1075 Pharmacology Jobs - Page 12

Overview The Clinical Assistant plays a vital role in supporting healthcare professionals in various clinical settings, including Level II trauma centers, outpatient facilities, and specialized units such as Pediatric Intensive Care Units (PICU) and medical-surgical departments. This position is essential for ensuring high-quality patient care and efficient operations within the healthcare environment. The Clinical Assistant will engage with patients, assist in medical procedures, and maintain a safe and organized clinical space. Duties Provide direct patient service by assisting with daily activities and ensuring comfort. Administer medications as prescribed while adhering to safety protocols. Support healthcare providers during medical procedures in the Operating Room (OR) and other clinical areas. Maintain accurate medical records and documentation using appropriate medical terminology. Assist with patient assessments and monitor vital signs as needed. Facilitate communication between patients, families, and healthcare teams to enhance patient care. Ensure cleanliness and organization of the clinical environment to promote safety and efficiency. Participate in training sessions to stay updated on best practices in patient care. Skills Knowledge of medical terminology relevant to various specialties, including geriatrics and hospital medicine. Experience or familiarity with working in a Level II trauma center or similar high-acuity settings. Ability to provide compassionate care in outpatient settings as well as during inpatient stays. Proficiency in medication administration techniques and understanding of pharmacology principles. Strong interpersonal skills to effectively interact with patients, families, and team members. Capability to work collaboratively within a multidisciplinary team while demonstrating flexibility in a fast-paced environment. Familiarity with pediatric care principles, particularly within PICU settings. The Clinical Assistant position is ideal for individuals seeking to make a meaningful impact on patient health outcomes while gaining valuable experience in the healthcare field. Job Type: Full-time Pay: ₹12,000.00 - ₹15,000.00 per month Schedule: Day shift Work Location: In person

Job Title: Regulatory Affairs Specialist Job Summary: The Regulatory Affairs Specialist/Manager is responsible for ensuring that the company’s products meet all regulatory requirements and standards. This role involves managing the regulatory submission process, collaborating with cross-functional teams, and ensuring compliance with local, regional, and international regulations throughout the product lifecycle. Key Responsibilities: Regulatory Submissions: Prepare and submit regulatory documents for product approvals, including applications, dossiers, and amendments. Ensure that all submissions meet the regulatory requirements of relevant authorities (e.g., FDA, EMA, etc.). Regulatory Strategy: Develop and implement regulatory strategies for product development and marketing. Provide regulatory advice to product development teams and senior management to ensure compliance and minimize risks. Compliance Monitoring: Monitor and interpret regulatory changes and industry trends, ensuring the company’s products remain compliant. Conduct periodic audits and reviews of regulatory practices within the company. Cross-functional Collaboration: Work closely with R&D, manufacturing, quality assurance, and marketing teams to ensure all regulatory aspects are considered in product design and commercialization. Liaise with external regulatory bodies as necessary to facilitate approvals. Regulatory Documentation: Maintain up-to-date knowledge of all regulatory documents, including product specifications, labeling, and promotional materials. Ensure timely reporting of adverse events and product recalls as required by authorities. Training and Guidance: Provide regulatory training and guidance to other departments within the company. Advise teams on the regulatory implications of business decisions. Qualifications: Bachelor’s degree in Life Sciences, Chemistry, Pharmacology, or a related field (advanced degrees preferred). 2+ years of experience in regulatory affairs, preferably in the relevant industry (pharmaceuticals, medical devices, etc.). Familiarity with international regulatory guidelines and standards (FDA, EMA, ICH, etc.). Strong written and verbal communication skills. Detail-oriented with strong organizational skills. Ability to work independently and manage multiple projects simultaneously. Preferred Skills: Experience with regulatory submissions such as IND, NDA, 510(k), CE Marking, etc. Knowledge of global regulations and market approval processes. Certification from regulatory bodies (e.g., RAC) is a plus. Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Schedule: Day shift Work Location: In person

Ophthalmologist Required Dist Hisar Haryana Salary 2.5 to 3 Lakhs + Share Accommodation Doctor couple can be adjusted in their respective field Or We can also help you to find out suitable job as per your preferred location

Anaesthesiologist Required Gadchiroli Maharashtra Salary 3 to 3.5 Lakhs + Accommodation + Food Sonipat Haryana For ICU IDCCM Preferred Salary 3 to 4 Lakhs Bharatpur Rajasthan Salary 3.5 Lakhs + Gurgaon Haryana Salary 2 Lakhs + Share Required Candidate profile Goalpara, Assam Salary 4 Lakhs + Accommodation Neemrana, Rajasthan Salary 3.5 - 4 Lakhs + Accommodation Batala, Punjab (Male Required) Salary: 3 to 3.5 Lakhs + Accommodation

