Hyderabad Healthcare Jobs

Role & Responsibilities • Lead medical affairs objectives and serve as a medical, technical, and scientific resource • Engage with physicians, academic centers, and researchers on AbbVie’s products • Ensure budget compliance and accurate documentation of activities • Collaborate with commercial leaders to set priorities and activities • Present AbbVie product data to healthcare professionals as required • Support research initiatives and develop medically accurate communications • Conduct training for internal teams and support Round Table/Advisory Board sessions • Represent AbbVie’s global medical office functions with 60% field time Qualifications & Experience • 2-3 years in Medical Affairs, clinical research, or the pharmaceutical industry • Strong presentation, teaching, and analytical skills • Experience in cross-functional collaboration and relationship development • Proficiency in Microsoft Office and medical database systems Education • MD/MBBS/Pharm D About AbbVie • AbbVie is a global biopharmaceutical company focused on discovering and delivering innovative medicines in immunology, oncology, neuroscience, and eye care.

Role & Responsibilities • Perform ICSR case processing, booking, triage, and data entry. • Conduct quality review (QC) of ICSRs as per SOPs and GVP. • Enter, code, and review safety data in Argus / ARISg / LSMV. • Prepare accurate case narratives and follow up on queries. • Identify and manage duplicate safety cases. • Perform MedDRA coding for events, indications, and products. • Handle literature screening and drug dictionary maintenance. • Support xEVMPD, SPOR / IDMP activities. • Ensure documentation compliance with TMF and PSMF. • Participate in internal and external PV audits. • Ensure adherence to ICH-GCP, GVP, and global safety regulations. Qualifications & Skills • Bachelor’s degree in Life Sciences / Pharmacy / Nursing. • 3+ years of experience in Pharmacovigilance case processing. • Mandatory experience in Clinical Trial, PMS, and Spontaneous cases. • Strong working knowledge of Argus Safety Database. • Proficiency in MedDRA coding and medical terminology. • Excellent communication, accuracy, and time-management skills.Why Join Syneos Health? • Work with a leading global organization involved in 94% of novel FDA-approved drugs. • Exposure to international clinical trials and post-marketing safety programs. • Career development with structured training and mentoring. • Inclusive culture promoting diversity and well-being. • Opportunity to work on cutting-edge drug safety projects.

Role & Responsibilities Medical review of ICSRs (investigational and marketed products) Perform seriousness, causality and consistency assessments of AEs Ensure compliance with global PV regulations and internal SOPs Collaborate with global safety teams and client medical counterparts Support signal detection and benefit–risk activities Mentor and train case processing and safety teamsQualification MBBS / MD (Mandatory) Knowledge of MedDRA and safety databases (Argus preferred)Experience Minimum 1 year pharmacovigilance experience Minimum 1 year clinical experienceSkills ICSR medical review and AE evaluation Regulatory and SOP compliance MedDRA terminology Argus safety database Strong analytical and communication skills Team mentoring and collaborationAbout the Company Syneos Health is a global biopharmaceutical solutions company delivering integrated clinical and commercial services to improve patient outcomes worldwide.

Role & Responsibilities • Execute medical affairs strategy in the assigned territory • Understand treatment practices, medicines, and therapeutic trends through KOL interactions, journals, and scientific symposia • Gather, analyze, and disseminate scientific information to internal and external stakeholders • Execute medical projects including IIS studies and key scientific initiatives • Support implementation of medico-marketing strategies • Identify and develop relationships with Key Opinion Leaders (KOLs) and External Experts (EEs) • Provide medical and scientific expertise for new product / indication registrations • Support regulatory defense of marketed products with scientific rationale and literature • Prepare, review, and revise labeling documents as per SOPs • Liaise with regulatory affairs teams and support EE access • Provide regular feedback to management on KOL development and field insights Qualification • Medical degree (MBBS / MD – Pharmacology preferred) • Life Sciences qualification (for experienced field professionals) Experience • 0–3 years of Medical Affairs / Pharmaceutical / Healthcare industry experience • Professionals without doctoral qualification require 10+ years of relevant field experience Skills • Strong scientific expertise in Diabetes therapeutic area • Excellent interpersonal and communication skills • Good presentation and scientific detailing skills • Basic IT knowledge (MS Office) • Ability to work independently in field-based roles About the Company Boehringer Ingelheim is a global biopharmaceutical company operating in human and animal health, focused on developing innovative therapies to improve and extend lives. With a legacy of research excellence since 1885, the company serves over 130 markets worldwide and is one of the largest investors in pharmaceutical R&D.

