Doctor Jobs in Mumbai

Why This Role MattersThe Medical Science Liaison (Oncology) at Astellas Pharma plays a critical role in connecting scientific knowledge with clinical practice. By engaging with key external experts, providing medical insights to internal teams, and supporting clinical research, this role ensures oncology products are used safely, effectively, and in line with medical and regulatory standards. MSLs contribute directly to advancing patient care and supporting evidence-based medical strategies.Job DescriptionAstellas Pharma, based in Mumbai, India, is seeking a proactive Medical Science Liaison (Oncology). This field-based, full-time role involves executing medical strategies, collaborating with cross-functional teams, engaging with healthcare professionals, and supporting investigator-sponsored research.Key Features of the Role• Position: Medical Science Liaison (Oncology)• Company: Astellas Pharma• Location: Mumbai, Maharashtra, India• Employment Type: Full-Time, On-Site• Experience Required: Minimum 1 year in Medical Affairs (Oncology)Responsibilities• Execute Core Medical Plan (CMP) activities, ensuring alignment with regional/global objectives• Deliver internal and external scientific presentations and lead advisory boards• Provide medical input to commercial teams, including promotional materials and product training• Gather insights from Key External Experts and clinical stakeholders to inform medical strategies• Evaluate Investigator Sponsored Research (ISR) proposals for scientific merit• Support clinical trials and regional/global research activities as needed• Build and maintain relationships with healthcare professionals, regulatory authorities, and funding bodies• Develop expertise in therapeutic areas through training, congresses, and self-study• Maintain compliance with local regulations, company SOPs, and ethical guidelinesRequired Qualification• Medical degree and advanced scientific degree in Life or Health Sciences, or relevant biological sciences• Minimum 1 year of experience in Medical Affairs within oncology• Strong scientific, analytical, and strategic skills• Excellent written and verbal communication, presentation, and interpersonal skills• Ability to work in a matrix environment and collaborate across teams• Knowledge of local and global industry laws, regulations, and complianceImportant Requirements• Field-based role requiring travel within India• Ability to engage effectively with Key External Experts and healthcare professionals• Proficiency in project management, planning, and organizational skills• Digital literacy and cross-cultural awarenessWhat We Offer• Opportunity to work with a leading global pharmaceutical company in oncology• Exposure to cutting-edge medical strategies and research• Collaborative and supportive professional environment• Professional growth and skill development in Medical AffairsExperience and Skills• Medical Affairs strategy execution• Scientific presentations and advisory board leadership• Clinical research support and ISR evaluation• Relationship-building with healthcare stakeholders• Regulatory compliance and medical communicationSalary Insights• Not specified; competitive based on experience and qualificationsCompany OverviewAstellas Pharma is a global, value-driven life sciences company focused on delivering innovative therapies to improve patient outcomes. The company emphasizes integrity, patient-centricity, collaboration, and ethical practices across all operations.FAQsWhat is the required qualification for this role?Medical degree + advanced scientific degree in Life/Health Sciences or related field.How much experience is required?Minimum 1 year in Medical Affairs, preferably oncology.What is the employment type?Full-time, on-site, field-based.Application Tips• Highlight experience in Medical Affairs and oncology therapeutic areas• Emphasize experience engaging with Key External Experts and advisory boards• Showcase understanding of regulatory compliance and ethical guidelines• Include relevant certifications, digital skills, or scientific training

Why This Role MattersThe Physical Medicine and Rehabilitation Specialist role plays a crucial part in improving the lives of patients with neurological conditions such as stroke, Parkinson’s disease, and spinal cord injuries. By combining clinical expertise with advanced medical technology, this role supports rehabilitation, enhances mobility, and contributes to innovative solutions that improve long-term patient care.Job DescriptionLifespark Technologies is seeking a Physical Medicine and Rehabilitation Specialist for a full-time, on-site role in Mumbai, Maharashtra. The specialist will conduct clinical assessments, develop rehabilitation plans, and support in-person as well as tele-rehabilitation programs. The role also involves contributing to clinical research and supporting the development and validation of digital health technologies and medical devices designed for neurological rehabilitation.Key Features of the Role• Position: Physical Medicine and Rehabilitation Specialist• Company: Lifespark Technologies• Location: IIT Bombay, Mumbai, Maharashtra, India• Employment Type: Full-Time• Workplace Type: On-site• Experience Level: Not specifiedResponsibilities• Conduct clinical assessments and rehabilitation planning for patients with neurological conditions• Support in-person rehabilitation and tele-rehabilitation sessions• Participate in clinical studies and validation of medical devices and digital health solutions• Perform outcome measurements and maintain structured clinical documentation• Collaborate with research, clinical, and product development teams• Contribute clinical insights to improve technology-enabled patient care• Assist in developing protocols for neurological rehabilitation programsRequired Qualification• MD / DNB / DPMR in Physical Medicine & Rehabilitationor• MPT in Neurological PhysiotherapyImportant Requirements• Understanding of neurological rehabilitation and patient assessments• Interest in clinical research and healthcare technology• Strong communication and documentation skills• Ability to collaborate with multidisciplinary teams including clinicians, researchers, and product developersWhat We Offer• Opportunity to work with advanced medical devices and digital therapeutics• Exposure to clinical research and neurological rehabilitation technologies• Collaboration with healthcare professionals, researchers, and engineers• Work environment focused on healthcare innovation and technology-driven careExperience and Skills• Neurological rehabilitation and clinical assessment• Rehabilitation program planning and patient monitoring• Tele-rehabilitation and remote patient care• Clinical research participation and documentation• Collaboration with clinical, research, and product teamsSalary Insights• Physical Medicine and Rehabilitation specialists in Mumbai typically earn ₹6 LPA to ₹20 LPA, depending on qualifications and experience..• Salaries may increase with research involvement, specialization in neurological rehabilitation, and experience in medical technology environments.Company OverviewLifespark Technologies is an Indian MedTech company developing innovative medical devices and digital health solutions for neurological conditions such as stroke, Parkinson’s disease, and spinal cord injury. The company focuses on home-based remote patient care, diagnostics, monitoring, and therapeutics. Its solutions include platforms for care management and fall prevention technologies designed to improve patient safety and rehabilitation outcomes. Lifespark has received several national and international recognitions and has been featured among Forbes Top 100 Startups in India for its contributions to healthcare innovation.FAQsWhat qualifications are required for this role?Candidates must have MD/DNB/DPMR in Physical Medicine & Rehabilitation or MPT in Neurological Physiotherapy.Where is the job located?The role is based at IIT Bombay in Mumbai, India.What type of work environment does this role offer?It is a full-time, on-site position with opportunities to work on clinical research and digital health technologies.What are the key responsibilities?Responsibilities include clinical assessments, rehabilitation planning, supporting tele-rehabilitation, participating in clinical studies, and collaborating with product and research teams.Application Tips• Highlight experience in neurological physiotherapy or rehabilitation medicine• Emphasize knowledge of stroke, Parkinson’s disease, or spinal cord injury rehabilitation• Showcase experience with clinical documentation and outcome measurement• Include any research participation, publications, or clinical studies• Demonstrate interest in digital health technologies and remote patient care solutions

