In this Role you will be Responsible for Should have experience in Radiology coding The coder reads the documentation to understand the patient's diagnoses assigned. Transforming of healthcare diagnosis, procedures, medical services, and equipment into universal medical alphanumeric codes Creating uniform vocabulary for describing the causes of injury, illness & death is the role of medical coders. Medical coding allows for Uniform documentation between medical facilities. The main task of a medical coders is to review clinical statements and assign standard Codes Requirements of the role include 1 Year of experience in any Healthcare BPO - University degree or equivalent that required 3+ years of formal studies in Life science/BPT/Pharm/Nursing Good knowledge in human Anatomy/Physiology 1+ year(s) of experience using a computer with Windows PC applications that required you to use a keyboard, navigate screens, and learn new software tools. Ability to work scheduled shifts from Monday-Friday 7:30 AM to 5:30 PM IST and the shift timings can be changed as per client requirements. Flexibility to accommodate overtime and work on weekend basis business requirements. It is Mandatory to return to office based on client or business requirement.

To dispense correct medicines from shelves against patient indents To issue medicines to employees against prescriptions by the authorized medical officer To arrange medicines on shelves according to expiry dates Male candidates preferred

"We are actively seeking a pharmacist to join our team at Mibo health & happiness care, a renowned premium psychiatric hospital." Preferably looking for candidates with at least 1 year experience in pharmacy setting Freshers with good knowledge of handling a pharmacy can also apply Salary will be decided according to experience *Valid license registered in Karnataka is mandatory* accommodation can be provided on request Duties & Responsibility - Accurately dispense prescribed medications to inpatients and outpatients. Ensure proper labeling and packaging of medications. - Maintain and manage pharmacy inventory, ensuring adequate stock levels and minimizing wastage. - Monitor expiration dates and remove expired medications from circulation. - Review medication orders for accuracy, appropriateness, and potential drug interactions. - Provide medication counseling to patients and family members, explaining dosage instructions, potential side effects, proper usage and the importance of adherence. Address patients' questions and concerns regarding their medications. - Work closely with other healthcare professionals, including doctors, nurses, and therapists, to provide comprehensive patient care. - Be prepared to provide medications and pharmaceutical support during medical emergencies and code situations. - Ensure compliance with Indian pharmaceutical laws, regulations, and hospital policies. Maintain electronic or paper records of all medication-related transactions and interventions. - Stay updated with the latest developments in pharmacology and healthcare by participating in continuing education programs. Job Types: Full-time, Permanent, Fresher Pay: ₹19,000.00 - ₹28,000.00 per month Schedule: Day shift Ability to commute/relocate: Bangalore, Karnataka: Reliably commute or planning to relocate before starting work (Required) Education: Diploma (Required) License/Certification: Pharmacist Registration (Required)

Hiring Fresh Pharmacy and Life Science Nursing Graduates Medical and Para Medical For Claims Associate Freshers Only Applicants should have good knowledge in Medical Coding Anatomy and Medical Terminology. Required Candidate profile Candidates Should have good knowledge in Medical Coding ICD 10, Anatomy Medical terminology Candidates with Excellent communication skills (verbal and written) Good typing speed

Radiologist, Pediatrics, Orthopedic, General Medicine

Hiring Fresh Pharmacy and Life Science Nursing Graduates Medical and Para Medical For Claims Associate Freshers Only Applicants should have good knowledge in Medical Coding Anatomy and Medical Terminology. Required Candidate profile Candidates Should have good knowledge in Medical Coding ICD 10, Anatomy Medical terminology and CPT Immediate Joiners Will be Preferred

