Hyderabad Healthcare Jobs

Role & Responsibilities • Contribute to a culture of process improvement and operational excellence • Review and process Serious Adverse Events (SAEs), spontaneous ADRs, and safety data • Perform safety review of clinical and diagnostic data • Ensure case processing accuracy as per SOPs, study procedures, regulatory and sponsor requirements • Maintain and review safety tracking systems for data quality and compliance • Liaise with investigational sites, reporters, sponsors, and cross-functional teams on safety issues • Attend project team meetings and sponsor teleconferences as required • Serve as a safety resource for investigational sites and internal teams • Assist in training and mentoring junior Drug Safety Associates • Support generation of study-specific procedures and identify out-of-scope activities • Act as Lead Drug Safety Associate for local or regional projects • Support MSS Functional Lead under supervision • Travel up to 10% (domestic/international) as required Qualification • Life Sciences / Pharmacy / Healthcare background preferred Experience • 4–10 years of experience in Pharmacovigilance / Drug Safety • Experience in Pharma, Biotech, CRO, or Clinical Research environments Skills • Strong knowledge of Pharmacovigilance processes • Hands-on experience with Oracle Argus • Knowledge of EudraVigilance and global safety databases • Exposure to aggregate reporting activities • Strong attention to detail and data quality focus • Effective communication and stakeholder coordination skills • Ability to work independently and lead safety activities About the Company • Covalent Trainings specialises in pharmacovigilance training and industry placements, Supports global PV projects across pharma, biotech, and CRO sectors

Role & Responsibilities:• Examine patients using X-rays and dental instruments to determine the type of dental prostheses required• Consult with patients to discuss their dental concerns and medical histories• Take impressions of patients' jaws and teeth to determine the dimensions of the dental prostheses to be fabricated• Send wax models of dental prostheses to the laboratory for fabrication• Fit newly-fabricated dental prostheses in patients' mouths and assess whether adjustments are required• Perform teeth whitening procedures to treat extrinsic tooth discoloration• Use bonding procedures to repair cracks and chips, fill small gaps between teeth, and alter the size of teeth• Collaborate with dental and healthcare specialists to develop suitable treatment plans for patientsQualifications:• BDS / MDS in Prosthodontics (Female candidates preferred)Experience:• 0 to 5 yearsSkills:• Strong clinical skills in prosthodontics• Excellent patient communication and consultation abilities• Ability to work collaboratively with dental and healthcare teams• Detail-oriented with precision in prosthetic fittingsAbout the Company:Oxiv is a reputed dental clinic based in Gachibowli, Hyderabad, focused on delivering advanced dental care with a patient-centric approach. The clinic provides a supportive and professional environment with access to modern dental technology, health insurance, and provident fund benefits.

Role & Responsibilities:• Manage the dental clinic independently• Perform dental procedures including root canal treatment, extractions, fillings, and crown preparation• Diagnose and treat patients with various dental conditions• Maintain accurate patient records and documentation• Educate patients on oral hygiene and preventive care• Ensure smooth clinic operations and patient flowQualifications:• Bachelor’s degree in Dentistry (BDS)Experience:• Minimum 1 year of relevant experience preferred• Freshers with strong practical skills may be consideredSkills:• Patient assessment and clinical diagnosis• Knowledge of dental terminology and documentation• Strong clinical and procedural skills• Ability to work independently and manage a clinicAbout the Company:Sun Shine Dental Care is a reputed dental clinic in Hyderabad focused on delivering high-quality dental care. The clinic emphasizes patient satisfaction, professional growth, and providing a supportive environment for dentists to excel in clinical practice.