Overview Please Note: 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 Senior 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 Taking ownership and responsibility for development (write, review, proofread, and data-check) of high-quality, client-ready scientific and medical materials like manuscripts, abstracts, posters, congress and meetings materials, and literature searches and reviews according to client and audience needs with excellent attention to detail Actively involved in reviewing materials developed by scientific writers to ensure strategic alignment and scientific accuracy as needed and providing clear constructive feedback, support, and supervision to writers. Mentor and train scientific writers by sharing best practices and client preferences, thereby contributing to skill development within the team Having excellent knowledge of product/accounts to enable meaningful interactions with clients and authors, including consultancy where necessary. Liaising and building and maintaining strong and long-standing 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. This includes educating and advising clients on how to best implement their strategic and tactical plans and proactively provide recommendations to clients on how to improve scientific content and propose new document types/ways to disseminate client date more effectively Effectively and proactively communicate with team members, authors/faculty, clients and vendors Attend workshops/seminars/training to hone your skills and contribute to organizational objectives Attending 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. Also, supporting with the development of visual content and materials using effective data visualization techniques and approaches. Contributing to innovative “out of the box” solutions for medical writing projects 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 Supporting with pitches, both during the preparation phase and the actual pitch Qualifications And Prerequisites 4+ years of experience in relevant fields of scientific writing in publications 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 Ability to multi-task and work under tight timelines 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. 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.

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description We are seeking a Senior Specialist, Intellectual Property for our North America Group (NAG). The incumbent will be based in India, and report to the Lead, Intellectual Property Counsel - North America. As a Senior Specialist in the IP department, you will collaborate with US Counsel and internal stakeholders to design and implement IP strategies to advance Dr. Reddy’s interest in providing affordable health care solutions. Roles & Responsibilities Work with US Counsel in managing ANDA, 505(b)(2), BPCIA, and PM(NOC) patent litigations, including post-grant patent office proceedings by developing and implementing claims and defenses. Assist in discovery, witness preparations, and competitive landscape analysis. Identify strategies related to Paragraph IV certifications and Section viii carve-outs. Work with US Counsel and DRL R&D in securing freedom-to-operate for Dr. Reddy’s products, including clearance of Orange Book and unlisted patents for the bulk API, route of synthesis, finished dosage form and polymorphs. Conduct prior art, patentability, landscape and freedom-to-operate searches. Examine patents, file histories, prior art, ongoing litigations, and citizen’s petitions for possible Paragraph IV and related strategies for ANDA and 505(b)(2) products. Develop and provide IP inputs as part of product selection. Provide IP prosecution strategy, including by collaborating with R&D on innovation and drafting patent applications. Conduct IP due diligence and provide IP support towards business development activities. Qualifications Educational qualification: Advanced Degree in pharmaceutics, pharmacology, pharmaceutical chemistry, or similar discipline required (MS or PhD); LLB preferred. Minimum work Experience: 14+ years of experience working with life science, biotechnology, and/or pharmaceutical companies in Intellectual Property is required, wherein 6+ years were spent assisting on complex intellectual property issues for the United States litigations. Skills & attributes: Technical Skills Experience in Intellectual Property (IP) domain Experience developing strategies for and assisting in the management of ANDA litigations in the US Skilled in infringement/invalidity analysis, freedom to operate, filing and prosecution, Market launch analysis. Experience leading product Identification and selection in perspective of complex Injectable, inhalation, OSDs in different geographies. Sound knowledge of technologies used in various dosage forms. Due diligence experience for North America region. Experience with both small molecules and biologics, not required, but preferred Behavioural Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Good Negotiation and Influencing skills. Ability to work collaboratively with Regulatory and cross-functional teams across US - India time zones. People management skills Additional Information Benefits Offered At Dr. Reddy’s we actively help to catalyze your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Qualifications: MBBS + MD/DNB in Ophthalmologywith minimum 3 years of expeience as an Assistant Professor in a recognised medical college Key Responsibilities: Conduct patient consultations to assess and address their eye health concerns and medical history. Prepare detailed medical reports and maintain accurate records for each patient. Perform specialized diagnostic tests (e.g., visual acuity tests, OCT, fundoscopy) to identify eye conditions. Develop and recommend treatment plans for various ocular diseases and disorders. Collaborate with a patient's primary physician to ensure integrated care. Carry out thorough physical examinations and assessments of patients eyes. Provide pre-operative and post-operative care for ophthalmic surgeries, ensuring optimal patient recovery. Monitor patient conditions and manage medications or treatments for eye conditions. Evaluate treatment progress and adjust care plans based on patient needs. Communicate daily with staff, including other specialists, administrative personnel, and healthcare professionals, to ensure coordinated care.

