Mumbai Healthcare Jobs

Roles & Responsibilities:• Conduct thorough physiotherapy assessments and diagnose patient conditions• Design and implement personalized treatment plans for orthopedic, physiotherapy, and wellness cases• Provide hands-on physiotherapy treatments and evidence-based rehabilitation care• 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 and timely patient records, treatment progress, and outcome reports• Mentor and guide junior staff and support overall clinical development• Develop, review, and follow clinical protocols and best practices• Build strong patient relationships through ethical, empathetic, and professional care• Guide patients on structured treatment packages and encourage continuity of careQualification:• Bachelor’s or Master’s degree in Physiotherapy (BPT / MPT)Experience:• Minimum 2+ years of clinical experience• Prior experience in a clinic, hospital, or wellness centre preferredSkills:• Strong physiotherapy assessment and diagnostic skills• Hands-on clinical treatment expertise• Excellent communication and interpersonal skills• Patient-centered and compassionate approach• Ability to work effectively in a multidisciplinary healthcare environmentAbout the Company:MY Pain Clinic Global is an advanced physiotherapy and wellness centre located in Bandra West, Mumbai. The clinic focuses on delivering high-quality, patient-centric care through integrated rehabilitation services, evidence-based treatment protocols, and a strong commitment to long-term wellness and recovery.

Roles & Responsibilities:• Conduct comprehensive dental examinations and accurately diagnose oral health conditions• Develop and implement effective treatment plans tailored to patient needs• Perform dental procedures including extractions, fillings, crowns, and other restorative treatments• Ensure high standards of patient care, comfort, and clinical excellence• Maintain accurate and detailed patient records and treatment documentation• Collaborate with other dental professionals and support staff to deliver comprehensive care• Stay updated with the latest advancements, techniques, and best practices in dentistry• Uphold clinic protocols, hygiene standards, and regulatory complianceQualification:• UG: Any Graduate• PG: Any PostgraduateExperience:• Minimum 2 years of clinical experience as a Dentist• Overall experience range: 2–7 yearsSkills:• Strong knowledge of dental procedures and clinical techniques• Excellent communication and interpersonal skills• Strong analytical and problem-solving abilities• Ability to work efficiently under pressure• Commitment to delivering high-quality patient careAbout the Company:Clove Dental is India’s largest network of dental clinics, established in 2011 with a mission to make world-class oral healthcare accessible across the country. Known for its standardized clinical protocols, advanced dental technology, and patient-centric approach, Clove Dental continues to set benchmarks in modern dentistry. The organization fosters a professional and inclusive work environment, offering dentists opportunities for continuous learning, growth, and excellence in clinical practice.

Roles & Responsibilities:• Conduct clinical diagnosis and short consultations (5–10 minutes) for walk-in customers• Assess posture, sleep habits, and musculoskeletal issues including back and joint pain• Provide expert recommendations on sleep ergonomics and posture correction• Clinically prescribe suitable SmartGRID products (Mattresses & Chairs) based on diagnosis• Support the sales team by offering health-based validation to assist in sales closure• Design and standardize customer engagement workflows from consultation to product recommendation• Track performance and improve product purchase conversion rates• Act as a core member of the West Region team and support expansion and training initiativesQualification:• UG: Any Graduate (BPT / MPT preferred)Experience:• 0 – 5 years of experience• 1 year experience preferred• Freshers can applySkills:• Physiotherapy and physical therapy expertise• Knowledge of spine, orthopaedics, posture correction, and ergonomics• Experience in community-based rehabilitation or ergonomic health• Strong communication and consultation skills• Ability to combine clinical assessment with customer interactionAdditional Details:• Working Schedule: Tuesday to Sunday, 2:00 PM – 9:00 PM (Monday fixed off)• Preferred Candidates: Women candidates and women returning to work• Industry Type: Miscellaneous• Department: Sports, Fitness & Personal Care• Role Category: Health & FitnessAbout the Company:The Sleep Company is a leading innovator in sleep solutions, dedicated to improving the way people sleep and live. By combining advanced technology with comfort-focused design, the company creates products that enhance well-being and promote restorative sleep. The organization fosters a collaborative and inclusive work culture where innovation, creativity, and impact-driven work are highly valued.

