Hyderabad Healthcare Jobs

Roles & Responsibilities• Support PV system compliance and SOP implementation• Conduct quality checks and internal audits• Assist in inspection readiness and CAPA tracking• Maintain pharmacovigilance quality standardsQualification• B.Pharm, M.Pharm, Pharm.D, Msc, BSc, or other Lifesciences degreeExperience• 4–6 years of relevant pharmacovigilance experienceSkills• Strong understanding of global pharmacovigilance regulations (ICH, GVP, FDA, EMA guidelines)• Experience with safety databases (Argus/ArisG preferred)• Strong analytical and documentation skills• Ability to work in a compliance-focused, quality-driven environmentAbout The CompanyMedifodil Smart Pharma Solutions is an expanding pharmacovigilance department offering high-growth opportunities in a quality-driven environment. With a focus on regulatory compliance and patient safety, Medifodil provides comprehensive solutions across ICSR, aggregate reporting, and PV Quality Assurance (QA).

Roles & Responsibilities• End-to-end ICSR case intake, processing, follow-up, and regulatory submissions• Provide medical review support and narrative writing• Perform MedDRA coding and case quality checks• Ensure compliance with global reporting timelines (FDA, EMA, MHRA)Qualification• B.Pharm, M.Pharm, Pharm.D, Msc, BSc, or other Lifesciences degreeExperience• 4–6 years of relevant pharmacovigilance experienceSkills• Strong understanding of global pharmacovigilance regulations (ICH, GVP, FDA, EMA guidelines)• Experience with safety databases (Argus/ArisG preferred)• Strong analytical and documentation skills• Ability to work in a compliance-focused, quality-driven environmentAbout The CompanyMedifodil Smart Pharma Solutions is an expanding pharmacovigilance department offering high-growth opportunities in a quality-driven environment. With a focus on regulatory compliance and patient safety, Medifodil provides comprehensive solutions across ICSR, aggregate reporting, and PV Quality Assurance (QA).

Roles & Responsibilities• Monitor and route incoming safety information to project teams• Perform accurate ICSR data entry and case processing in safety databases• Track and record all safety documentation per sponsor guidelines• Redact patient-identifiable data as per ICH-GCP and GVP requirements• Support literature and clinical trial (CT) case processing• Assist in translation coordination for safety source documents• Support query follow-up and safety submission processes• Maintain case files (electronic and paper)• Conduct daily workflow reconciliation activities• Follow SOPs, WIs, global PV regulations, and study plansQualification• B.Pharm / M.Pharm / PharmD / BDSExperience• Minimum 1 year of Pharmacovigilance case processing or full data entry role (mandatory)• Experience in Clinical Trial (CT) cases and Literature cases preferred• Knowledge of safety databases and medical terminology preferredSkills• Strong documentation accuracy• Ability to manage multiple tasks• Team collaboration• MS Office (Word, Excel, PowerPoint, Outlook) proficiency• Familiarity with document management systems• Understanding of ICH Guidelines, GVP Modules, and global drug safety regulationsAbout The CompanySyneos Health is a global, mid-sized Contract Research Organization (CRO) providing integrated biopharmaceutical solutions to help customers accelerate the development of their drugs. With operations in over 110 countries, Syneos Health has been involved in 94% of novel FDA-approved drugs in the last five years, offering unparalleled exposure to global regulatory standards and drug safety regulations.

Roles & Responsibilities• Handle pharmacy operations and ensure the availability of medicines• Oversee medication dispensing and ensure proper storage• Monitor inventory levels and manage procurement for the pharmacy• Provide pharmaceutical care and counseling to patients• Ensure compliance with PCI and hospital standards• Collaborate with healthcare providers for effective patient careQualification• D.Pharm / B.Pharm• Valid Telangana PCI RegistrationExperience• Freshers may applySkills• Strong knowledge of pharmaceutical practices and medication management• Excellent communication and interpersonal skills• Ability to manage inventory and handle procurement• Good organizational skills and attention to detailAbout The CompanyAnkura Hospital for Women & Children, Hyderabad, is committed to clinical excellence and providing quality healthcare to women and children. As part of our growth, we are expanding our pharmacy department and are seeking dedicated professionals who share our vision for patient care and operational excellence.

