Mumbai Healthcare Jobs

Roles & Responsibilities • Lead regulatory affairs for assigned franchise(s) from clinical development through lifecycle management • Develop and implement regulatory strategies, including risk mitigation and accelerated approval pathways • Drive SEC preparedness and support India’s inclusion in global clinical trials • Ensure 100% regulatory compliance, including post-approval commitments, labeling, site transfers, and biologics • Act as GRP Lead and ensure adherence to Good Regulatory Practices and quality management systems • Lead internal and external audits, ensuring deviations and CAPAs are addressed effectively • Collaborate cross-functionally with business, medical, QA, supply, and global regulatory teams • Support regulatory policy shaping, health authority advocacy, and industry association initiatives • Provide regulatory support to business development projects and oversee regulatory intelligence • Manage and develop regulatory team members (direct and indirect reports) Qualifications • Bachelor’s degree in Pharmacy (mandatory) • Post-graduate qualification in Pharmacy (preferred) Experience • Proven experience in regulatory affairs, drug development, and clinical trials • Prior people management and team leadership experience • Experience with innovative treatment modalities (desirable) Skills • Strong knowledge of Indian regulatory requirements • Strategic regulatory planning and risk management • Effective stakeholder management and cross-functional collaboration • Strong communication, leadership, and decision-making skills About the Organisation AstraZeneca is a global, science-led biopharmaceutical company focused on the discovery, development, and commercialization of innovative medicines. With a strong commitment to patient safety, scientific excellence, and ethical practices, AstraZeneca fosters an inclusive culture that encourages continuous learning, collaboration, and growth while advancing the future of healthcare worldwide.

Roles & Responsibilities • Perform publishing and technical validation of regulatory submissions (eCTD/CTD/NEES/Paper) for the US market • Conduct final technical quality review of submission dossiers • Dispatch submissions to health authorities or affiliates as per regulatory timelines • Handle post-submission activities including acknowledgements, receipts, and metadata capture in RIM systems • Upload and manage health authority correspondence, commitments, and related documentation • Ensure compliance with ICH and FDA guidelines in a regulated, process-driven environment • Coordinate with internal stakeholders and ensure timely communication of submission status Qualification • Bachelor’s degree in Pharmacy, Medicine, Chemistry, or related Life Sciences discipline Experience • Relevant experience in Regulatory Affairs Operations / Regulatory Publishing within the pharmaceutical industry Skills • Strong knowledge of ICH and FDA guidelines (US market) • Hands-on experience with eCTD, CTD, NEES, and paper submissions • Expertise in publishing tools such as Liquent, DocuBridge, or similar systems • Advanced English communication skills • Good understanding of RIM systems and regulatory workflows • Time management, organizational, and multitasking skills • Attention to detail and quality-focused mindset • Flexibility to adapt in a fast-changing environment About the Organisation Genpact is a global advanced technology services and solutions company that helps leading enterprises drive digital transformation through data, technology, and AI. Known for its strong regulatory, life sciences, and operations expertise, Genpact supports global pharma companies with end-to-end regulatory and compliance solutions while fostering innovation and continuous growth.

Roles & Responsibilities:• Perform digital scans and conduct teeth alignment consultations• Assist orthodontists in aligner-based orthodontic procedures at Toothsi retail centres• Carry out minor dental procedures such as scaling, fillings, and OPG assessments• Provide oral hygiene guidance and recommend teeth whitening and related dental products• Handle day-to-day store and clinic operations• Support business and sales objectives at the assigned centre• Travel across multiple centres within the city as per operational requirements• Manage individual appointments in case of emergencies• Learn and perform aligner delivery and related orthodontic proceduresQualifications:• Bachelor of Dental Surgery (BDS) from a recognized institution• Valid Dental Council registrationExperience:• Freshers or candidates with relevant clinical experience can apply• Willingness to work in a fast-paced, high-growth clinical environmentSkills Required:• Strong clinical and diagnostic skills• Confidence in patient handling and case management• Excellent communication and interpersonal abilities• Ability to self-learn and adapt quickly• Sales orientation and basic understanding of clinic/store operations• Flexibility to travel between centres as requiredWork Schedule:• 6 days working per week• Rotational weekly off (weekday only; no Saturday or Sunday off)About the Company:Ampa Orthodontics Pvt. Ltd. operates Toothsi, India’s leading tech-enabled clinical beauty platform revolutionizing smile makeovers and aesthetic care. Backed by advanced technology and expert clinicians, Toothsi is present in over 17 cities across India and 2 cities in the UAE. The brand has designed over 1,50,000 smiles, completed 44,000+ laser hair reduction sessions, and served nearly 2,00,000 customers through clinics, flagship centres, and home visits.

