Hyderabad Healthcare Jobs

Role & Responsibilities • Conduct detailed skin and hair consultations, including medical history assessment and accurate diagnosis of dermatological and trichological conditions. • Recommend and explain personalised treatment plans based on clinical suitability, safety, and client expectations. • Perform or supervise aesthetic and cosmetology procedures including Laser Hair Reduction, Laser Skin Treatments, Chemical Peels, PRP Therapy, Microneedling, Botox, Fillers, Threads, and other injectables as per training and competency. • Ensure proper documentation of treatment parameters, consent forms, progress notes, and follow-up records. • Educate clients about procedures, risks, outcomes, timelines, and post-treatment care. • Build long-term client relationships through ethical guidance, empathy, and transparent communication. • Collaborate with clinic staff, technicians, and consultants to ensure smooth clinical operations. • Support ethical treatment conversions while prioritising medical suitability and patient safety. • Participate in internal training programs and contribute to SOP and process improvements.Qualification • MBBS / BDS / MDS from a recognised institution. • Valid registration with relevant Medical or Dental Council. Experience • MBBS: 1–2 years of experience (dermatology / cosmetology exposure preferred). • BDS / MDS: 3–5 years of experience in cosmetology, dermatology, or trichology.Skills • Strong expertise in skin and hair consultation, counselling, and aesthetic procedures. • Hands-on experience with lasers, chemical peels, PRP, injectables, and blood extraction. • Excellent communication, client counselling, and interpersonal skills. • Ethical, confident, and patient-centric approach to aesthetic medicine. • Ability to work collaboratively in a high-volume clinical environment.About Company • Berkowits Hair & Skin Clinic is one of India’s leading and fastest-growing aesthetic and trichology clinic chains, with 45+ clinics PAN India and over 30 years of excellence. Trusted by more than 1,00,000 clients, Berkowits is a pioneer in non-surgical hair replacement and advanced hair & skin solutions.

Roles & Responsibilities• Provide comprehensive dental care to patients, including diagnosis and treatment of dental issues• Perform routine dental procedures and treatments• Educate patients on oral hygiene and preventive care• Maintain accurate patient records and treatment plans• Collaborate with other dental professionals to ensure high-quality patient care• Contribute to service improvement and adherence to clinical protocolsSkills Required• Strong clinical knowledge in dentistry• Excellent communication and interpersonal skills• Ability to work collaboratively with dental teams• Organizational skills for maintaining records and treatment plans• Commitment to patient-centred care and professional standardsQualifications• BDS or MDSExperience After Qualification• Minimum 3 years of relevant experience as a dentistAbout the CompanyThe Tooth Story Dental Clinic is dedicated to providing high-quality, patient-centred dental care. The clinic emphasizes modern dental practices, compassionate patient interactions, and professional excellence. The organization fosters a collaborative environment for dental professionals to deliver effective and safe oral healthcare.

Roles & Responsibilities:• Provide comprehensive dental care to patients• Conduct patient examinations, diagnosis, and treatment planning• Perform routine dental procedures and clinical treatments• Ensure proper patient care, safety, and comfort during procedures• Maintain accurate patient records and clinical documentation• Follow clinic protocols, hygiene, and sterilization standards• Communicate effectively with patients regarding treatment and oral health careQualifications:• Bachelor of Dental Surgery (BDS) from a recognized institutionExperience:• Freshers and experienced candidates can applyKey Skills:• Patient care and patient assessment• Basic Life Support (BLS) knowledge• Understanding of physiology and clinical practices• Good communication and interpersonal skills• Ethical and patient-focused approachAbout the Company:Srikanth Multi-speciality Dental Clinic is a patient-centric dental healthcare provider in Hyderabad offering comprehensive dental treatments. The clinic focuses on quality care, ethical practice, and accessibility, with additional support facilities such as food and accommodation for dentists relocating from distant locations.

