Pune Healthcare Jobs

Role & Responsibilities • Assess international patient medical requirements and treatment pathways • Coordinate with globally accredited hospitals for treatment plans and cost estimates • Support senior consultants in managing complete patient journeys • Communicate professionally with international patients • Maintain accurate documentation and case continuity • Address patient queries with clinical clarity • Support workflow and patient experience improvements Qualifications & Experience • MBBS / BDS / PharmD / BAMS / BHMS mandatory • Excellent English communication skills • Based in Pune or willing to relocate preferred • Immediate joiners preferred • Comfortable with day and night shifts Skills • Strong interpersonal and communication skills • Emotional intelligence • Ability to work in fast-paced corporate healthcare environment Salary & Benefits • Stipend ₹20,000 per month • Cab facility for night shifts • Exam leaves allowed • PPO opportunity based on performance • Competitive PPO compensation About the Company • Luxora Experiences is a global medical tourism and healthcare consulting company operating across four continents

Roles & Responsibilities: • Prepare summary reports for medical devices • Perform trend analysis on customer complaints and product performance • Conduct monthly and ad-hoc data analysis from complaints, sales, and trending databases • Carry out literature searches and review clinical, scientific, and medical references • Identify, interpret, and evaluate data from medical literature, clinical studies, and post-market sources • Compile and submit clinical and post-market surveillance (PMS) documents • Support international regulatory submissions in line with global medical device regulations • Contribute to PMS plans and safety reports for assigned device portfolios Qualification: • Relevant degree in Life Sciences, Biomedical Engineering, Pharmacy (B.Pharm, D.Pharm, M.Pharm) , or related discipline Experience: • 3-6 years of experience in Medical Devices domain • Hands-on experience in medical review and post-market surveillance Skills: • Strong knowledge of medical device regulations and PMS requirements • Experience in complaint trending and safety data analysis • Expertise in literature search and regulatory documentation • Excellent analytical, documentation, and communication skills • Ability to work in a fast-paced, office-based environment • Immediate joiners preferred About the Company: ANRI Solutions is a leading recruitment partner connecting skilled professionals with top pharmaceutical, medical device, and healthcare organizations across India and globally.

Role & Responsibilities • Perform medical review of Individual Case Safety Reports (ICSRs) • Ensure medical accuracy, completeness, and regulatory compliance of safety cases • Apply clinical judgment for case assessment, seriousness, causality, and expectedness • Support global pharmacovigilance and regulatory reporting activities • Ensure adherence to GVP, ICH guidelines, and internal SOPs Qualifications & Experience • MBBS / MD with valid MCI registration • Minimum 1 year of hands-on experience in ICSR medical review Skills • Strong knowledge of pharmacovigilance and clinical terminology • Understanding of regulatory reporting requirements • Good analytical and documentation skills About the Company • Indegene is a global life sciences solutions provider delivering pharmacovigilance, medical affairs, and regulatory services across worldwide markets

Role & Responsibilities • Recruit and enroll eligible study participants • Coordinate patient visits, procedures, and follow-ups as per study protocol • Enter and maintain clinical research data in electronic data capture (EDC) systems • Address protocol-related queries from study participants • Ensure compliance with ICH-GCP, ethical guidelines, and regulatory requirements • Prepare, maintain, and update essential study documentation • Archive Case Report Forms (CRFs) and trial-related documents properly • Coordinate with sponsors, ethics committees, investigators, and study sites • Support Principal Investigators (PI) for smooth study conduct Qualifications & Experience • Bachelor’s or Master’s degree in Biotechnology, Biochemistry, Microbiology, Biology, Life   Sciences, Nursing, or Pharmacy • Diploma in Clinical Research (optional) • 1–5 years of experience in clinical research coordination • Strong understanding of clinical trial processes and documentation • Proficiency in MS Word and MS Excel • Good communication and interpersonal skills About the Company • Indira IVF Hospital is one of India’s leading fertility and reproductive healthcare organizations,    known for its hospital-based clinical research and patient-centric trials.