Hi We are hiring for ITES Company Role -Medical Reviewer Qualification : MBBS/MD only (MCI Certification is not mandate**) Experience Range : 1 to 7 Years Preferred Experience: Minimum of 1 years of experience in PV/ Clinical Research (drug safety) Job Description: Author a company clinical comment (CCC) for case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Edit the Periodic Report Comment, if applicable, directly within the Periodic Report Comment field in the Patient Safety database. Perform the following actions within the Comments field of the GSP Review Workflow step in the Patient Safety database: -Review and respond to any queries/comments from the Case Owner, which are recorded in the Comment field of the GSP Review Workflow step in the Patient Safety database. -Detail any requests for changes to the case, including the narrative. -Detail any follow-up information that is required and not already noted within the Query Manager in the Patient Safety database. Provide product advice as required, especially with regards to case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Review the company causality assessment provided by Medical Advisor. • Review the medical sense including seriousness and coding of the case in the global context of the drug or clinical project, including the narrative, AE/SAE terms, suspect drugs, concomitant medications, laboratory data, and medical history. To provide documentation of the review and case comments in Sapphire in Medical Review workflow. Maintain knowledge of the marketed drug currently under litigation. Maintain knowledge of the company disease and therapeutic areas for marketed drugs and drugs in development through periodic medical review training held by client medical staff. Skills required: Computer Literate (good knowledge of MS Office) Sound understanding of the Drug Safety and Regulatory process Good problem solving and decision-making skills Capability to lead by motivation and example Ability to prioritize schedule and organize Excellent interpersonal and communication skills To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Medical Reviewer Mumbai (Job Code # 47) b) For Position in Pune Search : Medical Reviewer Pune (Job Code # 48) c) For Position in Bangalore Search : Medical Reviewer Bangalore (Job Code # 51)

We are currently hiring for DSA I role with a minimum of 3 to 5 years Of experience in Pharmacovigilance Perform triage & intake of ICSR received daily in ARGUS databases. Ensure data entry of ICSR in ARGUS Knowledge In Aggregate Reporting is Must Required Candidate profile Require 3 to 5 years of pharmacovigilance case processing experience. Responsible for coding events using MEDDRA Any Life Sciences(B pharm/M Pharm/ Pharm D, Life Sciences, Nursing, BDS, BPT)

Job Title: Ayurveda Consultant (Dravyaguna ) Location: Remote (Chandigarh, Mohali, Panchkula) Job Type: Freelance Education: BAMS + MD (Dravyaguna) Availability: Immediate We are seeking a highly qualified and motivated Ayurveda Consultant and Product Formulator with a strong academic background in Dravyaguna (Ayurveda Pharmacology) and hands-on experience in herbal product innovation. With proven expertise in medicinal plant research, drug standardization, and product formulation, this professional brings both traditional Ayurvedic knowledge and modern application skills to the table. Job Type: Freelance Schedule: Day shift Work Location: Remote

We are currently hiring for DSA I role with a minimum of 1 year experience in Pharmacovigilance Perform triage & intake of ICSR received daily in ARGUS databases. Ensure data entry of ICSR in ARGUS Required Candidate profile A minimum of 1 year pharmacovigilance case processing experience. Responsible for coding events using MEDDRA Any Life Sciences(B pharm/M Pharm/ Pharm D, Life Sciences, Nursing, BDS, BPT) are Eligible

Urgent vacancies for Faculties AP & Associate with good experience in medical college at a medical college in Meerut, UP Qualification as per NMC Norms Salary as per industry Norms,

Key Responsibilities: Dispensing Medications: Accurately review and fill prescriptions. Ensure compliance with legal and ethical standards in dispensing medicines. Patient Counseling: Provide clear instructions on medication usage, potential side effects, and interactions. Advise patients on the management of their health and wellness. Medication Management: Oversee and manage stock levels to ensure the availability of essential drugs. Maintain records of all prescriptions and inventory. Collaboration: Work closely with doctors, nurses, and other healthcare professionals to ensure optimal patient care. Offer expertise on drug selection, dosage, and potential interactions. Regulatory Compliance: Stay updated on pharmaceutical regulations and guidelines. Ensure proper labeling and storage of medications. Education and Awareness: Provide information about vaccinations and health screenings. Educate patients and communities about preventive healthcare measures. Research and Development (Optional): Contribute to research on new medications or healthcare products. Participate in clinical trials, if applicable. Skills and Qualifications: Educational Requirements: Bachelor’s or Doctorate degree in Pharmacy (B.Pharm or Pharm.D). Licensure: Valid pharmacy license as per local regulations. Technical Skills: Proficiency in pharmaceutical software and tools. Soft Skills: Excellent communication, attention to detail, and problem-solving abilities. Knowledge Base: In-depth understanding of pharmacology, drug interactions, and medical terminology. Job Type: Full-time Pay: ₹14,000.00 - ₹18,000.00 per month Schedule: Day shift Education: Diploma (Preferred) Work Location: In person

