613 Biomedical Jobs - Page 8

Oversee various biomedical engineering projects, including planning, execution, monitoring, and reporting of progress. Manage budgets for different projects and ensure that all expenses and invoices are processed accurately, within the given budget limits. Supervise the work of a team of biomedical engineers, ensuring that they remain motivated, focused, and aligned with project objectives. Ensure that all biomedical engineering projects meet regulatory compliance, quality, and safety standards.

Job Title Sr Image Quality Specialist Job Description Senior Image Quality Specialist In this role, you have the opportunity to be part of center of expertise on Image Quality (IQ) for Philips Image Guided Therapy -Mobile Surgery products and design, enhance IQ for new projects. This role supports Architects/designers, Application Specialists, Field Service specialists and Marketing. Global headquarter of Mobile Surgery, Philips HIC, Pune is playing a key role in Philips global strategy for Image-Guided Therapy. With Philips HIC, the foundation was laid to touch billions of lives and reiterate Philips commitment towards Indian and growth healthcare markets. Your role: Improve Image Quality (IQ) knowledge and expertise. Integral system IQ design Deliverable: IQ path system design. Contribute to Innovation/PRP studies from IQ specialism viewpoint System IQ requirements and decomposition of IQ to subsystem requirements Deliverable: IQ requirements are incorporated in the System and Subsystem requirements specifications Realizing that the system IQ is optimized per application area Deliverable: Optimized System IQ tuning sets. Integral system IQ verification and validation . Providing line support for IQ related issues in the field Deliverable: Solutions for IQ field issues / questions System engineering specific responsibilities. Carrying out System Engineering activities of assigned product(s)/product line(s) as per the global system engineering processes Define system architecture with focus on imaging chain under considerations of platform constraints Specify image chain requirements as part of a development project and document those requirements in various tools Be responsible for selection of image chain components and subsystems Analyze project ideas regarding realization options; evaluate impact on running projects with respect to image quality & product cost Test and verify selected components and subsystems against the requirements Be responsible to integrate image chain components, adjustment & calibration and verify the system with respect to meeting the safety, functional, performance, reliability and image quality requirements Evaluate the quality of X-ray Fluoroscopy images during the product development Evaluate new and competitive technology in terms of image chain subsystems Participate and perform risk analysis according to applicable medical device standards Youre the right fit if: M.Tech/ME in bio-medical engineering having IQ specialization with 5 -9 years of experience. In depth understanding of system wide IQ, combining IQ related theory (e.g. x-ray physics, image processing, visual perception, etc.) with understanding of relevant products and the application by the end-user. Good team player and ability to work independently & act pro-actively. Analytical, creative and abstract thinker. Ability to communicate (both written and verbal) on different levels. Is capable to introduce efficiency improvements on project level (change management). How we work together We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company s facilities. Field roles are most effectively done outside of the company s main facilities, generally at the customers or suppliers locations. This role is an office-based role. If you re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care here . #LI-PHILIN

Key Responsibilities: Lead and supervise the maintenance team including electrical, plumbing, HVAC, biomedical, civil, and general services personnel. Ensure smooth operation and maintenance of all hospital infrastructure including lifts, generators, water supply, HVAC systems, electrical systems, firefighting systems, and medical gas pipelines. Develop and implement preventive maintenance schedules for all critical equipment and infrastructure. Ensure timely resolution of all facility-related breakdowns and issues with minimal disruption to clinical operations. Oversee biomedical engineering support for maintenance and calibration of medical equipment. Monitor energy usage, initiate energy-saving measures, and manage utilities effectively. Ensure facility operations are in compliance with NABH, Fire Safety, Pollution Control Board, Biomedical Waste, and other statutory norms. Liaise with government agencies, external vendors, and contractors for facility upgrades, AMC/CMC, repairs, and inspections. Manage maintenance budgets, vendor contracts, and ensure cost-effective service delivery. Maintain accurate records of maintenance work, equipment history, and compliance documentation. Lead facility-related initiatives during hospital expansions, renovations, or new project implementations. Ensure safety protocols are followed by the maintenance team and that hospital infrastructure meets health and safety standards. Qualifications & Skills: Bachelor s degree/Diploma in Mechanical, Electrical, Civil Engineering or relevant technical field (mandatory). Minimum 8 12 years of experience in hospital/facility management, with at least 3 5 years in a supervisory or leadership role. Strong knowledge of hospital engineering systems, fire safety, HVAC, medical gases, and biomedical equipment. Familiarity with NABH and healthcare regulatory compliance standards. Ability to lead cross-functional teams and coordinate with clinical/non-clinical departments. Excellent troubleshooting, project management, and vendor management skills. Strong communication, analytical, and documentation abilities.

The Principal Biostatistician will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans (SAP), programming specifications for analysis datasets and provide QC done data packages including tables, figures, and listings for use in publications (ie, abstracts, posters, oral, presentations, manuscripts and ad-hoc data analysis requests) and to investigate the natural history of a TA diseases and long-term treatment outcomes of observational data using clinical trials and / or Registries as applicable; The Principal Biostatistician will ensure SOPs are followe'd, communications, timelines and quality metrics are met.; Collaboration of Local biostatistics and programming teams, Global Medical Affairs biostatisticians and / or programmers, and Global Medical Affairs Scientific Communications personnel. People: 1) Develop and maintain effective relationships and collaborations with the end stakeholders (Medical community) and local biostatistics and programming team members within the allocated Global business unit and product with an objective to develop statistical data outputs. 2) Support Sanofi Business Operations Leadership Team in understanding of stakeholders needs & expectations and provide end to end solutions for TAs/indications. 3) Coach/mentor new team members to support efficient and quick onboarding. 4) Support graduate hiring program as needed. Performance / Process: 1) Conduct appropriate post-hoc or ad-hoc statistical analyses of clinical trial data and / or registry (ie, Observational) data. 2) Design, develop, test, implement, and document statistical programming in high-level software packages eg SAS. 3) Produce we'll documented data packages that include tables, listings, and figures. 4) Work closely with the Team Lead Biostatistician and/or Team Lead Programmer to develop and implement project QC plans, timelines and KPIs. 5) Learn, implement, and share through lecture series at least one indication of disease and product (Immunology, Multiple Sclerosis and Neurology, Rare Diseases, Rare Blood Disorders and Oncology) expertise. 6) Review appropriate biomedical and clinical research literature related to assigned project(s). 7) Active participation and Effective contributing in project governance meeting to proactively discuss risks, issues related to timelines and quality of deliverables. 8) Present your selected / assigned topic in lecture series internal and / or across line functions thereby improving the statistical knowledge and presentation skills. 9) Use Advanced analytical methods & tools to provide dashboards to the stakeholders. Customer: Work closely with Global Medical Affairs biostatisticians and/or programmers to identify statistical analysis needs and assist in developing assigned deliverables About you Experience : Masters degree 8 years (M.Sc.) of experience required /Ph.D. in biostatistics or statistics or epidemiology (preferred) and 4 years. Soft skills : Stakeholder management, Ability to manage timelines and Ability to work independently and within a team environment, High proficiency in statistical methods used in the pharmaceutical industry, Autonomy in the management of activities; ability to manage multiple conflicting high priority deadlines. Technical skills : Advance SAS programming skills, SDTM & ADaM (CDISC) and other statistical computing software skills in a clinical data environment across multiple therapeutic areas. Education : Master of Science degree or equivalent in Statistics/ Ph.D. in biostatistics or statistics or epidemiology Languages : Excellent English language knowledge written and spoken

