464 Biomedical Jobs - Page 16

This role involves significant collaboration and communication across organizational boundaries to deliver the right information to Product Teams at the right time and deliver information from Product Teams to stakeholders to ensure we develop smooth processes that work well for the needs of BR and RX. Job Description Key Responsibilities: In collaboration with Product Line leadership, Product Teams, Engineering, Operational Excellence, Infrastructure, Security/Compliance, Technology and User Services, and other key stakeholders, the Application Operations Coordinator is accountable to ensure efficient and effective execution of prioritized operational activities for Product Teams. This is a coordination role, working across teams to spread better practices, ensure clear communications, and to create an environment where teams can succeed and measure their success in delivering on operational priorities. Specifically, this role is accountable to: Serve as the primary point of contact at the interface between infrastructure and security/compliance teams and Product Lines and Product Teams for application operations related activities relevant to applications in scope of product teams Promote and enable effective bi-lateral relationship and collaboration between colleagues in RX engineering, RX operational excellence, RX user support groups, and RX problem management. Ensure seamless and efficient execution patterns between Product Teams and Product Lines, for example, identifying vulnerabilities common across product lines and ensure an efficient and effective approach to addressing them. Provide timely and effective communication in to help teams deliver on operational priorities (including but not limited to vulnerability remediation, disaster recovery, backup/restore testing, and end-of-life activities for operating systems, databases and hardware). Coordinate across teams to ensure sustainable and effective process adoption, working with Operational Excellence to develop and drive improvement of key operational value metrics, and ensuring up-to-date application documentation. Be the primary point of contact for execution of monthly and quarterly maintenance activities for Product Teams, ensuring smooth maintenance windows, coordination with corporate IT and frequent, clear communication of key actions, information, and updates to Product Teams. Facilitate and support our cultural mindsets and organizational culture of operational excellence. Use metrics and data to derive insights and recommendations for systemic improvement. The Application Operations Coordinator contributes to shaping a culture of operational excellence by exemplifying excellence in product operations, and by combining a mindset of ethics, risk, compliance with a drive to deliver business outcomes. Together with Products Teams and collaborators within and beyond RX, the Application Operations Coordinator ensures Product Teams are effectively delivering on operational activities in the most efficient way possible. Essential Requirements 8+ Years of relevant experience. The Application Operations Coordinator is passionate about and experienced in product operations in complex business environments and has (or can quickly develop) domain knowledge in drug discovery. This role requires an intrinsic drive to improve the quality, speed, and impact of scientific research by ensuring teams can deliver on operational priorities efficiently and effectively. The role is highly collaborative, requires frequent, clear, and effective communication to a broad audience of ~300 members of our 30+ Product Teams, and dozens of other stakeholders in RX, BR, and corporate IT. The Applications Operations Coordinator is skilled driving incremental operational delivery in complex and ambiguous environments, providing information and coordination to help Product Teams succeed, and then holding teams to account to deliver. In addition, the Application Operations Coordinator brings many of the following types of expertise and capabilities, and the drive to grow into the rest: Domain expertise Product Operations or Application Management, ideally in the drug discovery Exceptional communication skills Incremental delivery mindset and experience with Agile software development The ability to influence without authority in a complex, matrixed organization Courage to constructively challenge the status quo, to experiment, and to take smart risks Quantitative skills and the ability to use data and metrics to inform decisions Creativity in identifying, encouraging, accelerating, and promoting innovative solutions, including in GxP regulated environments Ability to effect change, manage conflict, and create consent through direct and indirect influence Proven ability to execute consistently, rapidly, and effectively Having a clear and visible set of values and acting with integrity Education and Qualification Requirements: You have relevant subject matter expertise, obtained through experience or education, in Leadership in an agile environment Software product operations in a complex matrix environment Drug discovery or a core supporting scientific field

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology At HemoCue, one of Danaher s 15+ operating companies, our work saves lives and we re all united by a shared commitment to innovate for tangible impact. You ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher s system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. HemoCue is a leading provider of point-of-care diagnostic solutions, enabling healthcare practitioners across clinical settings and geographies to improve patient outcomes and clinical workflows. For more than four decades we ve been advancing what s possible at the point of care. HemoCue offers point-of-care testing for hemoglobin, glucose and HbA1c as well as total and differential white blood cell count. As Inside Sales Representative for HemoCue, you will play a key role in qualifying leads and scheduling meetings with potential customers. This position is part of the you will be part of a small team working closely with the sales and marketing departments. Located in Mumbai/Bangalore and will be on site. At HemoCue, our vision is to do things easier, to do things better, and to do them right. You will be a part of the Inside Sales Team and report to the Director Public Health and Commercial Excellence responsible for the Inside Sales Department. If you thrive in a fast paced, solution-oriented, customer-facing role and want to work to build a world-class Sales organization read on. In this role, you will have the opportunity to: Contact potential customers to verify interest and coordinate/schedule meetings with local sales representatives (direct or through channel partner) Document and qualify incoming leads using Salesforce Customer Relationship Management (CRM) software Respond to basic products and services inquiries and collaborate with the sales and marketing teams to optimize processes The essential requirements of the job include: 2+ years experience in customer service or client interaction role (e.g., healthcare, pharmacy, pharmaceuticals, sales, or support) Fluency in English, both spoken and written in addition to fluency in one of the following languages: Spanish, German, or French Strong computer literacy and experience working in a PC environment It would be a plus if you also possess previous experience in: Working knowledge of Customer Relationship Management (CRM) systems (preferably Salesforce) Previous experience working in biomedical, pharmaceutical, or healthcare-related fields Join a winning team today. Together, we ll accelerate the real-life impact of tomorrow s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com . Join our winning team today. Together, we ll accelerate the real-life impact of tomorrow s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Roles and Responsibilities As a Biomedical Engineer, you will be responsible for supporting patients by developing biomedical equipment based on the specifications. You will also be responsible for troubleshooting and maintaining the equipment on a regular basis. Planning and developing biomedical equipment. Conducting various tests on devices and equipment. Setting up the biomedical equipment. Educating and training the team members on using the systems. Calibrating the equipment as per the requirements. Maintaining and repairing biomedical devices. Providing training to the clinicians and other personnel on how to use the equipment. Resolving issues faced by the professional team. Maintaining proper inventory levels and restocking them as and when needed. Offering technical assistance to the person using the equipment. Preparing technical documentation on how to use the equipment. Researching on new techniques to be used in the biomedical industry. Writing reports and documents detailing procedures and policies. Attending meetings and conferences organized by the company. Complying with the rules and regulations of the company. Staying updated with the latest trends in the biomedical industry.