Role & Responsibilities • Process Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs). • Log and track Adverse Events (AE) and Serious Adverse Events (SAE). • Write patient narratives and code events using MedDRA. • Support safety report submissions and maintain safety databases. • Assist in quality review, reconciliation, and audit readiness. • Train and mentor junior staff.Qualifications & Experience • PharmD, MS/MA in Life Sciences, or BS/BA in related fields. • 1-2 years of experience in safety, pharmacovigilance, or clinical research.Skills • Knowledge of AE/SAE processing and safety databases. • Strong attention to detail and data accuracy. • Proficiency in MS Office and Windows.About the Company Fortrea is a global leader in clinical research and pharmacovigilance, providing safety and regulatory services to biopharmaceutical companies worldwide.

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 • Author, review, and approve Clinical Evaluation Reports (CER) in compliance with EU MDR • Prepare and maintain Periodic Safety Update Reports (PSUR) • Develop Post-Market Clinical Follow-up (PMCF) plans and evaluation reports • Create Trend Reports and other post-market surveillance documentation • Ensure compliance with global medical device regulations in regulatory documents • Collaborate with cross-functional regulatory, clinical, and quality teams • Maintain document traceability, version control, and audit readiness • Support regulatory submissions and responses to health authority queries Qualification • Graduate in Pharmacy or Biomedical Engineering, OR • Post-Graduation in Life Sciences Experience • 2 to 15 years in medical device medical writing • Proven hands-on experience in CER, PSUR, PMCF, and post-market documentation Skills • Strong understanding of EU MDR, post-market surveillance, and regulatory writing standards • Experience with regulatory document creation and management • Excellent written communication skills • Ability to collaborate effectively across teams About the Company • Hiring through Wipro • Pune-based, multinational organization • Focused on global medical device regulatory projects and post-market surveillance

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 • Initiate communication with internal business teams and subsidiaries for SDEA requirements • Follow up with third-party partners to establish and maintain SDEAs • Perform timely exchange of safety data with business partners • Conduct adverse event reconciliation with partners • Support case processing and safety writing activities • Ensure compliance with global pharmacovigilance standards • Stay updated with current PV regulations and scientific developments Qualification • B.Pharm / M.Pharm / BAMS / BHMS Experience • 3–4 years of experience in pharmacovigilance • Hands-on experience in case processing, safety writing and SDEA management • Experience in safety data exchange and reconciliation activities Skills • Knowledge of global pharmacovigilance regulations • SDEA management & reconciliation • Case processing & safety writing • Strong written and verbal communication skills • Presentation & documentation skills About the Company • A leading life sciences organization engaged in delivering high-quality pharmacovigilance and drug safety solutions across global markets

Role & Responsibilities • Review published biomedical literature for identification of adverse reaction case reports and non-individual case reports • Apply regulatory and internal guidance to determine case validity and reportability • Perform relevancy assessment based on accepted pharmacovigilance guidelines • Provide training and guidance to literature scanners on inclusion criteria • Collaborate with subject matter experts to ensure team capability and compliance • Perform additional pharmacovigilance tasks as assigned by lead or manager Qualification • MBBS or MD Experience • 0–3 years of experience in Pharmacovigilance / Drug Safety Skills • Strong knowledge of global PV regulatory guidelines • Narrative writing and medical case assessment • MedDRA coding proficiency • Understanding of pharmacological concepts About the Company Wipro is a leading global information technology, consulting, and business process services company that delivers innovation-led solutions to clients across industries, including life sciences and healthcare. With a strong presence worldwide, Wipro supports pharmaceutical organizations in ensuring drug safety, regulatory compliance, and patient-centric healthcare delivery.Interested candidates can share their resumes at varsha.kamalapurkar@wipro.com

Role & Responsibilities • Dispense prescribed medications accurately to inpatients and outpatients • Ensure safe storage, handling and inventory control of medicines • Review prescriptions for dosage accuracy and drug interactions • Provide medication counselling to patients • Support clinical teams in safe medication use practices • Maintain pharmacy documentation and regulatory compliance • Perform night shift pharmacy operations from 9 PM to 9 AM Qualification • D.Pharm or B.Pharm from a recognized institution • Registered Pharmacist with State Pharmacy Council Experience • Freshers can apply • Prior hospital pharmacy experience preferred Skills • Knowledge of hospital pharmacy operations • Prescription review and dispensing accuracy • Inventory and stock management • Good communication skills • Attention to detail About the Company • Hospital-based pharmacist role focused on safe medication dispensing, night duty operations and direct patient care in a super speciality urology institute