Genpact (NYSE: G) is a global professional services and solutions firm delivering outcomes that shape the future. Our 125,000+ people across 30+ countries are driven by our innate curiosity, entrepreneurial agility, and desire to create lasting value for clients. Powered by our purpose the relentless pursuit of a world that works better for people we serve and transform leading enterprises, including the Fortune Global 500, with our deep business and industry knowledge, digital operations services, and expertise in data, technology, and AI. Inviting applications for the role of Business Analyst, Medical Coding In this role, you need to work as Medical coder for Provider Coding. Responsibilities Review medical records, patient medical history and physical exams, physician orders, progress notes, consultation reports, diagnostic reports, operative and pathology reports, and discharge summaries to verify the pertinent CPT and ICD 10 CM codes. To code on Medical reports by assigning appropriate CPT & ICD 10 CM codes based on the documentation and per the client specification. Follow project-specific guidelines without any deviation. Check the LCD policy per insurance specification. Performs assigned tasks/complete targets with speed and accuracy as per client SLAs Compliance with client/project guidelines, business rules, and training provided the company's quality system and policies. Communication / Issue escalation to supervisor if there is any in a timely manner. Willing to learn and keep self-updated with the updated codes. Work cohesively in a team setting. Assist team members to achieve shared goals. Qualifications we seek in you! Minimum Qualifications Must have relevant experience in Medical Coding any (ED, E/M, Urgent Care, Ancillary (Path/Lab/Rad) Thorough knowledge of CPT and ICD-10-CM/PCS, HCPCS Level II, Medicare, Medicaid, and Insurance guidelines. Coding certification: Mandatory CPC (AAPC) and/or CCS (AHIMA) Science graduate/BAMS/BHMS/BPT/BUMS and/or relevant equivalent and relevant work experience Preferred Qualifications/ Skills Relevant years general medical coding experience. Must possess computer skills including, but not limited to, Word, Excel, and PowerPoint. Experience with 3M and encoder preferred. Experience with an EPIC preferred. Must be able to use the internet and other electronic resources for the purpose of research. Advanced understanding of Professional coding guidelines, medical terminology, pharmacology, body systems/anatomy, physiology, and concepts of disease processes Job Business Analyst Primary Location India-Gurugram Schedule Full-time Education Level Bachelor's / Graduation / Equivalent Job Posting Apr 1, 2025, 8:46:35 PM Unposting Date Ongoing Master Skills List Operations Job Category Full Time,

Jeevan Rekha Hospital 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.

Renai Medicity is looking for Senior Neuro Surgeon to join our dynamic team and embark on a rewarding career journeySpecializes in the surgical treatment of conditions affecting the brain, spinal cord, and nervesResponsibilities include evaluating patients, ordering and interpreting diagnostic tests, developing treatment plans, and performing surgeries.Prescribing medication and performing follow-up evaluations.Must have strong surgical skills, as well as a thorough understanding of anatomy, physiology, and medical technologies.

Role & responsibilities 1. Medication Review and Optimization:Review medication orders to ensure appropriateness, safety, and effectiveness of drug therapy 2.Identify and resolve medication-related problems, including drug interactions, contraindications, and duplications 3. Adjust medication regimens based on patient-specific factors, such as age, weight, renal/hepatic function, and concomitant medications 4. Patient Counseling:Educate patients and their caregivers about their medications, including dosage instructions, potential side effects, and precautions Address patient concerns and provide guidance on medication adherence 5. Clinical Rounds and Consultations:Participate in multidisciplinary rounds with healthcare teams to discuss patient progress and medication-related issues 6.Collaborate with physicians, nurses, and other healthcare professionals to develop individualized treatment plans 7.Drug Information and Education:Stay updated on the latest drug therapies, treatment guidelines, and pharmacotherapy developments 8. Provide drug information to healthcare professionals and assist in evidence-based decision-making 9. Medication Safety and Quality Improvement:Implement medication safety initiatives to prevent medication errors and adverse drug events 10.Participate in quality improvement programs to enhance patient care and medication-related processes 11.Research and Clinical Trials:Participate in research projects and clinical trials related to medication therapies and outcomes 12.Regulatory Compliance:Ensure compliance with all relevant laws, regulations, and hospital policies regarding medication use and distribution Preferred candidate profile