Role & Responsibilities • Perform signal detection activities across global safety databases • Conduct medical review and assessment of aggregate safety reports (PSUR, PBRER, DSUR) • Perform medical evaluation of Individual Case Safety Reports (ICSRs) • Support benefit–risk evaluation and safety decision-making • Ensure compliance with global pharmacovigilance regulations and guidelines • Collaborate with pharmacovigilance, regulatory, and cross-functional teams • Maintain high standards of documentation and medical review quality Qualification • MBBS or MD (mandatory) • Registered medical practitioner in India Experience • Minimum 1 year of experience in pharmacovigilance or drug safety • Hands-on exposure to signal detection and aggregate reporting preferred Skills • Strong knowledge of signal detection methodologies • Experience with aggregate safety reports (PSUR, PBRER, DSUR) • Understanding of global PV guidelines (ICH, GVP) • Good analytical and medical writing skills • High attention to detail and compliance orientation Availability • Immediate joiners or candidates with up to 1 month notice period preferred About the Company • OrciMed Life Sciences is a growing pharmacovigilance and life sciences services organisation

Roles & Responsibilities: • Carry out API production activities as per SOPs and batch manufacturing records. • Handle day-to-day production operations in a regulated pharmaceutical environment. • Follow GMP, safety, and quality standards during manufacturing processes. • Support smooth shift operations and documentation activities. • Coordinate with team members to ensure timely production targets. Qualification: • B.Sc / M.Sc / B.Pharmacy Experience: • 0 to 6 years of experience in API / pharmaceutical production • Freshers with strong subject knowledge can also apply Skills: • Basic knowledge of API and pharmaceutical manufacturing processes. • Understanding of production operations and documentation practices. • Willingness to work in rotational shifts. • Good learning attitude and team coordination skills. Walk-In Interview Details: • Date: January 30 & 31, 2026 • Time: 09:30 AM to 04:00 PM • Venue: Honour Lab Limited – Unit-IX, Sy.No. 332, 335, 336 & 341, Veliminedu, Chityala (M), Nalgonda (Dt.), Telangana – 508114 • Documents to Carry: Updated resume, educational certificates, experience letters (if applicable), and recent photographs. • Contact: 9949043874 / 9154840911 About the Organisation: Established in Hyderabad, Telangana, Honour Lab Limited is a leading pharmaceutical manufacturer specializing in APIs and intermediates, operating multiple manufacturing units with global regulatory approvals and offering stable career growth in a quality-driven, regulated environment.

Roles & Responsibilities:• Diagnose oral diseases and dental conditions accurately• Create comprehensive treatment plans based on patient needs• Perform restorative and cosmetic dental procedures• Carry out treatments such as tooth extractions, root canals, fillings, and minor dental surgeries• Educate patients on oral hygiene practices and preventive dental care• Ensure patient comfort and deliver high-quality dental care• Maintain accurate patient records and treatment documentation• Collaborate with other healthcare professionals when required• Uphold high standards of clinical care, safety, and hygieneQualifications:• Bachelor of Dental Surgery (BDS) or equivalent degree from a recognized institution• Valid licensure and certifications to practice dentistryExperience:• Prior clinical experience in general dentistry preferred• Experience with dental technologies and tools is an added advantageSkills Required:• Proficiency in diagnosing and treating oral health conditions• Strong knowledge of restorative and cosmetic dentistry procedures• Hands-on experience in extractions, root canals, and dental procedures• Excellent communication skills for patient education and consultation• Strong organizational and record-keeping abilities• Commitment to staying updated with advancements and best practices in dental care• Professional, patient-focused, and detail-oriented approachAbout the Company:Laasyam Dental Clinic is a dental care facility based in Hyderabad, committed to providing quality oral healthcare services. The clinic focuses on patient comfort, modern dental practices, and maintaining high standards of clinical excellence and hygiene.

Elmed Life Sciences Pvt Ltd, a leading USFDA-registered pharmaceutical formulation unit specializing in probiotics and OSD manufacturing, is hiring experienced professionals for its Oral Solid Dosage (OSD) department in Cherlapally, Hyderabad.Date: Saturday, 6th December 2025 Time: 10:00 AM – 3:00 PM Venue: Plot No. 36, Phase V, IDA Cherlapally, Hyderabad, Telangana – 500051 Available Positions – OSD Department Only1. Production Assistant Manager (OSD)Qualification: B.Pharm / M.Pharm / B.Sc / M.ScExperience: 8–10 years in pharma manufacturingSalary Range: ₹7 – 9 LPAKey Skills Required:Hands-on experience in upstream & downstream fermentation (preferred)Complete production planning & execution in OSDRegulatory compliance (USFDA, WHO-GMP)Team handling & cross-functional coordinationDocumentation oversight, CAPA, change controlYield improvement & process optimizationWhy Join Elmed Life Sciences?USFDA & WHO-GMP certified facilityState-of-the-art probiotic & OSD manufacturingAttractive salary + statutory benefitsFast-track growth for performersJob stability with expanding export orders