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Self Supportive Training ll be provided for Fresher Required Candidate profile UG / PG in Life Science, Medical, Paramedical Dental, Pharmacy, Physio, Nursing, Microbiology, Biochemistry, Biotechnology, Biology, Bio-Medical, Zoology, Bioinformatics, Botony, Nutrition & Dietetics Perks and benefits 12700/- to 14600/- PM Excluding Special Allowances

We are URGENTLY Hiring Product Specialist for Mumbai based Medical Device MNC Products : ULTRASOUND / Ventilator / ECG / Patient Monitors Vacant Location : PUNE, NAGPUR, MUMBAI, AYODHYA, DIBRUGARH, MUZAFFARPUR, JAIPUR, JAMMU, CHANDIGARH, NOIDA, DELHI and many more HQ's Job Description : Promoting the products and generating business Achieving assigned Area and Brand wise sales target Conduct activities and programs as per company strategy - OPD campaigns, Symposiums, CMEs etc to generating revenues. Enjoying excellent relationship with all leading customer in the area. To ensure full placement of products in entire market To increase market reach and visibility Conducting doctors meet/ conferences training programs and other marketing activities. Follow up with customers to resolve any issues and ensure satisfaction URGENTLY Share your CV at resume@aplepharma.com Qualification : Any Graduate (BE Biomedical / B.Pharma /B.sc preferable) Essential Skills: Hard worker with good market knowledge Self-starter with Initiative and Result Oriented Positive Attitude Good Communication & Good Documentation skills Good Analytical & Interpersonal Skills Committed & Ambitious Person who would be ready to take on challenging responsibilities. HR APLE PHARMA Deepika Whatsapp : 7015693171, 8950062647

We are Hiring Medical Sales Representative for the for renowned MNC Vacant Head Quarters : CENTRAL MUMBAI (Sion to Mulund), NAVI MUMBAI (Airoli to Panvel), SOUTH MUMBAI (Khar to Mahalaxmi), GURUGRAM, CHENNAI, HYDERABAD, BANGALORE, CUTTACK, BARODA, COIMBATORE, THANJAVUR and many more HQ's Qualification : Any Graduate JOB DESCRIPTION 1. Meeting doctors, Retailers & wholesalers, promotion and demand generation for the requisite product portfolio. 2. To implement the sales strategies in the respective territory of the Company. 3. To collect the various relevant market information & submit it to the ABM. 4. To respect and work within the systems and the values of the company. Thanks & regards HR APLE PHARMA Aastha Mishra / Arpita 7015693171, 8950062647 Share your CV at resume@aplepharma.com Required Candidate profile Should be confident, good in communication skills, Note: Share references for Medical representatives position for various other locations at te above numbers.

Collaborate with healthcare teams to streamline information flow. Assist in maintaining patient data integrity in a fast paced environment. Undergo comprehensive, hands on experience with industry experts.

