Doctor Jobs in Ahmedabad

Why This Role MattersPharmacovigilance systems play a vital role in ensuring that drug safety information is properly collected, managed, and reported to regulatory authorities. A Pharmacovigilance System Specialist helps maintain the integrity of safety databases and supports compliance with global pharmacovigilance regulations. This role ensures that adverse event data is handled accurately and efficiently, allowing pharmaceutical companies to monitor product safety and protect patient health.At Amneal Pharmaceuticals, professionals in this role contribute to maintaining strong pharmacovigilance operations by supporting safety database management, ensuring regulatory compliance, and facilitating effective reporting processes.Job DescriptionThe Pharmacovigilance System Specialist is responsible for managing pharmacovigilance systems, particularly the Oracle Argus Safety database. The role involves system configuration, workflow setup, user access management, compliance monitoring, and reporting activities.The professional works closely with pharmacovigilance teams, regulatory departments, and IT support teams to ensure that drug safety databases operate smoothly and comply with global pharmacovigilance guidelines such as ICH and GVP. The position also includes system validation, documentation, troubleshooting, and providing training or support to team members who use the pharmacovigilance system.Key Features of the RoleThis role provides exposure to advanced pharmacovigilance systems and global safety regulations. Professionals in this position gain experience in database administration, safety data management, and compliance monitoring.The role also offers opportunities to collaborate with multiple departments, including drug safety operations, regulatory affairs, and quality assurance teams. It is ideal for candidates interested in combining pharmacovigilance knowledge with technical system management.Responsibilities• Configure and maintain pharmacovigilance systems such as Oracle Argus Safety.• Manage user access, roles, and permissions within safety databases.• Set up workflows and system configurations according to pharmacovigilance requirements.• Monitor compliance with global pharmacovigilance regulations including ICH and GVP guidelines.• Generate safety reports and maintain system documentation.• Support system validation and ensure regulatory compliance of pharmacovigilance databases.• Provide troubleshooting support for pharmacovigilance system issues.• Ensure accuracy and quality of pharmacovigilance data entry.• Maintain documentation and ensure adherence to Standard Operating Procedures (SOPs).• Conduct training sessions and provide support to pharmacovigilance team members.Required QualificationsEducational RequirementsCandidates should possess one of the following qualifications:• Bachelor’s degree in Life Sciences• Bachelor of Pharmacy (B.Pharm)• Master of Pharmacy (M.Pharm)• Master’s degree in Life Sciences or related healthcare fieldExperience and SkillsCandidates should have knowledge or experience related to pharmacovigilance systems and drug safety processes.• Strong knowledge of pharmacovigilance processes• Experience with Oracle Argus Safety system• Understanding of ICH and GVP pharmacovigilance regulations• Database administration and configuration skills• Analytical and troubleshooting abilities• Attention to detail and accuracy in safety data management• Ability to follow SOPs and maintain proper documentation• Strong communication and training skills• Organizational and time management abilitiesSalary InsightsThe salary for a Pharmacovigilance System Specialist in India varies based on experience, organization size, and technical expertise.• Salary rang: ₹ 4.5 -₹ 8 LPA (estimated)Additional benefits may include health insurance, professional development programs, performance incentives, and career growth opportunities.Company OverviewAmneal Pharmaceuticals is a global pharmaceutical company focused on developing, manufacturing, and distributing high-quality generic and specialty medicines. The company operates across several international markets and is known for its commitment to affordable healthcare solutions and regulatory compliance. With advanced research, manufacturing, and pharmacovigilance systems, Amneal continues to expand its presence in the global pharmaceutical industry while maintaining strong standards for product safety and quality.FAQs1. What does a Pharmacovigilance System Specialist do?A Pharmacovigilance System Specialist manages drug safety databases, supports regulatory compliance, and ensures accurate handling of adverse event data.2. What is Oracle Argus Safety?Oracle Argus Safety is a widely used pharmacovigilance database designed for managing adverse event reporting, safety case processing, and regulatory submissions.3. Is pharmacovigilance system experience necessary?Experience with safety databases such as Argus Safety is highly preferred for this role, especially for system configuration and administration tasks.4. What career opportunities are available after this role?Professionals can advance to roles such as Senior PV Systems Specialist, Pharmacovigilance Operations Manager, Drug Safety Manager, or Global Safety Systems Lead.Application Tips• Highlight experience with pharmacovigilance databases like Oracle Argus Safety.• Demonstrate knowledge of ICH and GVP safety regulations.• Emphasize technical skills related to database administration and system configuration.• Mention experience with SOP compliance, documentation, and system validation.• Showcase communication skills and the ability to train or support pharmacovigilance teams.

