Mumbai Healthcare Jobs

Role & Responsibilities • Develop and deliver scientific communication strategies for healthcare professionals • Translate complex clinical, biomedical and real-world data into actionable insights • Interpret and summarize clinical trial data, safety information and medical literature • Validate medical content and ensure scientific integrity for AI research projects • Review and evaluate AI-generated medical outputs and datasets • Support global AI and life-science research initiatives Qualifications & Experience • Background in Medical Affairs, Clinical Research or Scientific Communication • Prior experience as MSL, Clinical Educator, Scientific Advisor or similar external-facing medical role • Strong ability to interpret clinical data, publications and regulatory materials • Experience engaging healthcare professionals Preferred • Exposure to data annotation, data quality or evaluation systems • Interest in AI-driven healthcare innovation Why Join Alignerr • Flexible freelance remote work • High hourly compensation • Exposure to advanced AI systems in healthcare • Global collaboration and contract extension opportunities About the Company • Alignerr partners with global AI research teams and life-science organizations to build scientifically grounded AI systems using real-world medical expertise

Role & Responsibilities • Lead global medical review and device safety pharmacovigilance operations • Oversee in-line medical assessment of ICSRs for expectedness, causality and reportability • Ensure compliance with global PV, ICH, and medical device safety regulations • Act as SME for audits, inspections and regulatory interactions • Lead and manage in-house and outsourced PV medical review teams • Oversee first-line signal detection and escalation of safety risks • Maintain KPIs, quality metrics and compliance dashboards • Drive process automation and PV innovation initiatives • Support regulatory responses, inspections and CAPA management • Collaborate cross-functionally with Clinical Development, Research and Global Safety teams Qualifications & Experience • MD / DO / PhD or equivalent medical degree • Minimum 7 years pharmacovigilance / clinical industry experience • Minimum 5 years leadership and people management experience • Strong expertise in global PV regulations and ICSR lifecycle • Experience in medical device safety monitoring and vendor oversight • Cross-cultural global team collaboration experience Skills • Advanced medical review and safety assessment expertise • Regulatory compliance and audit readiness • Leadership, stakeholder management and decision-making • Metrics, KPIs and quality governance About the Company • Organon is a global $6.5B healthcare company focused on Women’s Health, biosimilars and established medicines

Roles & Responsibilities • Publish and dispatch regulatory submissions (eCTD/NeeS) for US, EU, and Canada markets • Handle post-approval and lifecycle management submissions with high quality and timeliness • Perform document-level publishing, QC checks, and troubleshoot submission issues • Collaborate with regulatory and scientific teams for planning and publishing activities • Ensure compliance with ICH guidelines and agency-specific publishing requirements • Maintain and update submissions using regulatory IT systems and tools Qualifications • Bachelor of Pharmacy (B.Pharm) • Master of Pharmacy (M.Pharm) • Master’s degree in Life Sciences Experience • 1-3 years of experience • Regulatory publishing exposure in US/EU markets preferred Skills • Knowledge of eCTD, NeeS, and regulatory submission standards • Hands-on experience with tools like Veeva Vault, Global Insight, ISI Toolbox, Adobe Acrobat, Lorenz Validator • Good understanding of regulatory IT systems • Strong written and spoken English communication • Ability to work in a global, culturally diverse environment About the Company Teva Pharmaceuticals is a global leader in generic medicines, operating in nearly 60 countries and providing affordable, accessible healthcare solutions. Every day, over 200 million people worldwide rely on Teva medicines, making a meaningful impact on global health through innovation, quality, and inclusivity.