As a Lead Customer Service Specialist, you will be responsible for developing and maintaining strong interpersonal relationships with customer representatives, carrying out installation and maintenance all GE HealthCare Imaging equipment like CT, MRI, Cath Lab, C-ARMs, PETCT, Ultrasound etc and ensuring customer satisfaction in the assigned area. Job Description Roles and Responsibilities Technical: Maintaining all models specific to Multi-Modality Imaging Equipment in the assigned area. Total system level troubleshooting on complex multi-symptom problems Customer satisfaction: Daily interface with doctors and technicians on equipment status issues. Acts to ensure satisfaction to primary customers Business growth: Assists in the growth and direction of business in his/her geographic area Productivity: Responsible for Warranty and PMS contract cost control Administration: Responsibly completes all administration tasks on time. Ensures timely completion of FMIs and PMS inspections documentation for assigned accounts Installation: Plays a leading role in complex and multifunctional rooms Shares best practices. Maintain effective quality systems and programs compliant with ISO 9001 standard, according to the GE Service Quality Policy Statement Assists in account sales visits; helps train others where necessary; identify sales opportunities and communicate to account team. Incumbent will be based out of Patna and will support Bihar and Jharkhand territory. Required Qualifications Bachelors degree in Electrical & Electronics Engineering, Biomedical Engineering, Instrumentation Engineering, or related field and 8+ years of experience in servicing medical equipments like CT, PET CT, MRI, Ultrasound, Vascular and Surgery and Nuclear Medicine Experience interfacing with both internal team members and external customers as part of a solution-based service process Experience diagnosing and repairing mechanical, electromechanical, and/or electronic equipment Ability to be available after-hours and/or work a rotating on-call schedule, including weekends Desired Skills Strong oral and written communication skills. Ability to document, plan, market, and execute programs Candidate has to be flexible to work in any location thats assigned to him/her depending on business requirement. Sought by others for guidance and advice. Proficiency in English. Ability to work independently with minimum direction High work standards and quality Initiative and motivation. Plans and organizes work effectively Excellent communications, listening and interpersonal skills Strong Customer skills; deals tactfully and effectively with differences of opinion, influences rather than directs

Required Education - Diploma / Degree in biomedical engineering Experience- 2-5 yr for Degree and 5 - 8 years of experience for diploma holder in minimum 250+ Bedded Hospital ; Knowledge and Specific Skills knowledge of maintenance of medical equipments. Location: Gurugram For inquiries, kindly reach out to Mr. Uma Shankar Mohanta via email uma.mohanta@fortishealthcare.com Job Profile - To maintain records of all the maintenance activities carried out in the respective area. To carry out maintenance activities according to the schedule drawn. To maintain assets register. To maintain a list of spares for all the equipments maintained by him. To make immediate action in reducing the breakdown time of the equipment in their area. To consult with Biomedical Engineering HOD for procurement of new equipments. To Coordinate the Installation / Upgradation of equipment with Vendors To co-operate with Biomedical Engineer in giving training for the trainee. To perform any other work assigned by the HOD

Position:- Biomedical Engineer Qualification:- Graduation / Diploma Experience:- 1-5 Years Immediate joiner preferred. Interested candidate can share their resume:- Email:-hrd@metrohospitalfaridabad.com OR 9999202119

Senior Clinical System Designer- Office based- Bangalore/ Chennai/ Trivandrum We are currently seeking a Senior Clinical System Designer to join our diverse and dynamic team. As a Senior Clinical System Designer at ICON, you will play a pivotal role in designing and implementing advanced clinical systems that enhance trial design and execution. Your expertise will be essential in driving innovation and ensuring that our clinical systems meet regulatory requirements and support operational efficiency. What You Will Be Doing: Leading the design and development of clinical systems, ensuring alignment with study protocols and operational needs. Collaborating with cross-functional teams to identify opportunities for system enhancements and innovations in clinical trial processes. Overseeing system configuration, integration, and testing to ensure optimal functionality and user experience. Providing strategic guidance on the implementation of new technologies and best practices in clinical system design. Staying current with industry trends and advancements in clinical technology to drive continuous improvement initiatives. Your Profile: Advanced degree in a relevant field such as computer science, biomedical engineering, or a related discipline. Extensive experience in the design and implementation of clinical systems within the clinical research industry. Strong leadership skills and proven ability to manage cross-functional teams effectively in a matrix environment. Expertise in data analysis and interpretation, with proficiency in clinical data management systems and software. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive change in a complex organization. A commitment to maintaining high standards of quality and compliance in all system-related activities. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Senior Clinical System Designer- Office based- Bangalore/ Chennai/ Trivandrum ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Clinical System Designer to join our diverse and dynamic team. As a Senior Clinical System Designer at ICON, you will play a pivotal role in designing and implementing advanced clinical systems that enhance trial design and execution. Your expertise will be essential in driving innovation and ensuring that our clinical systems meet regulatory requirements and support operational efficiency. What You Will Be Doing: Leading the design and development of clinical systems, ensuring alignment with study protocols and operational needs. Collaborating with cross-functional teams to identify opportunities for system enhancements and innovations in clinical trial processes. Overseeing system configuration, integration, and testing to ensure optimal functionality and user experience. Providing strategic guidance on the implementation of new technologies and best practices in clinical system design. Staying current with industry trends and advancements in clinical technology to drive continuous improvement initiatives. Your Profile: Advanced degree in a relevant field such as computer science, biomedical engineering, or a related discipline. Extensive experience in the design and implementation of clinical systems within the clinical research industry. Strong leadership skills and proven ability to manage cross-functional teams effectively in a matrix environment. Expertise in data analysis and interpretation, with proficiency in clinical data management systems and software. Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive change in a complex organization. A commitment to maintaining high standards of quality and compliance in all system-related activities. What ICON can offer you: Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Job Category: Maintenance Technician Job Type: Full Time Job Location: Bangalore Qualification: ITI or Diploma Experience: 4 to 7 years of work experience Daily tasks include electrical and DG checks, patient room and utility area rounds, plumbing and electrical issue resolution, meter readings, and ensuring hot water availability. Waste management, wheelchair inspection, housekeeping coordination, and shifting of equipment are handled regularly. Responsibilities also cover biomedical equipment repairs, pest control follow-up, and purchasing of materials for maintenance needs. PG maintenance includes electrical/plumbing work, cot fixing, pest control, and bill collection. Vendor coordination is done for AMC services, waste management, and civil-related works.