Role & Responsibilities • Manage and lead a team of Medical Reviewers • Allocate work, monitor productivity and review assignments • Perform quality review of medical record summaries in client-specific formats • Train and onboard new team members • Handle client communication via email and coordination calls • Ensure timely and accurate delivery of assigned projects • Plan and support cross-training initiatives • Maintain compliance with internal quality and documentation standards Qualification • MBBS • MD / MS / Doctorate in any specialization Experience • 5 – 10 years of relevant medical review / healthcare documentation experience Skills • Team management and leadership • Medical record summarization and quality review • Client communication and coordination • Training and mentoring • Strong documentation and analytical skills About the Company The organization provides specialized medical review and clinical documentation services supporting global healthcare and life sciences clients with high-quality medical data review and compliance solutions.

Role & Responsibilities • Perform initial assessment and medical review of ICSRs in safety databases • Review seriousness, causality, labeling, narratives, MedDRA coding and medical history • Verify suspect drug, concomitant medications and laboratory data • Respond to case owner queries and document medical review comments • Identify and escalate complex case issues to team leads or line managers • Determine follow-up requirements and ensure proper documentation • Train and mentor PV associates on safety conventions and event capturing • Maintain current knowledge of product safety profiles across therapeutic areas Qualification • MBBS / MD (PG degree preferred) Experience • Minimum 8 years of experience in Pharmacovigilance / Drug Safety Skills • Strong knowledge of ICSR medical review • Good understanding of MedDRA coding and global PV regulations • Excellent communication and documentation skills • Strong organizational and mentoring abilities • Ability to work under pressure and meet timelines About the Company • Cencora is a global healthcare solutions organization delivering regulatory, pharmacovigilance and medical safety services through its affiliate PharmaLex India Private Limited, supporting safer medicines and improved patient outcomes worldwide

Role & Responsibilities • Perform end-to-end ICSR case processing including case booking and triage • Handle spontaneous, clinical trial and literature safety cases • Perform accurate medical coding and safety data entry • Ensure compliance with ICH-GCP guidelines, regulatory standards and SOP requirements • Work on global safety databases such as Argus, ARIS-G and LifeSphere Multi-Vigilance (LSMV) • Collaborate with cross-functional pharmacovigilance teams • Support timely and high-quality safety reporting activities Qualification • B.Pharm / M.Pharm • BDS / BMS / MBBS (BSc / MSc candidates are not eligible) Experience • 2.6 – 4 years of hands-on ICSR case processing experience Skills • Strong knowledge of medical terminology • ICSR processing & triage • Medical coding and safety database handling • Knowledge of ICH-GCP and regulatory compliance • Good written and verbal communication skills About the Company Syneos Health is a leading global contract research organization (CRO) providing integrated biopharmaceutical solutions across clinical development, pharmacovigilance, medical affairs and commercialization. The company supports global safety surveillance and regulatory compliance for pharmaceutical and biotechnology products worldwide.

Role & Responsibilities • Perform medical review of Individual Case Safety Reports (ICSRs) • Conduct signal detection and interpret emerging safety trends • Develop and review aggregate safety reports including PSURs, PBRERs and DSURs • Support benefit–risk assessments and safety strategy discussions • Ensure compliance with global pharmacovigilance regulations (ICH, EMA, US FDA) • Provide medical evaluation of case narratives and literature reports • Collaborate with cross-functional safety and quality teams • Contribute to clinical risk management and regulatory safety activities Qualification • MBBS / MD (Registered Medical Practitioner in India) Experience • Minimum 1+ year experience in Pharmacovigilance / Drug Safety Skills • Signal detection & aggregate reporting • ICSR medical review • Global PV regulatory knowledge • Analytical thinking & medical interpretation • Strong written and verbal communication About the Company • OrciMed Life Sciences is a pharmacovigilance and drug safety organization providing global safety services, signal detection, aggregate reporting and regulatory compliance solutions to pharmaceutical companies