Welcome to the era of Velsera! Seven Bridges, Pierian UgenTec have combined to become Velsera. Velsera is the precision engine company. We empower researchers, scientists, and clinicians to drive precision RD, expand access to, and more effectively leverage analytics at the point of care. We unify technology-enabled solutions and scientific expertise to enable a continuous flow of knowledge across the global healthcare ecosystem. This interweaves diverse biomedical communities, allowing them to build upon each other s success and accelerate medical breakthroughs that positively impact human health. With our headquarters in Boston, MA, we are growing and expanding our team which located in 14 different countries! Designation: Scientific Lead Location: Pune, India (Hybrid) As a Scientific Lead, you will report to the Manager KB and your tasks will consist of application on strong molecular biology and cancer biology background to curate, interpret and represent data from variety of sources into logical rules that form the core of our clinical genomics knowledgebase. What will you do Technical/Scientific - Demonstrate clear understanding of rules in KB and the rule firing logic. - Association between gene test and clinical findings - Predicates and attributes, how it impacts rule firing. - Patient management impact - Therapeutic / Prognostic / Diagnostic - Understanding of disease ontology and how it impacts rule firing. - In disease/out of disease concept - Understanding of different disease ontologies that is currently used by KB and its implication. - Different Rule firing engines - CGW vs TPS vs Lotus - Variant classification classification hierarchy (precedence logic) - WashU CAP/AMP/ASCO - Demonstrate clear understanding of respective source curation workflow for the given KB team. - Contribute as reviewer of the curated content. - Existing curation strategies and the clinically significant data that is curated. - Understanding of QA/QC process - How the curated data is used downstream and how it impacts patient care. - Create/design workflow for new curation strategy or extrapolate existing curation strategies to a similar new scenario. - Be the content owner of the respective source and be responsible for overall QC/QA of the data curated by the team, ensuring delivery of high-quality data. - Create/design SOPs /or Work Instruction (WI) generation. - Demonstrate new ideas and ability to present and defend ideas in team or CCC meetings. - Problem solving mindset - provide clear solutions or take decisions to resolve blockers in day-to-day tasks and be able to support/justify them in scientifically acceptable way or by providing necessary evidence. - Identify potential risks of process, project or design, and report deviation from SOP or WI - For deviations, we expect impact analysis to be conducted and some solution to be proposed. - Identify gaps or misalignment between written WI and workflow implementation and propose solutions. - Initiate and drive QMS/SQA related discussions to ensure quality compliance of KB content. - Identify tooling requirements/enhancements to improve source curation workflow and initiate discussion with KBMS team. - Have a basic understanding of other KB team s workflow and strategies - SME reviewer for other KB team s annotation WIs - Provide inputs in other team s strategy design. Collaborate wherever possible to increase efficiency and quality of the overall KB product. - Mentorship: provide mentorship to juniors and reviewers on content strategies helping them to scale up. - Thought leadership: You should be seen as a reference and go-to person for niche expertise. - Open to self-training and exploring new technologies. Communications - Should be able to initiate discussions and communicate issues within team or across teams with clear background understanding to achieve outcome or conclusions. - Initiate or engage in clear communication (slack, email, and verbal) regarding any blockers/issues with members of (other) teams, follow-up and conclude. - Ability to develop documentation, power point presentations, flowcharts, diagrams etc. to communicate technical solutions. Operational - Should have a strong sense of ownership urgency. - Follow/execute daily/weekly tasks till completion based on SOP with ownership and responsibility. - Self QC of work - demonstrate a high standard with each deliverable. - Commitment to delivery of day-to-day tasks and projects involved as per the project timelines. - Clear communication of daily work progress/status to the team lead - Decision making: In scenarios where the team is blocked because of some issue/gap, you should be able to provide a logical path forward to the team. - Identify needs, gather supporting evidence to devise or come up with proposals for newer processes/workflows. - Identify ways to increase team velocity and efficiency. For example, identify areas where automation would help and accordingly provide requirements for tool development. - Create plans for projects or processes on their own whenever required. - Plan and execute POC for new projects or sub tasks. - Content documentation - document and review content related approach in scientific and methodical manner - Manage different types of complexities in the workflow. - Trainings. - Design, document and execute existing or revised training workflows and conduct trainings as per SOP/WI - Identify the training needs within the team or specific team member to improve efficiency and quality of the data delivered. - Take a lead in solving problems or small projects, be proactive and own results. - Should provide regular peer feedback to the team/functional leads. - Demonstrate strong adherence to Velsera core values. What do you bring to the table - Ph.D. in genetics, genomics, molecular biology, or an equivalent with 4+ years of postdoc or work experience OR - Master s degree in molecular biology, genetics, biotechnology, or biochemistry with 8+ years of work experience - Genetic and molecular understanding of human disease. - Good understanding of genomic databases and their annotations (For example: GenBank, RefSeq, dbSNP etc.). - Basic understanding of cancer biology and signaling pathways. - An understanding of bioinformatics analysis to identify variants within genomic data sets is desirable. - Proficiency in communicating and understanding of genetic variant details. - An enthusiastic "can-do" mentality with leadership skills, a dedicated team-worker, having good verbal and written communication skills. - Previous experience as an experimental scientist in applied science or hands-on experience in oncogenomic diagnostic laboratories is a big plus. - Experience with open-source bioinformatics tools and publicly available variant databases is a plus. - Personal initiative and ability to work effectively as part of a team. - Excellent communication skills. Our Core Values People first. We create collaborative and supportive environments by operating with respect and flexibility to promote mental, emotional and physical health. We practice empathy by treating others the way they want to be treated and assuming positive intent. We are proud of our inclusive diverse team and humble ourselves to learn about and build our connection with each other. Patient focused. We act with swift determination without sacrificing our expectations of quality . We are driven by providing exceptional solutions for our customers to positively impact patient lives. Considering what is at stake, we challenge ourselves to develop the best solution, not just the easy one. Integrity. We hold ourselves accountable and strive for transparent communication to build trust amongst ourselves and our customers. We take ownership of our results as we know what we do matters and collectively we will change the healthcare industry. We are thoughtful and intentional with every customer interaction understanding the overall impact on human health. Curious. We ask questions and actively listen in order to learn and continuously improve . We embrace change and the opportunities it presents to make each other better. We strive to be on the cutting edge of science and technology innovation by encouraging creativity. Impactful. We take our social responsibility with the seriousness it deserves and hold ourselves to a high standard. We improve our sustainability by encouraging discussion and taking action as it relates to our natural, social and economic resource footprint. We are devoted to our humanitarian mission and look for new ways to make the world a better place. Velsera is an Equal Opportunity Employer: Velsera is proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, colour, gender, religion, marital status, domestic partner status, age, national origin or ancestry.