Why This Role MattersThe Physiotherapist at Prachi Shah Arora's Aquatic and Physiotherapy Clinic plays a vital role in delivering advanced sports, aquatic, and holistic rehabilitation services. This position supports athletes and patients across musculoskeletal, pediatric, neurological, and geriatric domains using modern and manual therapy techniques in a multidisciplinary clinical setup.Job DescriptionDr. Prachi Shah Arora's Physiotherapy and Aquatic Centre in Malad, Mumbai is hiring a full-time Physiotherapist to join its rehab team. The clinic is equipped with a heated hydrotherapy pool, indoor gym, modern treatment rooms, and massage therapy facilities. The role involves designing customized rehabilitation plans, applying diverse therapeutic modalities, and working with athletes and special patient populations. A 2-year commitment is required.Key Features of the Role• Position: Physiotherapist – Sports, Aquatic & Holistic Rehab Specialist• Organization: Prachi Shah Arora's Aquatic and Physiotherapy Clinic• Location: Malad, Mumbai, Maharashtra• Employment Type: Full-Time, Permanent• Salary Range: ₹20,000 – ₹45,000 per month• Work Mode: In-personResponsibilities• Conduct detailed patient assessments• Develop customized rehab and fitness programs• Perform manual therapy and joint mobilization• Apply cupping, dry needling, and advanced taping techniques• Deliver sports rehab, MSK rehab, aqua rehab, geriatric, pediatric & neuro aquatic therapy• Guide patients in aerial yoga, aqua fitness, HIIT, and related wellness programs• Maintain patient documentation and monitor recovery progress• Collaborate with multidisciplinary team membersRequired Qualification• Bachelor’s Degree (BPT) or Master’s Degree (MPT) in PhysiotherapyEducational Requirement• Bachelor’s Degree (Mandatory)• Master’s Degree preferredImportant Requirements• 1–5 years of experience preferred (Freshers with strong clinical interest may apply)• Strong communication and teamwork skills• Interest in holistic and aquatic rehabilitation techniques• Willingness to commit for 2 years• Knowledge of physiology and medical terminologyEmployment Options• Full-time permanent role• Exposure to sports and celebrity clientele• Growth in holistic and aquatic rehabilitationWhat We Offer• ₹20,000 – ₹45,000 monthly salary• 33 paid leaves per year (including Birthday Leave)• Employee health benefits (Massages, X-rays, Blood Tests)• Free swimming training• Food provided• Paid sick leave and paid time off• Flexible scheduleExperience and Skills• Sports and musculoskeletal rehabilitation• Aquatic therapy techniques• Manual therapy and taping expertise• Strong interpersonal and counseling skills• Team collaboration and documentation skillsSalary Insights• ₹20,000 – ₹45,000 per month• Salary based on experience, skills, and value additionCompany OverviewPrachi Shah Arora's Aquatic and Physiotherapy Clinic is one of the reputed physiotherapy clinics in India, offering modern infrastructure including a heated hydrotherapy pool, indoor gym, and advanced rehab facilities. The clinic specializes in sports, aquatic, and holistic rehabilitation services.FAQsWho can apply for this role?Candidates with BPT or MPT. Freshers with strong clinical interest are also welcome.Is experience mandatory?1–5 years preferred, but not compulsory for motivated freshers.Is aquatic therapy experience required?Preferred, but training and learning opportunities are available.Is there a commitment period?Yes, a 2-year commitment is required.What types of patients will be treated?Athletes, MSK cases, pediatric, neuro, geriatric, and holistic rehab patients.Application Tips• Highlight sports or aquatic therapy exposure clearly.• Mention certifications in dry needling, cupping, or taping if available.• Showcase experience with athletes or special populations.• Emphasize communication skills and teamwork abilities.• Clearly mention willingness for a 2-year commitment.

Why This Role MattersThe Consultant Physiotherapist at Stemrx Hospital and Research centre serves as a clinical bridge between frontline patient care and broader medical strategy. This leadership role ensures advanced clinical decision-making, manages complex multi-system cases, and strengthens the physiotherapy team through mentorship, training, and consultant-level expertise.Job DescriptionStemrx Hospital and Research Centre is hiring a full-time, permanent Consultant Physiotherapist for its Navi Mumbai facility. The role involves managing complex caseloads requiring advanced diagnostic reasoning, providing consultant-level second opinions, acting as a clinical lead for physiotherapists, identifying team skill gaps, and contributing to academic and training initiatives.Key Features of the Role• Position: Consultant Physiotherapist• Organization: Stemrx Hospital and Research Centre• Location: Navi Mumbai, Maharashtra• Employment Type: Full-Time, Permanent• Salary Range: ₹12,845.02 – ₹45,000 per month• Role Level: Consultant / Clinical LeadResponsibilities• Manage patients with complex, multi-system pathologies• Apply advanced diagnostic reasoning for treatment planning• Provide consultant-level second opinions to senior and junior physiotherapists• Act as a clinical lead and mentor within the physiotherapy department• Identify skill gaps and develop internal training programs• Liaise with academic institutions as guest lecturer or trainer• Support alignment between clinical practice and medical strategyRequired Qualification• Bachelor’s Degree in Physiotherapy (BPT)• Master’s Degree in Physiotherapy (MPT) preferredEducational Requirement• BPT mandatory; MPT or higher qualification preferredImportant Requirements• Strong clinical judgment and advanced assessment skills• Experience managing complex rehabilitation cases• Leadership and mentoring abilities• Excellent communication and academic presentation skills• Ability to develop training modules and clinical protocolsEmployment Options• Full-time permanent role• Leadership opportunity within hospital setting• Academic and training exposureWhat We Offer• Opportunity to handle advanced and complex cases• Leadership and consultant-level responsibilities• Professional growth in clinical and academic domains• Competitive salary based on experienceExperience and Skills• Advanced physiotherapy assessment and intervention skills• Complex case management expertise• Team leadership and mentoring capabilities• Clinical documentation and quality assurance knowledge• Academic training and presentation skillsSalary Insights• ₹12,845.02 – ₹45,000 per month• Salary based on experience and expertise levelCompany OverviewStemrx Hospital and Research centre is a healthcare institution based in Navi Mumbai, Maharashtra, focused on delivering advanced medical and rehabilitation services. The hospital emphasizes clinical excellence, interdisciplinary collaboration, and academic engagement in healthcare practice.FAQsWho can apply?Candidates with BPT (MPT preferred) and strong clinical experience.Is this a leadership role?Yes, this is a consultant-level position with team leadership responsibilities.What type of cases will be managed?Complex, multi-system rehabilitation cases requiring advanced diagnostic reasoning.Is this a permanent role?Yes, full-time permanent employment.How do I apply?Apply via Indeed using the link below.Application Tips• Highlight experience with complex and multi-system cases.• Mention leadership or mentoring experience.• Showcase academic involvement or guest lecturing roles.• Emphasize advanced clinical reasoning skills.