Why This Role MattersMedical Advisors play a critical role in bridging scientific knowledge with strategic business decisions in the pharmaceutical industry. This role ensures that medical strategies, product communication, and clinical insights are aligned with patient needs and evidence-based practices. By collaborating with healthcare professionals (HCPs), key opinion leaders (KOLs), and internal teams, Medical Advisors help shape responsible product positioning, support new product launches, and strengthen scientific credibility within therapeutic areas such as cardiology, diabetes, neurology, gastroenterology, gynaecology, and orthopaedics.Job DescriptionA growing Medical Affairs team is hiring Executive – Medical Affairs and Assistant Manager – Medical Affairs roles based in Ahmedabad. The position focuses on medico-marketing strategy, clinical research coordination, scientific communication, and collaboration with cross-functional teams to support pharmaceutical brands and patient-focused healthcare initiatives.Key Features of the Role• Job Title Options: Medical Advisor / Executive – Medical Affairs / Assistant Manager – Medical Affairs• Work Location: Ahmedabad• Department: Medical Affairs / Medico-Marketing• Experience Required: 1–3 years (Executive) | 4–6 years (Assistant Manager)• Qualification: Pharm.D or M.Pharm• Industry: Pharmaceutical / Healthcare• Travel Requirement: 30–40% for meetings and field interactionsResponsibilities• Provide medical and scientific input for product strategies and brand development.• Gather insights from Key Opinion Leaders (KOLs) and Healthcare Professionals (HCPs).• Collaborate with marketing and sales teams to develop patient-focused strategic plans.• Support new product launches through scientific materials such as monographs, FAQs, and presentation slides.• Review and validate visual aids (VA) and leave-behind literature (LBLs).• Organize and participate in advisory board meetings and KOL interactions.• Manage medical information requests and provide scientific responses.• Lead non-interventional studies (NIS) and clinical research projects from conceptualization to publication.• Prepare study documents, coordinate ethics committee approvals, and oversee investigator meetings.• Ensure accurate documentation and publication management related to pharmaceutical brands.• Work with cross-functional teams to ensure alignment between scientific evidence and commercial strategy.Required Qualifications• Doctor of Pharmacy (Pharm.D) or Master of Pharmacy (M.Pharm).• Strong understanding of medico-marketing and pharmaceutical product strategy.• Experience interacting with healthcare professionals and key opinion leaders.Educational RequirementsCandidates must hold one of the following degrees from a recognized institution:• Pharm.D (Doctor of Pharmacy)• M.Pharm (Master of Pharmacy)These qualifications provide the scientific foundation required for handling clinical data, medical communications, and pharmaceutical research initiatives.Experience and Skills• 1–3 years of medico-marketing experience for Executive role.• 4–6 years of experience managing medical strategy for Assistant Manager role.• Knowledge of therapeutic areas such as cardiology, diabetes, neurology, gastroenterology, gynaecology, and orthopaedics.• Strong communication and presentation skills.• Ability to work with cross-functional teams in a fast-paced environment.• Experience managing clinical studies, investigator meetings, and scientific publications.• Strong analytical and problem-solving abilities.• Ability to prioritize tasks and manage multiple projects simultaneously.Salary InsightsThe compensation for Medical Affairs roles typically varies based on experience and expertise. Industry standards for similar roles in India range from mid-level to senior-level salary packages depending on the position (Executive or Assistant Manager), therapeutic expertise, and previous industry experience.Company OverviewThe hiring organization is expanding its Medical Affairs team to strengthen scientific engagement and research-driven strategies in the pharmaceutical sector. The company focuses on evidence-based product development, medical education, and collaborative engagement with healthcare professionals to improve patient outcomes.FAQsQ1. What qualifications are required for this role?Candidates must have a Pharm.D or M.Pharm degree.Q2. Is prior medico-marketing experience required?Yes. Executive roles require 1–3 years of experience, while Assistant Manager roles require 4–6 years.Q3. Which therapeutic areas are relevant for this role?Cardiology, diabetes, neurology, gastroenterology, gynaecology, and orthopaedics.Q4. Does the role involve travel?Yes, approximately 30–40% travel may be required for meetings and professional interactions.Q5. Where is the job location?The role is based in Ahmedabad.Application Tips• Highlight medico-marketing and clinical research experience in your resume.• Mention therapeutic area expertise if applicable.• Include examples of working with KOLs or conducting medical education programs.• Demonstrate experience in preparing scientific documents and product launch materials.• Emphasize communication skills and ability to collaborate with marketing, sales, and research teams.

