9 Blockchain Architecture Jobs

You will be responsible for leading the development and implementation of blockchain technologies within the organization as a Chief Blockchain Officer. This full-time on-site role is based in Chennai. Your day-to-day activities will include designing blockchain protocols, developing smart contracts, managing back-end development, implementing cryptographic security measures, and maintaining cryptocurrency mechanisms. It is crucial to collaborate with stakeholders to align blockchain initiatives with business objectives and ensure the security and efficiency of blockchain systems. To excel in this role, you should possess extensive knowledge and experience in Blockchain Architecture and Blockchain technologies. Proficiency in Cryptography and Cryptocurrency is essential, along with a strong background in Back-End Web Development. Strong leadership and project management skills are required to drive the success of blockchain projects. The ability to work effectively in a team is crucial for this position. Previous experience in a similar leadership role would be advantageous. A Bachelor's degree in Computer Science, Information Technology, or a related field is a mandatory qualification for this role.,

Opus Bloc Inc. is dedicated to utilizing blockchain technology and artificial intelligence (AI) to tackle intricate global issues. The company envisions a future where decentralized systems and intelligent automation provide secure, transparent, and efficient solutions that are accessible to all. Unlike other firms that solely focus on cryptocurrency, Opus Bloc places emphasis on real-world applications, merging blockchain and AI to deliver substantial, tangible advantages. This impact-oriented approach distinguishes Opus Bloc, as it strives to integrate advanced technology into daily life to benefit billions globally. The company's objective is to democratize the accessibility of secure, intelligent systems and promote trust and collaboration across various sectors. This full-time on-site position is for a Chief Blockchain Officer (CBO) located in Bengaluru. The CBO will be responsible for supervising the development and execution of blockchain strategies and systems, guaranteeing seamless integration with AI technologies. Daily responsibilities involve spearheading blockchain projects, overseeing a team of developers, collaborating with other departments to address business challenges using blockchain, and keeping abreast of industry trends and regulations. Additionally, the CBO will ensure the security and scalability of blockchain solutions and offer strategic insights to propel innovation and expansion. Qualifications: - Proficiency in Blockchain Architecture, Blockchain, and Cryptocurrency - Strong background in Cryptography - Competence in Back-End Web Development pertaining to blockchain technology - Exceptional leadership and team management skills - Robust problem-solving and analytical capabilities - Ability to remain informed about emerging technologies and industry developments - Experience in the field of AI is advantageous - Bachelor's or Master's degree in Computer Science, Information Technology, or a related field,