Roles & Responsibilities • Lead and manage a portfolio of brands across key therapeutic segments • Define long-term brand vision, strategy, and growth roadmap • Oversee product managers and ensure alignment with business objectives • Drive product lifecycle management, including launches and extensions • Plan and execute integrated marketing campaigns and brand promotions • Conduct market research, competitor analysis, and performance reviews • Collaborate with sales, medical, regulatory, and supply chain teams • Develop and monitor marketing budgets and ROI metrics • Train, mentor, and motivate the PMT and field force teams Qualification • Graduate in Science or Pharmacy Experience • Minimum 8 years of experience in Product Management Team (PMT) • Proven track record in domestic pharmaceutical marketing Skills • Strong leadership and brand strategy expertise • Excellent analytical, communication, and presentation skills • Market insight, forecasting, and portfolio management • Ability to manage multiple brands and cross-functional teams About the Organisation IPCA Laboratories is a leading pharmaceutical company with a strong presence in domestic and international markets. The organization is known for its focus on quality, innovation, and sustained brand growth, offering professionals a dynamic environment and excellent career progression.

Roles & Responsibilities • Lead product strategy and brand planning for domestic pharma brands • Develop and execute marketing campaigns and promotional strategies • Prepare product positioning, visual aids, and marketing collaterals • Coordinate with sales teams to drive product performance • Analyze market trends, customer insights, and competitor activity • Manage product lifecycle including launches and line extensions • Conduct training programs for field force and internal teams • Collaborate with cross-functional teams such as sales, medical, and supply chain Qualification • Graduate in Science or Pharmacy Experience • Minimum 4 years of experience in Product Management Team (PMT) • Proven experience in domestic pharmaceutical marketing Skills • Strong brand management and strategic planning skills • Market analysis and competitive intelligence • Excellent communication, presentation, and leadership abilities • Ability to manage multiple products and projects effectively About the Organisation IPCA Laboratories is a leading Indian pharmaceutical company with a strong presence in domestic and global markets. The organization is known for its quality-driven manufacturing, robust brand portfolio, and commitment to innovation in healthcare.

Roles & Responsibilities • Support product planning and execution for domestic pharma brands • Develop promotional strategies and marketing campaigns • Prepare product literature, visual aids, and training materials • Coordinate with sales teams for product launches and campaigns • Analyze market trends, competitor activities, and product performance • Assist in brand positioning and lifecycle management • Work closely with cross-functional teams including sales, medical, and supply chain Qualification • Graduate in Science or Pharmacy Experience • Minimum 2 years of experience in Product Management Team (PMT) • Experience in domestic pharmaceutical marketing required Skills • Strong understanding of pharma marketing and brand management • Market analysis and competitive intelligence skills • Good communication and presentation abilities • Ability to work cross-functionally and manage multiple projects About the Organisation IPCA Laboratories is a leading Indian pharmaceutical company with a strong domestic and international presence. The company is recognized for its quality-driven approach, robust brand portfolio, and consistent growth in the pharmaceutical market.