Role & Responsibilities Maintain global oversight of unresolved sample discrepancies for incoming and outgoing shipments Coordinate with internal teams to resolve discrepancies within defined TAT and OTIF timelines Perform QC verification of biospecimen data in LIMS and inventory systems Conduct advanced QC checks and trend analysis on sample data Support study close-out activities including reconciliation of sample disposition Monitor patient sample collection schedules and protocol assessment windows Support study setup activities in LIMS including workflows and protocol configuration Prepare operational reports including inventory, kit tracking and site performance metrics Participate in RCA and CAPA activities Ensure compliance with QMS, SOPs and data privacy regulations Support ad-hoc analysis and cross-functional operational requests Qualification Bachelor’s or Master’s degree in Life Sciences or related discipline Experience Minimum 2–3 years of experience in clinical research, sample management or data operations Skills Strong understanding of drug, device and biologic development processes Hands-on experience with clinical databases and LIMS systems Expertise in data quality and compliance standards Proficiency in MS Excel, Word, PowerPoint and Outlook Excellent written and verbal communication skills Knowledge of GDPR, HIPAA and data privacy regulations About the Company Precision For Medicine is a global precision medicine organization supporting international clinical trials, biospecimen management and advanced clinical data operations

About the role & responsibilities • Perform medical review of adverse events for investigational and marketed products • Ensure accurate medical assessment using MedDRA, WHO-DRL and ARGUS safety database • Maintain compliance with global pharmacovigilance regulations and internal SOPs • Identify, communicate and manage potential safety risks and safety signals • Provide medical review for aggregate safety reports including PSURs, PADERs and annual reports • Collaborate with safety and pharmacovigilance teams for consistent case assessment • Interact with sponsor safety and medical teams when required • Support training and mentoring of pharmacovigilance associates • Maintain continued medical education and PV expertise Qualification • MD / MBBS / DO • Completed accredited residency Experience • 1–2 years of clinical practice • Minimum 1 year experience in Pharmacovigilance / Drug Safety in pharma, CRO or biotech Skills • Knowledge of global PV regulations • MedDRA and WHO-DRL coding understanding • ARGUS safety database exposure • Safety signal identification and risk assessment • Strong documentation and communication skills About the company • Syneos Health is a global biopharmaceutical solutions organization operating in 110+ countries, supporting clinical development, medical affairs and commercialization worldwide Location & travel • Location as per project | Travel up to 10%

Roles & Responsibilities• Diagnose and treat patients with physiotherapy needs• Provide physiotherapy care to manage pain, injuries, and mobility issues• Monitor patient progress and update treatment plans accordingly• Maintain basic patient records and documentation• Ensure patient comfort and safety during therapy sessionsQualifications• Bachelor’s degree in Physiotherapy from a recognized institution• Valid PT license requiredExperience• Minimum 1 year of experience in physiotherapy preferred• Freshers with at least 6 months of internship experience can applySkills• Good physiotherapy and clinical skills• Patient-friendly and empathetic approach• Good communication and interpersonal skills• Ability to work independentlyShift & Schedule• Evening shift (4:00 PM – 9:00 PM)Benefits• Paid sick time• Performance bonusAbout the CompanyApex Physiotherapy Clinic & Wellness Center, located in Baner, Pune, Maharashtra, provides professional physiotherapy and wellness services focused on patient recovery, pain management, and improved mobility. The clinic emphasizes quality care, patient satisfaction, and a supportive working environment.

Roles & Responsibilities • Generate and convert leads from pharmaceutical, nutraceutical, MedTech, and healthcare organizations • Promote market access services, pricing intelligence, product launch support, and healthcare research solutions • Build and maintain strong client relationships by understanding customer needs and business objectives • Prepare business proposals, presentations, and conduct follow-ups to close deals • Maintain and monitor the sales pipeline to achieve assigned business development targets • Coordinate with internal consulting, research, and delivery teams to ensure smooth project execution • Track market trends and identify new business opportunities in healthcare and life sciences Qualification • Graduate or Postgraduate in Pharmacy, Life Sciences, Healthcare, or Business Management Experience • 1–3 years of experience in business development, healthcare sales, or consulting services Skills • Basic understanding of pharmaceutical drugs, nutraceutical products, and healthcare markets • Strong communication, negotiation, and client relationship management skills • Ability to work in a target-driven, client-facing environment • Good presentation and proposal development skills • Self-motivated with a proactive approach to business growth About the Company Mark8Access is a leading healthcare intelligence and market access consulting firm that partners with pharmaceutical, nutraceutical, MedTech, and healthcare organizations. The company supports clients across pricing intelligence, market access strategy, product launch planning, scientific content services, and healthcare research, helping them make informed decisions and achieve successful market entry and growth.