Why This Role MattersThe Consultant Physiotherapist plays a vital leadership role in delivering high-quality, evidence-based physiotherapy care while enhancing patient recovery outcomes. This position strengthens integrated clinical services by combining expert diagnosis, structured treatment planning, and patient education to promote long-term wellness and functional independence.Job DescriptionMy Pain Clinic - Bandra, Mumbai is hiring a full-time Consultant Physiotherapist based in Mumbai, Maharashtra. The role involves conducting detailed clinical assessments, designing personalized treatment plans across orthopedic and general wellness cases, supervising junior staff, and ensuring adherence to evidence-based protocols. The consultant will also collaborate with allied health professionals to deliver comprehensive patient care.Key Features of the Role• Position: Consultant Physiotherapist• Company: My Pain Clinic – Bandra, Mumbai• Location: Mumbai, Maharashtra, India• Employment Type: Full-Time• Salary: ₹40,000 – ₹50,000 per Month• Work Setting: Physiotherapy & Wellness Clinic• Focus Area: Orthopedic & General Wellness CareResponsibilities• Conduct comprehensive clinical consultations and assessments• Diagnose musculoskeletal and orthopedic conditions• Design personalized treatment plans• Provide patient education and preventive care guidance• Collaborate with physiotherapists, rehabilitation experts, and wellness consultants• Maintain accurate patient records and documentation• Mentor junior medical staff and provide second opinions• Develop and implement clinical protocols aligned with best practices• Build strong patient relationships through ethical and empathetic service• Guide patients on structured treatment packages and renewalsRequired Qualification• Bachelor’s or Master’s Degree in Physiotherapy• Relevant professional license to practiceEducational Requirement• BPT / MPT from a recognized institutionImportant Remarks• Strong expertise in orthopedic physiotherapy preferred• Leadership and mentoring ability required• Strong clinical reasoning and decision-making skills essential• Excellent patient communication and relationship management skills• Commitment to evidence-based clinical practiceWhat We Offer• Opportunity to work in a specialized pain and wellness clinic• Leadership exposure within a growing clinical team• Stable monthly salary structure• Professional growth in orthopedic and wellness physiotherapyExperience and Skills• Advanced orthopedic assessment and rehabilitation skills• Strong consultation and treatment planning ability• Documentation and reporting proficiency• Team collaboration and leadership skills• Ethical, empathetic, and patient-focused approach• Ability to promote long-term treatment adherenceSalary Insights• ₹40,000 – ₹50,000 per month• Compensation based on experience and expertiseCompany OverviewMy Pain Clinic - Bandra, Mumbai is a physiotherapy and wellness center located in Mumbai, Maharashtra, specializing in pain management, orthopedic rehabilitation, and preventive care. The clinic focuses on integrated treatment approaches, combining clinical expertise with patient-centered care to build long-term recovery and wellness outcomes.FAQsWho can apply?Qualified Physiotherapists with relevant clinical experience and valid license.Is this a part-time role?No, this is a full-time position.What is the salary range?₹40,000 – ₹50,000 per month.Is leadership experience required?Mentoring and supervision skills are highly desirable.How do I apply?Apply through the Indeed job link below.Application Tips• Highlight orthopedic and consultation experience clearly• Emphasize leadership and mentoring exposure• Showcase patient communication and relationship management skills• Mention experience in protocol development if applicable• Include measurable patient outcomes or success cases in your resume

Why This Role MattersThe Medical Specialist role at Medulla Communications is critical for bridging the gap between scientific accuracy and creative healthcare communication. This position ensures that all medical content is scientifically precise, regulatory-compliant, and creatively compelling. The individual contributes directly to client success by developing materials that effectively communicate complex medical information to diverse target audiences, including healthcare professionals, patients, and internal stakeholders. By combining scientific expertise with creative thinking, the role enhances the agency’s reputation as a global leader in healthcare advertising, ensuring clients’ campaigns are both informative and impactful.Job DescriptionThe Medical Specialist will be responsible for developing and delivering high-quality medical communications for leading pharmaceutical, consumer healthcare, and medical device clients. The role involves understanding clients’ medico-marketing requirements, conducting detailed literature searches, creating scientifically accurate and engaging content, and collaborating with internal and external teams for seamless execution. This role requires a combination of scientific knowledge, creative aptitude, and project management skills to deliver communications across multiple media, including print, digital, video, CME-certified content, and scientific publications.Key Features of the Role• Develop innovative medical content that is both scientifically accurate and creatively engaging.• Collaborate with client servicing, creative, and external teams to deliver integrated healthcare campaigns.• Conduct literature searches and translate scientific insights into clear, compelling communication.• Ensure compliance with regulatory guidelines and scientific accuracy in all communications.• Participate in brainstorming and ideation sessions to provide medical expertise and insights.• Manage multiple projects across media channels, including websites, videos, print collaterals, CME modules, and presentations.• Review content produced by creative teams for accuracy, clarity, and relevance.• Stay updated with clinical, scientific, and industry trends to enhance content quality and innovation.Responsibilities Required• Create and develop medical communications that combine scientific rigor with creative presentation.• Collaborate with internal teams and external vendors to ensure timely and high-quality content delivery.• Conduct extensive literature searches and integrate relevant research findings into communications.• Develop content across multiple media including print, digital, video, scientific publications, CME collaterals, and presentations.• Attend brainstorming and ideation sessions to contribute scientific insights to creative campaigns.• Ensure that all content meets regulatory, legal, and scientific standards.• Manage timelines and prioritize tasks to meet project deadlines.• Mentor and guide junior team members on best practices in scientific writing and medical communication.Qualifications• MBBS – Medicine• Other Graduate – Any Specialization• PG – Any course, any specialization• M.Pharm – Pharmacy• M.Sc – Life Sciences, Biotechnology, Zoology, Botany, Microbiology, or related fieldsEducational Requirements• MBBS, M.Pharm, or M.Sc in Life Sciences or related disciplines.• Postgraduate qualifications in a relevant field are an advantage.Experience and Skills• 2-4 years of experience in medical or scientific writing is preferred.• Strong command of English grammar, composition, and creative writing.• Excellent research skills with the ability to translate complex scientific data into simple, engaging content.• Ability to work collaboratively with internal and external teams.• Flexibility and willingness to learn in a dynamic environment.• Strong project management skills and the ability to handle multiple assignments simultaneously.• Creative thinking, problem-solving, and attention to detail.• Knowledge of medico-marketing, healthcare regulations, and CME content development is an added advantage.Salary Insights• The salary is competitive and commensurate with experience, role responsibilities, and industry standards.• Performance-based incentives may be applicable depending on project outcomes and client satisfaction.Company OverviewMedulla Communications is a global leader in healthcare advertising and communications, recognized for combining scientific rigor with creativity. Since 2015, the agency has won over 20 international awards, including a Grand Prix at Cannes Lions Health, Clio, Global, LIA, and Spikes. Medulla offers end-to-end services, including creative development, advertising, digital solutions, and CME-certified content for pharmaceutical, consumer healthcare, and medical device brands. Its philosophy, “Inhale science, exhale creativity,” emphasizes collaboration among Client Servicing, Medical, and Creative teams to deliver accurate, effective, and innovative healthcare communications globally.FAQs• Q: Is prior medical writing experience mandatory?A: Preferred but not mandatory; strong scientific knowledge and communication skills are essential.• Q: Does this role involve client interaction?A: Yes, occasional client interactions may be required alongside internal collaboration.• Q: Is remote work allowed?A: The role is primarily based in Santacruz, Mumbai, with flexibility depending on project requirements.• Q: What types of media will the content cover?A: Content spans websites, videos, print collaterals, scientific publications, CME modules, and presentations.• Q: Are CME certifications part of the responsibilities?A: Yes, developing CME-certified content may be part of the role.Application Tips• Highlight relevant medical or scientific writing experience in your resume.• Showcase ability to translate complex scientific data into creative and impactful communication.• Demonstrate collaboration and teamwork skills in previous projects.• Include examples of multi-platform content creation if available.• Clearly present your qualifications, experience, and skills.• Emphasize adaptability, continuous learning, and innovative thinking in your application.