Roles & Responsibilities: • Provide scientific inputs for new product development and evaluate product claims • Review, validate, and approve product claims and medico-marketing materials • Plan and conduct claim substantiation studies and scientific training for marketing teams • Coordinate with third-party manufacturers for timely licenses and maintain license archival • Respond to medical, regulatory, and consumer queries with accurate scientific information • Monitor Adverse Events (AEs) and ensure pharmacovigilance and materiovigilance compliance • Ensure quality, integrity, and regulatory compliance of all information shared with stakeholders • Collaborate with internal teams including Marketing, QA, R&D, Supply Chain, and Business Development • Liaise with external stakeholders such as KOLs, legal teams, consultants, and manufacturing partners • Support business growth through regulatory strategy and compliance adherence Qualification: • M.Pharm or M.Sc in Pharmaceutical Sciences Experience:• 5-8 years of experience in Regulatory Affairs • Prior experience in OTC drugs preferred • Practical exposure to Pharmacovigilance and Materiovigilance processes Skills: • Strong knowledge of Indian regulations: D&C Act, DMR Act, UCPMP, ASCI Codes • Ability to critically review scientific and regulatory documents • Good analytical, communication, and presentation skills • Strong coordination and stakeholder management abilities About the Company: Piramal Pharma Ltd., part of the diversified Piramal Group, is a leading global healthcare organization with a strong presence in consumer healthcare, pharmaceuticals, and life sciences. Guided by the values of Knowledge, Action, Care, and Impact, the company focuses on ethical practices, innovation, and inclusive growth. Through its Consumer Healthcare division, Piramal touches millions of lives across India with trusted OTC brands and a robust distribution network, while fostering a people-centric and high-growth work culture.

Role & Responsibilities: • Internalize and adhere to Standard Operating Procedures (SOPs) in pharmacy operations • Prepare purchase orders and coordinate procurement of medicines and supplies • Receive medicines from suppliers and verify quantity, batch, and expiry details • Prepare Goods Receipt Notes (GRN) for received materials • Store and arrange medicines as per manufacturer-recommended storage conditions • Process purchase returns for rejected, expired, damaged, or spoiled materials • Receive and process indents from departments and inpatient units • Dispatch medicines to inpatients and attend to outpatient dispensing requirements • Accept and process medicine returns from patients in accordance with hospital policies • Maintain accurate pharmacy records and documentation Qualification: • D.Pharm or B.Pharm from a recognized institution • Diploma or Graduation in Pharmacy Experience: • Freshers or candidates with hospital pharmacy experience are welcome Skills: • Knowledge of hospital pharmacy operations and SOP compliance • Good understanding of inventory, procurement, and dispensing processes • Attention to detail and accuracy in documentation • Basic computer and pharmacy management system knowledge • Good communication and coordination skills About the Company: Wockhardt Hospitals is a leading chain of multi-specialty healthcare hospitals in India, known for its clinical excellence, advanced medical infrastructure, and patient-centric approach. Committed to quality care and safety, Wockhardt Hospitals provides a professional environment that supports continuous learning, adherence to best practices, and career growth for healthcare professionals.

Role & Responsibilities: • Assist the pharmacist in dispensing medicines as per doctor prescriptions and ensure complete prescription fulfillment through in-house pharmacy coordination • Consult doctors before any medicine substitution • Cross-check dispensed medicines with billing details including patient name, medicine, quantity, and expiry • Monitor stock availability and raise indents as required • Counsel patients and customers on medication usage, reactions, and general health guidance • Handle inbound calls related to drug information, patient education, and home delivery orders • Maintain home delivery records and ensure timely dispatch of medicines • Handle billing, cash collection, and system entries when required • Ensure proper storage of medicines including cold chain management • Receive, verify, and enter stock details including quantity, batch number, MRP, and expiry • Coordinate stock transfers between branches or distribution centers during shortages • Maintain records for out-of-stock items and follow up for replenishment • Perform regular physical stock verification and daily checks for fast-moving items • Ensure proper shift handover and focus on achieving pharmacy sales targets • Perform additional tasks as assigned by the in-charge Qualification: • Any Graduate Experience: • Freshers or candidates with relevant pharmacy experience are welcome Skills: • Strong prescription handling and dispensing skills • Good patient counseling and customer service abilities • Attention to detail in billing and inventory management • Basic computer and pharmacy software knowledge • Ability to work in shifts and a fast-paced environment About the Company: Apollo Pharmacy is one of India’s largest and most trusted pharmacy retail chains, dedicated to delivering quality medicines and healthcare services with a strong focus on patient safety and customer satisfaction. With a wide national presence and structured career growth opportunities, Apollo Pharmacy provides a professional and supportive work environment for pharmacy professionals.