We are looking for Medical Science Liaison- Oncology for a Global Pharmaceutical MNC. Position: Medical Science Liaison- OncologyQualification: MBBS/ MD PharmacologyExperience: Minimum 6 months of experience in Oncology as MSL/RMA (Freshers with MD Pharmacology degree can apply too)Location:Kolkata / Delhi 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 RequirementsA] Minimum Requirements:Education: MBBS/MDMinimum 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

Job Description :- Clinical Work Provide direct & indirect patient care in emergency care situations. Provide any & every detail about the procedures, medications, and answer patient queries & subsequent follow-up. Reporting & documenting USG findings/treatment plan in File/Portal. Documenting the prescribed mediation/Stimulation/HRT drugs etc. & in file/portal/ providing Trigger time. Executing all Donor Related Activity, in association with Donor Coordinator. Administer injection to patient/donor, as prescribed in file. Maintain stock of all required injections/drugs. Elicit accurate & relevant patient/donor medical history Co-ordinate procurement of necessary documents from patient/donor, per PCPNDT regulations. Update all patient records in both physical, as well as digital format. File all regulatory forms/consents before each procedure. Submit PCPNDT forms timely, as required by PCPNDT office. Identify & provide for physical, emotional, and developmental needs of patients. Counsel patients & their families; explain procedures planned for them. Ensure all procedures are carried out as per the SOP, and are compliant with the Policies on Universal Protection, Biomedical Hazard & Infection Control. Should have valid state registration Only immediate joiners apply for the role

Department Hierarchy Drugs Content Job posted on May 06, 2025 Employee Type Intern Experience range (Years) 0 - 1 year Designation- Intern Duration- 3 to 4 Months Location- Gurugram, Haryana About Tata 1mg: Tata 1mg is a trusted health partner for end consumers and large institutions. Our Mission is to make healthcare understandable, accessible, and affordable for all Indians. Over the past three years, we've worked to build a healthcare platform that guides customers to the right and affordable care. Today, Tata 1mg is present in 1000+ cities– And we’re just getting started. Leading the chart as one of the top consumer health platforms through ePharmacy, eDiagnostics, e-consult and offline stores, Tata 1mg has delivered over 15M ePharmacy orders, 2M eDiagnostics orders & 1M+ organic users/day in 2022 and we are just getting started. Our strongest asset is our 6400+ people enabling us to deliver on our mission consistently. Know more about us: https://www.1mg.com/aboutUs What are we looking for: We are looking for a detail-oriented and proactive Regulatory & Data Associate with a strong foundation in pharmacology and regulatory compliance to support our pharmaceutical operations. The ideal candidate should have a good understanding of the Drugs and Cosmetics Act, strong data documentation and validation skills, and be comfortable using digital tools for research and analysis. Key Responsibilities: Ensure compliance with the Drugs and Cosmetics Act for product-related documentation. Apply pharmacological knowledge to validate drug information and related data. Maintain accurate and organized documentation for regulatory submissions and internal use. Use intermediate-level Excel (e.g., VLOOKUP, data validation) for data analysis and reporting. Create and format documents in MS Word for compliance and communication needs. Conduct smart and efficient research using Google search and other online tools. Support cross-functional teams with data checks and regulatory documentation. Requirements: Bachelor's degree in Pharmacy, Life Sciences, or related field. Solid understanding of the Drugs and Cosmetics Act and basic regulatory requirements. Strong foundation in pharmacology. Proficiency in Excel, Word, and online research tools. Excellent attention to detail and organizational skills. Please note- NOC from respective college is mandatory at the time of joining