Responsibilities and Primary Activities Scientific Expertise : Develop and maintain a comprehensive understanding of the companys products, particularly in the cardiovascular therapeutic area, while staying updated on the latest medical advancements, clinical guidelines, and treatment protocols. Stakeholder Engagement : Build and maintain relationships with Scientific Leaders (SLs), Key Decision Makers (KDMs), healthcare professionals, and academic institutions. Engage in scientific discussions, present clinical data, and provide educational support to Key Opinion Leaders (KOLs) regarding the companys products and therapeutic areas. Support to Medical Strategy : Collaborate with the line manager to provide strategic inputs and expertise to product management. Medical Education : Deliver scientific and medical education to internal stakeholders, including sales and marketing teams. Collaborate with the Medical Affairs team to develop and present training materials. Scientific Exchange : Facilitate knowledge transfer between the company and external stakeholders by participating in medical conferences, advisory boards, and scientific meetings to gather insights and share data. Clinical Data Communication : Interpret and communicate clinical trial data, real-world evidence, and other scientific information to healthcare professionals and regulators, ensuring compliance with regulations and company policies. Clinical Research Support : Provide medical support for local studies, including identifying study sites for Investigator Initiated Trials. Cross-Functional Collaboration : Work closely with Clinical Development, Regulatory Affairs, Marketing, and Market Access teams to provide scientific input, support clinical trial design, and align on medical communication plans. Medical Initiatives : Support and lead medical projects aligned with the therapy area, involving strong stakeholder interaction. Medical Information : Address medical inquiries and provide timely, accurate responses to healthcare professionals and other stakeholders, ensuring that medical information materials are current and compliant. Sales Force Training : Train sales colleagues on assigned therapy areas and assist in pre-launch and launch training for new products. Compliance : Adhere to legal, regulatory, and compliance guidelines, ensuring all activities are conducted ethically and in accordance with applicable laws. Overall, the RMA in Medical Affairs acts as a scientific expert and liaison between the company and external stakeholders, playing a crucial role in building scientific credibility, fostering relationships, and supporting the companys strategic objectives in the healthcare industry. Values and Behaviours Consistently demonstrate company values with a focus on excellence. Collaborate harmoniously with internal and external stakeholders. What You Must Have Educational Background : A strong academic foundation in life sciences, such as a medical degree (MD) or doctorate (Ph.D.). Industry Experience : At least 1 year of experience in the pharmaceutical cardiovascular therapy area, including roles in clinical research or medical affairs that expose the candidate to scientific and medical aspects of the industry. Therapeutic Area Expertise : Demonstrated knowledge and expertise in the relevant cardiovascular therapeutic area, including experience with clinical trials and publications. Scientific and Clinical Knowledge : Strong understanding of medical and scientific principles, including clinical trial design, data analysis, and interpretation, along with familiarity with relevant disease states and treatment guidelines. Communication and Relationship-Building Skills : Excellent interpersonal, communication, and presentation skills are essential for effectively conveying scientific information to various stakeholders. Analytical and Problem-Solving Skills : Ability to analyse complex scientific data, identify insights, and provide recommendations, particularly in interpreting clinical trial results and addressing medical inquiries. Adaptability and Flexibility : Capability to work in dynamic environments, adapt to changing priorities, and travel frequently to engage with external stakeholders. Regulatory and Compliance Knowledge : Familiarity with legal, regulatory, and compliance guidelines, including Good Clinical Practice (GCP) and ICH guidelines, as well as local regulations governing medical communications.

Responsibilities and Primary Activities Scientific Expertise : Develop and maintain a comprehensive understanding of the companys products, particularly in the cardiovascular therapeutic area, while staying updated on the latest medical advancements, clinical guidelines, and treatment protocols. Stakeholder Engagement : Build and maintain relationships with Scientific Leaders (SLs), Key Decision Makers (KDMs), healthcare professionals, and academic institutions. Engage in scientific discussions, present clinical data, and provide educational support to Key Opinion Leaders (KOLs) regarding the companys products and therapeutic areas. Support to Medical Strategy : Collaborate with the line manager to provide strategic inputs and expertise to product management. Medical Education : Deliver scientific and medical education to internal stakeholders, including sales and marketing teams. Collaborate with the Medical Affairs team to develop and present training materials. Scientific Exchange : Facilitate knowledge transfer between the company and external stakeholders by participating in medical conferences, advisory boards, and scientific meetings to gather insights and share data. Clinical Data Communication : Interpret and communicate clinical trial data, real-world evidence, and other scientific information to healthcare professionals and regulators, ensuring compliance with regulations and company policies. Clinical Research Support : Provide medical support for local studies, including identifying study sites for Investigator Initiated Trials. Cross-Functional Collaboration : Work closely with Clinical Development, Regulatory Affairs, Marketing, and Market Access teams to provide scientific input, support clinical trial design, and align on medical communication plans. Medical Initiatives : Support and lead medical projects aligned with the therapy area, involving strong stakeholder interaction. Medical Information : Address medical inquiries and provide timely, accurate responses to healthcare professionals and other stakeholders, ensuring that medical information materials are current and compliant. Sales Force Training : Train sales colleagues on assigned therapy areas and assist in pre-launch and launch training for new products. Compliance : Adhere to legal, regulatory, and compliance guidelines, ensuring all activities are conducted ethically and in accordance with applicable laws. Overall, the RMA in Medical Affairs acts as a scientific expert and liaison between the company and external stakeholders, playing a crucial role in building scientific credibility, fostering relationships, and supporting the companys strategic objectives in the healthcare industry. Values and Behaviours Consistently demonstrate company values with a focus on excellence. Collaborate harmoniously with internal and external stakeholders. What You Must Have Educational Background : A strong academic foundation in life sciences, such as a medical degree (MD) or doctorate (Ph.D.). Industry Experience : At least 1 year of experience in the pharmaceutical cardiovascular therapy area, including roles in clinical research or medical affairs that expose the candidate to scientific and medical aspects of the industry. Therapeutic Area Expertise : Demonstrated knowledge and expertise in the relevant cardiovascular therapeutic area, including experience with clinical trials and publications. Scientific and Clinical Knowledge : Strong understanding of medical and scientific principles, including clinical trial design, data analysis, and interpretation, along with familiarity with relevant disease states and treatment guidelines. Communication and Relationship-Building Skills : Excellent interpersonal, communication, and presentation skills are essential for effectively conveying scientific information to various stakeholders. Analytical and Problem-Solving Skills : Ability to analyse complex scientific data, identify insights, and provide recommendations, particularly in interpreting clinical trial results and addressing medical inquiries. Adaptability and Flexibility : Capability to work in dynamic environments, adapt to changing priorities, and travel frequently to engage with external stakeholders. Regulatory and Compliance Knowledge : Familiarity with legal, regulatory, and compliance guidelines, including Good Clinical Practice (GCP) and ICH guidelines, as well as local regulations governing medical communications.