Roles & Responsibilities:• Assess and treat children with physical challenges to improve mobility, strength, and overall development• Design and implement individualized therapy plans based on patient assessments• Monitor patient progress and adjust treatment strategies as needed• Collaborate with caregivers, families, and other healthcare professionals to ensure comprehensive care• Educate families on exercises, posture, and rehabilitation techniques for children• Stay updated on advancements in pediatric physical therapy and apply evidence-based practices• Maintain accurate patient records and follow clinic protocolsQualification:• Bachelor’s or Master’s degree in Physiotherapy (BPT / MPT), preferably with pediatric specialization• Relevant certifications or licensure in Physical TherapyExperience:• Experience working with pediatric patients is highly desirableSkills:• Pediatric physiotherapy assessment and treatment techniques• Designing and implementing individualized therapy programs• Communication and collaboration with children, families, and healthcare teams• Knowledge of medicine, pediatrics, and rehabilitation• Professionalism, patience, and patient-centered care• Commitment to continuous learning and developmentAbout the Company:Movement By Design, based in Mumbai, specializes in pediatric physical therapy, focusing on enhancing children’s mobility, strength, and overall development. The clinic emphasizes personalized, evidence-based care, collaborative approaches with families and healthcare professionals, and ongoing professional development for therapists.

Roles & Responsibilities:• Diagnose and treat a wide range of dental conditions• Perform general dental procedures including cleanings, fillings, extractions, and root canal treatments• Develop and explain personalized treatment plans to patients• Educate patients on oral hygiene, preventive care, and overall oral health• Ensure high standards of patient comfort, care, and safety during treatments• Maintain accurate patient records and follow clinical protocols• Collaborate with the dental team to deliver quality, patient-centric careQualification:• Bachelor’s degree in Dental Surgery (BDS) or equivalent qualificationExperience:• Minimum 5 years of experience as a General DentistSkills:• General dentistry procedures and clinical expertise• Strong diagnostic and treatment planning skills• Excellent communication and interpersonal skills• Patient-focused approach with emphasis on comfort and care• Knowledge of dental instruments, materials, and clinical protocols• Valid dental license to practice in MumbaiAbout the Company:Neevwellbeing LLP, through its venture The Dental Clinic, is committed to delivering high-quality and affordable dental healthcare services in Mumbai. Offering comprehensive dental solutions under one roof, the clinic emphasizes modern technology, ethical practice, and a patient-centric approach to improve the oral health and overall well-being of the community

Roles & Responsibilities • Prepare ANDA Annual Reports, supplements and amendments in compliance with US FDA guidelines. • Support change control evaluations and review supporting documents including batch manufacturing records, analytical methods, specifications and validation documents. • Maintain regulatory databases, trackers and submission logs in real time. • Assist senior regulatory staff in FDA filing determinations and submission strategies. • Ensure approved applications remain compliant with FDA regulations throughout the product lifecycle. • Participate in cross-functional regulatory and quality projects as assigned. Qualification • M.Pharm in Regulatory Affairs or Quality Assurance (preferred). Experience • Minimum 2 years of experience in Regulatory Affairs, OR • Experience in QC, Analytical, R&D, Manufacturing or Pharmaceutical Production with regulatory exposure. Skills • Strong knowledge of FDA regulations and ANDA processes. • Hands-on experience with regulatory documentation and submissions. • Proficiency in MS Word, Excel and regulatory documentation tools. • Strong written and verbal communication skills. • High attention to detail with ability to manage multiple priorities. • Ability to work independently and collaborate with cross-functional teams. About the Company Teva Pharmaceuticals is a global leader in generic and specialty medicines, committed to improving patient health by delivering high-quality, affordable healthcare solutions, with a strong global presence and robust regulatory and compliance systems supporting markets worldwide.