About Turing:Turing is an AI-powered tech services company on a mission to accelerate the advancement and deployment of AGI. Recently backed by $111M in Series E funding, we’re scaling our efforts to connect exceptional global talent with transformative projects in AI. Role Overview:We are seeking candidates with strong medical knowledge and diagnostic abilities in various fields of medicine.The ideal candidate should have a deep understanding of medical concepts, particularly at the level required for medical school or professional practice.You should be able to break down complex medical cases into simple, clear explanations and work efficiently. What does day-to-day look like:You would spend time solving a variety of advanced medical problems, including those at the medical school or professional level, and creating detailed explanations. You’ll regularly work with a mix of medical content—combining text with images, simulations, and visual aids. Here are a few examples of the kinds of tasks you might handle day to day:Diagnostic Analysis: Review a complex patient case, analyze symptoms, and propose a diagnosis, supported by explanations and relevant medical imaging (e.g., X-rays, MRIs).Medical Pathophysiology: Explain the underlying mechanisms of a disease, utilizing diagrams, charts, and simulations to illustrate key concepts.Clinical Decision-Making: Solve clinical scenarios involving patient management, including the interpretation of lab results and imaging, and explain the rationale behind the chosen course of action. Candidate Requirements:Candidates pursuing UG (MBBS, BDS), PG (MD/MS/DNB/MDS), or Post PG (DM, MCh) are eligible and encouraged to apply for this program.Strong knowledge of core medical subjects like anatomy, physiology, pathology, pharmacology, and clinical medicine.Ability to analyze and solve complex medical problems with a structured approach.Ability to explain medical concepts clearly using simple language, visuals, and simulations when needed.Strong written and verbal communication skills in English.A laptop/desktop with stable internet and essential tools for collaboration and content review.Knowledge of medical-related software and tools is a plus (e.g., DICOM viewers, medical simulation software, electronic health records). What We Offer:A collaborative environment with top-tier talent and thought leaders in the AI industry.Flexible working hours and fully remote work setup.The chance to contribute to groundbreaking AI projects for global leaders like OpenAI, Meta, NVIDIA, DELL, and others.Well-compensated contractual roles with the potential for longer-term engagement. Application Process:Shortlisted candidates will be sent an online medical assessment tailored to their specialization.Candidates who pass the assessment will be invited for an interview.

About Turing:Turing is an AI-powered tech services company on a mission to accelerate the advancement and deployment of AGI. Recently backed by $111M in Series E funding, we’re scaling our efforts to connect exceptional global talent with transformative projects in AI. Role Overview:We are seeking candidates with strong medical knowledge and diagnostic abilities in various fields of medicine.The ideal candidate should have a deep understanding of medical concepts, particularly at the level required for medical school or professional practice.You should be able to break down complex medical cases into simple, clear explanations and work efficiently. What does day-to-day look like:You would spend time solving a variety of advanced medical problems, including those at the medical school or professional level, and creating detailed explanations. You’ll regularly work with a mix of medical content—combining text with images, simulations, and visual aids. Here are a few examples of the kinds of tasks you might handle day to day:Diagnostic Analysis: Review a complex patient case, analyze symptoms, and propose a diagnosis, supported by explanations and relevant medical imaging (e.g., X-rays, MRIs).Medical Pathophysiology: Explain the underlying mechanisms of a disease, utilizing diagrams, charts, and simulations to illustrate key concepts.Clinical Decision-Making: Solve clinical scenarios involving patient management, including the interpretation of lab results and imaging, and explain the rationale behind the chosen course of action. Candidate Requirements:Candidates pursuing UG (MBBS, BDS), PG (MD/MS/DNB/MDS), or Post PG (DM, MCh) are eligible and encouraged to apply for this program.Strong knowledge of core medical subjects like anatomy, physiology, pathology, pharmacology, and clinical medicine.Ability to analyze and solve complex medical problems with a structured approach.Ability to explain medical concepts clearly using simple language, visuals, and simulations when needed.Strong written and verbal communication skills in English.A laptop/desktop with stable internet and essential tools for collaboration and content review.Knowledge of medical-related software and tools is a plus (e.g., DICOM viewers, medical simulation software, electronic health records). What We Offer:A collaborative environment with top-tier talent and thought leaders in the AI industry.Flexible working hours and fully remote work setup.The chance to contribute to groundbreaking AI projects for global leaders like OpenAI, Meta, NVIDIA, DELL, and others.Well-compensated contractual roles with the potential for longer-term engagement. Application Process:Shortlisted candidates will be sent an online medical assessment tailored to their specialization.Candidates who pass the assessment will be invited for an interview.