Brief Description about the Project The ICMR-funded SecureUltrasound (SecureUS) Project is an innovative initiative focused on developing and validating a screenless ultrasound device aimed at addressing critical challenges in maternal healthcare. This project is driven by the need to improve the accessibility of Ultrasound and the ease of use in primary care settings and also overcome the shortage of skilled ultrasound operators in rural Indian health centers. This project is undertaken by Division of Medical Informatics at St. John s Research Institute and the India Institute of Science in Bangalore, which makes use of innovative tools and techniques to drive health systems research and healthcare innovation for improving healthcare outcomes with meaningful use of data. Project Research Scientist - I (Non-Medical) No. of Vacancy: Preferred Qualifications: MBBS with MPH (OR) BDS/ AYUSH with MPH/ Ph.D Maximum Age Limit Kannada, Telugu, Tamil (Optional) Experience: MBBS with MD Community Medicine (1 -2 years experience) MBBS with MPH (2 3 years experience) BDS/ AYUSH with MPH (5-6 years experience) 1. Experience in clinical research, medical device validation, or public health studies. 2. Experience in working on medical device research, maternal health, or community-based healthcare projects is preferred. 3. Experience in working in government health facilities is preferred. 4. Proficiency in data analysis software (SPSS, R, STATA, NVivo, or similar). 5. Experience in qualitative and quantitative research methodologies, data management, and literature review. 6. Prior experience in manuscript writing and research grant applications is desirable. 7. Familiarity with ethics approval processes and Good Clinical Practice (GCP) guidelines. 8. Experience in collaborating with national and international research organizations is an advantage. Employment Status: Contract (Initially for 6 month, extendable based on performance) Roles and Responsibilities: 1. Support the field implementation and clinical validation of the secure ultrasound device. 2. Assist in the design, implementation, and management of research activities related to the SecureUS Project. 3. Travel to project sites for field validation and stakeholder studies 4. Support data collection, management, and preliminary analysis for the evaluation of the screenless ultrasound device. 5. Work closely with the Project Research Scientist - Medical to coordinate field validation studies involving 192 pregnant women. 6. Collaborate with biomedical engineers, data scientists, and healthcare professionals to refine device features and research methodologies. 7. Develop survey instruments, interview guides, and research tools for stakeholder consultations, including hospital administrators and healthcare workers. 8. Conduct literature reviews and assist in drafting research papers, reports, and presentations. 9. Monitor project timelines, data quality, and regulatory compliance under the guidance of the medical research scientist. 10. Assist in grant writing and proposal development for securing additional funding. 11. Organize and participate in stakeholder meetings, workshops, and training sessions for research staff and healthcare workers. 12. Support field teams in troubleshooting data collection challenges and ensure adherence to ethical research practices. 13. Analyze qualitative and quantitative data using statistical software and visualization tools. 14. Maintain detailed project documentation, including research protocols, consent forms, and ethics committee submissions.

Job Title Norm Compliance Officer Job Description Norm Compliance Officer The purpose of this position is to handle end-to-end Norm Compliance activities for Diagnostic X-ray systems as part of the Research and Development team, with all relevant mandatory international and national regulations. Your role: Defining all applicable global product safety certification, product safety, EMC and environmental (if applicable) standards like IEC, EN, and ISO standards required to comply with all applicable international regulations. Define and review product requirements related to guidance, codes and standards to assure norm compliance and decomposition of standard requirements to the individual system or sub-systems. Preparation of norm compliance test plan that include applicable relevant clauses from standards (standards mainly include IEC60601-1, IEC60601-1-2, IEC60601-1-3, IEC60601-2-54, ISO 10993 etc.). Support in risk assessment related to product safety for achieving mitigation. Support usability and software teams to deliver documentation required for certification Support design and procurement team to ensure third party component level compliance Execute testing (witnessing, reporting and approval) of all specified product safety requirements. Arrangements of DXR product and required documents to test/certification agencies (like TUV/CSA/Any other lab) as part of submission and completion of certification activities. Support in preparing technical file deliverables (like GSPR and Compliance Data Record) in support to MDD, MDR, RED, REACH, RoHS regulations. Achieve certification of DXR products with all relevant global standards and regulations. Ensure timely delivery of all approbation activities / documentation adhering to Philips processes. Support the Regulatory team to achieve all regulatory approvals. Support all audits (FDA, Notified Body, INMETRO, etc). Review standard updates and provide standards gap assessment / technical support to the Regulatory team. Provide Training and guide all cross-functional teams on regulatory standards, update and execution. Maintain DXR compliance lab and its qualifications with CSA & Intertek as per ISO17025. Identification of approbation consequences due to change requests. Support factory inspections by certification agencies and address all audit observations in a timely manner (if applicable). Keep abreast of future upcoming regulatory & standards by interacting with notified body and standard organizations. Youre the right fit if: BE, BTech, ME, MTech degree (preferably in Biomedical/ Electrical/ Electronics/ Instrumentation). Minimum 10 to 15 years experience in product safety. Understanding of global mandatory / voluntary regulations like CE Marking, FDA, Health Canada, UL, CSA, INMETRO. Understanding of relevant standards (General Safety, EMC, Radiation Safety, Risk Management, Environmental, Sustainability, ISO17025, etc.). Knows how to participate in Design Reviews from norm compliance perspective Knowledge of regulatory submissions. Knowledge of X-ray systems will be an added advantage. Prior experience in product design will be preferrable. Excellent Communication skills. Understanding and implementation of good document practice (GDP). Strong hold on Compliance standards. Knowledge of Product safety and regulatory. How we work together We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company s facilities. Field roles are most effectively done outside of the company s main facilities, generally at the customers or suppliers locations. This role is an office-based role. If you re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care here . #LI-PHILIN