Why This Role MattersPharmacovigilance Agreements (PVAs) are critical legal and operational documents that define safety responsibilities between marketing authorization holders and partners. A well-drafted and compliant PVA ensures clear accountability, regulatory compliance, and seamless safety data exchange across global stakeholders.At Tata Consultancy Services (TCS), this role supports global clients within Business Process Services by drafting, reviewing, and managing PVAs in alignment with international pharmacovigilance regulations and company standards.Job DescriptionTCS is hiring experienced Pharmacovigilance professionals for the role of Executive / Senior Executive – Pharmacovigilance Agreements Specialist in Mumbai.The position focuses on drafting, reviewing, maintaining, and monitoring Global and Local Pharmacovigilance Agreements while ensuring compliance with ICH guidelines and Good Pharmacovigilance Practices (GVP).Key Features of the Role• Draft and review Global and Local Pharmacovigilance Agreements (PVAs)• Ensure compliance with ICH and global GVP regulations• Manage PVA trackers, repositories, and reconciliation activities• Monitor compliance of effective PVAs and prepare dashboards• Coordinate with cross-functional and client stakeholders• Manage PVA mailbox and communication workflows• Support project documentation and operational updatesResponsibilities• Draft new PVAs and revise existing agreements as per company standards• Review PVAs for quality, completeness, and regulatory alignment• Address internal and collaborating company comments on agreements• Manage dedicated PVA mailbox and ensure timely communication• Announce new or revised PVAs to relevant stakeholders• Maintain and update global PVA trackers including reconciliation activities• Perform compliance monitoring of active PVAs and prepare dashboards• Upload and maintain PVA documentation in company repository systems• Assist Project Manager or designee in updating project trackers and documentation• Attend team meetings and provide updates on PVA status and operational issuesRequired Qualifications• 3–7 years of experience in Pharmacovigilance• Strong knowledge of global pharmacovigilance regulations (ICH, GVP Modules)• Hands-on expertise in drafting and managing Global and Local PV Agreements• Experience handling contractual pharmacovigilance arrangementsEducational Requirements• Bachelor of Pharmacy (B.Pharm)• Master of Pharmacy (M.Pharm)• Bachelor of Science (B.Sc)• Master of Science (M.Sc)Experience and Skills• Strong understanding of contractual PV obligations• Experience managing PVA trackers and compliance dashboards• Knowledge of global regulatory frameworks and safety exchange processes• Excellent documentation, communication, and stakeholder coordination skills• Proficiency in MS Office tools• Ability to manage multiple agreements and timelines simultaneouslySalary Insights• Competitive compensation aligned with experience• Opportunity to work with global pharmaceutical clients• Exposure to international contractual pharmacovigilance frameworksFAQsQ: Is prior PVA drafting experience mandatory?Yes, hands-on experience with Global and Local PV Agreements is required.Q: Does the role involve client interaction?Yes, coordination with collaborating companies and internal stakeholders is part of the role.Q: Is regulatory knowledge important?Strong understanding of ICH and GVP modules is essential.Application Tips• Clearly mention PVA drafting and review experience• Highlight exposure to global pharmacovigilance regulations• Include examples of compliance monitoring or dashboard preparation• Emphasize stakeholder coordination and documentation management skills

Why This Role MattersDrug Safety Specialists play a crucial role in ensuring accurate reconciliation, regulatory compliance, and effective exchange of global safety information. Strong reconciliation and compliance monitoring processes protect patient safety and maintain regulatory trust.At Fidelity Health Services, this role supports global pharmacovigilance operations by managing safety reconciliation activities, reference safety information updates, and regulatory database reviews.Job DescriptionFidelity Health Services is hiring an Executive / Senior Executive – Drug Safety Specialist for its Navi Mumbai location. The role focuses on safety reconciliation, compliance monitoring, global safety information exchange, and regulatory data review.The selected candidate will coordinate with internal PV teams and global stakeholders to ensure accurate reconciliation of safety data and timely documentation updates.Key Features of the Role• Exposure to global pharmacovigilance operations• Hands-on experience in safety reconciliation and compliance monitoring• Interaction with regulatory safety databases• Involvement in global product lifecycle safety management• Opportunity to grow within drug safety operationsResponsibilities• Manage safety reconciliation and compliance monitoring activities for clients• Perform reconciliation of Reference Safety Information (RSI) for client products• Conduct data mining and review of FDA’s Adverse Event Reporting System (FAERS) and other regulatory databases• Edit, review, and reconcile Consolidated Global Product Lists• Manage global exchange of safety information for product approvals, launches, cancellations, and RSI updates• Maintain and update documentation related to safety reconciliation• Coordinate with cross-functional teams for issue resolution• Ensure regulatory compliance and audit readinessRequired Qualifications• 5–8 years of experience in the Pharmacovigilance domain• Strong experience in safety reconciliation and compliance monitoring• Proficiency in MS Excel• Experience in mailbox management and safety communication trackingEducational Requirements• Bachelor of Pharmacy (B.Pharm)• Master of Pharmacy (M.Pharm)Experience and Skills• Strong understanding of pharmacovigilance processes• Experience with global safety information exchange workflows• Knowledge of FAERS and regulatory safety databases• Analytical and detail-oriented approach• Good documentation and coordination skills• Ability to manage multiple client deliverables and timelinesSalary Insights• Competitive compensation based on experience• Exposure to global drug safety projects• Career progression opportunities in reconciliation and complianceCompany OverviewFidelity Health Services provides end-to-end pharmacovigilance and regulatory services to global pharmaceutical companies. The organization specializes in safety reconciliation, aggregate reporting, compliance monitoring, and regulatory documentation support.FAQsQ: Is prior reconciliation experience mandatory?Yes, hands-on experience in safety reconciliation is required.Q: Does the role involve regulatory database review?Yes, including FAERS and other global safety databases.Q: Is this a client-facing role?The role involves coordination with clients and internal PV teams.Application Tips• Highlight reconciliation experience clearly• Mention exposure to FAERS or regulatory databases• Showcase Excel proficiency (pivot tables, tracking sheets)• Include examples of compliance monitoring or audit support experience

