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Role & Responsibilities • Exchange and disseminate scientific, educational, and research-related information with Thought Leaders (TLs) proactively and reactively • Provide clarification and education of scientific data, study protocols, meeting abstracts, and professional literature, both on-label and off-label, in alignment with local regulations • Answer medical/scientific queries from Medical Societies regarding Bayer products • Organize, support, and participate in advisory boards • Attend congresses and conventions, interact with TLs, establish new contacts, and gather competitive intelligence • Plan and organize scientific education and training events with TLs within specific therapeutic areas or products • Contribute to internal understanding of specific TL interests and expertise within the medical community • Submit timely reports and track activities against agreed objectives • Provide external scientific support, training, and education where needed Qualification • Qualification in natural sciences or a medical background (MD, MBBS, BAMS, BDS, MDS) Experience • Basic knowledge of the concerned therapy area and related molecules • Basic understanding of clinical trials, their design, and rationale • Experience working independently and within a team environment • Ability to build productive relationships both internally and externally Skills • Excellent presentation and written and verbal communication skills • Ability to engage and influence thought leaders and stakeholders effectively • Proficiency in managing scientific data and presenting it clearly to diverse audiences About The Company • Bayer – A global leader in life sciences, Bayer is dedicated to driving innovation and improving lives through advanced solutions in healthcare and agriculture. The company values dynamic shared ownership (DSO) and fosters a work environment that prioritizes higher productivity, faster innovation, and better results. Bayer is committed to diversity and inclusivity, promoting fairness and respect at work.
Roles & Responsibilities:• Assess patients’ physical conditions and rehabilitation needs• Plan and execute physiotherapy treatment programs• Support patient recovery and rehabilitation through therapeutic exercises and interventions• Maintain accurate patient records and progress reports• Collaborate with doctors and other healthcare professionals for holistic patient care• Educate patients on preventive care and post-treatment exercisesQualifications:• Bachelor’s Degree or Diploma in Physiotherapy (BPT/DPT)• Valid registration with the relevant physiotherapy councilExperience:• Freshers or experienced candidates may applyKey Skills:• Strong knowledge of physiotherapy principles and rehabilitation techniques• Patient-handling and communication skills• Ability to work in a hospital or clinical environment• Compassionate and ethical approach to patient careKey Attributes:• Dedication, patience, and professionalism• Team-oriented with willingness to learn and adaptAbout the Company:Apollo Clinic, Beliaghata, is part of India’s trusted Apollo Healthcare network, committed to delivering high-quality medical services and patient-centered care. The clinic focuses on modern treatment methods, preventive healthcare, and professional development for its staff.
Role & Responsibilities • Provide medical leadership and oversight for medical safety and medical monitoring activities across assigned programs. • Ensure compliance with applicable federal, local, and international regulations and guidelines related to clinical research, safety, and Good Clinical Practice (GCP). • Review, assess, and interpret safety data from clinical trials and post-marketing sources. • Provide expert medical consultation and advice across multiple projects and assignments. • Establish priorities, manage deadlines, and ensure timely delivery of safety-related objectives. • Collaborate effectively with internal teams, senior management, and external clients. • Demonstrate leadership in project planning, execution, and financial management where applicable. • Support strategic decision-making related to safety risk assessment and benefit-risk evaluation. Qualifications • Medical degree from an accredited and internationally recognized medical school with curriculum relevant to general medical education. • Valid medical license or equivalent from the country or region of practice. • Strong understanding of clinical research, pharmaceutical development, and safety regulations. Experience • Minimum 5 years of clinical practice experience after award of medical degree, or equivalent combination of education, training, and experience. • Graduate medical training may be considered toward clinical practice experience. • Alternatively, 3 years of clinical practice experience with an additional 2 years as a pharmaceutical physician in any role. • Minimum 5 years of medical safety or medical monitoring experience in the pharmaceutical or related industry. Skills • Strong knowledge of clinical trial processes, pharmaceutical research, and safety regulations. • Excellent ability to manage priorities, objectives, and timelines effectively. • Strong consultation, advisory, and decision-making skills across multiple assignments. • Proven leadership skills with aptitude for project and financial management. • Ability to build and maintain effective working relationships with coworkers, managers, and clients. • Excellent written and verbal communication skills in English. About the Company • IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence, IQVIA creates intelligent connections to accelerate the development and commercialization of innovative medical treatments.