Bio Medical Engineer BACKGROUND The Hans Foundation (THF), established in 2009, is a Public Charitable Trust that works towards creating an equitable society to enhance quality of life for all through the empowerment of marginalized and underprivileged communities in India. The Hans Foundation works for the Health and Wellbeing of remote and under-served groups, with an additional focus on children, persons with disabilities and women. THF also works for holistic Education and Livelihood development of our communities. Our Two-Fold Strategy involves identifyinging and working within Aspirational Districts and high poverty index in the North, North-East and East regions within specific states, as well as catering to lower-income and migratory populations in cities, through urban programs. Over its 15 years of existence, THF has reached more than 35 million beneficiaries through its programs. THF works with communities through direct implementation of projects on the ground in addition to providing local management and monitoring support to not-for-profit organisations in India funded through THF USA and RIST. PROJECT The Hans Foundation has been operating more than 25 Hans Renal Care Centers on self-Implementation mode since January 2022. HRCC intervention is an innovative model of healthcare delivery that could help alleviate health disparities among vulnerable populations and individuals with chronic Kidney diseases. GENERAL Location of Job: Ranchi 1. JOB PURPOSE The role of a biomedical engineer is pivotal in the smooth functioning of equipment at HRCC. The biomedical engineer will take diligent care for the smooth functioning of medical devices and also manages maintenance of the same. This position will be based in one of the HRCC in Garhwal region and will extend the service and support for all the HRCCs in Uttarakhand. 2. KEY ACCOUNTABILITIES Pre-purchase Evaluation & Negotiation in Procurement of the consumables for HRCC. Commissioning and Installation Post Procuring the equipment and machineries at HRCC. Training: biomedical engineers give training to HRCC staff with the device to teach them the complete functioning and application of the device. Breakdown Management: This includes various categories like management of maintenance contracts, analysis of equipment failure, assessment of repair cost, scheduling of repair/PM visits, monitoring and documentation Support and facilitating the Inspection of Equipment : This includes various audits done by internal or external team. Equipment Risk Management to reduces the preventive maintenance requirement and internal device surveillance along with changes in standards. Documentation of all Condemnation-if not repaired or out of use: The devices which cannot be used or repaired should be labelled as condemned devices, such category devices need to be listed and documented. Maintains supplies inventory by checking stock, anticipating needs, placing and expediting orders, and verifying receipt. Prepares biomedical reports by collecting, analysing, and summarizing information and trends. Maintains patient confidence by keeping information confidential. Maintains safe and healthy working environment by conducting safety tests, recommending and complying with procedures, training and guiding medical and healthcare personnel and complying with codes. DOCUMENTATION Ensure that documents like AMC, consumables, medicines and reagents consumption, Machines etc. are updated and maintained regularly where you will visit. Supervise and inspect the requisition the availability of inventory and supplies of drugs, reagents, medical equipment & instruments as required at HRCC Centre. Attend the periodic review meeting organized by THF team. Maintain the confidentiality of the patient data and adhere the IPHS/IMC protocols for the treatment. Share the success stories/anecdotes from the field. 4. Reporting to : Project Manager/Project Coordinator/Sr. Associate Programme 5. Other Indicative Requirements Educational Qualifications B.Tech- Bio Technology Functional / Technical Skills and Relevant Experience & Other requirements (, Language, Certifications etc.) Minimum of 5 years of experience in public health programs with good team management skills. Candidate must have good communication skills in Hindi & English.

Macgence is a leading AI training data company at the forefront of providing exceptional human-in-the-loop solutions to make AI better. We specialize in offering fully managed AI/ML data solutions, catering to the evolving needs of businesses across industries. With a strong commitment to responsibility and sincerity, we have established ourselves as a trusted partner for organizations seeking advanced automation solutions. Fueled by our human expertise, our team has executed projects enabling cutting-edge technology that has revolutionized automation in many sectors. We do this by harnessing the power of human-generated AI and ML thus facilitating seamless global business automation and enhancing efficiency and productivity. At Macgence, we are committed to providing our customers with high quality, timely solutions that address their specific needs and challenges. We understand the crucial role of accurate, reliable human-generated data in driving AI and ML systems. As a result, we leverage our expertise to curate high-quality ~ 95%+ accuracy datasets . These datasets fuel innovation and deliver tangible results. Partnering with Macgence means gaining a trusted ally in your journey towards leveraging the power of AI and ML. We are dedicated to empowering businesses, optimizing processes, and driving growth through our innovative data solutions. Job Overview: We are looking for a dedicated and detail-oriented individual to join our team as a Medical Annotation Specialist. In this role, you will play a critical part in the development of machine learning algorithms for medical imaging analysis and healthcare applications. Your primary responsibility will be to annotate medical images and data accurately to support the training and validation of AI models for diagnosis, treatment planning, and research purposes. Key Responsibilities: Annotate medical images such as X-rays, CT scans, MRI scans, histopathology slides, and other modalities with annotations including anatomical structures, abnormalities, and clinical findings. Follow established annotation guidelines and protocols to ensure consistency and accuracy in the annotated datasets. Utilize annotation tools and software to perform tasks efficiently while maintaining high-quality annotations. Collaborate closely with radiologists, pathologists, clinicians, and other healthcare professionals to understand annotation requirements and clinical context. Verify and validate annotations to ensure they meet quality standards and are suitable for training machine learning models. Keep detailed records of annotation tasks, including documentation of annotation guidelines, specifications, and any issues encountered. Provide feedback and suggestions for improving annotation workflows, tools, and processes. Stay updated on developments in medical imaging technology, AI in healthcare, and annotation methodologies. Qualifications: Bachelor s degree in a relevant field such as Biology, Bioinformatics, Biomedical Engineering, Computer Science, or a related discipline. Advanced degrees are a plus. Strong understanding of medical imaging modalities, anatomy, and pathology. Familiarity with medical terminology, clinical concepts, and healthcare practices. Proficiency in using annotation tools and software for medical image annotation. Excellent attention to detail and ability to maintain accuracy while working with complex medical data. Effective communication skills with the ability to collaborate with multidisciplinary teams and healthcare professionals. Ability to work independently, manage time effectively, and meet project deadlines. Previous experience in medical imaging, healthcare, or data annotation is preferred but not required. Why Join Us: Opportunity to contribute to the advancement of medical technology and improve patient care through AI-driven solutions. Collaborative and supportive work environment with opportunities for professional growth and development. Competitive compensation and benefits package. Make a meaningful impact on healthcare outcomes and medical research with your annotation expertise. If you are passionate about healthcare, medical imaging, and leveraging AI to address healthcare challenges, we encourage you to apply for the position of Medical Annotation Specialist and join our dedicated team. For more enquiry: https: / / www.linkedin.com / company / macgence / Job Category: operations Job Type: Full Time Job Location: noida