Roles & Responsibilities:• Provide evidence-based water-based physiotherapy (aquatherapy / hydrotherapy) treatments in a dedicated therapy pool• Assess patients and design individualized rehabilitation programs• Treat orthopedic, post-operative, sports injury, chronic pain, women’s health, and related conditions• Monitor patient progress and modify treatment plans as required• Ensure patient safety during pool-based therapy sessions• Maintain pool hygiene standards and follow safety protocols• Deliver high-quality, patient-focused careQualifications:• Bachelor’s or Master’s degree in Physiotherapy (BPT / MPT)• Certification or formal training in Aquatherapy / Hydrotherapy is highly desirableExperience:• Prior hands-on experience working with patients in a hydrotherapy pool• Senior-level clinical exposure preferredSkills Required:• Strong practical expertise in aquatherapy and hydrotherapy• Sound clinical assessment and rehabilitation planning skills• Ability to manage diverse conditions including orthopedic, post-op, sports, and chronic pain cases• Professional communication and patient-handling skills• Strong focus on safety, hygiene, and quality careWhat We Offer:• Opportunity to work in a newly established clinic with a dedicated hydrotherapy pool• Supportive, growth-oriented work environment• Opportunity to help shape and grow aquatic therapy servicesAbout the Company:Horizon Physiotherapy Studio is a newly established physiotherapy clinic in Mumbai focused on delivering specialized, evidence-based rehabilitation services. With dedicated facilities for aquatherapy and hydrotherapy, the clinic aims to provide safe, effective, and patient-centered treatment solutions while building advanced aquatic therapy services for long-term clinical excellence.

Roles & Responsibilities:• Work collaboratively with the clinic team and cross-functional teams to ensure excellent patient treatment and experience at all times• Demonstrate high levels of patient ownership and represent the organization professionally in front of patients• Continuously engage in learning to excel clinically and grow as a healthcare professionalQualifications:• Bachelor of Physiotherapy (BPT) with completion of 6 months compulsory internship• Master of Physiotherapy (MPT)Experience:• Freshers and experienced candidates can applySkills Required:• Strong patient care and clinical handling skills• Willingness to learn and adapt to specialized spine care protocols• Good communication and interpersonal skills• Professional attitude with a patient-centric approachTraining & Bond:• Comprehensive 1-month structured training focused on developing Spine Specialists• Post-training mentorship for an additional 2 months• Mandatory 1.5-year deed of indemnity applicable towards training providedAbout the Company:Qi Lifecare Pvt. Ltd. is a growing healthcare organization focused on delivering high-quality, patient-centric spine and physiotherapy care. The company emphasizes continuous learning, structured training, and professional development, offering physiotherapists an opportunity to build expertise in spine rehabilitation while working in a supportive and collaborative clinical environment.

Roles & Responsibilities:• Diagnose and treat patients with musculoskeletal and spine-related conditions• Deliver evidence-based physiotherapy care focused on spine rehabilitation• Recommend appropriate therapy plans, services, and products to support patient recovery• Apply advanced manual therapy and rehabilitation techniques as per clinic protocols• Maintain accurate patient records and track treatment progress• Ensure high standards of patient care, comfort, and clinical outcomesTraining:• One month structured training at Ghatkopar / Bandra• Hands-on training in MTD Techniques, McKenzie, Maitland, Mulligan, Neurodynamics, Kinetic Control, and moreQualifications:• Bachelor’s or Master’s degree in Physiotherapy (BPT / MPT)• Completed 6 months compulsory internship (for BPT)Experience:• 0–1 year of physiotherapy experience preferred• Freshers are welcomeSkills Required:• Strong understanding of musculoskeletal physiotherapy• Willingness to learn advanced spine rehabilitation techniques• Fluency in English• Good communication and patient-handling skillsSelection Process:• Two interview rounds:– Clinical Round– Management RoundAbout the Company:QI Spine Clinic is India’s first chain of clinics dedicated exclusively to spine rehabilitation, using advanced German technology and globally accepted physiotherapy protocols. With a strong focus on non-surgical spine care, QI Spine provides structured training, career growth, and exposure to specialized spine rehabilitation practices.