Welcome to the era of Velsera! Seven Bridges, Pierian UgenTec have combined to become Velsera. Velsera is the precision engine company. We empower researchers, scientists, and clinicians to drive precision RD, expand access to, and more effectively leverage analytics at the point of care. We unify technology-enabled solutions and scientific expertise to enable a continuous flow of knowledge across the global healthcare ecosystem. This interweaves diverse biomedical communities, allowing them to build upon each other s success and accelerate medical breakthroughs that positively impact human health. With our headquarters in Boston, MA, we are growing and expanding our team which located in 14 different countries! What will you do Governance and Policy Development - Develop, implement, and maintain governance policies, SOPs, and related documentation. - Ensure all policies align with industry standards (e.g., FedRAMP, NIST SP 800-53, ISO 27001 family, and HIPAA). - Monitor policy effectiveness and recommend updates based on organizational changes or regulatory updates. Risk Management - Conduct risk assessments to identify vulnerabilities, threats, and compliance gaps. - Collaborate with cross-functional teams to design and implement remediation strategies. - Maintain risk registers and monitor mitigation efforts. Compliance Oversight - Support the organization in achieving and maintaining FedRAMP certification. - Manage periodic audits, security assessments, and readiness activities for compliance frameworks. - Track and report on compliance metrics, audit findings, and resolution status. Training and Awareness - Develop and deliver training programs to enhance employee understanding of compliance policies and procedures. - Act as a point of contact for compliance-related queries within the organization. Incident Response and Reporting - Support incident response processes to ensure effective investigation and reporting of compliance-related incidents. - Collaborate with stakeholders to implement corrective actions and prevent recurrence. Vendor and Third-Party Risk Management - Assess third-party vendors for compliance with organizational policies and standards. - Ensure contracts include appropriate compliance requirements. What do you bring to the table Education Experience - Bachelors degree in Information Technology, Cybersecurity, Risk Management, or related field (Master s preferred). - 3+ years of experience in governance, risk, and compliance roles, with specific experience in FedRAMP compliance. Knowledge Skills - Strong understanding of FedRAMP, NIST SP 800-53, ISO 27001, and other relevant frameworks. - Experience in drafting policies, procedures, and SOPs. - Familiarity with GRC tools and platforms (e.g., Archer, ServiceNow GRC). - Excellent communication and documentation skills. - Analytical mindset with attention to detail. Certifications (Preferred) - Certified Information Systems Security Professional (CISSP) - Certified Information Systems Auditor (CISA) - Certified Information Security Manager (CISM) - ISO 27001 Lead or Internal auditor Our Core Values People first. We create collaborative and supportive environments by operating with respect and flexibility to promote mental, emotional and physical health. We practice empathy by treating others the way they want to be treated and assuming positive intent. We are proud of our inclusive diverse team and humble ourselves to learn about and build our connection with each other. Patient focused. We act with swift determination without sacrificing our expectations of quality . We are driven by providing exceptional solutions for our customers to positively impact patient lives. Considering what is at stake, we challenge ourselves to develop the best solution, not just the easy one. Integrity. We hold ourselves accountable and strive for transparent communication to build trust amongst ourselves and our customers. We take ownership of our results as we know what we do matters and collectively we will change the healthcare industry. We are thoughtful and intentional with every customer interaction understanding the overall impact on human health. Curious. We ask questions and actively listen in order to learn and continuously improve . We embrace change and the opportunities it presents to make each other better. We strive to be on the cutting edge of science and technology innovation by encouraging creativity. Impactful. We take our social responsibility with the seriousness it deserves and hold ourselves to a high standard. We improve our sustainability by encouraging discussion and taking action as it relates to our natural, social and economic resource footprint. We are devoted to our humanitarian mission and look for new ways to make the world a better place. Velsera is an Equal Opportunity Employer: Velsera is proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, colour, gender, religion, marital status, domestic partner status, age, national origin or ancestry.

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Self Supportive Training ll be provided for Fresher Required Candidate profile UG / PG in Life Science, Medical, Paramedical Dental, Pharmacy, Physio, Nursing, Microbiology, Biochemistry, Biotechnology, Biology, Bio-Medical, Zoology, Bioinformatics, Botony, Nutrition & Dietetics Perks and benefits 12700/- to 14600/- PM Excluding Special Allowances

Work Mode- Work from Office Noida ( Candor Tecspace Sector 135, Noida ) Work Timeline - Monday To Saturday (1st and 3rd Saturday off) Summary: This role provides critical support to authors, editors, and other stakeholders by responding to inquiries and escalating complex issues. The ideal candidate will possess strong communication and problem-solving skills, and a commitment to providing high-quality service. Responsibilities: 1. Respond to a wide range of inquiries from authors and other stakeholders, utilizing standard operating procedures (SOPs) and internal knowledge bases. 2. Escalate complex or non-standard inquiries to the appropriate team or individual. 3. Maintain accurate records of all interactions and inquiries. 4. Provide timely and helpful responses to inquiries, ensuring a positive user experience. 5. Assist authors with various manuscript-related queries. 6. Collaborate with internal teams to ensure efficient resolution of inquiries. 7. Contribute to the continuous improvement of support processes. 8. Identify and document common issues and suggest improvements to SOPs and knowledge base content. Qualifications: The candidate should have an undergraduate degree in any life science discipline with following skills. 1. Excellent communication skills (written and verbal). 2. Strong problem-solving and analytical skills. 3. Ability to work independently and as part of a team. 4. Knowledge of journal publishing processes (preferred). 5. Ability to handle multiple tasks and prioritize effectively. 6. Ability to work in a fast-paced environment.