Roles & Responsibilities• Conduct medical evaluations and clinical assessments for study participants• Ensure subject safety and adherence to clinical trial protocols• Review and interpret clinical data and medical reports• Support BA/BE studies and clinical trial activities• Maintain compliance with ICH-GCP, DCGI, and regulatory guidelines• Collaborate with clinical research, QA, and operations teamsQualification• MBBSExperience• 0–3 YearsSkills• Strong knowledge of clinical trial protocols and ICH-GCP guidelines• Excellent communication and interpersonal skills• Ability to interpret clinical data and medical reports• Proficiency in using clinical research software and toolsAbout The CompanyNoah Therapeutics Pvt. Ltd. is a growing Clinical Research Organization (CRO) committed to quality, compliance, and innovation in the healthcare sector. We specialize in clinical trials, research, and testing, aiming to contribute to the medical field with high standards and expertise.

Roles & Responsibilities:• Lead complex neuro-rehabilitation cases with a focus on evidence-based recovery• Conduct detailed clinical assessments and develop individualized treatment plans• Implement specialized physiotherapy interventions to improve patient outcomes• Work collaboratively with a multidisciplinary healthcare team• Maintain accurate patient records and monitor progress• Provide patient-centric care to support rehabilitation goalsQualifications:• Master of Physiotherapy (MPT) in Neurology – MandatoryExperience:• Minimum 3+ years of clinical experience in neuro-rehabilitationSkills:• Strong clinical assessment and decision-making abilities• Patient-focused approach to treatment• Excellent communication and teamwork skills• Ability to manage complex rehabilitation cases• Professional and ethical practiceAbout the Company:MnD Consultation Services Pvt. Ltd. is dedicated to delivering high-quality rehabilitation services through advanced clinical practices and a collaborative work culture. The organization offers a state-of-the-art facility focused on improving patient outcomes and supporting professional growth.

Roles & Responsibilities:• Liaise with business partners, country medical teams, and medical leads• Maintain strong relationships with internal stakeholders across regions• Coordinate regularly with FMV leads and tier validators• Ensure accurate transfer of HCP data into tiering systems• Perform data quality checks and remediation of identified errors• Prepare monitoring, verification, and compliance reports within timelines• Support quarterly scientific expert and customer engagement reporting• Manage and prioritize requests via centralized mailbox/platform• Review HCP and non-HCP tiering documentation• Analyze expert credentials to determine appropriate tier levels and FMV• Support local process training, tools, and continuous improvementsQualification:• Bachelor’s or Master’s degree required• B.Pharm / M.Pharm / Life Sciences preferredExperience:• 1–2 years of experience in pharma or life-science companiesSkills:• Strong proficiency in MS Excel, Word, PowerPoint, Outlook, Access• Experience in data handling, reporting, and documentation• Stakeholder and project management skills• Strong communication (written & spoken English)• Analytical thinking, planning ability, and teamwork mindsetAbout The Company:Sanofi is a global pharmaceutical leader, centralizing and streamlining global medical processes to reduce dependency on external vendors and strengthen internal expertise. The company focuses on improving the quality of life for patients worldwide by delivering innovative medicines and therapies. Sanofi offers an inclusive, diverse, and equal-opportunity workplace with structured career growth and skill development opportunities.