Job Title: Study Director (Toxicology, Analytical, Gen Tox) Company: Vivo Bio Tech Ltd Location: Hyderabad Experience: 4-10 Years Education: Postgraduate (Life Sciences/Pharmacology/Toxicology or related fields) Vivo Bio Tech Ltd is seeking experienced Study Directors to lead and manage preclinical studies in accordance with GLP and regulatory guidelines. The role involves planning, execution, monitoring, and reporting of toxicology, pharmacology, or biocompatibility studies. Requirements: Postgraduate degree in Life Sciences or related discipline. 4-10 years of relevant experience in preclinical/GLP studies. Strong understanding of regulatory guidelines and data integrity practices. Excellent analytical, communication, and project management skills. Thanks and Regards, G Naga Sravani HR-Recruiter nagasravani.g@virinchi.com

Applications are invited for the post of Senior Resident in the following disciplines: Anatomy, Physiology, Biochemistry, Pharmacology & Microbiology Eligibility for Senior Resident: 1. Postgraduate degree in the subject Doctor of Medicine (MD) or Diplomate of National Board (DNB) in the subject. 2. Postgraduate Medical degree in Master of Science (MSc) with Doctor of Philosophy (PhD) shall be eligible for appointment as a Senior Resident. For further information kindly contact at 82889-69200 Mail your CV at principal@dmch.edu by 25th July 2025

Job Title: Pharmacist Department: Pharmacy Reports to: Medical Superintendent / Hospital Administrator Location: [Insert Location] Job Summary: The Pharmacist is responsible for dispensing medications, providing drug information, maintaining pharmacy inventory, and ensuring the safe, effective, and rational use of pharmaceutical products in accordance with legal and medical standards. Key Responsibilities: Dispense prescriptions accurately and ensure proper labeling. Review and interpret physician orders and detect potential drug interactions. Counsel patients on correct medication usage, side effects, and storage. Maintain and manage pharmacy inventory and place orders as required. Ensure compliance with all applicable regulations and licensing requirements. Maintain records of controlled substances and ensure proper documentation. Collaborate with healthcare professionals for medication therapy management. Monitor expiry dates and dispose of expired or damaged drugs appropriately. Maintain cleanliness and organization of the pharmacy area. Qualifications: Bachelor’s or Diploma in Pharmacy (D.Pharm / B.Pharm). Registered with the State Pharmacy Council. Minimum 1–2 years of experience in a hospital or retail pharmacy (preferred). Skills & Competencies: Strong knowledge of pharmacology and drug interactions. Attention to detail and accuracy. Excellent communication and counseling skills. Good organizational and inventory management abilities. Familiarity with pharmacy management software. Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.40 per month Benefits: Health insurance Provident Fund Schedule: Day shift Evening shift Morning shift Work Location: In person

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 POSITION TITLE Technical Lead REPORTING TO: IT Manager REPORTING LOCATION: Bangalore WORKING LOCATION: Bangalore, India SUMMARY OF POSITION AND OBJECTIVES: 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 Principal QA Engineer, you will be a crucial part of our delivery team, ensuring the product features are completely automated and reducing the idea to live time to Business. 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 IT Manager. Required Experience and Skills Required Qualifications: Engineering graduate/post graduate with at least 9 years of experience in total and at least 3 years as a technical lead your joining. Experience: 9 to 12 years of experience with developing end –to- end web applications using Microsoft stack of Technologies. Strong working knowledge of Web application development using ASP.NET technologies Strong working knowledge of SOLID principles and design patterns Good understanding of UML, object-oriented programming (OOP) and Object Oriented Design principles Should have worked on at least one SOA (Service Oriented Architecture) project Strong experience in designing and working with n-tier architectures Uncompromising attitude towards quality TDD, BDD, UML Should have worked in an AGILE practice methodology (preferably SCRUM) Able to provide technical recommendations and solve technical problems Must be a quick learner Technology skills: Strong working knowledge of .NET Core, C#, MVC, WCF Rest and WebAPI, nUnit/MsUnit, EF Working knowledge of JavaScript, TypeScript, JQuery, Angular 2 or above, Jasmine, HTML5 and CSS3 technologies Working knowledge of MS SQL Databases , Powershell Working knowledge of ESB or Message Queuing (MSMQ) is an added advantage Well versed with Unit testing frameworks Familiarity with UI testing framework Familiarity with WPF Qualifications Engineering graduate/post graduate with at least 9 years of experience in total and at least 3 years as a technical lead Additional Information Personal Skills: Excellent analytical and problem solving skills Excellent verbal and written communication skills Ability to articulate and present different points-of-views on various topics related to project and otherwise. Eager to learn and continuously develop personal and technical capabilities.