Why This Role MattersIn the pharmaceutical industry, regulatory approval is the gateway to market access. Without a well-prepared, technically accurate, and guideline-compliant dossier, even the most effective formulation cannot reach patients. The Regulatory Affairs Executive plays a central role in compiling and reviewing regulatory submissions in alignment with international standards such as the Common Technical Document (CTD) and ASEAN Common Technical Dossier (ACTD) formats.This role directly supports global product registrations across ROW (Rest of World), LATAM, and African markets. Each region has unique regulatory expectations, documentation standards, and technical review procedures. A well-prepared dossier ensures faster approvals, reduced queries, and successful product launches.By preparing high-quality technical documents, validating analytical data in line with International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use guidelines, and responding to regulatory authority queries, this position contributes significantly to the company’s international expansion and regulatory credibility.Job DescriptionThe Regulatory Affairs Executive is responsible for preparation, compilation, review, and submission of pharmaceutical dossiers as per CTD/ACTD formats and country-specific requirements. The role involves coordination with manufacturing, quality assurance, analytical development, and R&D teams to gather technical data for regulatory submissions.The candidate will handle documentation for multiple dosage forms including oral solids, liquids, injectables, ophthalmic, and topical formulations. Additionally, this role involves responding to regulatory authority queries, reviewing Drug Master Files (DMFs), and supporting product development documentation aligned with global regulatory standards.The position requires strong technical writing skills, attention to detail, regulatory knowledge, and the ability to manage multiple submissions simultaneously.Key Features of the Role• Preparation of CTD and ACTD dossiers for global markets• Exposure to ROW, LATAM, and African regulatory frameworks• Handling diverse dosage forms• Interaction with cross-functional technical teams• Direct involvement in regulatory query managementResponsibilities• Prepare and compile dossiers in CTD and ACTD formats (Modules I, II, III, IV, and V) as per country-specific regulatory requirements.• Draft and review technical documents including raw material specifications and finished product specifications.• Document manufacturing processes and product development reports.• Compile and review stability study reports and process validation documents.• Review analytical method validation documents in compliance with ICH guidelines.• Conduct Drug Master File (DMF) review to ensure completeness and regulatory compliance.• Prepare and submit Product Dossiers (PD) for product registration in international markets.• Respond to technical queries raised by regulatory authorities.• Coordinate with Quality Assurance, R&D, Production, and Analytical teams for data collection.• Ensure accuracy, consistency, and completeness of regulatory submissions.• Maintain regulatory documentation archives and version control systems.• Monitor updates in global regulatory requirements and adapt documentation accordingly.Dosage Forms Handled• Oral Solid Dosage Forms (Tablets, Capsules)• Liquid Formulations• Injectable Products• Ophthalmic Preparations• Topical Dosage FormsMarket Exposure• ROW (Rest of World) Markets• Latin American (LATAM) Countries• African Regulatory MarketsRequired Qualifications• Bachelor’s degree in Pharmacy (B.Pharm) or Master’s degree in Pharmacy (M.Pharm).• 1–5 years of experience in pharmaceutical regulatory affairs or dossier preparation.• Strong understanding of CTD and ACTD formats.• Knowledge of ICH guidelines for analytical validation and stability studies.Educational Requirements• B.Pharm / M.Pharm (Regulatory Affairs, Pharmaceutics, Pharmaceutical Analysis preferred).• Additional training in international regulatory documentation is advantageous.Experience and Skills• Hands-on experience in dossier preparation for international markets.• Strong knowledge of CTD Modules I–V.• Familiarity with ACTD requirements for ASEAN and other regions.• Experience reviewing analytical method validation reports.• Understanding of stability study requirements and process validation documentation.• Ability to draft high-quality technical responses to regulatory authority queries.• Strong documentation and technical writing skills.• Excellent coordination skills for cross-functional collaboration.• Ability to handle multiple submissions with strict deadlines.• High level of accuracy and attention to detail.Salary InsightsThe offered salary range of ₹18,000 to ₹60,000 per month depends on:• Years of regulatory experience• Exposure to global markets (LATAM, Africa, ROW)• Technical expertise in CTD/ACTD preparation• Experience handling regulatory queries independentlyIn addition to base salary, the company provides Provident Fund benefits as per statutory requirements.Company OverviewThe organization operates within the pharmaceutical manufacturing and export sector, focusing on regulatory-compliant product registration across international markets. With a growing footprint in LATAM, African, and ROW markets, the company emphasizes technical excellence and adherence to global regulatory standards.The regulatory affairs team plays a crucial role in ensuring that all submissions meet international guidelines and local regulatory authority expectations. Through accurate documentation and efficient query resolution, the team supports timely product approvals and global business expansion.FAQsWhat formats will the candidate work with?CTD and ACTD formats covering Modules I to V.Is experience in multiple dosage forms required?Yes, experience handling oral, liquid, injectable, ophthalmic, and topical dosage forms is preferred.Does the role involve query response handling?Yes, preparing and submitting technical responses to regulatory authorities is a key responsibility.Which markets will be handled?ROW, LATAM, and African countries.Is ICH knowledge mandatory?Yes, knowledge of ICH guidelines for method validation and stability studies is essential.Application Tips• Highlight direct experience with CTD/ACTD dossier preparation.• Mention specific markets handled (LATAM, Africa, ROW).• Provide examples of technical query responses you have prepared.• Emphasize experience with stability data and process validation documentation.• Showcase strong documentation and regulatory coordination skills.