Role & Responsibilities • Lead therapeutic area (TA) medical strategy and act as core scientific member of cross-functional franchise team • Plan and execute medical affairs strategy including publications, medical education, research, and patient support programs • Engage Key Opinion Leaders and Thought Leaders for scientific exchange and advisory activities • Drive regional medical affairs execution including product education and special projects • Provide scientific training and medical insights to sales and marketing teams • Serve as TA scientific expert for interpretation and communication of clinical and real-world data • Ensure compliance with Indian regulations, UCPMP, MCI code, and Drugs & Cosmetics Act • Support development of long-term medical affairs strategic plans Qualification • MBBS with MD (Pharmacology/Medicine) or full-time postgraduate medical qualification Experience • 2–4 years as Medical Advisor in pharmaceutical or research organizations Skills • Strong therapeutic area knowledge and research methodology understanding • Medical writing and clinical trial knowledge (ICH-GCP preferred) • Strategic thinking and scientific communication skills • Regulatory compliance knowledge (Indian regulations) • Excellent stakeholder engagement and presentation abilities About the Company Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company operating in 66 countries, driven by the purpose “Good Health Can’t Wait.” With strong R&D, manufacturing, and commercial presence, Dr. Reddy’s focuses on access, affordability, and innovation to serve over 1.5 billion patients worldwide by 2030 while maintaining sustainability, integrity, and people-centric work culture.

Role & Responsibilities • Perform medical review of company, literature, and regulatory ICSRs • Select and assess adverse events for seriousness and expectedness • Conduct MedDRA coding review of adverse events • Review causality assessments and perform label assessment • Classify product role (suspect, concomitant, interacting) • Review medical history, concomitant conditions, and laboratory data • Evaluate case narratives for medical accuracy and completeness • Perform medical review and quality review of aggregate safety reports (PSURs, PADERs) • Conduct medical review of Risk Management Plans (RMPs) • Review Signal Management Reports and support signal evaluation Qualification • MBBS or MD (Pharmacology preferred) Experience • Relevant experience in pharmacovigilance medical review or drug safety preferred Skills • Strong knowledge of pharmacovigilance regulations and safety reporting standards • MedDRA coding proficiency • High attention to clinical detail and document quality • Strong written and verbal communication skills • Ability to work with global safety documentation and regulatory timelines About the Company The hiring organization operates in regulated pharmacovigilance and drug safety domains, supporting global pharmaceutical safety surveillance, aggregate reporting, and risk management activities aligned with international regulatory standards.

Role & Responsibilities • Perform dental examinations, diagnosis, and routine oral procedures • Repair, extract, and restore damaged teeth • Fill cavities and perform root canal treatments • Develop and implement patient-specific treatment plans • Prescribe and administer medications for pain management and infection control • Evaluate dental X-rays and oral health conditions • Educate patients on oral hygiene and preventive dental care • Measure, fit, and place dental appliances • Refer patients to specialists when required Qualification • BDS (Bachelor of Dental Surgery) Experience • Minimum 4+ years of clinical dental experience • RCT experience preferred Skills • Clinical dentistry and oral surgery skills • Diagnosis and treatment planning • Patient communication and counseling • X-ray interpretation and documentation • Time management and chairside efficiency About the Company The hiring dental clinic in Hyderabad is a growing healthcare facility committed to delivering quality oral care services with a patient-centric approach, providing modern dental treatments in a professional clinical environment.

Role & Responsibilities • Perform accurate data entry of safety and pharmacovigilance cases • Ensure completeness and correctness of case-related information • Follow SOPs, quality standards and regulatory timelines • Identify, document and escalate data discrepancies • Maintain data confidentiality and integrity • Support workload management during high-volume periods Qualification • B.Pharm / M.Pharm / Pharm.D Experience • 2 – 3 years in pharmacovigilance case processing or safety data entry Skills • Strong data accuracy and documentation skills • Good knowledge of SOPs and regulatory requirements • Attention to detail and time management skills • Ability to work in quality-driven environments About the Company Mitocon Biopharma is a Hyderabad-based pharmaceutical organization focused on regulated pharmacovigilance operations, offering pharmacy professionals structured growth, compliance exposure and a professional work environment.