Role & Responsibilities • Drive sales of Dualto and advanced endosurgery capital equipment • Promote high-value surgical devices to hospitals and surgical centers • Build strong professional relationships with surgeons and hospital decision-makers • Identify new business opportunities in assigned territory • Conduct product demonstrations and clinical discussions with surgeons • Support surgeons during evaluations, trials, and product adoption • Manage key hospital accounts and procurement processes • Coordinate with internal teams for logistics, service, and product support • Track market trends, competitor activity, and customer needs • Ensure achievement of sales targets and business growth objectives • Maintain compliance with company policies and medical device regulationsQualification • Bachelor’s degree in Science / Pharmacy / Biomedical / Life Sciences (preferred) • MBA (Sales/Marketing) – Added advantageExperience • Experience in capital equipment or high-value medical device sales preferred • Experience working with surgeons, OTs, and hospital purchase teams • Experience in handling institutional / hospital salesSkills • Strong consultative selling and negotiation skills • Excellent communication with medical professionals • Ability to engage surgeons in clinical discussions • Good understanding of surgical procedures and OT environment • Relationship-building and account management skills • Target-driven and result-oriented mindset • Ability to manage territory independentlyAbout Company • Johnson & Johnson MedTech is a global leader in medical technology,   Ethicon division specializes in advanced surgical and endosurgery solutions

Role & Responsibilities • Provide scientific and medical support for AbbVie Oncology portfolio • Execute Medical Affairs strategy and initiatives in India • Engage Key Opinion Leaders (KOLs), physicians, and academic stakeholders • Deliver fair, balanced, and evidence-based scientific information • Conduct scientific education, presentations, and training programs • Support advisory boards, round tables, and medical meetings • Facilitate clinical research and investigator-initiated studies • Serve as internal medical/scientific expert for disease-state and product knowledge • Collaborate cross-functionally with Medical, Commercial, R&D, and Clinical teams • Document all medical activities accurately and on time • Maintain compliance with ethics, PV, regulatory, and company SOPs • Manage medical activities within assigned budget • Provide training to internal teams (medical, sales, cross-functional) • Travel extensively (~60%) for field medical engagementQualification • MD (Preferred) • MBBSExperience • 2–3 years post-qualification experience in Medical Affairs • Experience in pharma industry or clinical research preferred • Experience working in matrix and cross-functional environments Skills • Strong scientific and clinical knowledge in Oncology • Excellent presentation and communication skills • Ability to translate complex data into clear medical insights • Strong relationship-building with KOLs and stakeholders • Analytical ability to interpret clinical data • Training and teaching capability • Proficiency in MS Office and medical systems • Compliance-driven and ethical work approachAbout Company • AbbVie is a global research-based biopharmaceutical company , Focus areas include Immunology, Oncology, Neuroscience, and Eye Care

Roles & Responsibilities:• Diagnose oral health conditions and develop appropriate treatment plans• Perform dental procedures including restorative treatments, extractions, and preventive care• Provide patient education on oral hygiene, treatment options, and preventive dentistry• Maintain accurate patient records, treatment notes, and clinical documentation• Follow strict sterilization, infection control, and safety protocols at all times• Collaborate with orthodontists, specialists, and other dental professionals for comprehensive care• Ensure ethical, transparent, and patient-centric dental practices• Deliver high standards of clinical care to achieve optimal patient outcomesQualification:• Bachelor of Dental Surgery (BDS) or Master of Dental Surgery (MDS) from a recognized institution• Valid dental license/registration to practice in IndiaExperience:• Prior clinical or hospital experience preferred• Freshers may also be considered based on clinical competencySkills:• Proficiency in restorative treatments, extractions, and basic oral surgical procedures• Strong diagnostic and treatment planning skills• Excellent communication and interpersonal abilities• Knowledge of sterilization standards and infection control practices• Ethical mindset with a strong commitment to patient care and quality standardsAbout the Company:Clove Dental is India’s largest dental network, operating over 500+ stand-alone clinics across the country with a team of 1,200+ skilled dentists and specialists. Serving more than 2 million satisfied patients, Clove Dental is known for its ethical, transparent approach and adherence to stringent sterilization protocols. The organization offers comprehensive dental treatments including orthodontics, implants, and oral surgeries, while fostering a professional environment focused on clinical excellence and continuous growth.