Roles & Responsibilities • Perform medical device complaint investigations in compliance with global regulatory standards • Conduct risk assessments and support product safety evaluations • Analyze device-related adverse events and technical complaints • Prepare, review, and maintain investigation reports with high documentation accuracy • Collaborate with cross-functional global teams for complaint resolution and root cause analysis • Ensure adherence to medical device regulations, quality systems, and SOPs Qualification • B.Pharm / M.Pharm • Biomedical Engineering / Mechanical Engineering • B.Sc Medical Imaging & Radiology Technology • Master’s in Molecular Biology • B.Sc Nursing • BDS (Bachelor of Dental Surgery) Experience • 0-5 years of experience in medical device investigation, complaint handling, or related safety/quality roles • Prior exposure to medical device safety processes preferred Skills • Strong knowledge of medical devices, complaint investigation, and risk assessment • Excellent verbal and written English communication skills • Good analytical, documentation, and problem-solving abilities • Willingness to work in rotational and night shifts • Ability to collaborate with global stakeholders Walk-In Details • Dates: 15th & 16th January 2026 • Reporting Time: 10:00 AM – 12:00 PM • Venue: Gate 1, Plot No. 8 & 9, Block DM, Sector V, Salt Lake, Kolkata, West Bengal – 700091 • Documents Required: Updated resume (CV) and original government ID proof About the Company Wipro is a global leader in IT, consulting, and healthcare & life sciences services, delivering end-to-end solutions across pharmacovigilance, medical devices, clinical research, and regulatory domains, with a strong focus on quality, compliance, and innovation.
Role & Responsibilities • Execute medical affairs strategy for the assigned geographic zone • Understand disease trends, treatment practices and therapeutic needs through KOL engagement, scientific meetings and journal reviews • Disseminate credible, non-promotional scientific information to internal and external stakeholders • Execute medical projects including IIS (Investigator Initiated Studies) • Support medico-marketing strategies and provide regular field insights to management • Identify and develop relationships with Key Opinion Leaders and Expert Experts (EEs) • Support registration of new products and indications by providing medical rationale, literature support and scientific presentations • Support defence of marketed products with regulators, NGOs and media as required • Write, review and revise labeling and scientific documentation as per SOPs • Support regulatory affairs activities and stakeholder engagement Qualifications • Medical degree (MD preferred, Pharmacology specialization preferred) or life sciences qualification Experience• 0–3 years of experience in Medical Affairs / Pharmaceutical / Healthcare industry (fresh MD Pharmacology graduates can apply) • Candidates without doctoral qualification require 10+ years of relevant field-based scientific experience • Strong scientific knowledge of Diabetes therapy area • Good interpersonal and communication skills Skills • Scientific communication and presentation skills • KOL relationship management • Medical writing and documentation skills • Analytical and field-insight generation ability • Basic IT proficiency (MS Office) • Ability to work independently in field medical roles About the Company • Boehringer Ingelheim is a global biopharmaceutical company active in human and animal health