Roles & Responsibilities: • Research, write, and review scientific response documents under the guidance of the Global Medical Information (GMI) team • Conduct comprehensive literature searches and extract, analyze, and summarize complex scientific data • Develop accurate, evidence-based, current, and fair-balanced medical information responses for assigned therapeutic areas • Adapt global medical information documents for local and regional markets • Prepare responses to escalated medical inquiries for supported countries • Contribute to US NDA Annual Reports and US compendia reviews • Participate in peer reviews and review content created by other medical writers • Collaborate closely with Global Medical Information, Pharmacovigilance, and Medical Affairs teams • Maintain and continuously enhance therapeutic area expertise • Support cross-functional projects and ensure timely delivery of assigned deliverables • Assist other medical information writers through knowledge sharing and mentoring • Ensure compliance with global and local regulatory requirements related to medical information Qualification: • Advanced degree in Life Sciences, Pharmacy, or related discipline • Medical degree or doctorate preferred (PharmD, PhD, MSc, MBA or equivalent) Experience: • More than 5 years of experience in medical writing within the pharmaceutical or healthcare industry or equivalent clinical experience • Minimum 2–3 years of direct Medical Information experience in a pharmaceutical company Skills: • Strong scientific and medical writing and editing skills • Expertise in literature evaluation and evidence-based content development • Excellent stakeholder management and cross-functional collaboration skills • Strong time management, risk management, and operational excellence abilities • Ability to work independently and in a team-oriented environment • High attention to detail and commitment to quality and timelines • Excellent written and spoken English proficiency About the Organisation: Sanofi Business Operations (SBO) is Sanofi’s global capability center in India, supporting Medical, Commercial, HEVA, R&D, and Digital functions worldwide. SBO plays a strategic role in delivering high-quality scientific, medical, and operational support across Sanofi’s Specialty Care, Vaccines, General Medicines, and Consumer Healthcare portfolios, helping advance patient care through innovation, collaboration, and scientific excellence.

Roles & Responsibilities: • Design and configure clinical databases using EDC systems such as Oracle Clinical and Medidata Rave. • Develop Case Report Forms (CRFs) aligned with formulation-specific clinical endpoints. • Perform data cleaning and query management, resolving discrepancies with clinical sites. • Conduct User Acceptance Testing (UAT) to validate database logic and edit checks. • Ensure data accuracy, consistency, integrity, and traceability throughout the clinical study lifecycle. • Support database lock activities and clinical data transfer to biostatistics teams. • Provide submission-ready clinical data to support global regulatory filings and formulation performance evaluation. • Collaborate with clinical, formulation R&D, and regulatory teams to ensure compliant data management practices. Qualification: • M.Pharm (Clinical) – Mandatory. Experience: • 2–5 years of experience in Clinical Data Management or Clinical R&D. Skills: • Hands-on experience with EDC systems (Oracle Clinical, Medidata Rave, or equivalent). • Strong understanding of GCP guidelines and clinical trial workflows. • Working knowledge of CDISC standards (SDTM/ADaM) preferred. • Excellent communication and cross-functional coordination skills. • Strong attention to detail and data quality mindset. About the Organization: Bachwell Pharma is a growing pharmaceutical company with a strong focus on formulation R&D for global regulatory markets. The organization supports development of tablets, injectables, and topical formulations, offering professionals the opportunity to work at the intersection of clinical research, data management, and regulatory submissions in a dynamic R&D environment.