Role & Responsibilities • Review pharmacovigilance case processing for accuracy, completeness and regulatory compliance • Perform quality checks and identify gaps, deviations and trends • Ensure adherence to SOPs, global PV guidelines and defined TATs • Maintain quality metrics, reports and compliance documentation • Provide feedback, mentoring and training to case processing teams • Support audits, inspections and continuous improvement activities Qualification • B.Pharm / M.Pharm / Pharm.D Experience • 3 – 5 years in pharmacovigilance case processing or quality review Skills • Strong understanding of PV regulations and SOP compliance • High attention to detail and analytical skills • Good documentation and reporting ability • Effective communication and mentoring skills About the Company Mitocon Biopharma is a Hyderabad-based pharmaceutical organization engaged in regulated pharmacovigilance operations, providing high-quality drug safety services with strong focus on compliance, audits and continuous quality improvement.

Role & Responsibilities • Serve as primary interface between sponsors, vendors and internal Safety & PV teams • Provide line management to Safety and Pharmacovigilance associates and managers • Oversee operational delivery as per Safety Management Plans and contracted scope • Monitor quality, productivity and KPIs and resolve performance gaps • Lead PV projects and ensure timely safety reporting submissions • Review and approve study budgets, invoicing and financial forecasts • Act as escalation point for sponsors and provide regular project updates • Coordinate with Clinical, Data Management, Regulatory and other functions • Develop, review and approve SOPs, work instructions and process improvements • Support business development activities, proposals and bid defenses • Review safety sections of protocols, CRFs and SAE forms • Ensure compliance with ICH-GCP, GVP modules, global regulations and internal SOPs • Participate in audits, inspections, CAPA management and inspection readiness • Provide PV training and expert consultation to internal teams and clients Qualification • Bachelor’s degree in Life Sciences, Pharmacy, Nursing or related healthcare discipline Experience • Extensive leadership experience in Safety & Pharmacovigilance within CRO or global PV environments Skills • Strong knowledge of GVP, ICH guidelines and global safety regulations • Proven people management and project leadership abilities • Financial acumen for budget management and invoicing • Proficiency in MS Word, Excel, PowerPoint, Visio and Outlook • Excellent communication, stakeholder management and presentation skills • Ability to manage multiple priorities in a fast-paced, matrix environment About the Company Syneos Health® is a global biopharmaceutical solutions organization delivering integrated clinical development, medical affairs and commercial services, partnering with leading pharmaceutical companies worldwide to accelerate drug development and improve patient outcomes through innovation, quality and compliance.

Role & Responsibilities • Review clinical trial protocols and data review plans • Prepare and contribute to Data Quality Management Plans • Perform detailed review of clinical data listings and prioritize critical data • Manage query generation, resolution and data cleaning activities • Execute CRF freezing and database lock activities • Track and review external data loads including SAE, biomarker and adjudication data • Liaise with external vendors for discrepancy resolution • File essential documents in eTMF in line with master plan requirements • Ensure compliance with FDA, ICH and global data management standards • Train and mentor junior Clinical Data Management team members • Collaborate with cross-functional clinical teams to meet study timelines Qualification • Bachelor’s degree in Life Sciences, Pharmacy or related discipline Experience • Minimum 4 years of experience in clinical data review and management Skills • Strong knowledge of clinical drug development process • Hands-on experience with EDC systems (Medidata RAVE preferred) • Proficiency in Microsoft Office tools • Excellent written and verbal communication skills • Strong analytical, coordination and problem-solving abilities • Ability to work collaboratively in cross-functional environments About the Company Bristol Myers Squibb (BMS) is a global biopharmaceutical leader focused on discovering, developing and delivering innovative medicines that help patients prevail over serious diseases, offering professionals a collaborative, ethical and patient-centered work culture with strong career growth opportunities.