Roles & Responsibilities• Compile, review, and author regulatory dossiers in CTD and eCTD format for global submissions• Perform eCTD publishing and manage submission sequences and lifecycle operations• Handle product lifecycle activities including variations, renewals, amendments, and compliance updates• Ensure regulatory submissions comply with current guidelines and country-specific requirements• Coordinate with cross-functional teams such as QA, CMC, Clinical, Pharmacovigilance, and Medical Writing• Act as a point of contact for Health Authorities, including handling deficiency letters and regulatory queries• Track submission status, approvals, regulatory commitments, and timelines• Maintain regulatory databases, trackers, and documentation in a compliant manner• Support regulatory audits, inspections, and internal assessments as requiredExperience• 4 to 6 years of hands-on experience in Regulatory Affairs within Pharma or Life Sciences• Strong exposure to CTD and eCTD dossier compilation and publishing• Experience in regulatory submissions, lifecycle management, and health authority communicationQualification• Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or a related disciplineSkills• Strong understanding of global regulatory requirements (US, EU, and ROW)• Hands-on experience with eCTD publishing tools and submission processes• Excellent documentation, coordination, and communication skills• Ability to manage multiple submissions independently• High attention to detail with a compliance-focused approach• Ability to work effectively in a fast-paced, service-oriented environmentAbout the CompanyMedifodil Smart Pharma Solutions is a growing pharmaceutical services organization providing regulatory and compliance support to global life sciences companies. The company focuses on delivering high-quality, efficient, and compliant regulatory solutions across multiple international markets.

Roles & Responsibilities• Support regulatory services activities aligned with Life Sciences R&D operations• Coordinate documentation and resources required for global regulatory submissions• Manage and process electronic submissions, including original applications and lifecycle management submissions• Handle submissions related to CMC, advertising and promotional materials, amendments, annual reports, and SPL submissions• Prepare, review, and maintain regulatory documentation in compliance with applicable laws and regulations• Assist in regulatory reporting and submissions to health authorities• Stay updated with changing regulatory guidelines and support compliance audits• Perform analysis and resolution of low to medium complexity regulatory problems• Interact primarily with internal Accenture peers and update supervisors on work progress• Follow detailed instructions for new assignments and moderate guidance for daily tasks• Ensure decisions made are accurate and maintain quality standards, impacting own work and team deliverables• Work as an individual contributor within a team-focused environment• Be flexible to work in rotational shifts as requiredQualification• Bachelor of Pharmacy (B.Pharm)Experience• 3 to 5 years of experience in Life Sciences Regulatory Operations or Regulatory Services• Hands-on exposure to global regulatory submissions and electronic publishing processesSkills• Strong understanding of life sciences regulatory requirements and submission processes• Ability to work effectively in a team-oriented environment• Adaptable and flexible to changing project needs• High commitment to quality and compliance• Good analytical and problem-solving skills• Basic understanding of regulatory lifecycle management and compliance auditsAbout the CompanyAccenture is a global professional services company with expertise in digital, cloud, and security. With over 784,000 professionals across 120+ countries, Accenture delivers strategy, consulting, technology, and operations services to help organizations drive innovation, improve outcomes, and create sustainable value across industries, including life sciences and healthcare.

Roles & Responsibilities:• Process and upload regulatory correspondence (letters, emails, meeting minutes) into RIM systems in alignment with eCTD structure• Ensure accurate metadata classification and identify regulatory commitments and health authority deadlines• Extract structured data from FDA Summary Basis of Approval (SBA) documents, including trial design, sample size, and dosing details• Capture clinical endpoints, statistical outcomes (P-values, Hazard Ratios, Confidence Intervals), and regulatory conclusions• Identify and document key regulatory milestones such as Breakthrough Therapy, Orphan Drug Designation, and RMAT• Review and summarize Advisory Committee meeting content, voting results, and key discussions• Maintain database consistency through cross-referencing FDA sources (e.g., Drugs@FDA) using standardized terminology• Support internal audits and health authority inspections through efficient document retrieval and data accuracy• Ensure RIM database serves as a single source of truth with 100% data integrityQualification:• Bachelor’s / Master’s degree or Pharm D in Life Sciences, Pharmacy, Clinical Research, or related disciplineExperience:• 2–4 years of experience in Regulatory Operations, Regulatory Information Management, Document Management, or Clinical ResearchSkills:• Strong understanding of drug development lifecycle and global health authorities (FDA, EMA, etc.)• Good knowledge of FDA CDER/CBER approval package structures• Ability to interpret clinical trial data (double-blind studies, ITT analysis, non-inferiority trials)• Hands-on experience with RIM tools such as Veeva Vault (preferred)• Proficiency in MS Excel, Google Sheets, and document management systems• Excellent written English with strong summarization skills• High attention to detail and ability to manage high-volume work under strict timelinesPreferred:• Certification or PG Diploma in Regulatory Affairs• Experience supporting audits and regulatory inspectionsAbout the Organization:Roche is a global healthcare leader committed to innovation, inclusion, and patient-centric solutions. Roche Services & Solutions enables Roche teams worldwide by delivering high-quality end-to-end business services with a OneRoche mindset.