Roles & Responsibilities • Perform medical device complaint investigations in compliance with ISO 13485 and ISO 14971 • Conduct risk assessments, hazard analysis, and FMEA • Support CAPA initiation, investigation, and closure activities • Prepare, review, and maintain high-quality investigation and compliance documentation • Ensure adherence to global regulatory and quality system requirements • Collaborate with cross-functional and global teams for complaint resolution • Support audit readiness and continuous quality improvement initiatives Qualifications • Any Life Science Graduate • For Kolkata location: B.Pharm / M.Pharm, Biomedical / Mechanical Engineering / B.Sc Medical Imaging & Radiology / M.Sc Molecular Biology / B.Sc Nursing / BDS Experience • Pune & Hyderabad: 3-9 years (Immediate joiners preferred) • Kolkata: 0-5 years (Relevant medical device investigation experience required) Skills • Medical Device Complaint Investigation • ISO 14971 Risk Management • ISO 13485 Quality Management Systems • CAPA, Root Cause Analysis • FMEA and Risk Assessment • Excellent English communication skills • Willingness to work rotational shifts and from office Walk-In Interview Details Hyderabad Dates: 12, 15 & 16 January 2026 Venue: Wipro Limited, Manikonda STPI, Tower 6, 3rd Floor, Gachibowli, Hyderabad – 500032 Contact: Pavan Pune Dates: 12, 14 & 16 January 2026 Venue: Unit 2, Plot No. 31, Hinjewadi Phase 2, Rajiv Gandhi Infotech Park, Pune – 411057 Contact: Riya / Varsha Kolkata Dates: 13, 15 & 16 January 2026 Venue: Gate 1, Plot 8 & 9, Block DM, Sector V, Salt Lake, Kolkata – 700091 Contact: Sarita Reporting Time: 10:00 AM – 12:30 PM Documents to Carry • Updated Resume • Original Government ID Proof • Mention source of walk-in information on top of CV About the Company Wipro Limited is a leading global information technology, consulting, and business services company with a strong presence in healthcare and medical devices. Wipro supports global clients with regulatory-compliant quality, safety, and post-market surveillance services, offering professionals exposure to international standards, advanced technologies, and long-term career growth opportunities.

Role & Responsibilities: • Manage the complete tendering process for pharmaceutical projects from identification to submission • Analyze tender documents to understand technical, commercial, and legal requirements • Prepare and compile tender documentation including technical, commercial, and statutory documents • Ensure compliance with client requirements and internal quality standards • Screen tenders from registered portals and the GeM (Government e-Marketplace) portal • Create quotations, BOQs, and tender schedules • Maintain accurate records of all tender documents, submissions, and outcomes • Lead pre-tender activities for government and institutional tenders • Analyze tender risks, opportunities, and pricing strategies • Coordinate and communicate with internal departments, vendors, and external stakeholders • Assess customer preferences and satisfaction related to tender outcomes • Implement departmental CES action plans as required Qualification: • Bachelor’s or Master’s degree in Pharmacy or Pharmaceutical Sciences • Master’s degree preferred Experience: • 1–3 years of relevant experience in pharmaceutical tendering • Hands-on experience in tendering of pharma products preferred Skills: • Pharmaceutical Tendering & Government Procurement • Documentation & Compliance Management • GeM Portal & Tender Screening • Quotation & Pricing Analysis • Stakeholder Coordination & Communication • Analytical & Organizational Skills About the Company: Inducare Pharma Private Limited is a pharmaceutical organization engaged in delivering high-quality healthcare products, with a strong focus on compliance, ethical practices, and participation in government and institutional healthcare programs through structured tendering processes.