Job Role & Responsibilities• Assist Senior Dentist during dental procedures• Counsel and explain treatment plans to patients• Independently manage clinic operations in the absence of Senior Dentist• Perform basic procedures like RCT and simple tooth extractions• Ensure patient comfort and maintain clinic hygieneQualifications• BDS from a recognized dental institutionExperience• 0–2 years (Freshers are welcome to apply)Skills Required• Proficiency in RCT and basic dental procedures• Good patient communication and counseling skills• Confidence to handle basic procedures independently• Professional and patient-focused approachAbout the Company• Dr. Priti K. Shetty – Reputed dental clinic in Bhandup (West)• Offers quality dental care with a patient-friendly approach• Supportive environment for learning and professional growth• Conveniently located 5 minutes from Bhandup Railway Station

Job Role & Responsibilities• Make outbound calls for appointment reminders, follow-ups, and treatment explanations• Handle inbound patient calls related to dental queries and post-treatment care• Provide basic, non-invasive dental guidance within tele-dentistry scope• Educate patients on oral hygiene, preventive care, and post-procedure instructions• Identify cases requiring in-clinic visits and guide patients accordingly• Schedule, reschedule, and confirm dental appointments• Maintain and update patient records in CRM/HMS systems• Explain treatment plans, procedures, and estimated costs clearly• Coordinate with clinic dentists and specialists for patient care• Maintain accurate call logs and ensure data confidentialityQualifications• BDS (Bachelor of Dental Surgery) – Mandatory• Valid Dental Council registrationExperience• Freshers and experienced dentists can apply• Experience in patient counseling or tele-dentistry is an advantageSkills Required• Excellent communication skills (English and local language preferred)• Strong patient counseling and interpersonal skills• Basic computer knowledge (CRM, EMR, Excel)• Ability to explain medical terms in simple language• Calm, empathetic, and patient-focused approachAbout the Company• Patient-centric dental healthcare organization• Focuses on tele-dentistry and patient engagement solutions• Uses structured systems for care coordination and follow-ups• Supportive work environment with career growth opportunities

Role & Responsibilities • Coordinate day-to-day clinical trial activities at the site • Assist investigators during study initiation, conduct, and close-out • Maintain essential trial documents including ISF, CRFs, and logs • Ensure compliance with ICH-GCP, SOPs, and study protocols • Support subject recruitment, informed consent, and follow-ups • Coordinate with monitors, sponsors, and ethics committees • Handle data entry, query resolution, and audit readiness Qualifications & Experience • Degree in Life Sciences, Pharmacy, Nursing, or related field • 6 months – 1 year of experience in clinical research or CRC role • Practical knowledge of clinical trials, GCP, and regulatory guidelines Skills • Strong documentation and organizational skills • Good patient coordination and communication abilities • Ability to work in compliance-driven clinical environments About the Company • JSS Research is a reputed clinical research organization supporting regulated clinical trials in metro cities across India

Role & Responsibilities • Assess and treat infants, children, and adolescents with developmental, neurological, and musculoskeletal conditions • Design and implement individualized paediatric physiotherapy treatment plans • Manage conditions such as cerebral palsy, developmental delay, autism, Down syndrome, torticollis, and gait abnormalities • Monitor patient progress and modify treatment plans accordingly • Educate parents and caregivers on home exercise programs and child handling techniques • Maintain accurate clinical documentation and progress notes • Collaborate with multidisciplinary teams including pediatricians, occupational and speech therapists • Ensure a child-friendly, safe, and engaging therapy environment Qualifications & Experience • Bachelor’s or Master’s degree in Physiotherapy • Experience in paediatric physiotherapy preferred Skills • Strong paediatric assessment and rehabilitation skills • Knowledge of developmental milestones and early intervention programs • Play-based therapy techniques • Good communication and documentation abilities Preferred • Experience with early intervention and child development centres About the Company • ReLiva Physiotherapy and Rehab is a reputed rehabilitation network delivering specialized paediatric and neuro-musculoskeletal physiotherapy services

Role & Responsibilities • Conduct comprehensive assessment of patients with neurological conditions • Develop personalized treatment and rehabilitation plans • Implement aquatic and land-based physiotherapy interventions • Improve patient mobility, strength, balance, and functional independence • Educate patients and families on aquatic therapy benefits and home exercise programs • Collaborate with senior doctors, occupational therapists, and multidisciplinary teams • Maintain accurate patient records, progress notes, and discharge summaries • Communicate patient progress with consultants and research teams • Participate in research, quality improvement, and professional development activities Qualifications & Experience • Bachelor’s or Master’s degree in Physiotherapy • Valid physiotherapy licensure in India • Minimum 1 year of clinical experience Skills • Strong neurorehabilitation and aquatic therapy skills • Excellent communication and patient handling abilities • Good documentation, organization, and time-management skills • Ability to work in a multidisciplinary team Preferred • Certification or specialized training in aquatic therapy About the Company • Specialized rehabilitation center delivering aquatic and neuro physiotherapy services