Work Mode- Work from Office ( Candor Tecspace Sector 135, Noida) Work Timeline - 9:30 Am -6:30 Am (Monday to Saturday Summary: This role is responsible for verifying potential collaborators and partners. The successful candidate will utilize various online resources and tools to locate and validate contact details, institutions, and countries associated with a list of contacts. The role will be instrumental in ensuring data accuracy and completeness. Responsibilities: 1. Utilize provided search methods and tools to locate and verify contact information for each contact. This may involve searching online databases, institutional websites, and academic publications. 2. Identify the country associated with each contact's institution. If the country is not readily available, the candidate will research and add it to the spreadsheet. 3. Employ AI-powered tools and Excel formulas to streamline the verification process for multiple contacts simultaneously. 4. Document any instances where contact information cannot be verified, including reasons for failure. This may involve re-verification or flagging for follow-up. 5. Maintain data accuracy and completeness throughout the verification process. Qualifications: The candidate should have a masters degree in any life science discipline with following skills. 1. Strong research and data entry skills. 2. Proficiency in Microsoft Excel or similar spreadsheet software. 3. Familiarity with online research tools and databases, like PubMed and Google Scholar. 4. Ability to work independently and meet deadlines. 5. Attention to detail and accuracy. 6. Experience with AI-powered tools or similar technologies is a plus. 7. Strong organizational skills.

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don t settle for the mediocre. Each of us is driven to help improve patients lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don t settle for the mediocre. Each of us is driven to help improve patients lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. Your role at Vantive: We are seeking an Associate Director to be the leader for our Peritoneal Dialysis (PD) Systems Engineering Team. You will directly be responsible for leading, building the high performing team required Systems engineering infrastructure. You will be leading a team of Research Development engineers of multi-faceted talent (such as Therapy experts, Requirement/Risk Management Owners, Systems Engineers, Lead System Designers, Product Design Owners etc.), providing Product Technical expertise guidance along with accountability of quality of the design deliverables to the business. You will ensure a holistic system design to deliver the PD therapy to the patient, working collaboratively across the design development team disciplines and cross functions by analyzing multiple input sources to define product requirements, develop architectures and designs, to identify, assess, and ensure proper mitigation of patient and user risks. What youll be doing: Business Understands customer, patient therapy needs, and product roadmaps for the business. Leads the strategic planning for the new product development roadmap. Takes ownership for the continuous improvement initiatives within the assigned function in alignment with business needs. Effectively communicates within the function, across cross functions, to the leadership and stakeholders. Organization: Sets policies for the staff in accomplishing and documenting projects. Assists in the development of overall engineering departmental policy. Identifies and builds strategic technical competencies in the RD organization to realize all aspects of the business product development needs. Create a culture and environment that attracts, develops, retains, and grows diverse and top talent aligned through an environment of mentoring, coaching, career growth and progression, and employee development are critical focus areas. Leads functional and technical team leaders in the group that ensures clear accountability and operational excellence. Ensures that succession planning and talent pipeline is in place. Leverages and supports cross functional teams including Sustaining engineering, the larger business unit, quality, program management, manufacturing, regulatory, medical and clinical, to achieve business results. Fosters an environment where mentoring, coaching, career growth and progression, and employee development are critical focus areas. Continuously improve department efficiencies to deliver best-in-class development output and optimize fiscal funding. Projects Leads new product developments and/or life cycle management of current products in the field for the Peritoneal Dialysis Therapy Systems. Effectively manages resources from planning through execution in close collaboration with Program management. Responsible for development of state-of-the-art industry expertise and technical competencies to achieve new product developments and to bring productivity/efficiency in enhancing and sustaining the products to meet the evolving Market needs Regulatory/Quality Standards. Applies knowledge of medical device lifecycle management to effectively drive specific phases of product development with high quality and predictability of timeline and budget. Adheres to FDA, ISO, and IEC design control procedures, regulations and standards and ensures appropriate design controls and are being adhered to. What youll bring: Graduate or Post-Graduate in Electrical, Mechanical, Biomedical or related Engineering. An advanced technical degree is desired. Experience should include 10-12 years of relevant technical experience in Systems Engineering, including 5 years of leadership experience. Prior experience in Renal Care domain is a plus. Must possess a strong knowledge of engineering disciplines and solid knowledge of related disciplines, Electro/Mechanical, Systems, Fluid Mechanics, Materials Science, etc. A demonstrated track record in electromechanical system development, preferably medical devices. Have a proven track record of management/leadership effectiveness and Influencing in a fast-paced environment. Experience in leading large multi-functional teams with diversified backgrounds covering Systems engineering, System verification validation. Strong foundation and experience in resource, project and budget management and strategy development. Proven ability to create results within budget, timeline, and product/project deliverables. Proven ability to make sound decisions, think critically, build realistic plans, and manage execution, including creating and implementing resource deployment strategies. Vantive is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. Reasonable Accommodation Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link Recruitment Fraud Notice Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice .

Welcome to the era of Velsera! Seven Bridges, Pierian UgenTec have combined to become Velsera. Velsera is the precision engine company. We empower researchers, scientists, and clinicians to drive precision RD, expand access to, and more effectively leverage analytics at the point of care. We unify technology-enabled solutions and scientific expertise to enable a continuous flow of knowledge across the global healthcare ecosystem. This interweaves diverse biomedical communities, allowing them to build upon each other s success and accelerate medical breakthroughs that positively impact human health. With our headquarters in Boston, MA, we are growing and expanding our team which located in 14 different countries! What will you doDesign, develop and maintain various Bioinformatics solutions for analyzing and managing Biological data as per our best practices and quality standards. Collaborate with Product Management and Software Engineers, to build bioinformatics solutions. Produce high quality and detailed documentation for all projects. Provide consultation and technical solutions to cross functional bioinformatics projects. Identify and/or conceive novel approaches to better and more efficiently analyze client and public datasets. Participate in defining the high-level application architecture for future roadmap requirements and features. Coach other team members by sharing domain and technical knowledge and code reviews. Participate in activities such hiring and onboarding. Work with cross-functional teams to ensure quality throughout the bioinformatics software and analytical pipelines development lifecycle. Ensure compliance with our SDLC process during product development. Stay up-to-date on technology to deliver quality at each phase of the product life-cycle. You take leadership in evangelizing technical excellence within the team. What do you bring to the tablePh.D. degree with 3-5+ years of postdoc or industrial experience or Masters Degree with 5-8+ years of industrial experience in Bioinformatics, Computer Science, Bioengineering, Computational Biology or related field Excellent programming skills in Python and Shell scripting Experience with Relational database such as PostgreSQL, mySQL or Oracle Experience with version control systems such as GitHub. Experience with Linux/UNIX/Mac OS X based systems Experience with high-performance Linux cluster and cloud computing (AWS is preferred). Deep understanding of analytical approaches and tools for genomic data analysis along with familiarity with genomic databases. Candidates with proven expertise in the analysis of NGS data generated on sequencing platforms such as Illumina, Oxford Nanopore, or Thermo will be prioritized. Experience with open source bioinformatics tools and publicly available variant databases. Ability to manage moderately complex projects and initiatives. Exceptionally strong communication, data presentation and visualization skills. Personal initiative and ability to work effectively with in a cross functional team. Excellent communication skills and ability to learn and work independently when necessary. High energy and inquisitive and strong attention to detail Our Core Values People first. We create collaborative and supportive environments by operating with respect and flexibility to promote mental, emotional and physical health. We practice empathy by treating others the way they want to be treated and assuming positive intent. We are proud of our inclusive diverse team and humble ourselves to learn about and build our connection with each other. Patient focused. We act with swift determination without sacrificing our expectations of quality . We are driven by providing exceptional solutions for our customers to positively impact patient lives. Considering what is at stake, we challenge ourselves to develop the best solution, not just the easy one. Integrity. We hold ourselves accountable and strive for transparent communication to build trust amongst ourselves and our customers. We take ownership of our results as we know what we do matters and collectively we will change the healthcare industry. We are thoughtful and intentional with every customer interaction understanding the overall impact on human health. Curious. We ask questions and actively listen in order to learn and continuously improve . We embrace change and the opportunities it presents to make each other better. We strive to be on the cutting edge of science and technology innovation by encouraging creativity. Impactful. We take our social responsibility with the seriousness it deserves and hold ourselves to a high standard. We improve our sustainability by encouraging discussion and taking action as it relates to our natural, social and economic resource footprint. We are devoted to our humanitarian mission and look for new ways to make the world a better place. Velsera is an Equal Opportunity Employer: Velsera is proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, colour, gender, religion, marital status, domestic partner status, age, national origin or ancestry.

To advise and assist the factory management in fulfilment of its obligations, statutory or otherwise, concerning prevention of personal injuries and maintaining a safe working environment. To advise concerned departments in planning and organizing measures necessary of the effective control of personal injuries. To advise safety aspects in all job studies and to carryout detailed job safety studies at selected jobs. To check and evaluate the effectiveness of actions taken or proposed to be taken to prevent personal injuries. To advise the purchasing and stores departments in ensuring high quality and availability of personal protective equipment. To advise on matters related to carrying out plant safety inspections. To carry out plant safety inspections in order to observe the physical conditions of work and the work practices and procedures followed by workers and to render advice on measures to be adopted for removing the unsafe physical conditions and preventing unsafe actions by workers. To render advise on matters related to reporting and investigations of industrial accidents and diseases. To investigate accidents/incidents, dangerous occurrences reportable under Rule 115 of The Maharashtra Factories Rules, 1963 and the cases of industrial diseases contracted by any workers employed in the factory reportable under rule 116 of the (said rule). To maintain records as are necessary relating to accidents, dangerous occurrences, and industrial diseases, investigation, and corrective actions. To promote setting up safety committees and act as advise to such committees, To organize in associated with the concerned departments, campaigns, competitions, contests and other activities, which will develop and maintain the interest of the workers in establishing and maintaining safe conditions of work and procedures, e.g. - National Safety Day/Week, Road Safety week, Fire service week, World environment day/week, World environment day/week, etc., To design and conduct suitable training, and educational programs for the prevention of personal injuries, conduct EHS induction of newly joined employees, refresher trainings, etc., Activities: Implementation of ISO 14001 and ISO 45001 at site. Ensure compliance to EHS legislation. Liaison with Government authorities in connection with EHS matters. Identify and communicate new legal requirements, notified as well as relevant to Loni factory. Maintain legal register stating applicable EHS legal requirements. Develop training module and conduct training programs for employees related to environment, occupational health and safety. Assist Management Representative in implementing EHS management system. Maintain and update Master List of controlled documents and records related to EHS Maintenance of the list of monitoring procedures opted to know the key parameters. Co-ordinate and monitoring key EHS parameters. It shall be the responsibility of respective EHS officer for proper collection, handling and disposal of hazardous, municipal and bio-medical waste. Stop production operation if it leads to EHS emergency and recommend corrective action and follow up for implementation. Record, Monitor and analyze incidences related to EHS issues. Reporting EHS performance to top management for review and as a basis for continual improvement Conduct walk through safety audits for all operations. Assist Safety Committee chairman to conduct safety Committee meetings periodically and maintain minutes of meeting. Share management review output with workers representatives. Ensure participation of workers while implementation of EHS, making process changes which impact health and safety. Consult workers representatives appropriately on OHS issues. Maintain and ensure up-keep of equipment s identified for emergency preparedness Authorized to issue work permits as per the job requirement