Roles & Responsibilities • Lead end-to-end clinical data management activities for global clinical trials • Collaborate with external vendors, internal teams, and trial stakeholders to align data management expectations • Gather, review, and finalize requirements for eCRFs and clinical data collection tools • Establish data quality standards, conventions, and ensure regulatory compliance • Set, track, and manage data management timelines and milestones • Ensure real-time inspection readiness and timely data deliverables • Review clinical data management documents, reports, and submission packages • Perform complex data reviews and manage queries in EDC systems • Work closely with Study Responsible Scientists (SRS), physicians, and clinical working groups • Contribute to process, system, and tool improvement initiatives Qualification • Bachelor’s degree (BS/BA) in Clinical Data Management, Health Sciences, Computer Sciences, or related field • Master’s degree or PhD preferred Experience • Around 2 years of experience in pharmaceutical, CRO, or biotech industry • Experience in clinical drug development and clinical data management Skills • Strong written and verbal communication skills (English) • Good understanding of clinical trial protocols and data management processes • Ability to work effectively with cross-functional and global teams • Knowledge of international clinical data management guidelines • Familiarity with data capture platforms, EDC systems, and data privacy regulations • Team leadership exposure preferred • Willingness to travel up to 10% (domestic/international) About the Organisation Johnson & Johnson is a global healthcare leader committed to transforming lives through innovative medicines, medical devices, and data-driven healthcare solutions. With a strong focus on clinical research and patient outcomes, the company plays a critical role in advancing global health through science, technology, and collaboration.

Roles & Responsibilities• Conduct comprehensive clinical assessments and diagnose physiotherapy-related conditions• Design and implement personalized treatment plans across orthopedic, physiotherapy, and wellness domains• Deliver hands-on physiotherapy treatments and monitor patient progress• Educate patients on diagnoses, treatment procedures, and preventive care for long-term wellness• Collaborate with physiotherapists, rehabilitation experts, and wellness consultants for integrated care• Maintain accurate medical records, reports, and treatment documentation• Mentor junior staff, provide guidance, and support clinical skill development• Develop, review, and follow evidence-based clinical protocols and best practices• Build strong patient relationships through ethical, empathetic, and professional care• Guide patients on structured treatment packages and encourage adherence to long-term recovery plansQualifications• Bachelor of Physiotherapy (BPT) or Master of Physiotherapy (MPT) — required• Valid registration with the relevant Physiotherapy CouncilExperience• Minimum 2+ years of clinical experience as a Physiotherapist• Prior experience in a clinic, hospital, or wellness centre is preferredSkills• Strong diagnostic and clinical assessment skills• Hands-on experience in physiotherapy treatment techniques• Excellent communication and interpersonal skills• Patient-centric and compassionate approach to care• Ability to work collaboratively in a multidisciplinary team• Good documentation and reporting skillsAbout the CompanyMY Pain Clinic Global is an advanced physiotherapy, pain management, and wellness centre located in Bandra West, Mumbai. The clinic follows a multidisciplinary and evidence-based approach to help patients manage pain, recover from injuries, and improve overall physical well-being. With a strong focus on ethical practice, personalized care, and long-term treatment outcomes, MY Pain Clinic Global provides a professional and growth-oriented environment for healthcare practitioners.