Role & Responsibilities• Interpret diagnostic imaging studies including X-ray, CT, MRI, Ultrasound, and Mammography• Provide accurate and timely radiology reports to referring physicians• Perform image-guided procedures such as biopsies and aspirations• Ensure adherence to radiation safety and quality control protocols• Supervise radiology technicians and support staff• Manage and operate modalities including 1.5T MRI, 128-slice CT, USG, Digital Mammography, Digital X-Ray, DEXA, and Digital OPG• Maintain proper documentation and reporting standardsQualification• MD / DNB – Radiology• Valid Medical Council registrationExperience• 1–3 years of relevant radiology experience requiredVacancies• 1 VacancySkills• Strong diagnostic and reporting skills• Expertise in multiple imaging modalities• Knowledge of radiation safety protocols• Attention to detail and clinical accuracy• Team supervision and coordination skillsAbout the CompanyOrion Healthcare Solution is a healthcare recruitment and staffing organization supporting diagnostic centres and hospitals across India. The organization focuses on connecting qualified medical professionals with reputed healthcare institutions to ensure quality patient care and operational excellence.

Roles & Responsibilities:• Prepare and manage documentation for ISO 13485 certification, CE marking (EU MDR), and USFDA submissions• Develop and maintain Technical Master Files for medical device products• Create and update Clinical Evaluation Reports (CERs) as per EU MDR requirements• Handle Design & Development documentation along with Risk Management files in compliance with EU MDR guidelines• Maintain and implement Quality Management Systems (QMS) for medical devices• Prepare and submit regulatory dossiers to authorities in India, Europe, and the US• Conduct internal quality audits to ensure ongoing regulatory compliance• Ensure compliance with European CE regulations (MDD & MDR) and USFDA 510(k) pathways• Monitor regulatory updates and implement necessary changes in documentation and processesQualification:• B.Pharm (Bachelor of Pharmacy) / M.Pharm (Bachelor of Pharmacy) or Bachelor’s / Master’s degree in Biomedical Engineering or relevant Science discipline• Specialized training in Medical Devices Regulatory Affairs preferredExperience:• 3–5 years of experience in regulatory affairs for medical devices (mandatory)Skills:• Strong knowledge of European CE marking (MDD & MDR) requirements• Hands-on experience with USFDA 510(k) submission process• In-depth understanding of Quality Management Systems (ISO 13485)• Excellent documentation and technical writing skills• Strong written and verbal communication abilities• Proficiency in MS Office and regulatory documentation tools• High attention to detail and compliance-oriented mindsetAbout the Organization:MJ Surgical is a leading manufacturer and exporter of orthopedic implants and instruments, committed to delivering high-quality medical devices that meet global regulatory standards and support international market access.