Role & Responsibilities • Perform and interpret diagnostic imaging procedures including X-ray, CT Scan, MRI and Ultrasound • Review and report imaging findings accurately within defined turnaround time • Provide E-reporting support for PPP units (MRI & CT Scan) • Consult with referring physicians regarding imaging results and recommendations • Ensure strict adherence to radiation safety and hospital compliance protocols • Maintain accurate imaging records and patient documentation • Participate in multidisciplinary case discussions for patient care Qualifications & Experience • DMRD / DNB Radiology / DMRE / DM Radiology / DRIT • 1–2 years of post-qualification radiology experience • Strong diagnostic interpretation and reporting abilities • Good communication and clinical coordination skills Skills • Diagnostic imaging and reporting proficiency • Analytical and problem-solving skills • High attention to detail and report accuracy • Patient interaction and clinical coordination • Time management and efficiency in report delivery About the Company • Eskag Sanjeevani Pvt Ltd is a healthcare services organisation providing diagnostic and clinical services across PPP healthcare units, focused on delivering accessible and high-quality radiology services
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: • Dispense medications accurately and provide clear instructions on proper usage and dosage • Conduct patient consultations to assess medication needs and offer personalized guidance • Develop and support medication therapy plans in collaboration with healthcare professionals • Work closely with the medical team to ensure effective patient care and medication adherence • Maintain accurate patient records including medication histories and treatment plans • Stay updated on new drugs, therapies, and best practices in pharmacy care Qualification: • Bachelor of Pharmacy (B.Pharm) or equivalent qualification from a recognized institution Experience: • Freshers or candidates with relevant hospital or clinical pharmacy experience are welcome About the Company: Fortis Healthcare is one of India’s leading integrated healthcare delivery providers, known for its clinical excellence, advanced medical infrastructure, and patient-centric services. With a strong presence across hospitals, diagnostic centers, and specialty clinics, Fortis Healthcare is committed to delivering high-quality care while offering a professional environment that supports learning, growth, and excellence in healthcare services.
Role & Responsibilities • Assist in processing Adverse Events (AE) and endpoint data, including intake, tracking, and workflow distribution • Track safety case timelines and ensure timely submissions to clients and stakeholders • Support Lifecycle Safety database entry, quality control, and report generation • Coordinate safety report submissions to regulatory authorities and investigators • Maintain project files, case folders, and document control systems • Assist with project start-up activities, system access, and administrative workflows • Archive safety data and manage records post-study closure • Support database validation, user testing, and ad-hoc data searches • Coordinate meetings, courier dispatch, and administrative logistics • Mentor junior administrative staff and support continuous process improvement Qualification • Degree in Life Sciences, Pharmacy, Healthcare, or an allied scientific discipline Experience • Minimum 1 year of relevant experience in pharmacovigilance, clinical research, or safety operations Skills • Good understanding of GCP, ICH guidelines, SOPs, and safety workflows • Working knowledge of medical terminology • Proficiency in Microsoft Office and web-based applications • Strong organizational, multitasking, and time-management skills • Excellent written and verbal communication skills • High attention to detail, accuracy, and compliance About the Company • IQVIA is a globally recognized leader in clinical research, pharmacovigilance, and healthcare intelligence, supporting life sciences companies in the development and commercialization of innovative medical treatments.
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.
