with networking and security protocols in Azure. Knowledge of database management in Azure Cosmos DB. Technology Stack: Azure Technologies (Azure Pipelines), PowerShell and C# Scripting, Azure artifacts & Azure Git Repos .Net, App Service Plans – App Services, Azure Functions, AKS, C#, SQL scripts COSMOS DB, SQL DB Elastic Search, Azure Service Bus, Redis Cache Qualifications Bachelors in Engineering, Computer Science or equivalent.

Site Name: India - Maharashtra - Worli Mumbai Posted Date: Apr 29 2025 Job Purpose: Provide scientific and technical expertise of the highest standards for local medical information, including interactions with Key External Experts (KEEs) and Key Opinion Leaders (KOLs) Provide medical and scientific input and information for business strategy for the region. Key Responsibilities : Develop and sustain credible networking with appropriate Health Care Practitioners (HCPs) Plan, facilitate and conduct CMEs, symposia, trainings, workshops, scientific meetings, speaker tours, and other product specific campaigns and deliver scientific presentations with consistent messages for key products at these meetings, as required. Support and deliver scientific presentations with consistent “on label” messages at medical education meetings. Understand principles of and support Scientific Engagement (SE) activities as per Medical Plans. Have clarity in understanding on Scientific Engagements and Promotional Code. Become an expert in oncology where GSK have brands and support associated activities related to those brands. Be updated on scientific knowledge on oncology; GSK molecules and its PI to ensure its ‘On Label’ communications on various platforms. Support in feasibility assessment of potential research sites, develop concept notes, proposals, budgets, data collection and monitoring tools for field studies. Provide medical inputs into development and execution of brand strategy. Pharmacovigilance: Support Named Safety contact in strengthening of oncology Pharmacovigilance; ensure self-learning. Knowledge/ Education / Previous Experience Required Educational Background :- Minimum Level of Education - MBBS with post graduate qualification Preferred Level of Education - Post graduate qualification in Pharmacology / Public Health Why is this Level of Education Preferred - To interact with specialized HCPs Job-Related Experience:- Minimum Level Of Job-Related Experience Required Excellent written and oral communication skills in English, local language Experience of presenting scientific topics at different settings A sound understanding of the principles and practice of ICH-GCP and internal SOPs. Well-demonstrated ability to understand scientific methods and experimental design. 1-2 years in the pharmaceutical industry preferably in the oncology therapy area. Hemato -oncology mandatory. Other Job-Related Skills/Background:- General Competencies Presentation skills at Scientific meetings Communication skills, both verbal and written Technical writing skills Keep up to date with new developments Ability to provide and receive constructive feedback Build and maintain relationships with colleagues Share knowledge with other team members Work as part of a team to reach common goals Deliver creative ideas for continuous improvement Develop good relationships with key opinion leaders Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology). Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way. GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable. If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing askus@gsk.com, so that we can confirm to you if the job is genuine. 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Dr.Medcare is looking for Pharmacist to join our dynamic team and embark on a rewarding career journey. Compounding and dispensing medications, as prescribed by physicians. Monitoring customers drug therapies, advising interventions, and informing customers of any potential side effects. Instructing customers on how and when to take prescribed medications. Conducting health and wellness screenings. Providing immunizations, and other medical services, such as taking blood pressure, temperature measurements, and checking blood sugar levels. Keeping accurate customer records. Ensuring a safe and clean working environment. Completing operational requirements of the pharmacy, including verifying order entries, maintaining records of controlled substances, charges, and removing expired and/or damaged drugs from the pharmacys inventory. Adhering to applicable legal rules, regulations, and procedures governing pharmaceutical practice. Performing other administrative tasks when needed.

Avron Hospitals Pvt. Ltd. is looking for Pharmacy Assistant / Pharmacist to join our dynamic team and embark on a rewarding career journey. Compounding and dispensing medications, as prescribed by physicians. Monitoring customers drug therapies, advising interventions, and informing customers of any potential side effects. Instructing customers on how and when to take prescribed medications. Conducting health and wellness screenings. Providing immunizations, and other medical services, such as taking blood pressure, temperature measurements, and checking blood sugar levels. Keeping accurate customer records. Ensuring a safe and clean working environment. Completing operational requirements of the pharmacy, including verifying order entries, maintaining records of controlled substances, charges, and removing expired and/or damaged drugs from the pharmacys inventory. Adhering to applicable legal rules, regulations, and procedures governing pharmaceutical practice. Performing other administrative tasks when needed.