Company Description 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 35 years, Eurofins has grown from one laboratory in Nantes, France to 62,000 staff across a network of over 1,000 independent companies in 61 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. 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 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 next-generation applications and Laboratory Information Management Systems (LIMS). As Senior Software Engineer, you will be a crucial part of our delivery team, ensuring the Eurofins Electronic Notebook application’s (which is part of BPT’s application labsuite and one of the significant application) operations in production is adequately supported with quick turnaround time there by reducing the impact on Business due to application related requests, and issues. 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 qualification 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 Core (6/7/8), C#, Asp.net Core, MVC, WebAPI, Postman. Strong Working knowledge of Angular 7 or above, JavaScript, TypeScript, jQuery, HTML5 and CSS3. Good working knowledge of Cosmos DB, Elastic Search, Redis, Azure Functions, Azure DevOps, CI/CD, Event Driven Architecture, Domain Driven Architecture, Microservices, MSSQL – SQL etc. Experience with usage of Azure DevOps Familiar UI testing and Unit Testing (MS Test/ Jasmine/ MOQ/ NUnit/ Karma etc.) Good understanding of object-oriented programming (OOP) 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 complex issues, performance-related issues, how to write efficient code and query Working knowledge Authentication and Authorization [Plus OAuth2, OpenIDC etc.] (5+) Should have worked on at least one SOA (Service Oriented Architecture) project Should have worked in an AGILE practice methodology (preferably SCRUM) Personal Skills: Excellent analytical and problem solving skills Excellent verbal and written communication skills Ability to articulate and present different points-of-views on various topics related to project and otherwise. Successful teamwork experience and demonstrated leadership abilities are required. Eager to learn and continuously develop personal and technical capabilities. Responsibilities Advanced Troubleshooting & Issue Resolution Investigate and resolve complex issues (or escalated issues from Level 1 and Level 2 support). Analyze logs, application behavior, and system performance to identify root causes. Handle incidents involving application crashes, data inconsistencies, or integration failures. Root Cause Analysis (RCA) & Permanent Fixes Conduct detailed RCA for recurring or high-impact issues. Collaborate with development teams to implement long-term fixes or enhancements. Application Monitoring & Performance Tuning Use monitoring tools (e.g., app insights, Grafana, kibana etc.) to proactively detect anomalies. Optimize application performance and scalability. Deployment & Release Support Support production deployments, hotfixes, and rollback procedures. Validate post-deployment stability and performance. Compliance & Validation Ensure support activities align with GxP , and any other applicabl regulatory requirements. Maintain audit trails and documentation for all changes and incidents. Collaboration & Communication Work closely with DevOps, QA, and product teams to resolve issues. Communicate technical findings to non-technical stakeholders when needed. Knowledge Management Document solutions, workarounds, and known issues in a knowledge base. Provide guidance and training to L1/L2 teams. Additional Information Personal Skills: Excellent analytical and problem solving skills Excellent verbal and written communication skills Ability to articulate and present different points-of-views on various topics related to project and otherwise. Eager to learn and continuously develop personal and technical capabilities. Required Qualifications: MCA or Bachelors in Engineering, Computer Science or equivalent. 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.

Company Description 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 35 years, Eurofins has grown from one laboratory in Nantes, France to 62,000 staff across a network of over 1,000 independent companies in 61 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. 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 QA Engineer Automation 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 Senior Automation Engineer, you will be a crucial part of our delivery team, ensuring the product features are completely automated and reducing the idea to live time to Business. 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 manager. Required Experience and Skills Experience: Experience between 5 to 8 yrs. Expertise in Automation Testing of Web and Windows-based applications Good experience in building and using automation frameworks using technologies: Java/ C#. Experience in doing in-sprint automation. Strong Automation background with experience in identifying and reviewing test cases and testing results. Ability to understand complex requirements and transform those into Test Scenarios, Test cases and Test Scripts. Proficient in Version Control tool (ex: GIT ) Worked on automating the CI/CD pipelines. Good Knowledge of Manual Testing of Web and Windows-based applications. Have an excellent understanding of SDLC and STLC lifecycles. Hands-on work experience in preparing Test Strategy, Test plans and Requirement traceability matrix. Exposure to different Testing types – Sanity, Functional, Integration, Exploratory and System testing. Understanding of Agile/Scrum methodology and working experience in an Agile environment. Proficient in creating Test Reports. Should know about analyzing the Risks. Prior experience in testing LIMS would be an added advantage. Specific skills required Expertise in Automation Testing using Selenium/Specflow/BDD/Protractor/WebDriver IO. Hands-on experience in programming languages (C#, Java, Python, JavaScript). Experienced in Creating VM for Automation and setting up the configuration in the test suite and runners. Hands-on experience in SQL to write medium complex queries (e.g. Joins/sub-queries etc.). Good understanding of JSON, XML, REST and experience in testing web services using POSTMAN, REST Assured, JSON Lint, SOAP UI. Experience with any defect tracking tool like Jira, TFS/MTM, Bugzilla, etc. Experience on any test management tools like TFS/MTM, ALM, etc Desirable Experience Knowledge of Performance testing. Knowledge of Security testing. Knowledge of Mobile Automation Testing. Additional Information Personal Skills: Excellent analytical and problem solving skills Excellent verbal and written communication skills Ability to articulate and present different points-of-views on various topics related to project and otherwise. Eager to learn and continuously develop personal and technical capabilities. Required Qualifications: Bachelors in Engineering, Computer Science or equivalent.