Roles & Responsibilities • Coordinate with global R&D sites to provide end-to-end support for stability testing. • Perform routine analysis and testing for new product formats using analytical instruments in cGMP labs. • Develop, optimize and validate analytical methods. • Troubleshoot analytical instrumentation and support transfer of analytical methods and new technologies. • Drive operational excellence initiatives to simplify and improve technical processes using statistical approaches and experimental design. • Maintain, calibrate, qualify and troubleshoot laboratory instrumentation. • Ensure accurate, updated and compliant laboratory documentation following ALCOA+ principles. Qualification • M.Sc in Analytical Science / Organic Chemistry or related discipline. • Masters in Pharmacy. Experience • Minimum 2 years of total experience. • At least 1 year of hands-on experience with HPLC / GC in a cGMP environment. Skills • Strong expertise in chromatography techniques (HPLC / GC). • Experience working as an analytical scientist in a multinational Pharma / FMCG organization. • Hands-on exposure to stability testing. • Thorough knowledge of ICH / WHO / FDA guidelines, cGMP requirements and ALCOA+ principles. • Ability to support analytical method validation, forced degradation studies and documentation. Preferred Skills • Experience with OpenLab software and compliance with 21 CFR Part 11 (electronic records). • Knowledge of eLN and LIMS systems. • Strong analytical thinking, decision-making and problem-solving skills. • Good business presentation and communication skills. • Ability to handle assigned programs independently with minimal supervision. About the Company Colgate-Palmolive Company is a global consumer products organization operating in over 200 countries, specializing in Oral Care, Personal Care, Home Care, Skin Care and Pet Nutrition, driven by its core values of Caring, Inclusive and Courageous, and committed to building a healthier future for people, pets and the planet.

Key Responsibilities• Diagnose and treat patients with musculoskeletal and spine-related problems• Conduct patient assessments and develop individualized rehabilitation plans• Deliver physiotherapy treatment as per clinic protocols• Educate patients on posture correction, exercises, and spine care• Monitor patient progress and update treatment plans accordingly• Maintain proper clinical documentation and records• Communicate treatment plans and recovery expectations clearly to patients• Work collaboratively with spine specialists and clinic staffTraining• Mandatory 1-month training at Bandra or Ghatkopar centerShift & Work Schedule• Morning Shift: 7:00 AM – 3:00 PM• Evening Shift: 1:00 PM – 9:00 PM• 6 working days per week, 1 weekly off• Flexibility with shifts is mandatoryQualifications• Bachelor’s in Physiotherapy (BPT) with completed 6-month internship• Master’s in Physiotherapy (MPT) preferredExperience• 0 – 1 year of experience in musculoskeletal physiotherapy• Freshers are welcome to applySkills Required• Strong knowledge of physiotherapy fundamentals• Excellent communication skills• Fluency in English is mandatory• Patient-focused and empathetic approach• Willingness to learn and follow structured rehabilitation protocolsBond Requirement• 1.5-year service bond is mandatory• Only candidates willing to sign the bond should applyAbout company:QI Spine Clinic is India’s first chain of clinics dedicated exclusively to spine rehabilitation. The clinic is known for its evidence-based, non-surgical approach to spine care and has been ranked #1 by the Times of India Survey for two consecutive years across Mumbai, Delhi, Gurgaon, Bangalore, and Pune.