Why This Role MattersPharmacovigilance reconciliation and compliance monitoring are critical to maintaining global drug safety standards. Accurate reconciliation of safety data ensures consistency between regulatory submissions, reference safety information (RSI), and global product databases—ultimately safeguarding patient health and maintaining regulatory compliance.At Fidelity Health Services, this role plays a key part in managing global safety information exchange, reconciliation activities, and compliance oversight for multiple clients.Job DescriptionFidelity Health Services is seeking experienced Pharmacovigilance professionals for its Navi Mumbai location. The position focuses on safety reconciliation, compliance monitoring, RSI management, and global exchange of safety information across product lifecycles.The selected candidate will support client-specific safety operations, manage global product listings, and ensure regulatory alignment with international pharmacovigilance requirements.Key Features of the Role• Exposure to global pharmacovigilance operations• Involvement in safety reconciliation and compliance monitoring• Interaction with international regulatory databases (e.g., FAERS)• Management of global safety information exchange• Opportunity to work with multinational client portfoliosResponsibilities• Manage safety reconciliation activities for assigned clients• Perform reconciliation of Reference Safety Information (RSI)• Conduct data mining and review of FDA’s FAERS and other regulatory databases• Edit, review, and reconcile Consolidated Global Product Lists• Manage global exchange of safety information related to product approvals, launches, cancellations, and RSI updates• Monitor compliance metrics and reporting timelines• Maintain and update safety reconciliation documentation• Ensure data accuracy and regulatory compliance• Coordinate with cross-functional PV and regulatory teams• Support audit readiness and documentation reviewsRequired Qualifications• 5–8 years of experience in Pharmacovigilance domain• Hands-on experience in safety reconciliation and compliance monitoring• Experience working with global regulatory databases• Proficiency in MS Excel and mailbox managementEducational Requirements• Bachelor of Pharmacy• Master of PharmacyExperience and Skills• Strong understanding of global PV regulations• Experience in RSI reconciliation and safety database review• Knowledge of FAERS and regulatory data mining• Good analytical and documentation skills• Strong attention to detail and compliance mindset• Ability to manage multiple client deliverables• Effective communication and coordination skillsSalary Insights• Competitive compensation based on PV experience• Exposure to global pharmacovigilance operations• Growth opportunities in safety compliance and regulatory functionsCompany OverviewFidelity Health Services is a pharmacovigilance and regulatory support organization providing end-to-end drug safety services to global pharmaceutical clients. The company specializes in safety operations, reconciliation management, and compliance monitoring in regulated markets.FAQsQ: Is reconciliation experience mandatory?Yes, hands-on experience in safety reconciliation is required.Q: Is FAERS knowledge important?Yes, data mining and review of FAERS and regulatory databases is a key responsibility.Q: Does the role involve global coordination?Yes, management of global safety information exchange is part of the role.Application Tips• Highlight reconciliation projects handled• Mention RSI management experience• Include exposure to FAERS or regulatory databases• Emphasize Excel proficiency and compliance monitoring expertise

Why This Role MattersIn today’s evolving food industry, regulatory compliance and supplier quality assurance are essential to ensure product safety, brand protection, and global market access. With increasing regulatory scrutiny across the India, Middle East, and Africa (IMEA) region, organizations must maintain strong oversight of raw material approvals, certifications, and supplier documentation.This role ensures that every ingredient and packaging material meets regional and international regulatory standards. By strengthening supplier compliance systems and collaborating cross-functionally, the position directly supports consumer safety, sustainability commitments, and operational excellence.Job DescriptionThe Senior Supplier Quality & Regulatory Compliance Manager – IMEA is responsible for managing supplier documentation, regulatory compliance, and raw material risk assessment across the region. The role works closely with Procurement, R&D, Quality, and global compliance teams to ensure materials meet food safety standards and regulatory requirements.The position focuses on supplier assurance, audit readiness, certification tracking, and documentation accuracy while driving continuous improvement initiatives.Key Features of the Role• Regional responsibility for supplier compliance across IMEA• Cross-functional coordination with R&D and Procurement• Oversight of supplier certifications and documentation systems• Risk assessment and mitigation planning• Audit preparation and sustainability documentation support• Exposure to global regulatory standardsResponsibilities• Manage supplier documentation including specifications, certifications, and compliance declarations• Ensure raw materials and packaging meet regulatory and food safety requirements• Support onboarding and approval of new suppliers and materials• Conduct supplier risk assessments and ensure corrective actions• Track certification validity and maintain updated compliance records• Communicate with suppliers to obtain regulatory and sustainability data• Support customer documentation requirements• Assist in internal and external audits• Monitor regulatory updates affecting raw materials• Ensure compliance with import and export requirements• Drive improvements in supplier quality systemsRequired Qualifications• Strong understanding of food regulatory compliance and supplier assurance• Knowledge of risk assessment frameworks• Familiarity with ISO standards such as ISO 9000 and ISO 14000• Ability to manage documentation across multiple geographies• Strong analytical and coordination skillsEducational Requirements• MSc in Food Science, Chemistry, Biotechnology, Biochemistry, Regulatory Affairs, or NutritionEquivalent scientific qualifications may also be considered.Experience and Skills• Minimum 8+ years of experience in supplier quality or regulatory compliance• Experience handling global customer and regulatory documentation• Familiarity with digital documentation management systems• Knowledge of IMEA regulatory frameworks• Experience supporting sustainability and compliance initiatives• Strong communication and stakeholder management skills• Problem-solving and risk assessment expertiseSalary InsightsCompensation is competitive and aligned with senior regulatory leadership roles within the food manufacturing sector. Final salary depends on experience, technical expertise, and regional exposure.Company OverviewGriffith Foods is a global, family-owned food product development company founded in 1919 and headquartered in Alsip. The company partners with food manufacturers worldwide to develop innovative seasonings, sauces, and coating systems.Guided by its purpose, “We Blend Care and Creativity to Nourish the World,” the organization focuses on sustainability, responsible sourcing, and collaborative innovation across global markets.FAQsIs this a team management role?Primarily an individual contributor role with strong cross-functional influence.Does it involve regional exposure?Yes, the role supports IMEA regulatory and supplier compliance activities.Is prior IMEA experience mandatory?Highly preferred for faster role effectiveness.Application Tips• Highlight supplier documentation and certification management experience• Emphasize regulatory exposure across multiple geographies• Mention audit and compliance system experience• Showcase measurable improvements in supplier quality performance• Demonstrate strong cross-functional coordination examples