Job Description Regional Medical Advisor THE OPPORTUNITY The RMA (Regional Medical advisor) will be a valued representative at our company working in the field to interact and engage key stakeholders. Our medical affairs team objective is to provide scientific expertise across their identified regions/products/therapy areas to these valued customers. What You Will Do The RMA will have the following key responsibilities Developing and implementing medical strategies Scientific leader identification development and engagement to build regional, national or international relationships to contribute to understanding of diseases, scientific trends, practice guidelines, and treatment patterns in areas relevant to our business Support to the health care providers by providing accurate and up-to-date medical information Education, training and periodic medical updates to the commercial team as demanded Ensuring compliance with local regulations and industry standards in all medical activities Responsibilities And Primary Activities Scientific Expertise Developing and maintaining an in-depth understanding of the company's products, therapeutic areas, and relevant scientific research. Staying updated on the latest medical and scientific advancements, clinical guidelines, and treatment protocols. SL & KDM Engagement Building and maintaining relationships with Scientific Leaders (SLs), Key decision makers (KDMs) healthcare professionals, and academic institutions. Engaging in scientific discussions, presenting clinical data, and providing educational support to KOLs regarding the company's products and therapeutic areas. Support to medical strategy In alignment with the line manager, provide strategic inputs, and expertise, to product management towards ethical promotion of assigned products Medical Education Providing scientific and medical education to internal stakeholders, including sales teams, marketing teams, and other cross-functional colleagues. Collaborating with the Medical Affairs team to develop and deliver training materials, presentations, and scientific symposia. Scientific Exchange Facilitating scientific exchange and knowledge transfer between the company and external stakeholders. Participating in medical conferences, advisory boards, and scientific meetings to gather insights, share data, and contribute to the scientific community. Clinical Data Communication Interpreting and communicating clinical trial data, real-world evidence, and other scientific information to healthcare professionals, regulators, and other relevant stakeholders. Ensuring accurate and compliant dissemination of scientific information in accordance with regulations and company policies. Clinical Research Provide medical support for local studies, including need-based visits to identify study sites Lead Investigator Initiated Trials Cross-functional Collaboration Collaborating closely with cross-functional teams, including Clinical Development, Regulatory Affairs, Marketing, and Market Access, to provide scientific input, support clinical trial design, contribute to regulatory strategies, and align on medical communication plans. Facilitate access to scientific leaders as appropriate. Support as well as own medical initiated projects in line with therapy area that would involve a strong stakeholder interface Provide scientific support to sales team Medical Information Addressing medical inquiries and providing timely and accurate responses to healthcare professionals, patients, and other stakeholders. Ensuring that medical information materials, such as medical letters and FAQs, are up to date and compliant. Sales Force Training Provide medical training to sales colleagues on the therapy areas assigned Assist in pre-launch and launch training to sales staff for new products. Compliance Adhering to relevant legal, regulatory, and compliance guidelines, including the organization's code of conduct and industry-specific regulations. Ensuring all activities and interactions are conducted ethically and in compliance with applicable laws and regulations. Overall, RMA in Medical Affairs acts as a scientific expert and liaison between the company and external stakeholders, playing a crucial role in building scientific credibility, fostering relationships, and supporting the company's strategic objectives in the healthcare industry. Values and Behaviors Consistently adhere to/demonstrate all company Values with focus on excellence Work in harmony with internal and external stakeholders What You Must Have To be successful in this role, you will have strong marketing skills as well as business capabilities Educational Background A strong academic background in life sciences, such as a medical degree (MD), doctorate (Ph.D.). Other relevant degrees in biology, pharmacology, or related fields may also be considered. Industry Experience 1 year experience in the pharmaceutical, biotechnology, or medical device industry is often preferred. This could include experience in clinical research, medical affairs, or related roles that have exposed the candidate to scientific and medical aspects of the industry. Therapeutic Area Expertise Demonstrated knowledge and expertise in the specific therapeutic area relevant to the position. This may involve experience working on clinical trials, publications, or direct patient care in that therapeutic area. Scientific and Clinical Knowledge A strong understanding of medical and scientific principles, including knowledge of clinical trial design, data analysis, and interpretation. Familiarity with relevant disease states, treatment guidelines, and emerging trends in the therapeutic area is also important. Communication and Relationship-Building Skills Excellent interpersonal, communication, and presentation skills are crucial for a RMA role. The ability to effectively communicate scientific information to various stakeholders, including Key Opinion Leaders (KOLs), healthcare professionals, and internal teams, is essential. Analytical and Problem-Solving Skills RMAs are often required to analyze complex scientific data, identify insights, and provide recommendations. Strong analytical and problem-solving skills are valuable for interpreting clinical trial results and addressing medical inquiries. Adaptability and Flexibility RMAs often work in dynamic and fast-paced environments, requiring the ability to adapt to changing priorities and work independently. Flexibility to travel frequently to engage with external stakeholders is also often required. Regulatory and Compliance Knowledge Familiarity with relevant legal, regulatory, and compliance guidelines, such as Good Clinical Practice (GCP), the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines, and local regulations governing medical communications. Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry professionals ensuring the scientific value of our products is realized. We engage and train internal employees to ensure that they thoroughly comprehend the science behind the medicine and review further unmet medical needs to bolster collaboration and further differentiate our portfolio. We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe. We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status Regular Relocation VISA Sponsorship Travel Requirements Flexible Work Arrangements Not Applicable Shift Valid Driving License Hazardous Material(s) Required Skills Preferred Skills Job Posting End Date 07/31/2025 A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID R339104