Role & Responsibilities • Develop and maintain professional relationships with internal and external customers to provide medical and scientific support for AbbVie initiatives in oncology • Execute the Medical Affairs plan for India and provide scientific education and training across AbbVie’s oncology portfolio • Lead scientific communication with key therapy leaders and stakeholders, organizing advisory boards, facilitating clinical trials, and serving as a medical resource • Provide fair and balanced scientific information to healthcare professionals (HCPs) on AbbVie products • Facilitate educational and research activities for physicians and healthcare professionals regarding current and future AbbVie therapies • Collaborate with commercial teams to ensure the information and training needs of healthcare professionals are met • Present AbbVie product data to healthcare professionals, academic institutions, and researchers • Support research initiatives requested by AbbVie R&D, Clinical Operations, and Medical Affairs departments • Serve as an internal medical and scientific resource for developing disease-state and product communications • Support Round Table and Advisory Board sessions to ensure scientific and clinical data accuracy • Conduct ongoing training for medical affairs, field sales, and internal teams • Travel approximately 60% of the time for field-based activities Qualification • MD or MBBS (Medical degree) Experience • 2-3 years of post-qualification experience in Medical Affairs • Experience in the pharmaceutical industry or clinical research preferred • Experience working collaboratively in a cross-functional matrix structure • Demonstrated ability to convey technical information to individuals with varying degrees of scientific knowledge • Strong presentation and teaching skills • Ability to build and maintain strong relationships with healthcare professionals and stakeholders Skills • Strong analytical skills to evaluate and communicate key clinical data • Proficiency in Microsoft Office and other relevant technology systems • Ability to engage and influence thought leaders and internal teams About The Company • AbbVie – A global biopharmaceutical company dedicated to improving lives through innovative medicines and solutions. AbbVie operates across key therapeutic areas such as immunology, oncology, neuroscience, and eye care, with a strong commitment to research and patient care. The company values diversity and inclusivity, fostering a collaborative and innovative environment to address the medical challenges of today and tomorrow.

Role & Responsibilities • Build and maintain strong scientific engagement with healthcare professionals • Communicate medical information and conduct clinical discussions with HCPs • Support medical affairs activities aligned with product strategy • Coordinate closely with Sales and Marketing teams for scientific support • Participate in scientific meetings, CMEs, and product training programs • Stay updated with latest clinical data, guidelines, and therapeutic developments Qualification • PharmD (Mandatory) • M.Pharm Experience • Minimum 1 year experience in Pharma / Clinical / Medical Affairs role preferred Skills • Strong scientific and clinical knowledge • Excellent communication and presentation skills • Ability to engage and influence healthcare professionals • Cross-functional collaboration skills • Willingness to travel for field-based scientific activities About the Company • A Novartis leading pharmaceutical company focused on bridging science, strategy, and patient care through strong medical and scientific engagement

Roles & Responsibilities:• Develop personalized treatment plans using physiotherapy techniques• Conduct regular assessments to monitor patient progress• Collaborate with the healthcare team to ensure integrated patient care• Educate patients on exercises, posture correction, and injury prevention• Maintain accurate patient records and documentation• Ensure clinic hygiene, safety protocols, and equipment maintenance• Provide high-quality patient care and achieve patient satisfaction targetsQualification:• Bachelor of Physiotherapy (BPT) in any specializationExperience:• 0 – 2 yearsSkills:• Physiotherapy techniques and rehabilitation exercises• Exercise prescription and physical training• Patient assessment and progress monitoring• Communication and interpersonal skills• Ability to work in a clinical team environmentAbout the Company:• Orthocare Physiotherapy Clinic & Rehab Centre, established in 2000 in Mulund West, Mumbai, is a premier center offering specialized, high-quality rehabilitation, orthopedic, and sports injury treatments.• Led by experienced professionals, the clinic focuses on patient-centered care, evidence-based physiotherapy, and achieving optimal outcomes for all patients.