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 businessSupport to the health care providers by providing accurate and up-to-date medical informationEducation, training and periodic medical updates to the commercial team as demandedEnsuring 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 productsMedical 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 TrialsCross-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 interfaceProvide scientific support to sales teamMedical 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 excellenceWork 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. 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. 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 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) Job Posting End Date 04/20/2025 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 R340678

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services–from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)–in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology,in-vivo,in-vitromodels and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology &In-vitroADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world’s leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com The Position Organization : - Jubilant Biosys Designation & Level: - SRA Function: - Purification Location: - Greater Noida Department: - Analytical Key Responsibilities Having exposure of 1-6 years in analytical chemistry, method development and purification of samples on chromatographic instruments (HPLC/Prep-HPLC/SFC/Prep-SFC). Candidate should be able to handle routine analysis independently on respective instrument and trouble-shooting of respective analytical instruments. Knowledge of instrumental technique/software with its application Should be able to handle routine analysis independently on respective instrument, Experience in method development on LCMS will be desirable but not necessary. Practice safe work habits including complying with all safety health and environmental rules and regulation. Person Profile Qualification: - M. Sc. (Analytical Chemistry)/ M. Pharm or related field from reputed university/institute. Experience: - 2-10 years of relevant experience for Masters (depending on level) Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.

Hiring Senior Resident Radiologist Location – Gaya (Bihar) Hospital Name- Medical College & Hospital Number of Bedded- 650 Number of Year- New Setup CTC- 1.5-2 Lacs (Negotiable) Qualification- MD About Hospital: About: New Hospital and medical college, started in january 2025. Going for LOP. Applying For 150 MBBS Seats New Departments: Anatomy, Physiology, Biochemistry, Pharmacology, Pathalogy, Microbiology, FMT, Community Medicine, General Medicine, Pediatrics, Derma, Psychiatry, General surgery, Ortho, ENT, Opthal, Gyne & Obs, Anasthesia, Radiology, Dentistry Nearest Airport: Gaya International Airport- 27 km Nearest Railway Station: Gaya Junction- 36 km Specialist Requirments: Vacancy of Radiologist as Senior Resident , - 1.5-2 Lacs , Associate Professor & 1 as Professor Assoc- 3.5 to 4 LacsProf- 4-5 lacs-*Male/Female Both can do-*Duty Hours: Mon to Fri- 9 AM to 4 PM (OPD timings)Sat- Half Day- 9 AM to 2 PMIf living in campus 24/7 doctor required as emergencies are there-*Sundays Off-*Accomodation provided in campus*For AP, ASP & professor hospital is okay to buy out the Notice period of candidate Job Type: Full-time Pay: ₹150,000.00 - ₹200,000.00 per month Work Location: In person

Assistant Professor:- Anatomy Pharmacology Biochemistry Physiology Microbiology Community Medicine Pathology Teach medical students in the classroom and clinical settings Participate in academic activities such as seminars, conferences, and workshops Supervise and mentor junior residents and medical students Perform administrative tasks as assigned by the department head Monitoring and providing general care to patients on hospital wards and in outpatient clinics. Admitting patients requiring special care, followed by investigations and treatment. Examining and talking to patients to diagnose their medical conditions. Teaching and supervising junior doctors and medical students. Qualification - MBBS, MD Free Accommodation within Campus Salary - 18 L - 24 L Share CV @ hr@amrach.com Thanks & Regards; Amrach Consulting Services LLP Call@ 9105521331 WhatsApp@ 9105521331