Roles & Responsibilities • Perform medical and scientific data review for hematology clinical trials (e.g., myeloma, lymphoma) • Review standard data listings including adverse events, concomitant medications, efficacy and safety data • Conduct patient profile reviews, safety narratives, PD analysis, and scientific data evaluations • Support Lead Clinical Scientist and Medical Director in medical data review activities • Develop and contribute to Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans • Author medical data queries, review responses, and support query closure • Participate in medical and safety review meetings, including slide preparation • Collaborate with Clinical Operations, Data Management, Pharmacovigilance, and Project Management teams • Identify data trends, risks, and subject safety issues; escalate concerns appropriately • Ensure compliance with ICH-GCP, data privacy standards, SOPs, and regulatory requirements • Support audits and trusted process meetings as required Qualification • Degree in Life Sciences: MSc, PharmD, PhD, MD, DMD or equivalent Experience • Relevant scientific or clinical research experience in clinical development • Exposure to medical data review, clinical trials, or drug development preferred Skills • Strong understanding of clinical trial data, scientific principles, and ICH-GCP guidelines • Excellent analytical, documentation, and problem-solving skills • Strong written and verbal communication abilities • Proficiency in MS Office (Word, Excel, PowerPoint) • Ability to manage multiple tasks in a regulated, fast-paced environment • Strong collaboration and stakeholder management skills About the Organisation Syneos Health® is a leading global biopharmaceutical solutions organization, supporting clinical development, medical affairs, and commercialization. With operations across 110+ countries and involvement in the majority of novel FDA and EMA approvals, Syneos Health partners with customers to accelerate the delivery of therapies that improve and save lives worldwide.

Roles & Responsibilities:• Assist in the day-to-day functioning of the dental clinic• Conduct basic dental examinations and patient consultations• Support senior dentists during dental procedures• Provide preventive dental care and oral hygiene guidance to patients• Maintain accurate patient records and clinical documentation• Ensure clinic hygiene, sterilization, and patient safety protocols• Deliver patient-focused and professional dental careQualifications:• Bachelor of Dental Surgery (BDS) from a recognized institution• Valid Dental Council registrationExperience:• Freshers are welcome to apply• 0–1 year of clinical experience preferredSkills Required:• Basic clinical and diagnostic dental skills• Good communication and patient-handling abilities• Willingness to learn and work in a clinical setup• Professional attitude and teamwork skillsBenefits:• Flexible work schedule• Paid sick leave• Leave encashmentAbout the Company:STAR Dental Clinic and Implant Center is a patient-focused dental care provider committed to delivering quality dental treatments in a safe and professional environment. The clinic offers comprehensive dental services with an emphasis on ethical practice, continuous learning, and patient satisfaction.

Roles & Responsibilities • Analyse large and complex datasets to identify trends and generate actionable insights • Support business and operations teams with data-driven decision-making • Troubleshoot data issues and resolve data quality problems • Automate recurring reports and streamline data workflows • Collaborate with cross-functional business and technical stakeholders • Capture and translate business requirements into analytics solutions • Improve reporting accuracy, efficiency, and data governance standards • Prepare dashboards, presentations, and insight summaries for leadership • Contribute to process optimization and performance improvement initiatives Qualification • Bachelor’s or Master’s degree in Computer Science, Engineering, Information Systems, or related fields • Pharmaceutical or Life Sciences background is an added advantage Experience • Minimum 1+ year experience in Data Analysis or Business Analytics Skills • Strong expertise in SQL and Advanced Excel • Hands-on experience with Python or PySpark • Working knowledge of data visualization tools (Power BI, Tableau, etc.) • Experience with ETL tools, data integration, and relational databases • Automation experience using Excel macros, Google Apps Script, or similar tools • Excellent communication and stakeholder management skillsAbout the Organization Roche is a global leader in pharmaceuticals and diagnostics, committed to advancing science to improve people’s lives. With a strong focus on innovation, data, and personalized healthcare, Roche leverages advanced analytics and digital solutions to drive better patient outcomes and smarter business decisions. Roche Services & Solutions India supports global Roche operations through high-impact analytics, automation, and technology-driven insights.