Roles & Responsibilities:• Conduct biomechanical assessments of patients to identify structural or functional issues affecting gait, posture, and movement• Provide customized orthotic solutions including insoles, footwear, and braces for alignment and pain relief• Deliver physiotherapy and rehabilitation for foot, ankle, knee, hip, back, and upper-limb musculoskeletal conditions• Implement functional and strengthening exercises to improve mobility and long-term musculoskeletal health• Conduct pediatric, adult, athlete, and geriatric evaluations and treatment programs• Educate patients on lifestyle protocols, foot hygiene, biomechanics, and preventive care• Collaborate with physicians, specialists, and other healthcare professionals to ensure integrated patient care• Manage patient records and monitor progress of interventionsQualifications:• Bachelor of Physiotherapy (BPT) in Orthopedic Physiotherapy• MPT in Physiotherapy or specialization in Podiatry/Rehabilitation preferredExperience:• 0 – 4 years of relevant experience in physiotherapy, rehabilitation, or podiatrySkills:• Strong knowledge of physiotherapy principles, techniques, and rehabilitation protocols• Expertise in podiatry, orthotics, gait and posture correction• Excellent patient communication and counseling skills• Ability to design and implement individualized treatment plans• Knowledge of functional training, sports therapy, and diabetic foot careAbout the Company:Orthofit Healthcare, founded in 1998, is a leading physical healthcare provider specializing in Podiatry, Foot & Ankle, and Lower Limb assessment and care. The organization delivers personalized, evidence-based treatments including biomechanical assessments, customized orthotics, orthotic footwear, functional strength training, physiotherapy, pain management, and diabetic foot care. Orthofit is recognized for state-of-the-art practices supported by international experts and has served over 200,000 patients, focusing on alignment, gait, posture, and lifelong musculoskeletal health.

Roles & Responsibilities: • Report safety information from India and India cluster (South Asia countries) to Global Safety • Follow up with reporters for additional safety information • Review and manage safety mailbox for incoming reports • Perform monthly reconciliation and compliance checks from a pharmacovigilance perspective • Prepare and submit Periodic Safety Update Reports (PSURs) to regulatory authorities as per regulations • Gather requirements and prepare regulatory dossiers for new products, clinical trials, variations, and renewals • Prepare responses to regulatory authority queries and coordinate with global teams • Support preparation for regulatory authority and expert committee meetings • Prepare and follow up on regulatory submissions for South Asia countries • Prepare and update product labeling materials • Review promotional materials for compliance with approved product registrations • Ensure timely updates to regulatory databases • Update and maintain local SOPs • Update and renew safety agreements with partners, manufacturers, and distributors • Coordinate price updates and ensure timely entry into NPPA pricing database • Manage lifecycle maintenance activities and update commercial teams on key milestones Qualifications: • Bachelor’s degree in Pharmacy, Life Sciences, Microbiology, Chemistry, or related field Experience: • Minimum 1+ year experience in India Regulatory Affairs and Pharmacovigilance • Experience within pharmaceutical or biotechnology industry preferred Skills: • Knowledge of Indian regulatory and pharmacovigilance requirements • Strong documentation and dossier preparation skills • Ability to coordinate with global and cross-functional teams • Good communication and regulatory compliance understanding • Attention to detail and ability to manage multiple submissions About the Organization: Ferring Therapeutics is a global, research-driven biopharmaceutical company committed to developing innovative treatments in areas of high unmet medical need. The company focuses on maintaining the highest standards of quality, regulatory compliance, and patient safety while delivering life-changing therapies worldwide.

Role & Responsibilities:• Conduct clinical consultations, orthodontic assessments, and treatment planning• Supervise and monitor aligner treatments (invisible braces) and other orthodontic appliances• Take impressions, perform IPR and attachments as needed• Manage patient follow-ups and monitor clinical progress• Ensure clinic hygiene, patient safety, and adherence to SOPs• Provide a smooth and professional experience to patients during each visit• Collaborate with internal teams including dental planners and customer supportQualifications:• BDS + MDS in Orthodontics (Mandatory)Experience:• 1–3 years of clinical orthodontic practice• Experience with aligners preferredSkills:• Strong clinical and diagnostic skills in orthodontics• Excellent communication and interpersonal skills• Tech-savvy with comfort in handling intraoral scanners and digital tools• Ability to work in a retail clinic setup with high patient interactionAbout the Company:MakeO toothsi, under Ampa Orthodontics, is India’s leading smile makeover brand offering at-home and in-clinic teeth straightening treatments with cutting-edge invisible aligner technology supervised by expert orthodontists. The company focuses on delivering high-quality orthodontic care with a tech-enabled, consumer-first approach, providing growth opportunities and exposure to advanced dental technologies.