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

Urgent vacancies for teaching faculties SR, AP, Asso. Professor & Professor with good experience in medical college at a medical college in Pilkhuwa, UP Qualification as per NMC Norms Salary as per industry Norms,

Technical Product Owner – Manufacturing System Let’s do this. Let’s change the world. In this vital role you will drive the implementation and expansion of new and evolving technologies across Amgen’s global network of manufacturing sites. You will collaborate closely with Architects, Development Teams, Business Owners, Subject Matter Experts and other stakeholders to deliver and maintain high-quality, high-value, scalable solutions. Manage a suite of custom internal platforms, commercial off-the-shelf (COTS) software, and systems integrations Translate complex scientific and technological needs into clear, actionable requirements for development teams Function as a Product Owner for Manufacturing Systems within a Scaled Agile Framework (SAFe) product team Develop and maintain a product roadmap that clearly outlines the planned features and enhancements, timelines, and milestones Collaborate with geographically dispersed teams, including those in the US and other international locations. Partner and ensure alignment of the Amgen India DTI site leadership and follow global standards and practices. Foster a culture of collaboration, innovation, and continuous improvement. Identify and manage risks associated with the systems, including technological risks, scientific validation, and user acceptance Develop documentation, communication plans and training plans for end users Ensure operational excellence, cybersecurity and compliance. Basic Qualifications: Doctorate degree OR Master’s degree and 4 to 6 years of Life Science/Biotechnology/Pharmacology/Information Systems experience OR Bachelor’s degree and 6 to 8 years of Life Science/Biotechnology/Pharmacology/Information Systems experience OR Diploma and 10 to 12 years of Life Science/Biotechnology/Pharmacology/Information Systems experience Preferred Qualifications: Experience in implementing and supporting manufacturing systems. Experience with Manufacturing Execution Systems (MES), Data Historians, Process Automation Systems or Industry 4.0 technologies. Experience with cloud (e.g., AWS, Azure), on-premises and hybrid architecture. Professional Certifications: SAFe for Teams certification (preferred) SAFe Product Owner and SAFe Product Manager (preferred) Must-Have Skills Excellent problem-solving skills and a passion for tackling complex challenges in manufacturing with technology Understanding of manufacturing technologies, systems, data and integrations. Collaborative spirit and effective communication skills to work seamlessly in a cross-functional team An ongoing commitment to learning and staying at the forefront of technology, digital and AI advancements. Experience creating impactful slide decks and communicating data Good-to-Have Skills: Experience with stakeholder management, managing a team, ensuring seamless coordination across teams and driving the successful delivery of technical projects Familiarity with databases and analytics platform such as Databricks and related programming languages like SQL, Python. Ability to drive projects/company initiatives using Agile methodology Soft Skills: Exceptional collaboration and communication skills. High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented with a focus on achieving team goals. Strong presentation and public speaking skills. Work Hours: This position requires you to work a later shift and may be assigned a second or third shift schedule. Candidates must be willing and able to work during evening or night shifts, as required. Potential Shifts (subject to change based on business requirements)Second Shift2:00pm – 10:00pm IST; Third Shift10:00 pm – 7:00 am IST. EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Education: * B.Pharmacy/M.Pharmacy/Pharma-D * BSC/MSC in Nursing * BPT / BHMS / BAMS * Candidates should be 2024/2023/2022 passed outs *Should have 60% (CGPA 6.5) and above throughout the academics Other Skills: * Should possess good clinical knowledge and have wide awareness around anatomy, pharmacology and disease process * Good analytical and problem-solving skills * Ability to work independently and be flexible to work in shifts (WFO) * Good verbal and written communication