Responsibilities and Primary Activities Scientific Expertise : Develop and maintain a comprehensive understanding of the companys products, particularly in the cardiovascular therapeutic area, while staying updated on the latest medical advancements, clinical guidelines, and treatment protocols. Stakeholder Engagement : Build and maintain relationships with Scientific Leaders (SLs), Key Decision Makers (KDMs), healthcare professionals, and academic institutions. Engage in scientific discussions, present clinical data, and provide educational support to Key Opinion Leaders (KOLs) regarding the companys products and therapeutic areas. Support to Medical Strategy : Collaborate with the line manager to provide strategic inputs and expertise to product management. Medical Education : Deliver scientific and medical education to internal stakeholders, including sales and marketing teams. Collaborate with the Medical Affairs team to develop and present training materials. Scientific Exchange : Facilitate knowledge transfer between the company and external stakeholders by participating in medical conferences, advisory boards, and scientific meetings to gather insights and share data. Clinical Data Communication : Interpret and communicate clinical trial data, real-world evidence, and other scientific information to healthcare professionals and regulators, ensuring compliance with regulations and company policies. Clinical Research Support : Provide medical support for local studies, including identifying study sites for Investigator Initiated Trials. Cross-Functional Collaboration : Work closely with Clinical Development, Regulatory Affairs, Marketing, and Market Access teams to provide scientific input, support clinical trial design, and align on medical communication plans. Medical Initiatives : Support and lead medical projects aligned with the therapy area, involving strong stakeholder interaction. Medical Information : Address medical inquiries and provide timely, accurate responses to healthcare professionals and other stakeholders, ensuring that medical information materials are current and compliant. Sales Force Training : Train sales colleagues on assigned therapy areas and assist in pre-launch and launch training for new products. Compliance : Adhere to legal, regulatory, and compliance guidelines, ensuring all activities are conducted ethically and in accordance with applicable laws. Overall, the RMA in Medical Affairs acts as a scientific expert and liaison between the company and external stakeholders, playing a crucial role in building scientific credibility, fostering relationships, and supporting the companys strategic objectives in the healthcare industry. Values and Behaviours Consistently demonstrate company values with a focus on excellence. Collaborate harmoniously with internal and external stakeholders. What You Must Have Educational Background : A strong academic foundation in life sciences, such as a medical degree (MD) or doctorate (Ph.D.). Industry Experience : At least 1 year of experience in the pharmaceutical cardiovascular therapy area, including roles in clinical research or medical affairs that expose the candidate to scientific and medical aspects of the industry. Therapeutic Area Expertise : Demonstrated knowledge and expertise in the relevant cardiovascular therapeutic area, including experience with clinical trials and publications. Scientific and Clinical Knowledge : Strong understanding of medical and scientific principles, including clinical trial design, data analysis, and interpretation, along with familiarity with relevant disease states and treatment guidelines. Communication and Relationship-Building Skills : Excellent interpersonal, communication, and presentation skills are essential for effectively conveying scientific information to various stakeholders. Analytical and Problem-Solving Skills : Ability to analyse complex scientific data, identify insights, and provide recommendations, particularly in interpreting clinical trial results and addressing medical inquiries. Adaptability and Flexibility : Capability to work in dynamic environments, adapt to changing priorities, and travel frequently to engage with external stakeholders. Regulatory and Compliance Knowledge : Familiarity with legal, regulatory, and compliance guidelines, including Good Clinical Practice (GCP) and ICH guidelines, as well as local regulations governing medical communications.