Roles & Responsibilities: • Develop, program, and validate ADaM datasets as per CDISC standards. • Create Tables, Listings, and Figures (TLFs) using SAS and/or R. • Implement Statistical Analysis Plans (SAP) and Statistical Programming Plans (SPP). • Ensure compliance with regulatory and industry standards (CDISC – SDTM, ADaM). • Collaborate closely with biostatisticians and clinical teams to ensure data accuracy. • Develop reusable macros and automate programming processes for efficiency. • Perform independent QC checks on statistical outputs and deliverables. • Support programming activities across multiple therapeutic areas including Oncology, Neuroscience, and Immunology. Qualifications • Graduate / Postgraduate in Life Sciences, Engineering, Statistics, or related disciplines.Experience: • 3 to 12 years of experience in clinical or biostatistical programming. • Hands-on experience in ADaM, TLF development, and clinical trial data analysis. Skills: • Strong expertise in SAS and/or R programming. • In-depth knowledge of CDISC standards (SDTM, ADaM). • Experience working with clinical trial protocols and regulatory guidelines. • Proficiency in TLF generation and data manipulation techniques. • Strong analytical, problem-solving, and attention-to-detail skills. • Exposure to additional tools such as Python or SQL (preferred). • Basic understanding of machine learning concepts applied to clinical data (preferred). About the Organisation: The organization is a leading clinical research and data analytics-driven company supporting global clinical trials across multiple therapeutic areas, offering a collaborative work environment, exposure to regulatory-compliant projects, and long-term career growth opportunities in statistical and clinical programming.

Role & Responsibilities:• Perform dental scans and conduct teeth alignment consultations• Assist orthodontists in aligner-based procedures at toothsi retail centres• Offer complete oral hygiene solutions including teeth whitening and related products• Perform minor dental procedures such as scaling, fillings, and OPG• Handle day-to-day store/centre operations• Ensure achievement of sales and business objectives at the centre level• Travel between centres within the city as per operational requirements• Learn and assist in delivery procedures and manage emergency appointments when required• Handle cases confidently and manage escalations effectivelyQualification:• BDS (Mandatory)Experience:• Freshers or experienced dentists may apply• Experience in aligners, orthodontics, or retail dental setups is an advantageSkills:• Strong clinical and consultation skills• Confidence in handling patients and dental cases• Ability to work in a fast-paced and dynamic environment• Good communication, sales orientation, and interpersonal skills• Willingness to travel between centres and work rotational shifts• Self-driven, quick learner, and adaptableAbout the Company:Toothsi, operated by Ampa Orthodontics Pvt Ltd, is India’s leading clinical beauty platform backed by experts and driven by technology. With brands like toothsi and skinnsi, the company is revolutionizing smile makeovers and aesthetic care. Present in 17+ cities across India and 2 cities in the UAE, toothsi has designed over 1,50,000 smiles and served nearly 2,00,000 customers through clinics, flagship centres, and at-home services.

Roles & Responsibilities: • Lead development and optimization of immunoassays based on fluorescence and chemiluminescence techniques. • Perform assay verification, validation, and robustness studies as per regulatory and quality requirements. • Support process transfer from R&D to manufacturing and ensure scale-up readiness. • Design, execute, and document experimental studies for immunoassay development. • Analyze data, troubleshoot assay issues, and implement improvements. • Prepare technical documentation, validation reports, and development summaries. • Collaborate with cross-functional teams including manufacturing, QA, and regulatory. • Ensure compliance with applicable quality systems and laboratory standards. Qualification: • M.Sc / M.Tech / PhD in Life Sciences or related disciplines. Experience: • 5–8 years of experience in development and optimization of immunoassays. • Hands-on exposure to fluorescence and/or chemiluminescence-based assay platforms. Skills: • Strong expertise in immunoassay development and validation. • Experience with assay verification, method validation, and process transfer. • Sound understanding of analytical techniques and data interpretation. • Strong documentation, problem-solving, and cross-functional coordination skills. • Ability to work independently in an R&D-driven diagnostic environment. About the Organization: Erba Mannheim Transasia is a global diagnostics leader and one of India’s largest diagnostic companies, delivering innovative solutions across clinical chemistry, immunoassays, hematology, and molecular diagnostics. With a strong focus on research, quality, and advanced technology, the organization plays a key role in shaping the future of diagnostics worldwide.