Additional Locations: India-Haryana, Gurgaon Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. About Role: Provides mechanical engineering support for developing innovative medical devices, ensuring designs meet customer and business needs. Applies principles of engineering, physics, and material science to optimize and evaluate mechanical and electro-mechanical components. Manages design risks, collaborates with internal and external teams, and ensures robust documentation and compliance with quality systems. Proficient in CAD design, GDT, material sciences, and statistical analysis, with a strong focus on process improvement and technical communication. Key Responsibilities: Responsible for providing mechanical engineering support in the creation and the development of new medical device products (invasive and non-invasive). Key Responsibilities Apply principles of Mechanical engineering, Physics, and Material Science to perform data driven development, optimization, and evaluation of novel or iterative designs of mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment, based on customer and business needs. Defines and implements specifications, inputs/outputs, working parameters, and test methods using current best practice engineering methods and technologies. Assesses design risks and mitigations through tools such as FMEA, Fault tree, etc. Works closely with key internal and external specialty resources to ensure to ensure robust holistic device / component design and to address complex design issues. Continuously improves process and work methodologies by interfacing with peers/cross-functional groups and analyzing activities to improve workflow and work processes. Provides clear communication to stakeholders for key technical updates. Creates robust documentation of requirements, protocols, evaluations, reports, etc. throughout all phases of research and development by writing clear and concise documents. Complies with site and department specific procedures on record keeping, use of log books, materials receiving, and inventory control. Completes time records and reports projects allocated time. Adheres to all EHS procedures and general housekeeping SOPs. Remains knowledgeable of technologies within functional area. Writes and submits intellectual property (patents). Reviews or coordinates vendor activities to support development. Contributes to a strong team culture around high expectations and high performance and Experience Qualifications and Skill-Set BE/B.Tech degree in Mechanical/ Biomedical Engineering. Minimum 3 years of RD / NPD experience, preferably in medical devices. Knowledge in medical grade material sciences and processing - Metals, Polymers Proficient in CAD Design, GDT, Tolerance stack-ups Knowledge of quality system processes that need to be applied for product development. Basic stats knowledge Requisition ID: 602001 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Review, evaluate, classify and perform follow up activities on all product complaints relative to the identity, quality, reliability, safety and effectiveness of medical devices. Evaluates for reporting criteria to Government Agencies to determine if the event reasonably suggests a device may have or could have caused or contributed to a death or serious injury Responsibilities may include the following and other duties may be assigned. Evaluates incoming complaint information and maintains the record in the electronic database. Performs follow up activities to obtain additional information. Use and maintain database(s), provide analysis and trending data all on complaints. Determines Reportability of complaints to Government Agencies. Identify and document appropriate complaint categories to assure trend accuracy within the complaint database. Writes investigation summaries based on technical product analysis information provided; Ensures record documentation is maintained in a constant state of audit readiness per internal policies. Liaison with groups who perform additional investigation and who prepare written record of investigation. Interact with Technical Service, Manufacturing, RD, and Quality Assurance, as needed, during the course of complaint processing. Provide basic technical expertise and assistance in handling complaints to comply with current FDA and International reporting regulations. Reviews and interprets risk management documentation as it applies to the complaint event. Interacts with multiple departments within Medtronic - MITG, such as Technical Services, Failure Investigation, R D, Manufacturing and Engineering. Interacts with groups external to Medtronic - MITG, such as customers, vendors, health care professional. SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects - from design to implementation - while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education. DIFFERENTIATING FACTORS Autonomy: Established and productive individual contributor. Works independently with general supervision on larger, moderately complex projects / assignments. Organizational Impact: Sets objectives for own job area to meet the objectives of projects and assignments. Contributes to the completion of project milestones . May have some involvement in cross functional assignments. Innovation and Complexity: Problems and issues faced are general, and may require understanding of broader set of issues or other job areas but typically are not complex . Makes adjustments or recommends enhancements in systems and processes to solve problems or improve effectiveness of job area. Communication and Influence: Communicates primarily and frequently with internal contacts . External interactions are less complex or problem solving in nature. Contacts others to share information, status, needs and issues in order to inform, gain input, and support decision-making. Leadership and Talent Management: May provide guidance and assistance to entry level professionals and / or employee in Support Career Stream. Minimum Qualifications Bachelor degree; Engineering or Science degrees preferred (e.g. SW,EE, ME, Biomedical Engineering) 4 to 8 years quality assurance or regulatory experience in medical or pharmaceutical industry. Computer literate with skills in Word, Excel, Access, PowerPoint and database trending analysis Strong typing skills and ability to write business documents with minimal supervision. Strong verbal and written communication skills and ability to work in a team oriented environment Ability to multitask. Ability to understand the functionality / intended use of complex medical devices. Minimum travel may be required Nice to Haves Knowledge of medical devices, their development and quality control. Knowledge of FDA, MEDDEV, Canadian Regulations. Technical Writing experience. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. Benefits Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. About Medtronic We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission to alleviate pain, restore health, and extend life unites a global team of 95,000+ passionate people. We are engineers at heart putting ambitious ideas to work to generate real solutions for real people. From the RD lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity here