Responsibilities and Primary Activities Scientific Expertise : Develop and maintain a comprehensive understanding of the companys products, particularly in the cardiovascular therapeutic area, while staying updated on the latest medical advancements, clinical guidelines, and treatment protocols. Stakeholder Engagement : Build and maintain relationships with Scientific Leaders (SLs), Key Decision Makers (KDMs), healthcare professionals, and academic institutions. Engage in scientific discussions, present clinical data, and provide educational support to Key Opinion Leaders (KOLs) regarding the companys products and therapeutic areas. Support to Medical Strategy : Collaborate with the line manager to provide strategic inputs and expertise to product management. Medical Education : Deliver scientific and medical education to internal stakeholders, including sales and marketing teams. Collaborate with the Medical Affairs team to develop and present training materials. Scientific Exchange : Facilitate knowledge transfer between the company and external stakeholders by participating in medical conferences, advisory boards, and scientific meetings to gather insights and share data. Clinical Data Communication : Interpret and communicate clinical trial data, real-world evidence, and other scientific information to healthcare professionals and regulators, ensuring compliance with regulations and company policies. Clinical Research Support : Provide medical support for local studies, including identifying study sites for Investigator Initiated Trials. Cross-Functional Collaboration : Work closely with Clinical Development, Regulatory Affairs, Marketing, and Market Access teams to provide scientific input, support clinical trial design, and align on medical communication plans. Medical Initiatives : Support and lead medical projects aligned with the therapy area, involving strong stakeholder interaction. Medical Information : Address medical inquiries and provide timely, accurate responses to healthcare professionals and other stakeholders, ensuring that medical information materials are current and compliant. Sales Force Training : Train sales colleagues on assigned therapy areas and assist in pre-launch and launch training for new products. Compliance : Adhere to legal, regulatory, and compliance guidelines, ensuring all activities are conducted ethically and in accordance with applicable laws. Overall, the RMA in Medical Affairs acts as a scientific expert and liaison between the company and external stakeholders, playing a crucial role in building scientific credibility, fostering relationships, and supporting the companys strategic objectives in the healthcare industry. Values and Behaviours Consistently demonstrate company values with a focus on excellence. Collaborate harmoniously with internal and external stakeholders. What You Must Have Educational Background : A strong academic foundation in life sciences, such as a medical degree (MD) or doctorate (Ph.D.). Industry Experience : At least 1 year of experience in the pharmaceutical cardiovascular therapy area, including roles in clinical research or medical affairs that expose the candidate to scientific and medical aspects of the industry. Therapeutic Area Expertise : Demonstrated knowledge and expertise in the relevant cardiovascular therapeutic area, including experience with clinical trials and publications. Scientific and Clinical Knowledge : Strong understanding of medical and scientific principles, including clinical trial design, data analysis, and interpretation, along with familiarity with relevant disease states and treatment guidelines. Communication and Relationship-Building Skills : Excellent interpersonal, communication, and presentation skills are essential for effectively conveying scientific information to various stakeholders. Analytical and Problem-Solving Skills : Ability to analyse complex scientific data, identify insights, and provide recommendations, particularly in interpreting clinical trial results and addressing medical inquiries. Adaptability and Flexibility : Capability to work in dynamic environments, adapt to changing priorities, and travel frequently to engage with external stakeholders. Regulatory and Compliance Knowledge : Familiarity with legal, regulatory, and compliance guidelines, including Good Clinical Practice (GCP) and ICH guidelines, as well as local regulations governing medical communications.