Why This Role MattersClinical trials are the foundation of medical innovation. In high-impact therapeutic areas such as Oncology and Immunology, precision, compliance, and patient safety are critical. Every monitoring visit, every data query resolved, and every protocol deviation addressed contributes to the development of potentially life-saving therapies.As a Clinical Research Associate (CRA) II at ICON plc, you play a direct role in ensuring that clinical trials are conducted ethically, safely, and in full compliance with regulatory standards. Your oversight ensures that complex oncology and immunology studies generate reliable data while protecting trial participants. This position is instrumental in advancing innovative treatments from development to regulatory approval.Job DescriptionThe Clinical Research Associate II is responsible for managing and monitoring assigned clinical trial sites in accordance with study protocols, sponsor expectations, ICH-GCP guidelines, and applicable regulatory requirements. This role requires strong on-site monitoring experience, therapeutic expertise in Oncology or Immunology, and the ability to independently manage site relationships.The CRA II acts as the primary liaison between the sponsor and investigational sites, ensuring that studies are conducted with integrity and operational efficiency. The role involves significant travel and requires strong organizational and communication skills to manage multiple responsibilities simultaneously.Key Features of the Role• Focus on Oncology and Immunology therapeutic areas• Independent on-site monitoring responsibilities• Exposure to complex, high-impact clinical trials• Significant travel opportunities (domestic and international)• Cross-functional collaboration with global teams• Career progression toward Senior CRA or Clinical Trial Manager roles• Compliance-driven and patient-focused environmentResponsibilities• Conduct site qualification, initiation, monitoring, and close-out visits in accordance with monitoring plans.• Ensure adherence to study protocols, ICH-GCP standards, and regulatory requirements.• Review source documents to verify data accuracy and completeness.• Ensure informed consent processes are conducted properly and documented accurately.• Monitor patient recruitment, enrollment progress, and retention metrics.• Identify protocol deviations, documentation gaps, and compliance risks.• Ensure timely and accurate reporting of adverse events and safety information.• Perform detailed data review and resolve queries in collaboration with site staff and data management teams.• Ensure case report forms (CRFs) are complete, accurate, and submitted within required timelines.• Collaborate with investigators and site personnel to facilitate smooth trial conduct.• Provide training and support to site staff regarding protocol requirements and study procedures.• Contribute to the preparation and review of essential study documentation, including protocols and clinical study reports.• Maintain accurate monitoring visit reports and follow-up documentation.• Manage multiple sites and ensure all milestones are met within study timelines.Required Qualifications• Strong understanding of clinical trial processes and lifecycle management.• In-depth knowledge of ICH-GCP guidelines and regulatory frameworks.• Proven experience in Oncology and/or Immunology therapeutic areas (mandatory).• Strong analytical skills for interpreting complex clinical data.• Excellent communication and stakeholder management abilities.• High attention to detail and documentation accuracy.• Ability to independently manage site activities and resolve issues proactively.Educational Requirements• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Medicine, Biotechnology, or related healthcare discipline.• Bachelor’s degree in Life Sciences, Pharmacy• Advanced clinical research certifications are an added advantage.Experience and Skills• Minimum 3 years of experience as a Clinical Research Associate.• Demonstrated on-site monitoring experience.• Experience handling Oncology or Immunology clinical trials (mandatory).• Strong administrative and documentation skills.• Proficiency in Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) platforms.• Experience managing safety reporting and regulatory documentation.• Ability to interpret clinical data and identify trends or discrepancies.• Strong problem-solving and risk mitigation skills.• Ability to work both independently and collaboratively within global teams.• Willingness and ability to travel at least 60% (domestic and international).• Valid driver’s license required.Salary InsightsCompensation for the Clinical Research Associate II role is competitive and aligned with industry benchmarks for Oncology-focused CRA positions. Salary may vary based on therapeutic expertise, travel flexibility, and geographic region.In addition to base salary, employees at ICON plc may receive:• Comprehensive health insurance coverage• Retirement savings programs• Performance-linked incentives• Annual leave entitlements• Life assurance benefits• Global Employee Assistance Programme (LifeWorks)• Flexible lifestyle and wellness benefitsICON’s total rewards framework supports career development, financial planning, and work-life balance.Company OverviewICON plc is a globally recognized leader in healthcare intelligence and clinical research services. The company partners with pharmaceutical, biotechnology, and medical device organizations to accelerate the development of innovative treatments across all phases of clinical development.With a strong presence worldwide, ICON supports complex clinical programs in therapeutic areas including Oncology and Immunology. The organization fosters an inclusive, performance-driven culture focused on scientific excellence and operational quality.Inclusion and belonging are core values at ICON. The company is committed to providing equal employment opportunities and maintaining a workplace free from discrimination and harassment.FAQs1. Is Oncology/Immunology experience mandatory?Yes, therapeutic area experience in Oncology or Immunology is mandatory for this role.2. Does this role require travel?Yes, the position requires approximately 60% travel, including domestic and international visits.3. Is on-site monitoring experience required?Yes, demonstrated on-site monitoring experience is essential.4. What growth opportunities are available?Career progression may include Senior CRA, Lead CRA, Clinical Trial Manager, or Project Management roles.5. Does this role involve data analysis?The role includes data review and query resolution but does not replace formal biostatistical analysis functions.Application Tips• Highlight Oncology/Immunology trial experience prominently in your resume.• Quantify monitoring experience (number of sites, visits conducted, countries supported).• Demonstrate strong knowledge of ICH-GCP and regulatory compliance.• Mention experience handling adverse event reporting and safety oversight.• Emphasize travel flexibility and independent site management capability.• Showcase examples of resolving complex site or data-related issues.

Why This Role MattersMedical Science Liaisons (MSLs) bridge scientific research and clinical practice. In Dermatology, MSLs support evidence-based engagement with Key Opinion Leaders (KOLs), contribute to medical strategy, and ensure accurate scientific communication in alignment with regulatory standards.Job DescriptionSun Pharma is hiring a Medical Science Liaison – Dermatology within the Medical Affairs function. The role involves scientific engagement with healthcare professionals, supporting clinical data discussions, and contributing to dermatology portfolio strategy.Key Features of the Role:• Company: Sun Pharmaceutical Industries Ltd.• Function: Medical Affairs• Therapy Area: Dermatology• Location: Mumbai, Maharashtra• Salary Range: ₹3,00,000 – ₹12,00,000 per year (as listed)• Field-based scientific roleResponsibilities• Engage with dermatologists and KOLs to discuss scientific data• Present clinical trial data and product evidence• Support advisory boards and medical education initiatives• Provide medical insights to internal cross-functional teams• Gather field intelligence and therapeutic insights• Ensure compliance with regulatory and ethical guidelines• Support investigator-initiated studies and clinical collaborationsRequired Qualifications• MBBS / MD / Pharm.D / M.Pharm or equivalent life sciences qualification• Experience in Medical Affairs or as an MSL preferred• Strong dermatology therapeutic knowledge preferredExperience and Skills:• Scientific communication and presentation skills• Understanding of clinical trial data interpretation• Stakeholder engagement and KOL management• Knowledge of regulatory compliance standards• Ability to work independently in field role• Strong analytical and interpersonal skillsSalary Insights• Listed salary range: ₹3,00,000 – ₹12,00,000 per annum• Compensation may vary based on experience and qualification• Additional field allowances may applyFAQsIs prior MSL experience required?Preferred, but strong Medical Affairs experience may also be considered.Is this a field-based role?Yes, MSL roles typically involve field engagement with KOLs.Is dermatology experience mandatory?Preferred for better alignment with therapy area.What department does this role belong to?Medical Affairs.Application Tips• Highlight therapy-area expertise in Dermatology• Mention KOL engagement or advisory board experience• Demonstrate ability to interpret and present clinical data• Include regulatory and compliance exposure• Specify total Medical Affairs experience clearly

