Job Description
Job Description
Senior Manager, Batch Integration Software Engineering
The Opportunity
• Based in Hyderabad, join a global healthcare biopharma company and be part of a 130-year legacy of success backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.
• Be part of an organisation driven by digital technology and data-backed approaches that support a diversified portfolio of prescription medicines, vaccines, and animal health products.
• Drive innovation and execution excellence. Be a part of a team with a passion for using data, analytics, and insights to drive decision-making, allowing us to tackle some of the world's greatest health threats.
Our Technology Centers focus on creating a space where teams can come together to deliver business solutions that save and improve lives. An integral part of our company’s IT operating model, Tech Centers are globally distributed locations where each IT division has employees to enable our digital transformation journey and drive business outcomes. These locations, in addition to the other sites, are essential to supporting our business and strategy.
A focused group of leaders in each Tech Center helps to ensure we can manage and improve each location, from investing in growth, success, and well-being of our people, to making sure colleagues from each IT division feel a sense of belonging to managing critical emergencies. And together, we must leverage the strength of our team to collaborate globally to optimize connections and share best practices across the Tech Centers.
Role Overview
Our Data and Analytics team plays a pivotal role in transforming data into actionable insights that drive strategic decisions and enhance business performance. We are dedicated to harnessing the power of data and integration capabilities to ensure seamless data flow, providing a deeper understanding of our operations, supporting innovation, and fostering a data-driven culture across the organization.
What Will You Do In This Role
• Develop comprehensive High-Level Technical Design and Data Mapping documents to meet specific business integration requirements.
• Own the data integration and ingestion solutions throughout the project lifecycle, delivering key artifacts such as data flow diagrams and source system inventories.
• Provide end-to-end delivery ownership for assigned data pipelines, performing cleansing, processing, and validation on the data to ensure its quality.
• Define and implement robust Test Strategies and Test Plans, ensuring end-to-end accountability for middleware testing and evidence management.
• Collaborate with the Solutions Architecture and Business analyst teams to analyze system requirements and prototype innovative integration methods.
• Exhibit a hands-on leadership approach, ready to engage in coding, debugging, and all necessary actions to ensure the delivery of high-quality, scalable products.
• Influence and drive cross-product teams and collaboration while coordinating the execution of complex, technology-driven initiatives within distributed and remote teams.
• Work closely with various platforms and competencies to enrich the purpose of Enterprise Integration and guide their roadmaps to address current and emerging data integration and ingestion capabilities.
• Design ETL/ELT solutions, lead comprehensive system and integration testing, and outline standards and architectural toolkits to underpin our data integration efforts.
• Analyze data requirements and translate them into technical specifications for ETL processes.
• Develop and maintain ETL workflows, ensuring optimal performance and error handling mechanisms are in place.
• Monitor and troubleshoot ETL processes to ensure timely and successful data delivery.
• Collaborate with data analyst and other stakeholders to ensure alignment between data architecture and integration strategies.
• Document integration processes, data mappings, and ETL workflows to maintain clear communication and ensure knowledge transfer.
What Should You Have
• Bachelor's degree in information technology, Computer Science or any Technology stream.
• 8+ years of working experience with enterprise data integration technologies – Informatica Intelligent Data Management Cloud Services (CDI, CAI, Mass Ingest, Orchestration) and Power center
• 5+ years of integration experience utilizing REST and custom API integration
• 8+ Years of working experience in relational database technologies and cloud data stores from AWS & Azure
• 2+ years of work experience utilizing AWS cloud well architecture framework, deployment & integration, and data engineering.
• Preferred experience with CI/CD processes and related tools, including - Terraform, GitHub Actions, Artifactory, etc.
• Proven expertise in Python and Shell scripting, with a strong focus on leveraging these languages for data integration and orchestration to optimize workflows and enhance data processing efficiency.
• Extensive experience in the design of reusable integration patterns using cloud-native technologies
• Extensive experience in process orchestration and Scheduling Integration Jobs in Autosys, Airflow.
• Experience in Agile development methodologies and release management techniques
• Excellent analytical and problem-solving skills
• Good Understanding of data modeling and data architecture principles
Our technology teams operate as business partners, proposing ideas and innovative solutions that enable new organizational capabilities. We collaborate internationally to deliver services and solutions that help everyone be more productive and enable innovation.
Who We Are
We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have bee Job Description
Regional Medical Advisor (RMA) – General & Specialty Medicine, South Region
The RMA will serve as a key representative for our company, engaging with essential stakeholders in the field. The objective of our medical affairs team is to provide scientific expertise across identified regions, products, and therapy areas to these valued customers.
Responsibilities And Primary Activities
• Scientific Expertise Develop and maintain a comprehensive understanding of the company's 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 company's 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 company's 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.
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status
Regular
Relocation
VISA Sponsorship
Travel Requirements
Flexible Work Arrangements
Not Applicable
Shift
Valid Driving License
Hazardous Material(s)
Required Skills
Advisory Board Development, Advisory Board Development, Clinical Development, Clinical Knowledge, Clinical Testing, Educational Program Development, Emergency Care, Good Clinical Practice (GCP), Healthcare Education, Health Economics Research, Investigator-Initiated Studies (IIS), Life Science, Management Process, Medical Affairs, Medical Communications, Medical Information Systems, Medical Marketing Strategy, Medical Policy Development, Medical Writing, Pharmacovigilance, Product Knowledge, Product Management, Regulatory Affairs Compliance, Regulatory Compliance, Regulatory Compliance Consulting {+ 5 more}
Preferred Skills
Job Posting End Date
06/30/2026
• A job posting is effective until 11 5+ 5+PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID R35073+