Roles & Responsibilities:• Examine patients’ oral health and diagnose dental conditions• Perform dental procedures including fillings, extractions, root canals, and scaling• Provide preventive dental care and oral hygiene education to patients• Prepare and maintain accurate patient records and treatment plans• Ensure compliance with clinic policies, safety standards, and infection control protocols• Work collaboratively with other healthcare professionals to deliver quality care• Maintain ethical, patient-focused clinical practiceQualifications:• BDS / MDS from a recognized institution• Valid Dental Council registrationExperience:• Minimum 6 years of clinical experience preferredKey Skills:• Strong clinical and diagnostic skills• Excellent communication and interpersonal skills• Patient counselling and education• Ability to work independently and as part of a team• Ethical and patient-centric approachAbout the Company:Aga Khan Health Centre is a trusted healthcare provider committed to delivering high-quality medical and dental services. The centre emphasizes ethical practice, patient safety, and comprehensive care through experienced professionals and standardized clinical protocols.

Roles & Responsibilities:• Diagnose and treat dental conditions and oral diseases• Perform dental examinations, scaling, fillings, and extractions• Develop and implement appropriate treatment plans for patients• Educate patients on oral hygiene practices and preventive dental care• Maintain accurate and detailed patient records and treatment progress• Collaborate with dental assistants, hygienists, and other healthcare professionals• Stay updated with latest dental procedures, techniques, and technologiesQualifications:• Bachelor of Dental Surgery (BDS) from a recognized institution• Valid Dental Council registration• Female candidates preferredExperience:• Minimum 1 to 4 years of clinical experienceKey Skills:• Clinical dentistry skills• Patient assessment and diagnosis• Communication and interpersonal skills• Treatment planning and execution• Record keeping and documentation• Team collaborationBenefits:• Health insurance• Provident FundAbout the Company:Oxiv is a growing healthcare organization focused on delivering quality dental services through patient-centric care and modern clinical practices. The clinic emphasizes ethical dentistry, continuous learning, and providing a supportive work environment for dental professionals.

Roles & Responsibilities:• Perform general dental procedures including extractions, root canals, fillings, and routine dental treatments• Examine patients using dental instruments such as drills, probes, mirrors, and brushes• Prescribe medications including pain relievers and antibiotics as required• Administer local anesthesia or sedatives prior to dental treatments when necessary• Handle patients independently and manage complete clinical workflow• Coordinate and communicate effectively with dental assistants and clinic staff• Ensure adherence to clinic protocols, hygiene, and safety standards• Maintain accurate patient records and treatment documentationQualifications:• Bachelor of Dental Surgery (BDS) from a recognized institution• Valid Dental Council registrationExperience:• Minimum 2+ years of clinical experience• Ability to manage clinic operations independentlyKey Skills:• Strong clinical dentistry skills• Patient handling and communication skills• Diagnostic and treatment planning abilities• Team coordination and clinic management• Ethical and patient-centric approachAbout the Company:Orthosquare Multispeciality Dental Clinic Pvt. Ltd. is one of India’s largest and fastest-growing dental chains, known for delivering comprehensive, technology-driven, and patient-focused dental care. With a strong presence across multiple locations, Orthosquare is committed to clinical excellence, standardized treatment protocols, and providing quality oral healthcare services.

Roles & Responsibilities• Handle day-to-day administrative and operational activities of the clinic• Ensure smooth functioning of clinic operations across multiple branches• Work on operational, administrative, and billing software• Monitor, verify, and resolve billing-related issues on a daily basis• Prepare daily accounts and revenue reports for all clinic branches• Manage patient leads and schedule appointments accordingly• Coordinate with administrative teams to streamline processes and improve patient experience• Train clinic staff and maintain discipline and operational standards• Provide administrative and operational support to the management and executive teamQualifications• BDS from a recognized institution• Strong interest in administrative and non-clinical roles• Bachelor’s degree mandatoryExperience• Minimum 1 year of experience in administrative / operations role preferred• Freshers with strong administrative aptitude can applyKey Skills• Strong organizational and administrative skills• Proficiency in MS Office• Working knowledge of billing and clinic management software• Excellent communication skills• Ability to manage multiple branches and reports efficientlyLanguages• English – Preferred• Hindi – Preferred• Telugu – PreferredBenefits• Cell phone reimbursement• Commuter assistanceAbout the CompanyDantam Dental Clinics is a leading dental care network in Hyderabad with multiple branches across key locations. The organization is committed to delivering high-quality dental services supported by efficient operations, ethical practices, and a patient-centric approach, ensuring excellence in both clinical and administrative functions.