Roles and responsibilities:• Assist physical therapists in implementing treatment plans• Guide patients through exercises and ensure proper techniques• Manage therapy equipment and ensure safety and correct usage• Help patients during therapy sessions and provide attentive support• Maintain a clean, organized, and safe clinic environment• Record patient progress and maintain accurate documentation• Collaborate effectively with the healthcare team to provide quality patient careQualification:• Proficiency in physical therapy methods and understanding of exercise physiology• High school diploma or equivalent (additional certifications in related fields preferred)• Strong communication skills and ability to work in a healthcare team environmentExperience:• Previous experience as a Physical Therapy Aide or in a similar role is a plus• Freshers with relevant skills may also applySkills:• Patient care and support skills• Customer service and interpersonal skills• Ability to follow instructions and assist therapists effectively• Organizational skills for managing equipment and clinic environmentBenefits:• Opportunity to learn and grow in a physiotherapy clinic• Exposure to patient care and rehabilitation practices• Hands-on experience assisting qualified physiotherapistsAbout the company:PhysioPad – Physiotherapy and Wellness provides patient-centered physiotherapy and wellness services, focusing on rehabilitation, exercise therapy, and promoting overall health. The clinic aims to ensure high-quality care through skilled therapists and supportive staff in a professional environment.

Roles and responsibilities:• Provide specialized physiotherapy services for children with developmental and physical challenges • Assess children’s physical needs and develop individualized treatment plans • Implement therapy sessions to improve motor and functional abilities • Collaborate with multidisciplinary teams including therapists, consultants, and caregivers • Maintain accurate patient records and progress reports • Assist and guide parents and educators in therapeutic practicesQualification:• Bachelor’s or Master’s degree in Physiotherapy or related field • Strong knowledge of movement therapy, sensory integration therapy, and rehabilitation practices • Proficiency in designing and implementing therapeutic strategies tailored for children • Excellent observation and assessment skillsExperience:• Prior experience in pediatric physiotherapy, early intervention, or related therapeutic services is desirable • Freshers with relevant training may also applySkills:• Strong communication and interpersonal skills to work with children, parents, and educators • Ability to collaborate effectively within a multidisciplinary team • Commitment to continuous professional developmentBenefits:• Professional growth through exposure to diverse pediatric therapy practices • Opportunity to work in a dedicated child development and early intervention setting • Supportive multidisciplinary team environmentWorking hours:• Typically 9:00 AM – 6:30 PM, Monday to Saturday (may vary as per clinic schedule)About the company:Ananya Child Development & Early Intervention Clinic focuses on providing comprehensive therapy services for children with diverse educational and developmental needs such as Autism Spectrum Disorder (ASD), ADHD, learning disabilities, and developmental delays. The clinic emphasizes early intervention programs and collaboration with parents, guided by values of knowledge sharing, integrity, and teamwork. It offers a range of therapies including physiotherapy, occupational therapy, speech therapy, sensory integration, and more to help children achieve functional independence and developmental progress.