Responsible for entire EHS in the Unit of Amneal Oncology Private Limited and supported by the other staff. Reporting and co-ordination with Unit Management, operation and maintenance of treatment / control equipment, delegation of day to day duties to the staff of EHS wing, liaison and correspondence with regulatory agencies and timely submission of data, reports, etc. to related Government and Regulatory Agencies, CETP, TSDF, monitoring and analysis including third party assessment, procurement of new equipment / instruments, preparation of documents and data-base, imparting training and identification of external training needs. Prepare and implement EHS specific SOP s as per site condition. Operation of ETP facilities without any major breakdowns. Hazardous Waste segregation, collection and disposal. Bio-Medical Waste Segregation, collection and disposal. To form Emergency Rescue Team (ERT) and provide training on Fire Fighting with Fire Extinguishers regularly as per Factory Act, 1948. To form First Aid Team members and organize External training by external agency as per Factory Act, 1948. Implementation Work Permit system and Responsible for issuance of work permit, checking appropriate PPEs & filling record. Responsible for timely submission of legal submission of legal/regulatory documents viz Environmental Audit Statement (Form-V), Returns for filing Hazardous Waste (Form - IV), Monthly Reports, etc. Responsible for filling logbooks related as per cGMP norms related to EHS. Regular inspection of Plant safety and working conditions. Investigation of Incidents/accidents. Safety instructions to employees for storage, handling & processing of chemicals. Responsible for coordinating with Environment Monitoring Team during their visit. External customer to Telangana State Pollution Control Board (TSPCB) Inspector of Factories Third parties Coordinate internal trainings for new joinee and existing employees including SOP related training. Coordinate with other department coordinators for compliance of cross functional Training. Responsible for training management activities Responsible as department training coordinator (DTC) Activities other than described in the job responsibility are to be done under the instruction of HOD.

Ideal Candidate Profile Manager (Device Equipment Sales) West Zone (Mumbai-Based | Individual Contributor Role) Company Overview We are a leading importer and distributor of advanced aesthetic and medical devices, proudly serving 2000+ doctors across India . With a robust presence in Mumbai, Delhi, Kolkata, Chennai, Hyderabad, Bangalore, Kerala, Gujarat, UP and Madhya Pradesh , we continue to innovate and shape the future of aesthetic healthcare in India. As part of the AgeLess Group , our diverse ecosystem includes: The AgeLess Clinic – Flagship premium aesthetic centers The AgeLess Institute – Education & training division HLYWD MD – Luxury skincare brand CliniNeo – In-house innovation & device manufacturing Ageless Retail – Online product selling platform Ageless Advance Hair Studio – Hair restoration & aesthetics Role Overview We are seeking a high-performing, self-driven Sales Manager to drive individual B2B sales of high-value aesthetic and medical devices. The ideal candidate will have a strong background in hardcore equipment sales and the ability to individually engage and convert doctors and clinics . Role Type: Individual Contributor (Hybrid Model – Field + Office) Location: Mumbai Head Office (West Zone Focus) Reports to: Group Company COO Working Hours: 10:00 AM to 7:00 PM Working Days: Monday to Saturday Experience Required: 7–20 years in device sales with leadership exposure CTC: 8 – 15 LPA + Attractive Incentive Scheme Monthly Target: - INR 50 TO 75 Lakhs (Male, preferred age bracket 25–50) Preferably: - selling electronic items, biomedical devices, and capital equipment across healthcare, industrial, or tech-driven sectors. Proven success in B2B sales, product demonstrations, installation support, and client relationship management. Industries from Which Candidates Are Preferred Medical Devices Surgical Equipment Biomedical Equipment Aesthetic Devices Electronic Equipment / Technology Solutions UPS & Power Backup Solutions (B2B High-Value Sales) Any electronic industries Devices & Aesthetic Equipment Suppliers Lumenis India – Laser and IPL technologies Alma Lasers India – RF, laser, and skin tightening platforms Hydrafacial India (authorized partners) Venus Concept – RF and aesthetic platforms Fotona India (Timewalker / Starwalker) – Q-Switch, Er:YAG lasers Cosederma Timeless Inmode Top Surgical Equipment Companies in India 1. B. Braun Medical India Pvt. Ltd. German-origin multinational with strong India presence Products: Surgical instruments, sutures, infusion therapy, OT solutions Known for: High-quality and innovation in surgery & healthcare 2. Johnson & Johnson Medical India Products: Surgical staplers, endo devices, orthopedic implants, sutures Key Segment: General surgery, minimally invasive surgery, orthopedics 3. Stryker India Global leader in surgical and medical equipment Products: Surgical instruments, endoscopy, surgical navigation, ortho implants Focus: Advanced surgical & robotic technology 4. Medtronic India Pvt. Ltd. Products: Energy-based surgical devices, staplers, electrosurgical units Known for: Cutting-edge technologies and devices in laparoscopy, neuro, and spine 5. Olympus Medical India Products: Surgical endoscopy, imaging systems, ENT, urology instruments Specialization: Minimally invasive surgical tools Leading Indian Surgical Equipment Manufacturers 6. Hindustan Syringes & Medical Devices Ltd. (HMD) Products: Syringes, surgical blades, catheters, needles Known for: DispoVan, trusted brand in hospitals & government procurement 7. Transasia Bio-Medicals Ltd. Products: Diagnostic + surgical/lab equipment Reputation: India's largest IVD company, with surgical diagnostics too 8. LifeLine Biz Pvt. Ltd. Products: Surgical instruments (orthopedic, general, ENT, neuro) Exporter and domestic supplier across India 9. GPC Medical Ltd. (Delhi) Products: Surgical instruments, orthopedic implants, hospital furniture Focus: One of India’s largest OEM & export players 10. Alan Electronic Systems Pvt. Ltd. Products: Electro surgical units, cautery machines, monitors Focus: Advanced Indian tech for OT and critical care Must-Have Skills & Attributes Proven Sales Record – Strong B2B track record in closing high-ticket equipment deals with hospitals, clinics, or medical professionals. Excellent Communication – Fluent in English (spoken & written); skilled in delivering demos and senior-level presentations. High Conversion & Objection Handling – Skilled in convincing decision-makers, handling resistance, and driving closures. CRM Proficiency – Hands-on experience with tools like Zoho CRM , Salesforce , or equivalent. Tech-Savvy – Proficient with Excel, PowerPoint, and Word for reporting and proposals. Target-Driven – Consistently delivered or exceeded INR 50 TO 70 Lakhs monthly sales targets . Preferred Attributes Experience selling to Electronic items, dermatologists, cosmetologists, or aesthetic clinics . Familiarity with channel/distributor management . Willingness to travel across the West Zone or pan-India. Prior experience managing zonal or regional sales teams (though this role is individual at present). Key Responsibilities 1. Sales Strategy & Execution Build and execute territory-wise strategic sales plans to meet/exceed targets. Conduct market research and competitor analysis to identify growth opportunities. Actively meet B2B doctors and clinics individually to convert sales. 2. Business Development Identify and onboard new clinic partners across West India. Present product demos and clinical benefits persuasively to drive product adoption. 3. Customer Relationship Management Cultivate strong, long-term relationships with doctors, clinic managers, and key stakeholders. Ensure excellent post-sales service and address escalations swiftly. 4. Sales Reporting & CRM Oversight Maintain accurate sales activity records and update CRM regularly. Generate monthly/quarterly sales reports and pipeline forecasts. 5. Cross-Functional Collaboration Liaise with marketing, training, and service teams for smooth execution of sales campaigns and after-sales support. Share market intelligence to support product positioning and enhancements. Requirements Proven experience as a Sales Manager / Individual Sales Contributor in device/equipment sales. Strong B2B selling skills, field sales exposure, and hands-on closing capabilities. Bachelor’s degree in Business, Science, or Healthcare field; Electrical/electronic engineer, Bio medical engineer, Science and physics preferred. High emotional intelligence, resilience, and self-motivation. Willingness to travel as needed (Mumbai-based with regional movement). What We Offer Competitive base salary + performance-linked incentives Health Insurance Career growth & learning opportunities in a rapidly expanding ecosystem A collaborative and innovation-driven work environment