About role & responsibilities • Execute Medical Affairs strategy for CVRM products • Engage with healthcare professionals and scientific experts • Deliver scientific exchange and product education • Organize advisory boards, symposiums and medical events • Support real-world evidence and investigator studies • Gather and share actionable medical insights • Ensure compliance with PV, GxP and ethical standards Qualification • Master’s degree in scientific discipline • MD / PhD / PharmD preferred Skills • Strong scientific communication • Presentation and stakeholder engagement • Analytical and project management skills • Knowledge of pharmacovigilance and compliance Experience • Pharmaceutical / clinical research / medical affairs experience • Therapeutic area experience preferred Salary • Salary Competitive Benefits • Global medical affairs exposure • Career growth opportunities • Inclusive and collaborative culture About the company • AstraZeneca is a global science-led biopharmaceutical company • Focused on innovative medicines for serious chronic diseases • Operates across 100+ countries with strong R&D leadership
Job ID: 25650 About the Role Execute medical affairs strategy in the assigned zone, driving scientific engagement, medical projects, and regulatory support to strengthen Boehringer Ingelheim’s diabetes portfolio. Key Responsibilities Engage with HCPs, attend scientific forums, and review literature to gather insights on therapy trends Deliver clear, non-promotional scientific communication to internal and external stakeholders Execute medical projects including IIS studies Support medico-marketing strategy implementation Identify and develop relationships with KOLs and expert experts (EEs) Provide medical support for product registrations, new indications, and defense of marketed products Prepare and review labeling and regulatory documentation Support regulatory affairs with expert access Eligibility Medical degree (Pharmacology preferred) or Life Sciences qualification 0–3 years pharma/healthcare experience (Fresh MD Pharmacology graduates can apply) 10+ years field experience acceptable for non-doctoral candidates Strong scientific knowledge in diabetes therapy area Good communication and MS Office skills
About the role & responsibilities • Engage with pathologists, geneticists, oncologists, surgeons and laboratory physicians to support biomarker-based diagnostics • Build diagnostic pathways to streamline testing within clinical decision-making • Provide field support in priority oncology accounts using data-driven insights • Analyze testing patterns, turnaround times and access barriers • Conduct scientific training on biomarker science, diagnostic workflows and test interpretation • Develop educational tools and conduct clinician and lab scientific programs • Build partnerships with diagnostic companies and laboratory networks • Support implementation of companion and complementary diagnostics • Promote precision medicine adoption and early biomarker testing Qualification • Life sciences / pharmacy / medical graduate (biomedical, biotechnology, M.Pharm, PharmD, MBBS or related) Experience • 2+ years in medical affairs, diagnostics, oncology, biomarker or molecular pathology roles Skills • Oncology & biomarker knowledge • Diagnostic workflow expertise • Stakeholder engagement • Scientific communication • Data interpretation • Field collaboration & training About the company • Global pharmaceutical MNC focused on precision medicine and oncology innovation
About the Company • Boehringer Ingelheim is a global, research-driven pharmaceutical company focused on innovative therapies across human and animal health • Strong presence in medical affairs, clinical research, and regulatory compliance worldwide About the Role & Responsibilities • Execute medical affairs strategy and scientific engagement activities • Engage Key Opinion Leaders (KOLs) and Healthcare Professionals (HCPs) • Support medical projects and Investigator Initiated Studies (IIS) • Provide scientific communication and medical education • Support advisory boards, CMEs, and scientific meetings • Provide field-based medical support Qualification • MD preferred (Pharmacology desirable) or Life Sciences degree Skills • Strong scientific communication and presentation skills • Medical affairs and clinical research understanding • KOL and HCP engagement skills • Medical strategy execution capability • Good documentation and reporting Experience • 0–3 years Medical Affairs / Pharma experience • Fresh MD Pharmacology graduates are welcome Salary • Competitive salary package Benefits • Exposure to global medical affairs projects • Career growth opportunities • Continuous learning and development
About the Company • Johnson & Johnson is a global healthcare leader delivering innovative medicines and medical technologies across multiple therapeutic areas • Strong presence in immunology, medical affairs, and patient-focused research worldwide About the Role & Responsibilities • Act as the scientific liaison for immunology therapeutic portfolio • Map and engage Key Opinion Leaders (KOLs) for scientific exchange • Conduct medical affairs initiatives and scientific data presentations • Respond to healthcare professional scientific queries • Support CMEs, advisory boards, and scientific meetings • Provide field-based medical support with 70–80% travel Qualification • MD / MBBS / Pharm D / BDS / MDS Skills • Strong immunology domain understanding • Scientific communication and presentation skills • KOL engagement and stakeholder management • Medical affairs knowledge • Good documentation and reporting skills Experience • MBBS / MD: 0–3 years pharma or healthcare experience • Pharm D / MDS / BDS: 2+ years relevant experience Salary • Competitive salary package Benefits • Exposure to global immunology medical affairs projects • Career growth and leadership opportunities • Continuous learning and development
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.