shroffsfoundation 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.

JOB DESCRIPTION Designation: Associate Scientist / Senior Associate Scientist Job Location: Bangalore Department: TM-TDDT About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Job Purpose (1-2 Lines) We are seeking motivated master s level scientists (MS, MTech, MSc, etc) to join the Translational Medicine team at the Biocon Bristol Myers Squibb Research Center in Bangalore, India. Key responsibilities of this role are to serve as an execution arm for the preclinical support of asset programs through mechanism of action-based studies, differentiation from standard of care and competitive therapeutics, combination rationale, new indications (life cycle management), and patient selection strategies. S/He will work directly with translational scientists, disease leaders within translational medicine, and will also interact with thematic research centers in early development within the company. Key Responsibilities: Conduct preclinical/laboratory experiments on late stage BMS portfolio compounds to support annual goals and objectives for Translational Medicine (for internal /external, collaborations, compound specific plans etc). Responsible for delivering data in support of translational strategies including biomarkers, patient selection hypotheses, dose and schedule, combination strategies, resistance mechanisms and differentiation. Interfaces with TM scientists across departments to ensure seamless flow of information for assets which are entering the remit of translational medicine. Assists in designing experiments and delivering data for collaborative projects along with TM scientists. Maintains comprehensive records, communicates regularly and makes presentations within the department, as required. Reports experimental finding in written nonclinical pharmacology study reports, to support regulatory filings. Educational Qualification: Masters with at least 2 years of relevant work experience across immunology, oncology, heme-oncology focus areas. Industry experience is a plus. Multiple positions can range upto 6 years of experience. Technical/functional Skills: Cell culture, primary cell isolation, cell transfection and single cell cloning; including siRNA / CRISPR / TALEN or HDR workflows Gene expression methods including qRT-PCR and/or familiarity with RNA sequencing, epigenomic methods including methylation analysis, ChIP etc Protein analyses and immunoassays, and cell phenotyping analysis (e.g. ELISA, MSD, Luminex, TSA, CBA, flow cytometry). Design, setup and execution of autoimmune, solid tumor oncology or heme-oncology in vivo pharmacology models. Excellent verbal and written communication skills, familiarity with standard or relevant software platforms, and scientific qualities are expected. Competence in analysis and solving of problems, keeping track of overall goals. Maintain a good understanding of the methodological basis and biological significance of assays performed. Forecast potential issues regarding support of assays for current and long term projects. Devise strategic solutions to identified and potential hurdles/issues and efficiently and proactively troubleshoot technical and experimental problems. Experience: 2-6 years Behavioral Skills: A self-starter, who is/can become technically proficient in a diverse set of techniques and assays with a focus on quality and speed, and will meticulously follow internal SOPs Good basic lab skills required (pipetting, balances, etc.) Highly detailed and meticulous, high standards of data entering and QC Must be highly adaptive to changing timelines and goals Must be comfortable taking on complex tasks with minimal direct supervision An excellent multitasker with an ability to be level-headed in a fast-paced lab setting Team-oriented and comfortable working in a highly dynamic matrix environment across multiple locations Prior experience working with patient samples (i.e. FFPE tissue, Fresh Frozen tissue, blood) or working in a CLIA/GCLP/clinical environment is a plus Must be comfortable and able to work with animal (rodent) or human derived samples Equal Opportunity Employer: .