Role & responsibilities Prepare and maintain operation theatre Maintain equipment support in an acute care environment Identify and move to maintain a sterile field Follow infection control policies and procedures Manage and maintain theatre equipment Prepare patient for operative procedures Provide intra-operative equipment and technical support Assist anesthetist in handling emergencies outside of OT Room Preferred candidate profile Qualification - Diploma / B. Sc. (Operation Theater) Experience - 0-2 yrs Perks and benefits As per market standards

India's Hiring for Big Healthcare Enterprise KTPL Technologies Private Limited. Position Hiring: Engineer Trainee for Rajasthan No. of Vacancies: 20 (Looking for Freshers Only) Company Profile: About KTPL Technologies Pvt. Ltd.: Founded in 1993 by the late Mr. Vikram Kirloskar with the name of Kirloskar Theratronics Pvt. Ltd. and further changed to KTPL Technologies (formerly Kirloskar Technologies Pvt. Ltd.) w.e.f . began its journey with a vision to transform Indias healthcare landscape through advanced medical technologies and solutions. What started as a modest venture with a team of 15 employees across three locations has evolved into a robust organization of 650+ professionals, delivering excellence across India and globally. Over the past 30 years, KTPL has built a reputation for reliability, customer focus, and pioneering spirit. The company has served more than 75,000 customers , spanning leading public and private healthcare institutions, and has successfully executed international healthcare technology projects. In 2024, KTPL entered an exciting new phase under the leadership of renowned businessman Mr. Kamal Gupta , who took over the company with a vision to scale new heights, strengthen the foundation, and accelerate KTPLs journey toward global excellence. Position Objective: Responsibilities include planning and managing the services of medical equipment and optimal use of resources. Job Responsibilities: Service Support: Responsible for providing periodic maintenance services, timely resolution for equipment malfunctions, troubleshooting, and repair of electronic and electromechanical equipment onsite service. Preventive and Corrective maintenance of Biomedical Equipment. Coordinate with service contractors for maintenance, calibration, and collection of service documents. Training customers on equipment operation, maintenance procedures and process related to the upkeep of equipment. Key Account/Customer Relationship Management: Responsible for building and managing key customers as well as building and strengthening customer relations by timely follow up and support to the customers. Responsible for the closure of all assigned calls. Timely submission of documents (service reports, PM reports, etc.) to the branch office. Responsible for the daily scheduling of engineers and providing daily updates to BSM. Follow up with the service coordinator for spares required to rectify the equipment. Responsible for grooming of Engineers technicians reporting to him. Education and Experience Requirements: B.E/B.Tech in Biomedical Engineering/ Medical Electronics/ Electronics & Electrical / Electronics & Telecommunication, and Instrumentation. Diploma in Electronics Engineering, Electronics & Telecommunications, or Electrical Engineering. Experience: Fresher Expertise in the repair, calibration, and maintenance of medical equipment. High level of customer focus and good communication skills with a pleasing personality. Self-motivated and self-directed with the ability to create and manage their own schedule. WE REQUIRE AMBITIOUS PEOPLE WITH PROFESSIONAL IMAGE, GOOD ATTITUDE, AND MENTALITY TO GROW WITH THE COMPANY. Salary Range: Salary will not be a constraint for the right candidate, and it may vary based on experience and skill set.