Roles & Responsibilities • Handle regulatory compliance workflows including SDS creation, labels, product registrations, notifications, and renewals • Author Safety Data Sheets (SDS) for multiple global geographies as per applicable regulations • Derive hazard classifications for substances and mixtures using GHS, CLP, OSHA, and other regulations • Perform raw material, formulation, and finished product compliance reviews • Maintain data accuracy and integrity in SDS authoring tools and ERP systems • Respond to regulatory queries from internal and external stakeholders within defined TATs • Coordinate with team leads and SMEs for resolution of complex or high-priority requests • Maintain regulatory records as per defined formats and standards • Support global regulatory compliance across Diversey’s product portfolios Qualification • Bachelor’s or Master’s degree in Chemistry, Chemical Engineering, Environmental Science, Pharmacy, or related discipline Experience • Experience working in a corporate regulatory affairs or chemical regulatory environment • Hands-on experience in SDS and label authoring • Exposure to product registration, regulatory compliance, or regulatory consulting • Proven interaction with competent authorities is preferred Skills • Strong knowledge of global chemical regulations and hazard communication (GHS, CLP, OSHA) • Experience with SDS authoring software and regulatory databases • Good analytical, documentation, and problem-solving skills • Ability to prioritize tasks and meet strict timelines • Excellent written and verbal communication skills in English • Ability to work independently and in cross-functional teams About the Organisation Diversey, a Solenis company, is a global leader in hygiene, cleaning, and sustainability solutions. Through its Global Regulatory Affairs Service Center (GRASC) in Mumbai, Diversey supports regulatory compliance across worldwide markets. Solenis values its people as its greatest asset, offering a collaborative, inclusive, and growth-oriented work environment with exposure to global regulatory operations.

Roles & Responsibilities • Manage end-to-end product lifecycle for US and Canada markets from launch to commercialization • Drive sales growth, profitability, and P&L ownership for assigned international markets • Coordinate with Regulatory Affairs, Manufacturing, Supply Chain, Planning, and Operations teams • Liaise with international customers to ensure optimal inventory planning and supply continuity • Analyze IQVIA and export data to prepare sales forecasts, demand plans, and profitability analysis • Prepare and circulate monthly MIS reports to track KRAs and business performance • Support alliance management and partner coordination in regulated markets • Monitor market trends, competition, and product performance to support strategic decision-making Qualification • Bachelor’s degree in Pharmacy or related science discipline (mandatory) • MBA or equivalent postgraduate qualification preferred Experience • 2–6 years of experience in International Business Development or Pharma Sales & Marketing • Hands-on exposure to regulated markets such as US and Canada • Experience managing finished formulations portfolios Skills • Strong analytical and data-driven decision-making skills • Proactive, result-oriented mindset with ownership attitude • Excellent verbal and written communication skills • Working knowledge of SAP or similar ERP systems • Proficiency in MS Excel, PowerPoint, and Word • Ability to manage risk, resolve conflicts, and coordinate cross-functional teams About the Organisation Umedica Laboratories Private Limited is a globally reputed pharmaceutical manufacturer with a strong presence in regulated markets, particularly the United States. With multiple USFDA-approved products already commercialized and a robust ANDA pipeline under development, Umedica continues to expand its footprint in the global generics space. The organization offers professionals strong exposure to international business strategy, product lifecycle management, alliance partnerships, and long-term career growth in a regulated market environment.