Roles & Responsibilities:• Schedule and manage patient appointments• Provide patient counselling and perform clinical diagnosis• Carry out basic dental procedures• Deliver post-procedure care and ensure proper follow-up• Maintain accurate patient records• Support smooth day-to-day clinic operationsQualifications:• Bachelor of Dental Surgery (BDS) from a recognized institutionExperience:• 1–2 years of clinical experience preferredSkills:• Strong patient management and counselling skills• Good clinical and diagnostic abilities• Effective communication skills• Organizational and time-management skills• Professional and compassionate approach to patient careBenefits:• Limited working hours (2:00 PM – 7:00 PM)• Weekly holiday on Friday• Supportive clinical environmentAbout the Company:Dr Romana's Dental Clinic & Implant Center is dedicated to delivering quality dental care with a patient-focused approach. The clinic provides a professional setting that encourages skill development and hands-on experience in modern dentistry.

Roles & Responsibilities• Manage end-to-end medical events in a project mode using the 1CRM events portal• Create, document, and track advisory boards, consulting services, symposia, speaker trainings, scientific education programs, stand-alone meetings, hospital/clinical staff meetings, and third-party sponsorships• Ensure all required information, approvals, and documents are available for event creation within 1CRM• Coordinate regularly with internal and external stakeholders until successful event execution and closure• Partner with event business requestors and engagement teams to secure timely approvals and documentation• Manage event communications, attendee registration, and data management within the 1CRM portal• Ensure adherence to company policies with a strong focus on transparency and compliance• Monitor KPIs and prepare metrics reporting to sustain operational synergies• Provide recommendations for process improvements to enhance efficiency and compliance• Mentor and train incoming 1CRM digital asset specialists and maintain training materials and guidelines• Stay updated on CRM system enhancements and participate in relevant trainingsQualification• Bachelor’s degree in a relevant discipline• Fluency in written and spoken EnglishExperience• 1–3 years of experience in event management preferred• Direct experience in pharmaceuticals or life sciences required• Hands-on experience with CRM systems; Veeva Vault proficiency preferredSkills• Strong stakeholder management and relationship-building ability• Excellent project management, organisation, and communication skills• High attention to detail with strong compliance orientation• Financial acumen and event operations knowledge• Digital literacy with proficiency in MS Office and CRM platforms• Ability to adapt quickly to changing priorities in a multicultural environment• Proactive, accountable, and solution-oriented mindsetAbout the CompanySanofi is a global healthcare leader focused on discovering, developing, and delivering medicines and vaccines across specialty care, general medicines, and vaccines. Through its Sanofi Business Operations hub in India, the company centralizes and scales support for Medical, HEVA, Commercial, and Digital functions worldwide, driving innovation, compliance, and operational excellence to improve patient outcomes globally.

Roles & Responsibilities:• Analyze oncology products using advanced analytical techniques and instruments• Handle and operate lab equipment including HPLC, GC, Dissolution apparatus, PSD, and other wet lab instruments• Perform sampling of raw materials, packaging materials, and cleaning samples• Conduct analysis and report results for working standards, raw materials, in-process, drug products, cleaning, and stability samples• Ensure proper calibration and maintenance of instruments and equipment• Maintain accurate documentation, compile analytical data, and follow GLP activities• Work with strong attention to detail in a regulated pharmaceutical environmentQualification:• Master of Pharmacy or Msc in Organic ChemistryExperience:• 3–5 years in pharmaceutical quality controlSkills:• Strong knowledge of analytical instruments (HPLC, GC, Dissolution, PSD, etc.)• Good understanding of GLP compliance• Proficiency in analytical methods and data documentation• Ability to work in a regulated pharma environmentAbout the Organization:Tiefenbacher Laboratories specializes in oncology and high-quality drug development, offering globally connected facilities and opportunities to contribute to critical pharmaceutical products.

Roles & Responsibilities:• Conduct dental awareness and screening camps at corporates, residential societies, schools, and institutions• Perform basic oral examinations and provide patient counselling• Educate individuals on oral hygiene, preventive care, and available treatment options• Maintain camp records and patient data accurately• Coordinate with the Park Dental Care team to ensure smooth camp execution• Refer patients to nearby Park Dental Care clinics when necessaryQualifications:• BDS (Mandatory) | MDS (Preferred but not mandatory)• Valid State Dental Council RegistrationExperience:• Freshers can apply• Prior camp or field experience is an added advantageSkills:• Strong communication and patient interaction skills• Interest in community dentistry and outreach programs• Ability to conduct screenings independently• Organized with good record-keeping abilities• Patient-focused and proactive approachBenefits:• Pay per camp or compensation based on experience• Additional incentives based on performance and referrals• Flexible working scheduleAbout the Company:Park Dental Care is dedicated to promoting oral health through preventive care, community outreach, and patient education. The organization conducts awareness and screening programs to improve dental health while providing accessible and quality dental services.