Roles & Responsibilities:• eCRF development, testing, and maintenance• Clinical data validation and query management• Preparation of CDM documentation (DMP, DVP, eCCG)• Data reconciliation activities and user training• Medical coding using standard dictionaries• Handling EDC systems and related tools (IWRS, ePRO)• Supporting end-to-end clinical data management activitiesQualification:• M.Pharm (Pharmacology / Quality Assurance)• BDS / BAMS / BHMSExperience:• Site-level experience as a Clinical Research Coordinator (CRC)• Hands-on experience in late-phase clinical trials• Working knowledge of EDC systems and CDM processes• Exposure to IWRS, ePRO, and clinical data toolsSkills:• Strong knowledge of clinical data management processes• Proficiency in handling eCRFs, IWRS, and ePRO systems• Expertise in medical coding using standard dictionaries• Strong analytical and problem-solving skills• Excellent communication and training skillsAbout The Company:Lambda Therapeutic Research Ltd. is a globally recognized full-service Clinical Research Organization (CRO) headquartered in Ahmedabad. Lambda operates across India, USA, Canada, UK, Spain, and Poland, offering clinical research services with a focus on late-phase clinical trials. With competitive compensation and global exposure, Lambda provides a structured career growth path in the clinical research industry.

Roles & Responsibilities:• Lead integrated, multi-modality drug discovery programs across chemistry disciplines• Solve complex synthesis and route-design challenges using advanced analytical approaches• Apply modern discovery platforms including ELNs, cheminformatics, and digital workflows• Collaborate closely with Biology, ADME/DMPK, and platform science teams for integrated delivery• Mentor and guide scientists to global standards of quality and scientific rigor• Build, manage, and represent o2h Discovery partnerships with global biotech and pharma clientsQualification:• Ph.D. / Postdoctoral training from a leading international university (US / UK / EU preferred)Experience:• 5–20 years of industrial experience in small-molecule drug discoverySkills:• Strong expertise in medicinal and synthetic chemistry with advanced problem-solving skills• Experience with advanced modalities (ADCs, peptides, covalent inhibitors, TPD)• Hands-on knowledge of modern productivity tools (HTE, flow chemistry)• Proficiency in digital chemistry platforms and data-driven discovery• Excellent scientific communication, leadership, and mentoring abilitiesAbout the Organization:o2h Discovery is a global co-discovery partner with integrated discovery platforms in the UK and India, enabling biotech and pharma clients to accelerate pre-clinical drug discovery through innovation and scientific excellence.

Roles and responsibilities:• Design and implement personalized rehabilitation programs for patients• Conduct biomechanics and functional assessments for neurological and orthopedic conditions• Monitor patient progress and modify treatments as needed• Educate patients and caregivers on exercises, injury prevention, and rehabilitation strategies• Collaborate with multidisciplinary healthcare team members• Maintain accurate patient records and documentation• Conduct comprehensive assessments of patients’ biomechanics, gait, and human performance• Use advanced assessment tools and motion analysis systems to evaluate patient conditions• Perform muscle assessments to identify weaknesses or imbalances• Stay updated with the latest physiotherapy practices and techniques• Apply AI/ML and data-driven approaches to optimize rehabilitation outcomesQualification:• Bachelor’s or Master’s degree in Physiotherapy or relevant field• Valid physiotherapy license/certification• Proficiency in neuro and orthopedic rehabilitation or sports physiotherapy• Familiarity with biomechanics, gait analysis, and human performance assessmentExperience:• Experience in neuro and orthopedic rehab or sports physiotherapy preferred• Freshers with strong clinical training may also be consideredSkills:• Strong communication and interpersonal skills for patient interaction and collaboration• Ability to work independently in a part-time consulting role• Competence in advanced technologies for motion capture and analysis• Analytical skills for interpreting gait and biomechanics data• Commitment to continuous learning and staying updated with industry trendsBenefits:• Flexible part-time work schedule• Opportunity to work with cutting-edge technology in motion analysis and rehabilitation• Exposure to a deep-tech, data-driven healthcare environmentWorking hours:• Part-time; 3–5 hours daily (flexible), may require on-site visits to clinics or rehab centersAbout the company:SynerSense® integrates sports, health & wellness, biomechanics, AI/ML, and data science to deliver advanced, data-driven human performance and rehabilitation solutions. The company leverages motion capture technology, digital human movement analysis, and edge computing platforms to provide precise assessment and rehabilitation services anywhere, across clinical, sports, and industrial settings.