Purchase Review of Comparative Quotes Conducting Negotiation Meetings Co coordinating for Approval for Negotiated Work/Purchases Ensuring timely release of Purchase/Work orders Vendor Management Procurement Planning Interaction with User department Team Management Commercial tie-ups for outsourced tests Inventory Setting up of Processes Review & Monitoring Stores activities to ensure the SOP is followed MIS Statutory compliance Vendor Dispute resolution Interaction with user Department Team Management Billing Planning & strategizing on Pricing Approval of Discount Handling Escalations on Billing complaints Interaction with Doctors on Billing related matters Team Management Job description: Manage end to end procurement process for high end medical equipment s to and low-end equipment s Work closely with Head of Technical Operations to evaluate alternate platforms for tests to minimise cost of consumption and wastage Receive and process procurement requests from Business units i.e Hospitals, clinics, Labs, Tele Health and new projects and provide frequent updates on status of requests. Participate in procurement committee meetings and provide management with weekly reports on status of procurement requests Prepare quarterly procurement performance reports and market research reports for review by management Develop and maintain a list of approved suppliers to track quality of supplies/equipment, encourage competitive pricing and ensure timely awards and execution of contracts Develop and maintain strong professional relationships with suppliers to encourage prompt responses to requests, open dialogue and cooperation in identifying best options that add value to purchasing decisions Develop Enterprise procurement strategy for Biomedical equipment procurement and AMC/CMC contracts Liaise with suppliers to ensure adherence to contract agreements and lead corrective action plans in the instance of breach of contract Preparation and upkeep of materials database / library Evaluate product / arrange the equipment demo to users before negotiation Take on any other related duties which may be assigned

The key responsibilities of this position are as given below: Maintaining dialysis machines and equipment. Cleaning dialysis machines and equipment Sanitizing and cleaning the machine are the dialysis treatment has taken place. Sanitizing and cleaning the surrounding area of the machine before the dialysis treatment can take place, so that the patient does not get infected. Monitoring the water treatment. The reprocessing of the dialyzer. Observing patients during treatment to monitor for signs of medical emergencies. Assisting with any patient questions or concerns. Educating patients on dialysis. Making alterations to treatment to maintain safe application. Working with nurses and doctors to administer the correct treatment for each Explaining the dialysis process to patients and their families. Monitoring the vascular access of the patient. Teaching patients about additional health care to enhance positive dialysis results. Prep patients and give local anesthesia. Create written reports on patient progress for doctors. Participating in the quality improvement of the centre. Taking good and efficient care of the patient. Document the pre- dialysis specifications, which are inclusive of the weight of the patient, the temperature of the patient, and the other vital signs of the patient. 2. Reporting to: Project Coordinator / Bio Medical Engineer 3. Other Indicative Requirements Educational Qualifications Degree / Diploma in Dialysis. Functional / Technical Skills and Relevant Experience & Other requirements (Behavioral, Language, Certifications etc.) 2 -5 years of experience in Dialysis Centre with good knowledge and skills. Good communication and documentation in English and Hindi Data analysis, reporting and presentation skills. Willingness to travel extensively in remote areas

The successful candidate will be responsible for ensuring the efficient and safe production of high-quality products.

The Biomedical Equipment Technician will be responsible for the maintenance and repair of medical equipment, ensuring all devices are calibrated and functioning correctly. Day-to-day tasks include conducting electrical safety checks, managing equipment spare parts, performing routine and emergency repairs, and documenting all maintenance activities. The technician will also collaborate with healthcare professionals to ensure all equipment meets regulatory and safety standards.

Roles and Responsibilities Perform routine maintenance, repairs, and troubleshooting of biomedical equipment such as ultrasound machines, X-ray machines, CT scanners, MRI machines, and other medical devices. Conduct quality control checks on equipment to ensure proper functioning and identify areas for improvement. Collaborate with healthcare professionals to understand their needs and provide technical support for new equipment installations or upgrades. Desired Candidate Profile 1-5 years of experience in biomedical engineering or a related field. Strong knowledge of biomedical equipment including ultrasound machines, X-ray machines, CT scanners, MRI machines etc. . Familiarity with medical device regulations and industry standards (e.g., FDA guidelines). Interested candidates can also mail me at siddhant.kanojia@sodexo.com

We are URGENTLY Hiring Product Specialist / Sales Manager for Medical Device MNC. Vacant Location : HYDERABAD /CHENNAI/ BANGALORE (Covering South India) Job Description : Promoting the products and generating business Achieving assigned Area and Brand wise sales target Conduct activities and programs as per company strategy - OPD campaigns, Symposiums, CMEs etc to generating revenues. Developing KOL, establish dealers infrastructure to drive the business in private and government sector. Enjoying excellent relationship with all leading customer in the area. Ready to work on new launches with innovative technologies. Aggressive in sales plan and execution to achieve the revenue goals. To ensure full placement of products in entire market To increase market reach and visibility Conducting doctors meet/ conferences training programs and other marketing activities. Follow up with customers to resolve any issues and ensure satisfaction URGENTLY Share your CV at resume@aplepharma.com Qualification : Any Graduate (BE Biomedical / B.Pharma /B.sc preferable) Essential Skills: Hard worker with good market knowledge Self-starter with Initiative and Result Oriented Positive Attitude Good Communication & Good Documentation skills Good Analytical & Interpersonal Skills Committed & Ambitious Person who would be ready to take on challenging responsibilities. HR APLE PHARMA Deepika 7015693171, 8950062647

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Self Supportive Training ll be provided for Fresher Required Candidate profile UG / PG in Life Science, Medical, Paramedical Dental, Pharmacy, Physiotherapy, Nursing, Microbiology, Biochemistry, Biotechnology, Biology, Bio-Medical, Zoology, Bioinformatics, Nutrition & Dietetics Perks and benefits 12700/- to 14600/- PM excluding Allowances

Skills and Qualifications: Education: A bachelor and Master degree in Biomedical Engineering related field is required. Ph.D is optional. (Fresher can also Apply). Technical Skills: Proficiency with CAD software, engineering design tools, and knowledge of medical device regulations. Problem-Solving: Strong analytical skills and the ability to troubleshoot complex technical issues. Communication: Excellent communication skills to collaborate with multidisciplinary teams and convey technical information to non-technical stakeholders.