Roles & Responsibilities:• Examine patients and diagnose oral and dental conditions• Perform dental procedures including fillings, extractions, scaling, and root canal treatments• Provide preventive dental care and oral hygiene education• Prepare and maintain accurate patient records and treatment plans• Ensure compliance with clinic policies, safety, and infection control standards• Follow sterilization and hygiene protocols strictly• Collaborate with healthcare professionals for integrated patient careQualifications:• BDS / MDS from a recognized institution• Valid Dental Council registration• Strong clinical and diagnostic expertiseKey Skills:• Clinical dentistry• Patient communication and counselling• Diagnostic and treatment planning skills• Ethical and patient-focused approach• Ability to work independently and in a teamAbout the Company:Aga Khan Health Centre is a trusted healthcare institution committed to delivering quality medical and dental services. The centre emphasizes ethical practice, patient safety, and holistic care, supported by experienced healthcare professionals and standardized clinical protocols.

Role & Responsibilities • Diagnose and treat patients and prescribe appropriate medications. • Develop and implement comprehensive patient care plans. • Monitor patient health and provide preventive care services. • Maintain high standards of clinical practice and patient safety. • Communicate effectively with patients, families, and healthcare staff. Qualifications • MBBS with valid medical licensing and certifications. Experience • 1–2 years of clinical or hospital experience preferred. Skills • Strong clinical diagnosis and patient care management skills. • Good knowledge of medical procedures, medications, and healthcare regulations. • Excellent communication, problem-solving, and attention to detail. • Compassionate, patient-centred approach to care. About the Company • Healthcare facility providing primary medical services with a focus on quality patient care.

Roles & Responsibilities • Ensure compliance with current Good Manufacturing Practices (cGMP) and applicable regulatory requirements • Manage and review QMS documentation including SOPs, batch manufacturing records, and quality reports • Support preparation and execution of internal, external, customer, and regulatory audits • Handle batch release activities in coordination with Production and Quality Control teams • Identify, investigate, and implement CAPA for deviations, OOS/OOT results, and quality complaints • Support data integrity practices and maintain accurate, traceable quality records • Participate in continuous improvement initiatives to strengthen quality systems Qualification • B.Pharm or M.Pharm from a recognized university Experience • 1–3 years of experience in a Quality Assurance role within the pharmaceutical industry Skills • Strong knowledge of GMP, GLP, and regulatory guidelines (USFDA, WHO, CDSCO preferred) • Hands-on experience with QMS, CAPA, deviations, and batch release activities • Good documentation, audit-handling, and compliance skills • Proficiency in MS Office and quality management systems • Effective communication and coordination abilities About the Company Ceph Lifesciences Pvt. Ltd. is a well-established pharmaceutical company specializing in the manufacturing of high-quality cephalosporin-based products, driven by robust quality systems, regulatory compliance, and a commitment to excellence in pharmaceutical manufacturing.

Role & Responsibilities • Develop and deliver high-quality, accurate, and innovative scientific and medical content (DSE, digital assets, MSL materials, FAQs, Medical Information Letters) tailored for global and US audiences • Draft and deliver publications including manuscripts, abstracts, posters, oral presentations, and enhanced content for scientific congresses and journals • Address complex medical information inquiries and escalations • Create content to support payer interactions and compendia submissions • Execute tactical scientific communication plans aligned with medical and product strategies across regions • Manage content workflows and approvals through established systems and processes • Partner closely with Scientific Communications Operations to drive standardization, innovation, and continuous improvement, including digital and omnichannel approaches • Track and report impactful KPIs related to scientific communications • Ensure compliance with enterprise SOPs, external guidelines, and regulatory requirements • Build, maintain, and influence strong cross-functional and global stakeholder relationships Qualifications • Advanced scientific degree such as MD, PharmD, PhD, DO, or equivalent • Doctorate with 7+ years of relevant experience OR • Master’s degree / MBBS with 10+ years of experience in Global Publications, Medical Communications, Medical Information, Medical Value & Access, or Medical Strategy OR • Bachelor’s degree with 10+ years of relevant experience OR • Associate degree with 15+ years of relevant experience Experience • Minimum 5+ years of experience in medical and publications content development • Experience in Medical Affairs or Clinical Development within the biopharmaceutical industry • Clinical or research experience within a relevant therapeutic area • Proven experience implementing publication guidelines and transparency standards such as ICMJE and GPP • Experience working in a global, matrixed environment with limited supervision Skills • Strong understanding of pharmaceutical commercialization and regulatory and legal guidelines for prescription products • Ability to critically analyze scientific literature and communicate insights cross-functionally • Demonstrated strategic execution and stakeholder management skills • Knowledge of emerging technologies in scientific communications including AI tools and digital/omnichannel platforms • Strong proficiency in Microsoft Office and related digital tools • Excellent written and verbal communication skills • Strong project management, prioritization, and self-direction abilities • Collaborative mindset with high accountability, adaptability, and initiative About the Company • Amgen is a leading global biotechnology company focused on discovering, developing, manufacturing, and delivering innovative human therapeutics