Roles & Responsibilities • Analyse drug development information from clinical trials, regulatory agencies, and scientific sources • Track new drugs, pipeline updates, development phases, indications, and sponsors • Perform primary and secondary research on global drug development activities • Summarize, edit, and validate scientific and pharmaceutical content with high accuracy • Conduct comprehensive online searches for drug and clinical intelligence • Maintain assigned production volumes, quality standards, and KPIs • Collaborate with global teams across regions and business units • Follow SOPs and contribute to process improvement initiatives • Adapt to workflow changes in a fast-paced research environment Qualification • M.Pharm / B.Pharm / D.Pharm Experience • Freshers or up to 6 months of relevant experience Skills • Strong understanding of drug development and clinical research concepts • Excellent written and verbal communication skills • Good content analysis, summarization, and editing abilities • Proficiency in MS Word, Excel, and PowerPoint • Strong attention to detail and time management skills • Exposure to AI tools for research or content analysis • Basic knowledge of SQL or Python • Interest in pharmaceutical analytics, clinical intelligence, and drug pipelines About the Team Clarivate’s Drug Development (CDDI) team delivers high-quality intelligence on clinical trials, regulatory pipelines, and drug research, covering MoA, development milestones, regulatory pathways, and disease focus to support global pharmaceutical decision-making.

Roles & Responsibilities • Perform quality control testing for OSD formulations • Conduct analysis using HPLC, GC, and microbiology techniques • Ensure compliance with GLP, SOPs, and cGMP requirements • Maintain accurate QC documentation and analytical records • Support routine testing, investigations, and lab activities • Ensure data integrity and timely reporting of results Qualification • M.Pharmacy / B.Pharmacy / MSc Experience • 1 to 5 years of experience in Quality Control for OSD formulation Skills • Hands-on experience with HPLC and GC • Knowledge of GLP and microbiology testing • Strong documentation and compliance skills • Attention to detail and quality-focused mindset Walk-In Interview Details • Date: 24 January 2026 (Saturday) • Time: 09:00 AM to 01:00 PM • Venue: Sy. No. 261, Plot No. 13 to 14, Annaram (Village), Jinnaram, Hyderabad • Contact No. for Queries: 9121185330 • Documents to carry: Updated resume, academic documents, ID proof, passport-size photo, latest increment letter and payslips (if applicable) About the Organisation Annora Pharma Pvt Ltd is a pharmaceutical company specializing in OSD formulations, with a strong focus on quality, compliance, and regulatory standards. The organization offers growth-oriented opportunities for professionals passionate about pharmaceutical quality systems and laboratory excellence.

Roles & Responsibilities • Support Clinical Data Services activities within the Life Sciences R&D vertical • Perform Clinical eTMF (Electronic Trial Master File) management across the clinical trial lifecycle • Conduct discrepancy review, query generation, and query resolution in clinical databases • Support data validation, quality checks, and database accuracy reviews • Assist in creation and review of: – CRF Completion Guidelines (CCG) – SAE reconciliation guidelines • Identify, document, and escalate protocol deviations in clinical databases • Perform edit check validation by creating test cases and test scripts • Execute database validation (UAT) against specified CRF/eCRF requirements • Conduct TMF quality and completeness checks including: – Trial Master File Table of Contents – Initial and amended Full Protocol Packages (FPP) – End-of-trial checklists – Essential document reconciliation – Clinical Study Report (CSR) appendices • Perform eCTD-compliant document format checks for regulatory submissions including: – PDF property verification – Bookmarking and hyperlink validation – Compliance with Good Documentation Practices (GDP) • Collaborate with internal and client stakeholders to ensure regulatory readiness Qualification • Bachelor of Pharmacy (B.Pharm) Experience • 1–3 years of experience in: – Clinical Data Services – Clinical Data Management – Clinical eTMF management – Regulated clinical or regulatory documentation Skills • Strong attention to detail and documentation accuracy • Problem-solving and analytical skills • Ability to work under pressure in a regulated environment • Adaptable and flexible mindset • Strong client relationship and stakeholder management skills About the Organisation Accenture is a global professional services company with leading capabilities in digital, cloud, security, and life sciences operations. With over 699,000 professionals serving clients in more than 120 countries, Accenture supports pharmaceutical and biotech organizations across research, clinical trials, regulatory services, pharmacovigilance, and patient solutions—helping bring innovative therapies to market while improving patient outcomes worldwide.