Role & Responsibilities • Perform dental scans and conduct teeth alignment consultations • Provide complete oral hygiene, whitening, and preventive dental solutions • Perform minor dental procedures such as scaling, fillings, and OPG • Assist orthodontists in aligner procedures at retail centres • Handle individual emergency dental appointments when required • Manage day-to-day clinic/store operations • Ensure store-level sales and business objectives are achieved • Travel between multiple centres within the city as per operational requirements Qualifications & Experience • Bachelor of Dental Surgery (BDS) • Comfortable working in a fast-paced clinical retail environment • Ability to self-learn, handle escalations, and manage patient cases independently Skills • Strong clinical and diagnostic skills • Good communication and patient handling abilities • Sales orientation and basic operational management skills • Ability to travel and adapt across multiple clinic locations Preferred • Experience in orthodontics or aligner procedures About the Company • AMPA Orthodontics Private Limited (toothsi) is India’s leading clinical beauty platform offering advanced smile makeover and skincare solutions across India

Role & Responsibilities • Communicate therapeutic area-related, product-related, and clinical information to external       stakeholders • Develop long-term relationships with opinion leaders and key stakeholders • Support clinical research, including investigator-initiated trials (IITs) and RWE projects • Capture market insights to support Field Medical Plans and business strategies • Provide medical expertise to commercial teams and assist in regulatory submissions • Ensure compliance with industry regulations and company policies • Support Patient Support Programs (PSPs) and patient awareness initiatives Qualification • MBBS, MD, or Pharm D Experience • 1-2 years in medico marketing or related field Skills • Strong communication and presentation skills • Excellent relationship-building ability with healthcare professionals • Proficiency in English and ability to manage cross-functional projects Why Join Domnic Lewis • Career growth in a leading healthcare company • Collaborate with experts in the therapeutic area • Contribute to global medical strategies and patient outcomes

Role & Responsibilities • Develop and execute medical strategy for Cardio Diabetic & Respiratory segments • Provide scientific support to commercial and marketing teams • Review promotional materials for medical and regulatory compliance • Engage with KOLs and healthcare professionals • Support clinical and post-marketing medical activities • Ensure compliance with medical affairs and pharmacovigilance standards Qualification • MBBS / MDS (Mandatory) Experience • Minimum 2 years of experience as Medical Advisor Skills • Medical affairs strategy • Scientific communication and interpretation • Regulatory and compliance knowledge • KOL engagement • Strong presentation and communication skills About the Company • Hiring through Gig Consultants • Mumbai-based pharmaceutical organization • Focused on Cardio Diabetic & Respiratory therapy segmentsInterested candidates may share their updated CV on deepali@gig-consultants.in or reach out via DM - 8800395116

Role & Responsibilities • Manage and execute ICSR regulatory submissions for clinical and post-marketing products • Perform global safety submissions within regulatory timelines • Handle case processing and submissions in ARGUS Safety database • Review AE data and local labeling for accurate scheduling • Monitor submission workflows and resolve pending or failed submissions • Perform major corrections and case distribution • Ensure compliance with global PV regulations, SOPs, WRKs, MANs, and BEDs • Maintain submission tracking and documentation • Identify data gaps and quality issues Qualification • B.Pharm or M.Pharm Experience • 1–4 years in Pharmacovigilance Submission • Experience with ARGUS, ICSR processing, and global regulatory reporting Skills • ARGUS Safety handling • ICSR submissions and distribution • Medical terminology and clinical interpretation • Quality control in PV • Documentation and workflow monitoring • Strong organizational and communication skills About the Company • A leading ITES organization hiring through Outpace Consulting Services • Focused on global pharmacovigilance and regulatory compliance • Provides exposure to international safety submissions and structured compliance processes