Role & Responsibilities • Hire, manage, mentor, and develop a team of Study Delivery Associates and Senior Associates. • Recruit, onboard, and train team members in collaboration with R&D Training. • Manage team performance, capacity, attrition risks, and continuous development. • Allocate resources effectively in partnership with Resource Points of Contact. • Ensure team readiness and high-quality operational support to clinical programs. • Drive continuous improvement, knowledge sharing, and best practice adoption. • Act as escalation point for performance issues and ensure stakeholder alignment. • Ensure compliance with SOPs, regulatory guidelines, and inspection readiness. Qualifications • Doctorate degree OR • Master’s degree with 8+ years of clinical execution experience OR • Bachelor’s degree with 10+ years of clinical execution experience Experience • Minimum 5 years’ experience in life sciences with strong clinical trial exposure. • At least 3 years of biopharmaceutical clinical research experience. • Proven people management and resource planning/allocation experience. Skills • Strong leadership, mentoring, and team development skills. • Solid understanding of clinical drug development and trial execution. • Experience with study budgets, financial oversight, and risk-based monitoring. • Excellent cross-functional communication and stakeholder management skills. About the Company • Amgen is a leading global biotechnology company focused on developing innovative medicines. • Amgen is committed to scientific excellence, compliance, and equal opportunity employment.

Roles & Responsibilities • Act as the US/EU local safety office representative and FDA/EMA point of contact • Prepare and submit Individual Case Safety Reports (ICSRs) to FDA, EMA, and business partners • Perform case review, quality checks, and escalation of case-level safety issues • Ensure timely expedited safety reporting in compliance with global regulatory timelines • Manage intake, triage, follow-up, and data entry queries related to ICSRs • Support vendor oversight for case intake, processing, reconciliation, and quality metrics • Conduct reportable event reconciliation for Amgen-sponsored clinical trials • Perform business partner safety reconciliations as per safety agreements • Provide LAO E2B support, including nullification and redistribution of cases • Review non-matching data across clinical and safety databases • Support audit readiness, health authority inspections, and internal audits • Undertake delegated activities from the QPPV in line with the PV System Master File • Assist in pharmacovigilance training and convention-related safety activities • Initiate unblinding requests and support literature case review processes Qualification • Bachelor’s degree in Pharmacy, Life Sciences, Biotechnology, Clinical Research, or related field Experience • Bachelor’s degree with 2+ years of pharmacovigilance experience, or • Associate degree with 6+ years of directly related experience, or • High school diploma/GED with 8+ years of pharmacovigilance experience Skills • Strong knowledge of global pharmacovigilance regulations (US FDA, EMA, ICH) • Hands-on experience in ICSR case processing and regulatory reporting • Familiarity with clinical development and safety reporting workflows • High attention to detail and strong case quality management skills • Proficiency in safety databases and Microsoft Office (Word, Excel, PowerPoint, Outlook) About the Company Amgen is a leading global biotechnology company committed to discovering, developing, and delivering innovative medicines for patients with serious illnesses. With a strong focus on quality, compliance, and patient safety, Amgen offers a collaborative work environment and global exposure across pharmacovigilance and medical services functions.