Role Overview The Connected Channel product line within our company's Digital Manufacturing Division is seeking a skilled and motivated Hyperledger Fabric Blockchain Administrator to join our dynamic team. The ideal candidate will be responsible for the deployment, management, and maintenance of Hyperledger Fabric networks. This role requires a deep understanding of blockchain technology, particularly Hyperledger Fabric, and the ability to work collaboratively with cross-functional teams to support our blockchain initiatives. What will you do in this role Network Deployment and Configuration : Set up and configure Hyperledger Fabric networks, including peers, orderers, and channels. Monitoring and Maintenance : Monitor network performance, troubleshoot issues, and ensure high availability and reliability of the blockchain infrastructure. Smart Contract and SDK Management : Assist in the development, deployment, and management of smart contracts (chaincode) and the SDK on the Hyperledger Fabric network. Security Management : Implement and maintain security protocols, including identity management, access control, and data privacy measures. Documentation : Create and maintain comprehensive documentation for network architecture, configurations, and operational procedures. Collaboration : Work closely with developers, business analysts, and other stakeholders to understand requirements and provide blockchain solutions. Upgrades and Patching : Plan and execute upgrades and patches to the Hyperledger Fabric network to ensure it remains up-to-date and secure. Training and Support : Provide training and support to team members and stakeholders on blockchain technologies and best practices. What should you have Experience : 3+ years of experience in blockchain administration, with a focus on Hyperledger Fabric. Proven experience in deploying and managing distributed ledger technologies. Technical Skills : Strong understanding of Hyperledger Fabric architecture and components. Proficiency in programming languages such as Go, NodeJs, SQL. Familiarity with containerization technologies (e.g., Docker, Kubernetes). Experience with cloud platforms (e.g., AWS, Azure) is a plus. Soft Skills : Excellent problem-solving and analytical skills. Strong communication and interpersonal skills. Ability to work independently and as part of a team. Preferred Qualifications Certifications in blockchain technologies or cloud computing. Experience with other blockchain frameworks like Ethereum

Description We are looking for a skilled Blockchain Developer to join our team in India. The ideal candidate will have 3-12 years of experience in blockchain development, with a strong understanding of various blockchain technologies and protocols. Responsibilities Design and develop blockchain-based applications and smart contracts. Collaborate with cross-functional teams to define, design, and ship new features. Implement security and data protection measures for blockchain systems. Maintain and optimize existing blockchain networks and applications. Research and assess new blockchain technologies and trends to improve product performance. Skills and Qualifications Proven experience with blockchain technologies such as Ethereum, Hyperledger, or Corda. Strong programming skills in languages such as Solidity, JavaScript, Go, or Python. Familiarity with cryptography and security protocols used in blockchain. Experience with distributed systems and peer-to-peer networks. Understanding of consensus algorithms and blockchain architecture.

We are seeking an experienced Blockchain Developer to join our team in India. The ideal candidate will have extensive experience in developing and implementing blockchain solutions, with a strong understanding of various blockchain technologies and protocols. Responsibilities Design, develop, and implement blockchain-based solutions. Collaborate with cross-functional teams to define, design, and deliver new features. Conduct research and analysis on blockchain technologies and trends. Write clean, maintainable, and efficient code. Troubleshoot, debug, and optimize existing blockchain applications. Stay updated with the latest developments in blockchain technology and propose innovative solutions. Skills and Qualifications 10-15 years of experience in blockchain development and implementation. Strong programming skills in languages such as Solidity, JavaScript, Python, or Go. Experience with blockchain platforms such as Ethereum, Hyperledger, or Corda. Knowledge of cryptographic protocols and security standards in blockchain. Familiarity with decentralized application (DApp) development and smart contracts. Understanding of consensus algorithms and blockchain architecture. Strong problem-solving skills and attention to detail. Excellent communication and collaboration skills.