Roles & Responsibilities: • Lead authoring and review of aggregate safety reports (PSUR/PBRER, DSUR, PADER, Annual Reports). • Prepare benefit–risk evaluations, signal detection reports, and ad hoc regulatory safety documents. • Author and review RMPs, safety update reports, addendum reports, and CTD summaries (Clinical & Non-Clinical Overviews, Clinical Summaries). • Develop and update product labeling documents (CDS, USPI, SmPC/SPC, Medication Guides). • Conduct scientific literature reviews, recommend label updates, and prepare justification documents. • Generate and review line listings, summary tabulations, CFIs, and CFCs. • Prepare medical information responses for healthcare professionals (HCPs). • Coordinate safety writing projects including resource planning, timelines, and cross-functional communication. • Act as primary client contact for safety writing deliverables and ensure quality, compliance, and audit readiness. • Support RFPs, resource estimation, metrics tracking, and mentor junior writers. Qualification: • Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or related field (Master’s/PhD preferred). Experience: • 5–7 years of experience in the pharmaceutical industry or minimum 4 years in medical/safety writing. Skills: • Strong expertise in pharmacovigilance regulations, ICH guidelines, and aggregate safety reporting. • Excellent scientific writing and communication skills. • Proficiency in MS Office and strong project coordination abilities. • Client-facing, leadership, and mentoring skills. • In-depth understanding of disease areas, drug safety lifecycle, and risk management. About the Organization: Fortrea is a global clinical development and pharmacovigilance services company supporting pharmaceutical and biotech organizations worldwide. With a strong focus on scientific excellence, regulatory compliance, and patient safety, Fortrea offers professionals the opportunity to lead complex global safety projects in a collaborative and growth-driven environment.

Roles & Responsibilities: • Perform daily website review and pharmacovigilance compliance monitoring for Europe, UK, WHO, and ROW markets (India, Kazakhstan, South Africa, Ukraine, etc.). • Identify safety-related updates and share with relevant stakeholders: ICSR updates with Case Processing team, PSUR updates with PSUR team, and signal-related updates with Signal Management team. • Draft, review, and update SOPs in line with evolving global pharmacovigilance regulations. • Coordinate with QPPV and Local Responsible Persons (LRPs) for regulatory queries and training activities. • Archive emails and documents as per pharmacovigilance compliance requirements. • Collect safety data from cross-functional teams for compliance report preparation. • Prepare, review, and circulate compliance reports as per approved templates and SOPs. • Conduct and support compliance meetings with QPPV, draft Minutes of Meeting (MoM), and track action items. Qualification: • M.Pharm in Pharmacology or Pharmaceutics. Experience: • 1–2 years of hands-on experience in Pharmacovigilance compliance, website review, and global regulatory reporting. Skills: • Strong knowledge of GVP Modules and global PV regulations (EU, UK, USFDA, India, MHRA, ROW). • Hands-on understanding of PSMF, ICSR, PSUR, and RMP. • Excellent written and verbal communication skills. • Strong documentation, time management, and coordination abilities. • Ability to work effectively in cross-functional pharmacovigilance teams. About the Organization: Macleods Pharmaceutical Ltd is a leading Indian pharmaceutical company with a strong global presence and a robust R&D focus. Known for its commitment to quality, compliance, and patient safety, Macleods operates across multiple regulated markets and offers professionals an opportunity to work on global pharmacovigilance systems in a dynamic and growth-oriented environment.