Roles & Responsibilities• Prepare and submit Ethics Committee (EC) applications and follow up for regulatory approvals• Upload, review, and maintain regulatory documents in electronic Trial Master File (eTMF) systems• Prepare and submit dossiers, justification notes, and applications to Zonal and Central regulatory offices• Coordinate and support BE-NOC, Test License (TL), and Clinical Trial (CT) application submissions• Prepare and submit CBN/NCB applications for controlled substances and track approval status• Prepare and manage CTRI registrations in coordination with Clinical Trial Project Managers• Draft responses to regulatory queries and maintain regulatory submission trackers• Prepare and circulate monthly regulatory affairs activity and status reports• Support system and vendor audits and prepare responses to audit observations• Ensure compliance with CDSCO regulations, ICH-GCP, Schedule Y, and applicable regulatory guidelinesQualification• Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related disciplineExperience• 1–4 years of experience in Regulatory Affairs within a CRO or clinical research environment• Hands-on experience with CDSCO submissions and clinical trial regulatory documentationSkills• Strong knowledge of CDSCO regulations, ICH-GCP, Schedule Y, and CTRI requirements• Experience in dossier preparation, regulatory submissions, and eTMF systems• Proficiency in regulatory documentation tracking and compliance monitoring• Excellent communication, coordination, and documentation skills• Strong attention to detail with the ability to manage multiple regulatory activities• Problem-solving mindset with a proactive regulatory approachAbout the OrganizationLambda Therapeutic Research Ltd. is a globally recognized Clinical Research Organization providing comprehensive clinical development and bioequivalence research services. Known for regulatory expertise and quality-driven clinical research, the company supports pharmaceutical and biotechnology clients across international markets.

Role & Responsibilities• Act as the primary scientific face of the organization for thought leaders and physicians in the assigned therapy area• Identify, map, and profile Key Opinion Leaders (KOLs) across the assigned geography• Engage KOLs through planned medical affairs activities aligned with strategic objectives• Execute the medical affairs plan including medical education, product education, evidence generation, advisory boards, and special projects• Serve as a therapeutic area scientific expert, discussing clinical data, treatment trends, and studies with healthcare professionals• Gather insights on disease trends and treatment patterns and share with therapy leads and commercial teams• Conduct disease trend analysis and contribute to annual Medical Affairs Strategy planning• Respond to and process scientific information requests from physicians• Represent the organization on internal and external scientific platforms• Collaborate with KOLs on reviews, meta-analyses, case studies, and publications in reputed journalsQualification• MBBS with full-time postgraduate qualification (minimum 2 years) in any medical disciplineOR• MBBS with MBA from a reputed instituteExperience• Fresh postgraduate or up to 2 years of experience in field-based Medical AffairsSkills• Strong scientific and therapeutic area knowledge• Research aptitude with understanding of research methodologies and data interpretation• Excellent scientific communication and presentation skills• Ability to build peer-to-peer relationships with leading specialists• Strategic thinking and strong analytical abilities• Integrity-driven decision making and compliance orientation• Strong collaboration skills in a matrix environment• Result-oriented mindset with high intellectual curiosity• Excellent interpersonal and stakeholder management skillsAbout The Company• Dr. Reddy’s Laboratories is one of India’s leading pharmaceutical companies with a strong presence in Global Generics India, Ranked among the top 10 pharma companies in the Indian Pharma Market. Strong leadership positions in oncology, anti-allergy, and gastrointestinal therapy areas.