Roles & Responsibilities • Develop, program, validate, and maintain clinical trial databases in compliance with company SOPs and regulatory standards • Design and maintain CDASH-compliant Case Report Forms (CRFs) and support the standard CRF library • Perform Medidata RAVE study build activities including database setup, edit checks, and custom functions • Develop and implement custom functions using C# programming within Medidata RAVE • Act as the primary technical point of contact for Data Management teams on assigned clinical studies • Ensure high-quality database design, validation documentation, and audit readiness • Provide technical support throughout the clinical trial lifecycle from study startup to database lock • Support global clinical trials across multiple therapeutic areas Qualification • Bachelor’s or Advanced degree in Life Sciences, Computer Science, or equivalent Experience • Minimum 3+ years of experience in Clinical Database Programming • Hands-on experience in Medidata RAVE study build and maintenance • Experience working in CRO, pharma, or biotech clinical research environments Skills • Strong expertise in Medidata RAVE (study build, edit checks, custom functions) • Proficiency in Custom Functions and C# programming • Knowledge of CDASH standards and CRF design principles • Familiarity with Veeva EDC is an added advantage • Understanding of clinical data management and regulatory requirements • Excellent documentation and validation skills • Strong attention to detail and quality mindset • Effective communication and cross-functional collaboration skills About the Organisation Medpace is a globally recognized Clinical Research Organization (CRO) with more than three decades of experience supporting Phase I–IV clinical trials across multiple therapeutic areas. Known for its scientific-driven approach and strong in-house expertise, Medpace offers a stable, growth-oriented environment where clinical research professionals can build long-term careers while contributing to global drug development programs.

Roles & Responsibilities • Maintain eCRF and Edit Check Specification templates in alignment with CDISC standards • Develop, review, and customize eCRF specifications from database build through database lock • Create and maintain Edit Check Specifications ensuring protocol and regulatory compliance • Perform User Acceptance Testing (UAT) and validation of eCRFs and edit checks with complete documentation • Collaborate with Clinical Database Programmers for accurate technical implementation • Coordinate with Data Managers and Sponsors to ensure EDC setup meets study expectations • Design and generate custom EDC reports using tools such as Business Objects and JReview • Lead and participate in internal and external eCRF specification review meetings • Ensure quality, consistency, and audit readiness of all database design deliverables Qualification • Bachelor’s or Advanced degree in Life Sciences, Pharmacy, Biotechnology, Computer Science, or equivalent Experience • Minimum 1 year of hands-on experience in Clinical Data Management • Experience in EDC database build, eCRF specification development, and edit checks or UAT activities • Experience with Medidata RAVE or similar EDC systems preferred Skills • Strong knowledge of EDC systems and clinical database design • Understanding of CDISC standards and clinical trial workflows • Expertise in eCRF design, edit check creation, and UAT execution • Excellent documentation and attention to detail • Strong written and verbal communication skills • Ability to collaborate effectively with cross-functional teams About the Organisation Medpace is a globally recognized Clinical Research Organization with over 30 years of experience supporting Phase I–IV clinical trials. Known for its scientific expertise and long-term stability, Medpace provides a growth-oriented environment for clinical research professionals, offering exposure to global studies and advanced clinical data management practices.

Roles & Responsibilities:• Provide physiotherapy care to patients at rehabilitation centers• Assess patients’ physical conditions and plan appropriate therapy programs• Deliver physiotherapy treatments as per rehabilitation protocols• Work across Thane (Balkum) and Kopar Khairane centers on alternate days• Monitor patient progress and modify treatment plans when required• Maintain proper clinical records and therapy documentation• Coordinate with the multidisciplinary rehabilitation team• Ensure adherence to safety, hygiene, and ethical care standardsQualification:• Bachelor of Physiotherapy (BPT) from a recognized institution• Master of Physiotherapy (MPT) preferredExperience:• 0 – 1 year of relevant physiotherapy experience• Freshers may apply• Immediate joiners onlySkills:• Strong understanding of physiotherapy and rehabilitation techniques• Good patient assessment and treatment planning skills• Effective communication and patient-handling ability• Ability to work across multiple locations• Team-oriented and professional approachAdditional Requirements:• Local candidates from Mumbai preferred• Willingness to work in both centers on alternate daysAbout the Company:Jagruti Rehabilitation Center is a renowned rehabilitation organization with a strong presence across India. With more than 15 branches and a team of over 400 professionals, the center is committed to delivering high-quality rehabilitation, mental health, and de-addiction services through a multidisciplinary and patient-focused approach.