Roles & Responsibilities • Coordinate GLP toxicology studies with CROs, including timelines, tracking, and review of study reports • Support CMC readiness by compiling specifications, development data, and technical documentation • Assist in preparation of IND/CTA submissions with focus on nonclinical and CMC sections • Manage cross-functional coordination with R&D, QA, CROs, and external partners • Maintain regulatory-ready documentation, trackers, and development logs • Support IND-enabling activities for late preclinical development programs Qualification • MS / M.Pharm / M.Sc in Life Sciences, Pharmacy, or Biotechnology Experience • 2-3 years of experience in clinical development, preclinical development, or regulatory support • Hands-on exposure to GLP toxicology coordination, CMC documentation, or IND submissions Skills • Strong understanding of GLP toxicology and CMC development workflows • Working knowledge of CDSCO and/or US FDA IND processes • Excellent documentation, organizational, and follow-up skills • Ability to work effectively in cross-functional and CRO-facing environments • Good communication and coordination abilities About the Company Utopia Therapeutics is an emerging biopharmaceutical company focused on advancing innovative therapies through robust preclinical and clinical development. With active IND-enabling programs and a science-driven culture, the company provides hands-on exposure, close collaboration with senior scientists, and strong career growth opportunities in clinical development and regulatory affairs.

 Roles & Responsibilities:• Perform routine dental procedures including scaling, restorations, and extractions• Take accurate dental impressions and diagnostic radiographs (IOPA)• Perform root canal treatments (anterior and posterior preferred)• Carry out crown and bridge preparation and cementation• Diagnose and plan treatment for common dental conditions• Maintain strict infection control and sterilization protocols• Communicate effectively with patients and ensure excellent chairside manner• Assist in implant and prosthodontic procedures (preferred)• Handle dental materials and equipment with proper care and knowledgeQualifications:• Bachelor of Dental Surgery (BDS) from a recognized institutionSkills Required:• Diagnosis and treatment planning• Routine dental procedures• Root canal treatment (RCT)• Crown and bridge procedures• Dental impressions and radiography• Infection control and sterilization• Patient communication and counseling• Knowledge of dental materials and equipmentAbout the Company:Vijay Multispeciality Dental Hospital is one of Hyderabad’s leading dental care centers, offering comprehensive, patient-centric dental services. Known for clinical excellence and advanced treatment facilities, the hospital provides a supportive environment for professional growth and skill enhancement.

Roles & Responsibilities• Assist in the overall management and operations of the Physiotherapy & Rehabilitation Centre• Supervise and coordinate daily clinical activities of the physiotherapy team• Ensure delivery of high-quality physiotherapy and rehabilitation services• Monitor patient care standards and ensure adherence to clinical protocols• Coordinate with doctors, therapists, and multidisciplinary teams for patient rehabilitation plans• Oversee scheduling, workflow management, and resource allocation• Support training, mentoring, and performance evaluation of physiotherapy staff• Ensure compliance with hospital policies, clinical SOPs, and regulatory standards• Maintain accurate documentation, reports, and departmental recordsOperational & Administrative Responsibilities• Assist in implementing departmental goals and quality improvement initiatives• Monitor equipment usage and ensure proper maintenance of rehabilitation facilities• Support patient satisfaction initiatives and service excellence standards• Participate in audits, reviews, and hospital accreditation processesQualifications• Master’s Degree in Physiotherapy from a recognized institutionExperience• Relevant experience in physiotherapy and rehabilitation services• Prior experience in a supervisory or assistant managerial role preferredSkills Required• Strong clinical knowledge in physiotherapy and rehabilitation• Leadership and team management skills• Effective communication and coordination abilities• Organizational and problem-solving skills• Ability to work in a fast-paced hospital environment• Knowledge of healthcare quality and compliance standardsAbout the CompanyApollo BGS Hospitals is a part of the Apollo Hospitals Group, one of India’s most trusted and leading healthcare providers. Known for clinical excellence, advanced medical infrastructure, and patient-centric care, Apollo BGS Hospitals delivers comprehensive healthcare services across specialties, including advanced rehabilitation and physiotherapy care.