Support the team in the development of route plan for the MMU; Provide preventive, promotive and curative health care and referral services to patients during MMU-OPDs; Document processes and maintain health records of patients as per project requirement; Utilize, supervise and manage stock of medicines, healthcare products and reagents for regular MMU services; Supervise safe disposal of biomedical wastes; Network with other medical professionals/ specialists in and around the project site and solicit their support as and when need arises; Encourage health literacy amongst the target audience; Supervise functions and quality of services of the MMU technical team; Provide regular need-based technical training to MMU team; Support the team in compilation and submission of progress report; and Perform other tasks which may be assigned by the reporting manager from time to time. MBBS Team Wok, Proactive

Position Title: HCOO Scope of Responsibility Operations India Country Department General Administration Services Position Level Others: Employment Status Full Time Work Location type Unit Reports to title: Group CEO Date Written/Revised 1 January 2022 Position Statement: The objective of this role is to facilitate the use of best practices with the latest technologies in the hospital to achieve optimum service satisfaction from both internal/external customers. Position Summary: KEY RESPONSIBILITIES Ensure a healthy profitability matrix through innovation cost optimization and revenue maximization measures and maintain a positive P&L Developing and implementing standardized processes for administration. Conducting inventory management of all branches and monitoring unit inventory utilization. Organizing and conducting events and workshops. Monitoring allocation of rooms/beds and their utilization. Coordinating with HR Department on manpower requirements, utilization, welfare, training and discipline. Developing and implementing policy and process manuals for administrative procedures. Handling media and preparation of media reports. Developing proposals for various donors. Overseeing deployment of biomedical engineering equipments. Creating a strong and empowered team at the hospitals to manage patient care. Coordinating with the quality consultants in developing and documenting quality management systems in the form of manuals, system procedures, departmental procedures and work instructions. Overseeing the day-to-day operations of all departments. Ensuring hospitals operate efficiently and provide adequate medical care to patients. Ensuring adequate and responsive fire-fighting and security arrangements. Ensuring that revenues are generated as per targets projected and expenditure is controlled as per legitimate requirements and within the annual projections. Maintaining all fixed and movable assets, their proper accounting and utilization. KEY PERFORMANCE INDICATORS High profitability and positive P&L Ensuring patient satisfaction levels. Overseeing bed occupancy and effective utilization. Enhancing operational efficiency. Monitoring internal customer satisfaction levels. Ensuring compliance to quality systems. Ensuring adherence to Standards Operating Procedures. Required Qualifications Preferred Behavior Skills Please list specific qualifications/experience, knowledge, skills and abilities needed for this position: MHM / MBBS Ability to handle a team of functional and technical professionals 15-18 years of relevant experience in hospital administration. . Project management and evaluation experience. Communication skills Observational, critical thinking and design thinking skills Teamwork and people skills Ability to take initiative Ability to deal with emotionally charged and difficult situations Resilience Empathy License/ Certificates - Years of related experience 15+ Years of management or supervisory experience 10+ Management or supervisory experience type General Manager Addl requirements (i.e. % of travel, etc.) 10% travel included I have read and acknowledge receipt of the above Job description. . Name & Signature of Team Member Date

Christian Medical College is looking for Physical Medicine and Rehabilitation to join our dynamic team and embark on a rewarding career journey Diagnose and treat patients with physical impairments Create therapy plans and oversee rehabilitation progress Work with physiotherapists and occupational therapists Promote recovery and pain management

Job Description: We are looking for a dynamic and motivated Sales Engineer to join our growing team in Coimbatore. This is an exciting opportunity for fresh graduates who are technically inclined and have an interest or background in the healthcare domain. You will play a key role in bridging the gap between technical products and customer needs. Please note: This role may involve on-the-road sales activities, including visiting clients for meetings, demonstrations, and support. Key Responsibilities: Engage with clients to understand their requirements and provide technical solutions. Present and demonstrate products to prospective customers. Collaborate with the sales and technical teams to craft customized proposals. Develop strong product knowledge and stay updated on industry trends. Follow up with leads and maintain long-term customer relationships. Provide post-sales support and customer training as needed. Travel to client locations for demos and meetings when required. Required Skills: Strong communication and interpersonal skills. Technical aptitude and eagerness to learn about product specifications. Ability to understand customer requirements and recommend solutions. Good presentation and negotiation skills. Willingness to travel for . for . We offer a dynamic work environment, opportunities for

Job Description Summary Job Summary: The Product Safety and Standards Compliance Engineer will be responsible for ensuring that all medical devices and related products adhere to applicable safety standards and regulations. The role involves conducting thorough safety assessments, identifying potential hazards, collaborating with design teams to mitigate risks, and maintaining compliance throughout the product lifecycle. This position is crucial for prioritizing patient safety and ensuring regulatory adherence within the healthcare industry. . Job Description Key Responsibilities: Risk Assessment and Hazard Identification: Perform detailed safety analyses on new and existing medical devices to identify potential hazards and assess their associated risks using methodologies like Failure Mode and Effect Analysis (FMEA) and other risk management tools. Conduct thorough reviews of product designs, materials, and manufacturing processes to identify potential safety concerns. Compliance with Regulatory Standards: Stay updated on relevant international and national healthcare regulations (e.g., FDA, ISO 13485, IEC 60601) and ensure products comply with all applicable standards. Develop and maintain compliance documentation, including technical files, risk management plans, and product safety reports. Design Input and Collaboration: Work closely with product development teams to integrate safety considerations into product designs from the early stages of development. Provide technical expertise on safety standards and regulations to engineering teams to ensure safe product design and implementation. Testing and Certification: Oversee product testing and certification processes to verify compliance with safety standards, including collaborating with external testing laboratories. Analyze test results and interpret data to identify potential safety concerns. Incident Investigation and Corrective Action: Investigate reported product safety incidents, analyze root causes, and implement appropriate corrective actions to prevent recurrence. Monitor post-market surveillance data to identify safety trends and take proactive measures to address potential issues. Training and Awareness: Conduct training programs for cross-functional teams on product safety principles, regulatory requirements, and risk management practices. Required Skills and Qualifications: Bachelors degree in Biomedical Engineering, Mechanical Engineering, or a related field. Strong understanding of medical device regulations and standards (e.g., FDA 21 CFR Part 820, ISO 13485, IEC 60601). Expertise in risk management methodologies and tools. Excellent analytical and problem-solving skills. Strong communication and collaboration skills to work effectively with cross-functional teams. Experience with product development lifecycle and design control processes. Ability to stay updated with emerging safety standards and regulatory changes. Preferred Qualifications: Master s degree in a related field. Certification in quality management systems or risk management. Prior experience in a similar role within the healthcare or medical device industry. Working Conditions: Office environment with occasional travel to manufacturing sites, testing laboratories, and industry conferences. Ability to work in a fast-paced and dynamic environment with strict regulatory timelines. Inclusion and Diversity . Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you d expect from an organization with global strength and scale, and you ll be surrounded by career opportunities in a culture that fosters care, collaboration and support. #LI-Hybrid #LI-MP2 #EveryRoleIsVital Relocation Assistance Provided: Yes