Why This Role MattersThe Consultant Physiotherapist at My Pain Clinic plays a pivotal role in helping patients manage pain, restore function, and improve mobility. This position focuses on providing expert physiotherapy interventions for musculoskeletal, neurological, and postural conditions. The role contributes to patient recovery, functional rehabilitation, and long-term wellness through evidence-based physiotherapy programs and personalised care.Job DescriptionThe Consultant Physiotherapist will assess, diagnose, and treat patients presenting with a variety of physical conditions. Responsibilities include developing tailored treatment plans, delivering hands-on therapy, prescribing exercises, and educating patients on self-management strategies. The role also involves monitoring progress, maintaining accurate clinical documentation, and collaborating with multidisciplinary teams to ensure comprehensive patient care.Key Features of the Role• Position: Consultant Physiotherapist• Company: My Pain Clinic• Location: Bandra, Mumbai, Maharashtra, India• Employment Type: Full-Time• Salary: ₹40,000 – ₹50,000 per month• Work Environment: Pain Management & Physiotherapy ClinicResponsibilities• Conduct comprehensive assessments of patients’ musculoskeletal, neurological, and functional conditions• Develop and implement personalised physiotherapy treatment plans• Provide hands-on therapy, corrective exercises, and rehabilitation interventions• Educate patients on pain management, posture correction, and injury prevention• Monitor progress and adjust treatment protocols as required• Maintain accurate clinical records and documentation• Collaborate with multidisciplinary teams for integrated patient care• Ensure compliance with professional, ethical, and safety standardsRequired QualificationCandidates must hold a recognised physiotherapy degree and demonstrate clinical competence.Educational Requirement• Bachelor’s or Master’s degree in Physiotherapy (BPT/MPT)• Valid professional license/registration preferredImportant Remarks• Clinical experience in physiotherapy preferred but fresh graduates may be considered• Strong communication, patient-centred care, and documentation skills required• Ability to work independently and collaboratively within a multidisciplinary teamExperience and SkillsExperience Required• Experience in clinical physiotherapy preferred• Fresh graduates with strong academic and clinical training may applyKey Skills Expected• Competence in assessment, diagnosis, and rehabilitation techniques• Hands-on therapy and exercise prescription skills• Effective patient education and counselling• Professionalism, organisation, and accurate documentation• Team collaboration and patient-centred approachSalary Insights• ₹40,000 – ₹50,000 per month depending on experience• Remuneration aligned with physiotherapy practice standards in MumbaiCompany OverviewMy Pain Clinic in Bandra, Mumbai, is a specialised physiotherapy and pain management centre providing evidence-based treatments for musculoskeletal, neurological, and functional conditions. The clinic emphasises personalised care, functional rehabilitation, and patient education to promote recovery, mobility, and long-term wellness.FAQs1. What qualification is required for this role?Bachelor’s or Master’s degree in Physiotherapy (BPT/MPT) is required.2. Can fresh graduates apply?Yes, fresh graduates with relevant clinical training may be considered.3. What type of patients will I work with?Patients with musculoskeletal, neurological, postural, and pain management needs.4. Where is the clinic located?Bandra, Mumbai, Maharashtra, India.5. Is professional registration required?Professional licensure is preferred to practise physiotherapy.Application Tips• Highlight BPT/MPT qualification and clinical training• Emphasise experience in musculoskeletal, neurological, or pain management physiotherapy• Showcase patient-centred care and rehabilitation outcomes• Include examples of hands-on therapy and exercise prescription• Tailor CV to demonstrate practical skills, teamwork, and professional competence

Role & Responsibilities• Conduct comprehensive medical examinations and clinical assessments• Diagnose and manage acute and chronic medical conditions• Prescribe medications and develop appropriate treatment plans• Provide counselling on lifestyle modification, preventive health, and disease management• Maintain continuity of care through regular follow-ups and chronic disease monitoring• Coordinate referrals to specialists and allied healthcare professionals when required• Respond to medical emergencies and stabilize patients prior to transfer if needed• Conduct health screenings and promote preventive healthcare practices• Collaborate with nurses, specialists, and multidisciplinary teams for integrated care• Maintain accurate and up-to-date Electronic Medical Records (EMR)• Ensure compliance with confidentiality and data protection regulations• Participate in quality improvement initiatives to enhance patient safety and care outcomes• Engage in community health programs and outreach initiatives• Maintain medical licensure and pursue continuous professional development• Uphold ethical standards in accordance with medical regulations and guidelinesQualification• Bachelor’s degree in Medicine (MBBS or equivalent)Experience• Relevant experience in general practice or primary healthcare preferredSkills• Strong clinical diagnosis and patient management skills• Proficiency in EMR systems and medical documentation• Effective communication and counselling abilities• Emergency response and critical decision-making skills• Collaborative team-working capability• Commitment to ethical medical practice and continuous learningAbout the CompanyMetropolis is a leading healthcare and diagnostic services provider in India, known for delivering high-quality pathology and medical services. With a strong network of laboratories and healthcare professionals, the organization is committed to accuracy, patient-centric care, and continuous innovation in medical diagnostics and primary healthcare services.

Serve as a scientific peer-to-peer resource to disease experts and healthcare professionals. Must have PhD, PharmD, or MD.

Roles and Responsibilities:• Conduct thorough clinical assessments, diagnose conditions, and design personalized treatment plans across orthopedic, physiotherapy, and wellness domains.• Provide clear patient education regarding diagnosis, procedures, treatment options, and preventive care strategies.• Collaborate with physiotherapists, rehabilitation experts, and wellness consultants to ensure integrated patient care.• Maintain accurate and timely documentation of patient history, treatment progress, and clinical outcomes.• Mentor junior medical staff, provide second opinions, and contribute to team clinical development.• Develop, review, and implement clinical protocols ensuring adherence to evidence-based practices.• Build strong patient relationships through ethical, empathetic, and professional service.• Guide patients on structured treatment packages, encourage long-term commitment to rehabilitation plans, and support timely renewals.Qualification:• Bachelor’s or Master’s Degree in Physiotherapy (BPT / MPT).Experience:• Relevant clinical experience in orthopedic and physiotherapy practice preferred.Skills:• Strong diagnostic and clinical reasoning skills.• Excellent communication and patient counseling abilities.• Leadership and mentoring capability.• Commitment to evidence-based practice and ethical care delivery.About the Company:My Pain Clinic – Bandra, Mumbai is a patient-focused physiotherapy and wellness centre offering integrated orthopedic and rehabilitation services. The clinic emphasizes evidence-based practice, structured treatment planning, and long-term patient recovery.