Role & Responsibilities • Perform bedside handover and takeover, ensuring proper knowledge about the assigned patient • Constantly observe and evaluate patient condition, providing prompt and effective bedside nursing care • Attend to patient needs immediately and report abnormalities promptly • Maintain proper documentation of patient care activities • Counsel patients and family members regarding health conditions • Follow consultant doctor’s rounds and implement their orders • Assist in bedside procedures and collect investigation reports • Provide pre and post-operative care, including managing nutritional needs • Ensure confidentiality of patient records and condition • Manage emergencies effectively and coordinate with other departments • Follow protocols for admission, discharge, death, and transfers • Maintain and sterilize equipment, manage inventories, and ensure proper storage • Report any abnormal values or changes in patient condition to the in-charge doctor Qualification • GNM / BSc Nursing (Diploma preferred) Experience • 2-4 years of experience in a hospital setting Skills • Patient observation and care skills • Strong communication skills in Hindi (preferred) • Ability to manage emergencies and patient needs effectively • Knowledge of hospital protocols and procedures About the Company • KIMS Hospitals is a leading healthcare provider in Hyderabad, dedicated to offering high-quality care and excellent medical services to patients across various specialties.

Roles & Responsibilities • Perform clinical and performance assessment of IVD manufacturers’ technical documentation in line with EU IVDR (Regulation (EU) 2017/746) • Review and assess Scientific Validity, Analytical Performance, and Clinical Performance data • Prepare and finalize detailed clinical assessment and evaluation reports • Evaluate Summary of Safety and Performance (SSP) documentation for high-risk IVD devices • Review and approve Performance Evaluation Reports (PERs) and supporting clinical evidence • Provide expert recommendations for conformity assessment, certification, and regulatory decisions • Ensure all assessments comply with Notified Body requirements and DNV quality standards • Interact with internal teams, manufacturers, and stakeholders to clarify technical and regulatory queries Qualification • Biology / Microbiology • Chemistry / Biochemistry • Biotechnology / Medical Technology • Biomedical Sciences (Hematology, Virology, Molecular Diagnostics) • Pharmacy / Pharmacology / Toxicology • Medicine / Veterinary Medicine / Nursing / Physiology • PhD in a relevant discipline may substitute part of the experience requirement Experience • Minimum 4 years of full-time experience in IVD medical devices, academia, or hospital settings • At least 2 years of hands-on experience in performance evaluation of IVD devices or assessment of scientific validity and clinical performance data • PhD holders may substitute 3 years of experience, provided 2 years are in performance evaluation Skills • Strong analytical and scientific assessment capability • Excellent technical writing and regulatory reporting skills • In-depth understanding of EU IVDR 2017/746 requirements • Ability to independently manage complex certification and assessment activities • Effective communication and stakeholder management skills About the Company DNV is a globally trusted assurance and risk management company, operating across healthcare, life sciences, energy, maritime, and industrial sectors. DNV supports organizations in managing risks, ensuring regulatory compliance, and improving safety and sustainability. With a strong focus on quality, integrity, and innovation, DNV provides professionals with structured training, global exposure, and long-term career growth in high-impact regulatory and compliance roles.

Roles & Responsibilities • Author and review regulatory medical writing documents including Clinical Study Reports (CSRs), protocols, Investigator’s Brochures (IBs), Informed Consent Forms (ICFs), and submission documents • Act as lead writer or submission coordinator for assigned projects • Manage and coordinate contributions from multiple writers across related deliverables • Serve as the primary point of contact for clients, ensuring clear communication and timely delivery • Drive process improvements and contribute to development of medical writing best practices • Mentor, train, and technically guide junior medical writers • Support business development activities by contributing to proposals and client interactions Qualification • Bachelor’s or advanced degree in Life Sciences, Healthcare, Pharmacy, or related discipline Experience • Minimum 6+ years of experience in regulatory medical writing • Proven expertise in authoring key clinical and regulatory documents • Experience across multiple therapeutic areas including vaccines, immunology, oncology, cardiovascular, neurology, infectious diseases, endocrine, gastrointestinal, autoimmune, and mental health Skills • Strong scientific, analytical, and regulatory writing skills • Excellent communication and stakeholder management abilities • Ability to lead projects independently and manage multiple timelines • High attention to detail with strong quality and compliance focus • Capability to work under pressure and manage variable workloads About the Company VUEVERSE is a specialized medical communications and regulatory writing organization delivering high-quality, compliant scientific and regulatory content to pharmaceutical and CRO clients across global markets, with a strong focus on expertise, innovation, and mentorship.