Creative Content & Growth Marketer (1–2 YOE) @ OnCourse Learning Location: India Experience: 1–2 Years (strictly enforced) Type: Full-time About Us OnCourse is an early-stage learning-tech startup reimagining how students prepare for high-stakes exams like NEET PG, INI-CET, and USMLE . We’re building a smart learning engine powered by AI and cognitive science to personalize, accelerate, and make exam prep radically more effective. We’re not building “just another edtech app.” We’re building the future of learning —and that story needs a voice as bold as our mission. Who We’re Looking For Y oung, hungry storyteller with 1–2 years of hands-on content and growth experience who: Lives inside students’ heads —you intuitively know what hooks a stressed-out NEET-PG aspirant at 11 p.m. and what sparks a share-fest in a USMLE Discord server. Is from a medical or life-sciences background (or has created for that audience) and can translate dense concepts into scroll-stopping nuggets. Crafts thumb-stopping content —Reels/Shorts, carousels, memes, threads—that earns shares, saves, and comments (show us proof!). Balances creative instinct with data —A/B tests, retention curves, cohort metrics are second nature. Possesses a global outlook —you grok why an anatomy meme explodes on TikTok in the US but a pharmacology carousel trends on Indian Insta. Is a self-starting creative who turns fuzzy ideas into shipped campaigns in days, not weeks. Thrives in ambiguity, embraces feedback, and iterates at startup speed. If you love turning insights into viral stories—and watching the metrics spike—this is your playground. What You’ll Work On Own OnCourse’s voice across Instagram, YouTube, TikTok, X, LinkedIn, email, push, and in-app surfaces. Ideate, script, shoot/animate, and publish daily short-form videos and carousel posts that make medical concepts binge-worthy. Build viral loops & share hooks inside product experiences (quizzes, streaks, leaderboards). Partner with AI, product, and design teams to turn raw features into narratives learners feel . Run growth experiments : headline tests, retention nudges, referral prompts—measure, learn, repeat. Curate & amplify UGC from toppers, resident doctors, and student creators worldwide. Track and report KPIs (views, watch time, CTR, activation, retention) to steer the content roadmap. Stack & Tools Creative : Adobe Suite / Figma / CapCut / Descript / Canva Distribution : Instagram, YouTube Studio, TikTok, LinkedIn, X, Discord, Substack Analytics : GA4 / Mixpanel / native platform dashboards AI Assist : ChatGPT, Midjourney, Runway, Descript overdub Collab : Notion, Slack, Linear, Loom Who This Role Is NOT For People who are not Doctors ; People who are not with Life Sciences background Folks without a portfolio or data-backed proof of content performance Marketers who need strict brand guidelines before creating Candidates with < 1 or > 2 YOE People who dislike rapid experimentation and public feedback loops Why Join Us Front-row seat : Shape the voice of a product already loved by thousands of medicos. Speed & autonomy : Ideate Monday, ship Tuesday, analyze Thursday. High-leverage learning : Work with AI engineers, cognitive-science experts, and growth hackers. Culture of writing & clarity : Ideas > hierarchy; outcomes > optics. Flexibility : Remote-friendly, async-friendly—own your craft, not just your hours. Apply If… You’ve grown an account from zero to thousands (or millions) of engaged followers—and have the screenshots to prove it. You live on creator Twitter, study hooks on LinkedIn, reverse-engineer viral Shorts, and know the difference between a US TikTok trend and an Indian Insta reel. You’re passionate about medical education and want to make learning addictive— and you’re ready to own that narrative . How to apply: Send us (1) your CV, (2) a portfolio or reel of your best-performing content with metrics, and (3) a quick Loom explaining one growth idea you’d try at OnCourse next month. Let’s make learning go viral.

Required community Medicines for Freshers MBBS MD or DNB

SENIOR RESIDENT IN PHARMACOLOGY JOB IN PERUMBALUR, TAMILNADU, INDIA Designation: SENIOR RESIDENT IN PHARMACOLOGY Qualification: MD PHARMACOLOGY Experience: As per NMC norms Male or Female doctors Tamil speaking doctors preffered

SENIOR RESIDENT IN PHARMACOLOGY JOB IN PERUMBALUR, TAMILNADU, INDIA Designation: SENIOR RESIDENT IN PHARMACOLOGY Qualification: MD PHARMACOLOGY Experience: As per NMC norms Male or Female doctors Tamil speaking doctors preffered

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 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 Healthcare Professional, such as 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. 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.***