Career Category Safety Job Description The Global Safety Therapeutic Areas serve as the safety experts for all Amgen products globally and are accountable for the safety strategy and major safety deliverables for each Amgen product. Leaders in the therapeutic area safety teams are accountable for the staff management and resource allocations in Global Patient Safety and support GPS in the establishment of a highly effective global safety organization in full compliance to worldwide regulations. The Global PV Sr. Scientist works with the Therapeutic Safety Teams for safety assessment activities for medical/scientific operations. This person will also provide scientific and compliance expertise as needed to GPS. Applicable tasks may vary by product(s) assigned. The Global PV Sr. Scientist is responsible for the following: Directs the planning, preparation, writing and review of portions of aggregate reports Organize and direct liaison for activities with affiliates and other internal Amgen partner regarding products Supports and provides oversight to staff with regards to safety in clinical trials to: Review and provide input and support on study protocols, statistical analysis plans and other clinical study-related documents Review of AEs/SAEs from clinical trials as needed Review standard design of tables, figures, and listings for safety data from clinical studies Participate in development of safety-related data collection forms for clinical studies Participate in study team meetings as requested or needed Signal detection, evaluation, and management- Perform data analysis to evaluate safety signals and write up analysis results Documents work as required in the safety information management system Author Safety Assessment Reports and other safety documents and regulatory responses in collaboration with the GSO Search and review adverse event data, literature, and other safety-relevant data for the purpose of signal detection Prepare presentation of the Global Safety Team s recommendations on safety issues to the cross-functional decision-making body Assist GSO in the development of risk management strategy and activities: Provides contents for risk management plans Develop or update strategy and content for regional risk management plans Assist GSOs to oversee risk minimization activities including tracking of activities as needed. Evaluate risk minimization activity Prepare response to regulatory inquiries related to risk management plans under the guidance of GSO Support activities related to new drug applications and other regulatory filings Assist GSO in developing a strategy for safety-related regulatory activities Provide safety contents for filings Inspection Readiness Undertake activities delegated by the QPPV as detailed in the PV System Master File and maintain a state of inspection readiness Be representative and point of contact for Health Authority Inspection and Internal Process Audits within the remit of role and responsibility Knowledge and Skills Processes and regulations for pharmacovigilance and risk management Drug development and lifecycle management Safety data capture in clinical development and post-market settings Safety database structure and conventions MedDRA and other dictionaries used in pharmacovigilance Methods of qualitative and quantitative safety data analysis Product and disease state knowledge Risk management and risk minimization Inter-relationship across various pharmacovigilance processes and documents, including reference safety information and product labelling Advanced understanding of interfaces across various pharmacovigilance and risk management processes Internal organizational and governance structure Pharmacovigilance skills-intermediate knowledge of the following: Signal detection, evaluation and management Aggregate data analysis, interpretation and synthesis Good clinical and scientific judgment Application of medical concepts and terminology Document writing and source document review Writing Risk Management Plans Ability to convey complex, scientific data in an understandable way Ability to analyze and interpret complex safety data Intermediate skills in application of statistical and epidemiological methods to pharmacovigilance Biomedical Literature-intermediate skills: Literature Surveillance: source document review knowledge and skills Literature search, evaluation and assessment skills-ability to search literature databases to identify safety literature for signal evaluation and assessment, interpretation and synthesis skills Other skills-intermediate skills in the following Organization, prioritization, planning skills Collaboration with cross-functional team settings Meeting management and time management skill Process and project management Critical scientific assessment and problem solving Strong Written and verbal communications skills, including medical/scientific writing Computer skills (e.g., MS Office Suite and safety systems) Strategic thinking Influencing and negotiation in a cross-functional, matrix environment Presentation skills for conveying complex technical contents to non-expert audiences KNOWLEDGE Broad PV knowledge with expertise within defined subject area Applies knowledge and broad understanding of multiple disciplines Understands impact of emerging scientific/technical trends and their implications for Amgen PROBLEM SOLVING Analyzes and forecasts scientific/technical trends Develops solutions to problems through in-depth analysis, coordination and negotiation with key decision makers Performs complex work-flow analysis on processes impacting multiple areas across the organization Adapts and integrates own experience with Amgen-wide strategy Develops innovative solutions to problems without precedent Proposes new processes to achieve strategic business objectives Works in partnership with GPS team to develop business plans that support the direction of the business AUTONOMY Guided by business plans and strategy Executes strategy, goals and changes within area of responsibility Contributes to strategic decisions affecting the discipline Guides ideas through development into a final product CONTRIBUTION Contributes to business results through quality of results, advice and decisions related to the operations of the discipline Designs and develops global processes, systems and/or applications Contributes to organizational through leadership May accomplish business results through leveraging a team of professionals and/or managers Develops mutually beneficial strategic alliances with internal and external contacts Education & Experience (Basic) Doctorate/Master s degree/Bachelor s degree and 12 to 17 years of directly related experience Education & Experience (Preferred) BS or BA in Life Science with a MS and 12 years of related experience And 2 years of managerial experience directly managing people and or leadership experience leading teams, project, programs or directing the allocation of resources Clinical/medical research experience 6 years of experience in a biotech/pharmaceutical/CRO setting Previous management and/or mentoring experience .

Develop and execute the product strategy for Drug Delivery Single Use Bags and Devices. Work closely with R&D, regulatory, and sales teams to ensure successful product development. Conduct market analysis to identify opportunities for new products and improvements. Define product specifications, pricing, and positioning. Manage product lifecycle, from conception to commercialization. Oversee regulatory compliance and quality standards. Develop sales training materials and marketing strategies. Build relationships with key industry experts and healthcare professionals. Qualifications & Requirements: Bachelor s/Master s degree in Biomedical Engineering, Biotechnology, or Life Sciences. 5+ years of experience in product management within the medical device industry. Expertise in Drug Delivery Single Use Bags and Devices. Strong knowledge of ISO 13485, FDA, and MDR regulations. Excellent project management and leadership skills.