Roles & Responsibilities• Manage all Medical Affairs activities for commercial and pipeline products across global markets (Critical Care portfolio)• Perform medical reviews and provide scientific insights to internal and external stakeholders• Address Medical Affairs queries from distributors, CMOs, business partners, and health authorities• Collaborate with Pharmacovigilance and Medical Information teams to ensure accurate and timely medical responses• Represent Medical Affairs in the Promotional Review Committee and review/approve promotional materials and labeling (US, EU, and global markets)• Support regulatory strategy implementation for ongoing and future clinical/development projects• Provide medical evaluation and due diligence support for business development initiatives• Interpret global regulations, guidelines, and compliance requirements and communicate effectively across departments• Generate, revise, and harmonize SOPs and work instructions globally• Effectively manage multiple priorities in a fast-paced, cross-functional environmentQualification• B.Pharm (Bachelor's degree in Pharmacy) or MS in a scientific discipline• MBBS / BDS / MD preferredExperience• Minimum 5 years of experience in Medical Affairs• Strong knowledge of medical strategy and global health authority requirements• Experience interacting with cross-functional and senior management teamsSkills• Strong leadership and strategic influencing abilities• Excellent written and verbal communication skills• In-depth understanding of regulatory and compliance frameworks (US, EU, global)• Cross-functional collaboration and stakeholder management• Ability to manage diverse responsibilities and multitask effectively• Decision-making skills in complex regulatory and medical environmentsAbout the CompanyPiramal Pharma Limited is a leading global pharmaceutical company with strong capabilities in APIs, complex generics, and critical care products, committed to innovation, regulatory excellence, and patient-centric healthcare solutions worldwide.

Roles & Responsibilities• Distribute medical safety documents to internal stakeholders, affiliates, and license partners• Process, format, and archive periodic safety reports and Risk Management Plans (RMP)• Perform eCTD formatting and document publishing as per global pharmacovigilance regulations• Act as GPV Business Administrator for the DARIUS Document Management System• Manage GPV-specific documents and oversee archiving activities in DARIUS• Maintain electronic archives, SharePoint drives, and document repositories• Support pharmacovigilance inspections and audits through back-office documentation support• Serve as Deputy PSMF Coordinator and assist in maintaining the Pharmacovigilance System Master File (PSMF)• Provide PSMF documentation to regulatory authorities upon request• Ensure compliance with global safety reporting requirements and document lifecycle management standardsQualification• B.Pharm, M.Pharm, Pharm.D, MSc, BSc (Life Sciences) or equivalent qualification• Industrial Business Management Assistant / Documentation Specialist qualification preferredExperience• Minimum 3 years of experience in pharmacovigilance documentation or safety reporting• Strong experience in eCTD formatting and publishing• Experience handling PSUR, DSUR, PBRER, and RMP documentation• Experience with DARIUS Document Management System• Experience in PSMF maintenance and regulatory documentationVacancies• 1 VacancySkills• Advanced knowledge of global pharmacovigilance terminology and regulations• Strong expertise in document management systems• Proficiency in Microsoft Excel, Word, PowerPoint, and Outlook• Knowledge of SharePoint and e-room technology• Basic HTML knowledge preferred• Strong multitasking and organizational skills• Detail-oriented approach with audit readiness exposure• Excellent written and verbal English communication skillsAbout the CompanyAbbott is a leading global healthcare and research-driven organization focused on innovation across pharmaceuticals, diagnostics, medical devices, and nutrition. With a strong presence in Research & Development, Abbott provides opportunities to work on global pharmacovigilance systems, regulatory compliance frameworks, and safety documentation processes aligned with international standards.

Roles and Responsibilities:• Conduct detailed physiotherapy assessments and develop personalized treatment plans.• Deliver evidence-based therapy to ensure optimal recovery outcomes.• Maintain accurate patient records including assessments, progress notes, and follow-ups.• Educate patients and caregivers on exercise programs, posture correction, and preventive care.• Coordinate with clinic and home-visit teams to ensure seamless patient service.• Participate in case discussions, training sessions, and professional development activities.• Achieve monthly performance targets to qualify for incentive benefits.• Maintain clinic hygiene, decorum, and uphold organizational standards.Qualification:• Master’s Degree in Physiotherapy (MPT) in Ortho/Neuro/Pediatric/Geriatric/Sports.Experience:• Relevant clinical experience preferred.Skills:• Strong assessment and treatment planning skills.• Knowledge of evidence-based physiotherapy practices.• Good communication and patient counseling abilities.• Ability to work independently and meet performance goals.• Professional and patient-centered approach.About the Company:Aries PhysioCare is a division of Aries HealthCare International Pvt. Ltd., providing premium clinic-based and home-visit physiotherapy services across Mumbai and other major Indian cities. The organization is expanding its healthcare services internationally to countries such as Canada, UK, and UAE, aiming to deliver high-quality, technology-driven, patient-centered care with strong growth opportunities for its clinical team.

Roles & Responsibilities• Devise strategies and planning for launch of new indications/products including KOL engagement and medical education initiatives• Liaise with professional associations and Key Opinion Leaders (KOLs) to build and drive scientific advocacy in the therapy area• Drive medical education and scientific dialogue in collaboration with cross-functional teams• Collaborate with the marketing department to develop evidence-based marketing strategies• Conduct analysis of products and product pipeline• Build and maintain professional rapport with KOLs and external medical experts• Support sales force training, present scientific updates, and execute activity plans• Provide pre-launch and launch training for new products• Deliver refresher training to sales and marketing teams through continuous education initiatives• Devise Phase IV post-marketing studies including registries, real-world evidence (RWE), and observational studies• Approve promotional materials in compliance with IFPMA guidelines• Resolve scientific queries from sales, marketing teams, and healthcare professionals with strong scientific backing• Present scientific content at CMEs, conferences, advisory boards, and academic meetings• Contribute to medical writing activities and scientific documentationQualification• MD Pharmacology / MD Medicine (Fresher MD candidates eligible)• MBBS with 2 years of experience in medico-marketing• MD Pharmacology/Medicine with 2+ years experience considered for Senior Manager roleExperience• Fresher MD Pharmacology / Medicine can apply• 2+ years experience in medico-marketing preferred for senior role consideration• 2 years medico-marketing experience required for MBBS candidatesSkills• Strong scientific knowledge and analytical capability• KOL engagement and stakeholder management skills• Medical writing and scientific presentation skills• Cross-functional collaboration ability• Knowledge of IFPMA promotional guidelines• Excellent interpersonal and communication skillsAbout The CompanyZydus Group is a leading global pharmaceutical organization headquartered in India, engaged in research, development, manufacturing, and marketing of healthcare therapies across multiple therapeutic areas. The company focuses on innovation, scientific excellence, and global healthcare advancement through strong medical affairs, research, and commercial strategies.