Role & Responsibilities • Oversee complete clinic operations and staff duties • Manage physiotherapy team and clinic management staff • Develop and implement procedures to ensure optimal patient care • Lead hiring, training and performance evaluation of staff • Manage internal and external communications and handle patient queries • Ensure smooth day-to-day clinic operations including appointments and records • Ensure compliance with healthcare rules, safety guidelines and regulatory standards • Manage budgeting, expenses, inventory and medical supply control • Handle patient grievances and maintain a positive clinic environment • Design and implement business strategies to achieve organizational goals • Assign and delegate tasks to improve staff productivity • Develop clinic protocols and operational procedures • Conduct quarterly and annual staff performance reviews • Monitor productivity, receivables and overall clinic performance Qualification • BPT / MPT (Physiotherapy) Experience • Minimum 10+ years Skills • Strong leadership and people management abilities • Excellent communication and interpersonal skills • Problem-solving and decision-making capability • Strong organizational and multitasking skills • Attention to detail and regulatory compliance knowledge • Patient care coordination and service quality management Salary • ₹45,000 – ₹65,000 per month About the Company MPC is a patient-focused physiotherapy and rehabilitation clinic committed to delivering high-quality, ethical and evidence-based physiotherapy services. The organization promotes a collaborative work culture with strong emphasis on clinical excellence, operational efficiency and patient satisfaction.

Role & Responsibilities • Maintain accurate, complete and inspection-ready Trial Master Files • Review and approve TMF documents for regulatory compliance • Manage version control and document consistency • Maintain eTMF system structure, folders and system health • Ensure continuous inspection readiness of TMF • Act as TMF point of contact during audits and inspections • Coordinate with CRAs for TMF updates • Perform periodic TMF gap analysis and share findings • Drive continuous improvement of eTMF workflows Qualification • Bachelor’s or Master’s degree in Life Sciences / Pharmacy / Nursing / Public Health / Related discipline • PG Diploma in Clinical Research (preferred) Experience • 0–2 years in Clinical Research • Freshers are eligible Skills • Knowledge of TMF/eTMF processes • Understanding of ICH-GCP and regulatory documentation • Strong attention to detail • Good communication and coordination skills • Proficiency in MS Office and document management systems About the Company Sun Pharma is India’s largest pharmaceutical company with a strong global presence, known for high-quality medicines and world-class clinical research standards.

Role & Responsibilities • Maintain study documentation including protocols, ICFs, CRFs and clinical reports • Organize and manage electronic and paper study files • Support meeting scheduling, minutes preparation and travel coordination • Assist in preparation and submission of regulatory documents • Support GCP compliance and regulatory requirements • Track site invoices and payment status • Handle vendor code generation and vendor tracking • Support site coordination and communication activities Qualification • Bachelor’s or Master’s degree in Life Sciences / Pharmacy / Nursing / Public Health / Related discipline • PG Diploma in Clinical Research (preferred) Experience • 0–2 years in Clinical Research • Freshers are eligible Skills • Basic understanding of GCP and clinical research documentation • Good organizational and coordination skills • Strong documentation and communication abilities • Proficiency in MS Office About the Company Sun Pharma is India’s largest pharmaceutical company and a global leader in specialty generics and innovative medicines.

Role & Responsibilities • Prepare and compile regulatory dossiers for drug registration submissions • Liaise with regional and global regulatory teams to obtain supporting documentation • Support DCGI and Health Authority submissions including PMS and Phase IV studies • Coordinate and review clinical study reports, stability protocols and non-clinical reports • Maintain regulatory dossiers, approvals and submission archives • Support lifecycle management activities for registered pharmaceutical products • Coordinate with regulatory consultants for effective submissions • Manage regulatory trackers and documentation for tenders • Ensure compliance with Indian regulatory requirements Qualification • Bachelor’s or Master’s degree in Pharmacy / Life Sciences / Related discipline Experience • Prior experience in Regulatory Affairs within pharmaceutical or healthcare industry • Hands-on exposure to DCGI submissions preferred Skills • Strong knowledge of Indian regulatory framework • Drug registration and lifecycle management expertise • Excellent documentation and coordination skills • Strong analytical and communication abilities • High attention to detail and compliance orientation About the Company Johnson & Johnson is a global healthcare leader committed to advancing patient care through innovative medicines, medical devices and regulatory excellence.