Job Responsibilities • Dispense medications accurately and safely • Review prescriptions for appropriateness and patient safety • Counsel patients on correct medicine usage, dosage, and precautions • Maintain pharmacy inventory, stock levels, and documentation • Coordinate with doctors and nursing staff for medication clarification and continuity of careEligibility Criteria • B.Pharm degree (Mandatory) • State Pharmacy Council Registration (Required) • Freshers & Experienced candidates can applyPreferred Skills • Knowledge of hospital pharmacy operations • Good verbal communication skills • Willingness to work in rotational shifts

Role & Responsibilities Oversee In-Process Quality Assurance (IPQA) activities for injectables and packaging operations Review and approve Batch Manufacturing Records (BMRs) and Batch Packaging Records (BPRs) Ensure compliance with cGMP, GDP and Quality Management Systems Handle deviations, investigations, CAPA and audit preparedness Lead QA team and drive continuous quality improvement initiatives Perform analytical testing of raw materials, in-process and finished products Operate analytical instruments such as HPLC, UV, IR and related equipment Maintain compliance with GMP, GLP and ISO regulatory standards Utilize LIMS for laboratory data management and documentation Qualification B.Pharm / M.Pharm / M.Sc (Organic Chemistry) Experience 6–8 years for Executive / Sr. Executive – Quality Assurance (IPQA) 3–5 years for Sr. Officer / Officer – Quality Control Injectables manufacturing experience preferred Skills Strong knowledge of pharmaceutical quality systems and regulatory compliance Proficiency in analytical testing and laboratory instrumentation Knowledge of CAPA, deviations and audit readiness Attention to detail and documentation accuracy Team leadership and coordination abilities Good communication and problem-solving skills About the Company Zenotech Laboratories, a subsidiary of the Sun Pharma Group, is a Hyderabad-based pharmaceutical manufacturer specializing in generic injectables, oncology and biotechnology products. The company is known for its focus on quality, regulatory compliance and innovation, offering professionals a structured and high-standard manufacturing environment.

Role & Responsibilities Perform medical review of individual case safety reports (ICSRs) from clinical trials, literature, spontaneous sources and regulatory authorities Ensure correct assessment of adverse events for seriousness, expectedness and listedness Review MedDRA coding for adverse events, medical history and concomitant medications Validate causality assessment and product role classification (suspect, concomitant, interacting) Review case narratives for medical accuracy, clinical coherence and regulatory completeness Draft and medically review aggregate safety reports including PSURs and PADERs Review Risk Management Plans (RMPs) and signal management documentation Support pharmacovigilance medical writing and regulatory submission activities Qualification MBBS or MD (preferably Pharmacology) OR PharmD or M.Pharm with drug safety medical writing experience Experience 2–4 years of experience in pharmacovigilance medical review or drug safety medical writing Hands-on exposure to PSURs, PADERs, DSURs, RMPs and signal management reports Skills Strong knowledge of pharmacovigilance regulations and safety reporting standards Proficiency in ICSR medical review and aggregate report writing Accurate use of MedDRA terminology High attention to clinical detail and documentation quality Strong written and verbal communication skills Good organizational and time management skills Working knowledge of MS Office tools About the Company MSN Group is a vertically integrated pharmaceutical company with strong capabilities across APIs, formulations and drug delivery systems. The company operates structured pharmacovigilance and regulatory compliance frameworks supporting global markets, with a strong R&D-driven focus on documentation quality, lifecycle safety management and regulatory excellence.

Key Responsibilities • Establish strategic growth plans, KPIs and performance roadmaps • Ensure strict compliance to hospital pharmacy policies & NABH standards • Manage high-value medicine consignment systems and vendor coordination • Handle internal & external audits and inventory risk mitigation • Maintain optimal stock levels and reduce wastage • Drive customer retention through superior pharmacy service • Evaluate, register and manage vendors • Streamline pharmacy processes and close operational gaps • Coordinate continuously with Quality department for compliance • Lead clinical pharmacy services and protocol implementation • Review medication therapy and improve patient safety • Provide drug information support to doctors and nursing teams • Supervise dispensing, compounding and documentation processes • Mentor clinical pharmacy team members • Participate in multidisciplinary patient care roundsKey Skills & Expertise • NABH Hospital Pharmacy Operations • Clinical Pharmacy & Medication Therapy Management • Inventory Optimization & Consignment Handling • Vendor Management • Audit & Compliance Management • Leadership & Team DevelopmentBenefits • Paid Time Off • Stable hospital environment • Leadership growth opportunityRole Overview We are hiring a Clinical & Hospital Pharmacy Manager to lead pharmacy operations, clinical pharmacy services, vendor management and inventory control while ensuring 100% NABH & quality compliance. This role combines strategic pharmacy leadership with hands-on clinical expertise and is ideal for experienced hospital pharmacists seeking growth into leadership positions.