Role & Responsibilities• Engage with identified thought leaders in the therapeutic area through medical affairs activities, aligning with the overall strategic plan• Execute strategic medical affairs plans, including medical education, product education, medical evidence generation, advisory boards, pre-license activities, and special projects• Serve as a therapeutic area scientific expert, discussing scientific data pertaining to products, treatment trends, and studies with leading specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies)• Support optimal patient outcomes through the communication of data, information, knowledge, and insights• Represent the organization in internal and external scientific platforms• Conduct disease trend analysis and gather insights from thought leaders to inform the medical affairs strategy• Ensure all activities are conducted in alignment with Dr. Reddy’s COBE (Code of Business Ethics) Policy and compliance guidelines• Contribute to medical writing, including publications, case studies, and patient-reported outcomesQualifications• MBBS with a post-graduate qualification in medicine or MBA from a reputed institute• Fresh postgraduates or candidates with up to 2 years of experience in Field-based Medical Affairs• Strong scientific acumen and understanding of medical data interpretationSkills• Strong academic background with deep knowledge of therapeutic areas• Experience in medical research methodologies and interpretation of medical data• Excellent communication skills, both verbal and written, with the ability to engage with top-tier specialists• Ability to develop strategic plans based on disease trends and treatment patterns• Strong analytical, strategic thinking, and decision-making skills• Experience in medical affairs and working with cross-functional teamsBenefits• Personalized learning programs and professional growth opportunities• Medical coverage for employees and their families• Life coverage for employees• Maternity and paternity benefits• Relocation and family support• Competitive compensation packageAbout The Company• Dr. Reddy's is one of the leading pharmaceutical companies in India, focused on making high-quality healthcare accessible globally. Dr. Reddy’s has been at the forefront of innovation and growth in the pharmaceutical industry, with a strong presence in oncology, anti-allergy, and gastrointestinal diseases. The company fosters a culture of empathy, dynamism, and individual growth, working to empower people to lead healthier lives.

Role & Responsibilities • Serve as a key representative of the Medical Affairs function, providing scientific and clinical expertise on Bioscan Research's technologies and innovations • Communicate complex medical and scientific information to healthcare professionals (HCPs) in a clear, accurate, and compliant manner • Establish and maintain strong relationships with key opinion leaders (KOLs), healthcare professionals, and other stakeholders in the field of traumatic brain injury • Collaborate with cross-functional teams to support clinical development, regulatory activities, and marketing efforts • Provide training and support to internal teams on the scientific and clinical aspects of the company's products • Monitor and report on trends in the field of traumatic brain injury and related medical advancements Qualification • Advanced degree in a relevant scientific or medical field (MD, PhD, or equivalent) Experience • Prior experience as a Medical Science Liaison or similar role in the pharmaceutical, biotechnology, or medical device industry • Experience in communicating scientific data to healthcare professionals • Knowledge in the area of traumatic brain injury or related fields Skills • Strong scientific and clinical knowledge, particularly in traumatic brain injury and neurotechnology • Excellent communication and interpersonal skills to engage with HCPs and KOLs • Ability to present complex scientific concepts in a clear and compliant manner • Strong problem-solving and critical thinking skills • Ability to work independently and collaboratively in a cross-functional environment About The Company • Bioscan Research – A company dedicated to improving traumatic brain injury patient outcomes through innovative technologies, including the machine learning-powered NIRS device, CEREBO, which aims to advance clinical understanding and treatment strategies for brain injury.

Roles & Responsibilities: • Perform medical assessments of client’s product ranges and evaluate adverse events • Conduct medical reviews of aggregate reports and prepare clinical expert statements • Detect signals for client’s medicinal products and manage risk management plans • Provide guidance and participate in follow-up of adverse events, offering backup medical support • Interact with staff at various levels to resolve issues during reviews • Contribute to enhancing pharmacovigilance processes and writing SOPs • Ensure compliance with local regulations and global pharmacovigilance requirements • Assist in developing SOPs for the department and clients, and communicate with clients and regulatory agencies if needed Qualifications: • Relevant degree in Life Sciences, Pharmacy, or related field Experience: • 0–1 year in pharmacovigilance or related field Skills: • Knowledge of local and national pharmacovigilance requirements • Strong communication and client interaction skills • Ability to work effectively with staff at various levels and functional areas • Marketing, business generation, direct sales, and client servicing skills About the Organization: This organization is a dynamic employment and recruitment services firm providing specialized healthcare and pharmacovigilance staffing solutions. They focus on regulatory compliance, quality processes, and client satisfaction while fostering a collaborative environment for professional growth.