Roles & Responsibilities:• Assess and develop children’s abilities across motor, cognitive, and sensory domains• Plan and implement individualized therapeutic and rehabilitation programs• Deliver evidence-based occupational therapy sessions to enhance overall well-being• Collaborate with families, caregivers, and other healthcare professionals• Monitor progress and maintain accurate therapy documentation• Support children’s functional development, school readiness, and daily living skillsQualifications:• Bachelor’s or Master’s degree in Occupational Therapy or related field• Valid licensure or certification to practice Occupational Therapy• Knowledge of pediatric therapy and rehabilitation principlesExperience:• Experience in healthcare or pediatric therapy settings is a plusSkills:• Expertise in occupational therapy, rehabilitation, and pediatrics• Strong communication and interpersonal skills• Patience, empathy, and passion for working with children• Ability to work collaboratively in a multidisciplinary teamBenefits:• Opportunity to work in a child-focused, holistic therapy environment• Exposure to pediatric therapy and evidence-based rehabilitation programs• Collaborative and supportive work cultureAbout the Company:Mini Milestone Child Development Centre, Hyderabad, focuses on enhancing children’s developmental skills through holistic, evidence-based occupational therapy programs. The Centre emphasizes functional growth, sensory integration, and overall well-being while fostering collaboration between therapists, families, and healthcare professionals.

Roles & Responsibilities• Manage volunteer registration and screening processes• Coordinate with diagnostic laboratories for clinical reports• Conduct and support the informed consent process for study volunteers• Perform volunteer enrolment activities as per study protocol• Monitor volunteers throughout the study duration• Support investigational product administration activities• Manage volunteer discharge activities as per protocol requirements• Compile, maintain, and update study documents and Trial Master File (TMF)Qualification• B.Pharm / M.PharmExperience• 2–3 years of relevant experience in clinical research or clinical pharmacology studiesNo. of Positions: 07Skills• Good understanding of clinical trial processes and GCP guidelines• Strong documentation and coordination skills• Attention to detail and ability to follow protocols• Effective communication and teamwork skillsAbout the OrganizationJeevan Scientific Technology Limited is a leading life sciences services company offering integrated solutions in clinical research, bioavailability and bioequivalence studies, regulatory, and quality services, supporting global pharmaceutical and biotech organizations.

Roles & Responsibilities• Plan, conduct, and manage internal audits including in-process, retrospective, and system audits• Perform vendor audits as per audit plans and regulatory requirements• Prepare and issue audit reports to auditees in a timely manner• Review and prepare SOPs, clinical study protocols, and clinical study reports• Assess audit responses and negotiate appropriate corrective and preventive actions (CAPA)• Review deviations and CAPA plans and ensure timely implementation and closure• Support preparation for client, sponsor, and regulatory inspections• Reconcile project and non-project documents and coordinate archival activities• Review equipment calibration and validation recordsQualification• Bachelor’s or Master’s degree in Life Sciences (B.sc, M.sc/ B.Pharm / M.Pharm)Experience• 2–5 years of experience in GCP Quality Assurance audits• Strong knowledge of ICH-GCP guidelines• Working knowledge of US, EU regulations, and applicable GxP standardsSkills• Strong written and verbal communication skills• Excellent analytical and problem-solving abilities• Good computer proficiency• Self-motivated with strong prioritization and time-management skillsAbout the OrganizationJeevan Scientific Technology Limited is a global life sciences services organization providing clinical research, quality assurance, regulatory, and medical writing services to pharmaceutical and biotechnology companies, ensuring compliance and quality across the product development lifecycle.