Roles & Responsibilities • Support Clinical Data Management (CDM) activities including discrepancy review, query management, and data validation • Perform data quality checks to ensure accuracy, completeness, and regulatory compliance • Manage Clinical eTMF (Electronic Trial Master File) lifecycle activities • Conduct completeness and accuracy checks for: – Trial Master File (TMF) Table of Contents – Protocol packages and protocol amendments – End-of-trial and essential document checklists • Assist with CRF/eCRF review, edit check validation, and User Acceptance Testing (UAT) • Identify, document, and escalate protocol deviations as per SOPs • Support eCTD-compliant document preparation including: – PDF property checks – Bookmarking and hyperlink validation • Ensure adherence to Good Documentation Practices (GDP) • Collaborate with global cross-functional teams to support inspection and regulatory readiness Qualification • Bachelor of Pharmacy (B.Pharm) Experience • 0–3 years of experience in: – Clinical Data Services – Clinical Data Management – eTMF management – Regulated clinical documentation Skills • Strong attention to detail and documentation accuracy • Analytical and problem-solving skills • Ability to work under pressure in regulated environments • Adaptability and willingness to learn clinical systems and processes • Effective client communication and stakeholder coordination skills About the Organisation Accenture is a global professional services company with deep expertise in digital, cloud, security, and life sciences operations. With a workforce of over 790,000 professionals across 120+ countries, Accenture supports pharmaceutical and biotech companies throughout the product lifecycle—from clinical trials and clinical data management to pharmacovigilance and regulatory submissions—helping organizations deliver compliant, high-quality healthcare solutions worldwide.

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

Roles & Responsibilities• Provide high-quality dental care in Prosthodontics, Pedodontics, or General Dentistry• Conduct patient assessments and develop appropriate treatment plans• Perform dental procedures including restorations, extractions, and preventive care• Educate patients on oral hygiene and post-treatment care• Maintain accurate patient records and clinical documentation• Collaborate with the dental team to ensure seamless patient care• Contribute to the growth and reputation of the clinicSkills Required• Strong patient assessment and clinical skills• Fluency in Telugu, Hindi, and English• Good communication and interpersonal skills• Ability to work independently and as part of a team• Compassionate and patient-focused approachQualifications• Bachelor’s degree in Dentistry (BDS); MDS preferred• Valid dental license to practice in India• Minimum 2 years of relevant clinical experienceBenefits• Provident Fund• Supportive work environment• Opportunities for professional growthAbout the CompanyMK Dental is a reputed multi-branch dental clinic located in Hyderabad, serving patients across KPHB, Nallagandla, Pragati Nagar, and Miyapur. The clinic focuses on delivering patient-centered dental care with experienced professionals and a collaborative team environment.

Roles & Responsibilities• Lead and manage the clinic operations at Dr Jaydev Dental, Jubilee Hills, Hyderabad• Conduct patient assessments and provide high-quality dental care• Diagnose oral health conditions and develop treatment plans• Perform routine and advanced dental procedures, including extractions, fillings, and restorative treatments• Maintain accurate medical records and documentation using proper medical terminology• Supervise and mentor junior dental staff• Ensure adherence to hygiene, safety, and clinical protocols• Handle patient interactions to ensure excellent patient experienceSkills Required• Strong expertise in patient assessment, treatment planning, and dental procedures• Excellent communication and interpersonal skills• Ability to manage a team and clinic operations efficiently• Proficiency in medical documentation and record-keeping• Patient-centered approach with a professional and compassionate attitudeQualifications• Bachelor’s degree in Dentistry (BDS) or Master’s (MDS) from a recognized institution• Minimum 5 years of clinical experience in dentistry• Valid dental license to practice in IndiaWhat We Offer• Competitive salary package• Opportunity to lead and manage a well-established dental clinic• Professional growth and leadership development• Supportive and collaborative work environment• Fixed Sunday holiday and work timings 10 AM – 6 PMAbout the CompanyDr Jaydev Dental, located in Jubilee Hills, Hyderabad, is a reputed dental clinic known for delivering high-quality, patient-focused dental care. The clinic emphasizes modern treatment protocols, advanced equipment, and professional development opportunities for its dental staff while maintaining a welcoming environment for patients.