דרושים Developer Iii Sap Btp ב-Boston Scientific ב-India, Gurugram

India-Haryana, Gurgaon

About the position:

Key Responsibilities:

• Lead the design, development, and deployment of scalable Salesforce solutions across initiatives like AOP Feedback, Tableau Integration, and Territory Action Planning.
• Collaborate with cross-functional teams including Admin, Marketing, and Analytics for solution alignment and delivery.
• Guide and mentor junior developers to ensure quality, consistency, and timely delivery.
• Take ownership of project timelines, task prioritization, and phased implementation planning.
• Work closely with the SFDC Product Owner to track progress using tools like Jira and participate in agile ceremonies.
• Serve as backup lead for critical activities including scrum master support, testing, and Jira process management during leadership absence.
• Remain flexible and responsive to ad-hoc development or configuration requests.

Basic Required:

• B.E./B.Tech (any field) OR BCA+MCA.
• 4-7.5 Years of experience to be considered.
• Hands-on Salesforce development experience (Apex, Lightning Components, Flows, SOQL).
• Strong knowledge of Salesforce configuration, declarative tools, and platform limits.
• Experience with integrations such as REST/SOAP APIs or Tableau.
• Familiarity with Agile methodologies and Jira project tracking.
• Ability to lead, mentor, and collaborate across teams.
• Excellent communication and problem-solving skills.
• Salesforce Platform Developer II certification is preferred.

India-Haryana, Gurgaon

Leader of information technology system project/program, directing all phases from inception through completion.

Role and responsibilities:

• Lead, manage, and drive the execution of global IT Data Center and Real Estate Facility projects from initiation through to completion. Ensure projects are delivered on-time, within scope, and on budget.
• Develop detailed project plans, timelines, and milestones. Establish realistic deadlines and ensure resources are aligned to meet project objectives.
• Define and manage project scope in collaboration with stakeholders. Continuously assess scope changes and communicate any adjustments to timelines, budgets, or deliverables.
• Act as the central point of contact for all teams involved in the project. This includes cross-functional collaboration with IT, Real Estate, Facilities Management, Procurement, Legal, and Finance teams.
• Regularly engage with senior leadership and stakeholders to provide updates on project progress, key decisions, risks, and other critical factors. Tailor communication to different stakeholder needs, from technical teams to senior executives.
• Coordinate with external vendors, contractors, and consultants for the delivery of equipment, services, and support. Manage third-party relationships to ensure contractual obligations are met and project quality standards are maintained.
• Budget Control and Cost Management: Develop detailed budgets for each project phase. Track project expenses against forecasts, ensuring that any deviations are identified and addressed early. Appropriately allocate resources and manage them efficiently.
• Work closely with resource managers to ensure the right skills are available and utilized for successful project delivery.
• Proactively identify potential risks or bottlenecks in project delivery. Develop risk management plans, ensuring that preventive measures are in place and contingency plans are prepared.
• Quickly identify project issues and work collaboratively with the project team to develop effective solutions to maintain project timelines and outcomes.
• Maintain comprehensive documentation for all projects, including project charters, status reports, meeting notes, and post-project reviews. Ensure all documentation is clear, accurate, and readily available to stakeholders.
• Provide regular and ad hoc project status reports to senior leadership, highlighting key achievements, challenges, and resource needs. Prepare detailed project updates and executive summaries.
• Ensure all projects comply with Boston Scientific’s internal policies, including regulatory requirements and industry best practices. This includes IT security, data governance, and sustainability standards for Real Estate facilities.
• Contribute to the continuous improvement of project management processes and methodologies. Implement best practices that align with organizational goals and improve overall project efficiency.
• Work effectively across different time zones, cultures, and markets within the APAC region. Understand regional challenges and adapt project management strategies accordingly.
• Support and coordinate with global teams, ensuring alignment of project goals and consistent execution across regions.

Experience:

• 8-12 years of proven experience in managing IT infrastructure projects, including IT Data Centers and Real Estate Facility projects.
• Experience in managing complex global projects across different geographic locations, particularly in the APAC region.
• Hands-on experience in managing large-scale projects involving cross-functional teams.
• Experience in the MedTech, healthcare, or life sciences industry is a significant advantage.
• Certifications: Project Management Professional (PMP), PRINCE2, or similar project management certification preferred.
• Technical Skills: Strong understanding of IT infrastructure, data center operations, and real estate facility management. Familiarity with data center design and construction is highly desirable.
• Proficiency in project management tools Like MS Project, Jira, and GoPMO) is a plus.

Educational Background:

• Bachelor’s degree in Engineering or Information Technology, A Master’s degree in Business Administration (MBA), or a related field, is a plus.

India-Maharashtra, Pune

Key Responsibilities:

• Design and implement SAP solutions that support finance and controlling processes, with a focus on product costing.
• Collaborate with business stakeholders to understand their needs and translate them into technical solutions.
• Lead the development and maintenance of the SAP architecture for FI/CO and product costing, ensuring integration with other business processes and systems.
• Provide technical guidance and support to project teams, ensuring successful delivery of SAP projects related to FI/CO and product costing.
• Conduct regular assessments of the SAP architecture to identify areas for improvement and implement necessary changes.
• Stay updated with the latest trends and technologies in SAP FI/CO and product costing to ensure the organization remains competitive.
• Develop and maintain documentation related to SAP architecture and product costing processes.

Qualifications:

• Bachelor's degree in Information Technology, Computer Science, Finance, or a related field.
• Minimum of 10 years of experience working with SAP Finance (FI) and Controlling (CO) modules.
• Proven experience in designing and implementing SAP solutions for product costing processes.
• Strong understanding of product costing principles and methodologies.
• Experience with SAP S/4HANA and SAP ECC product costing components is highly preferred.
• Excellent problem-solving skills and the ability to diagnose and resolve technical issues.
• Strong communication and interpersonal skills, with the ability to work effectively with cross-functional teams.
• Experience with project management and the ability to lead multiple project activities simultaneously.

Preferred Qualifications:

• Experience with SAP S/4HANA and SAP ECC
• Knowledge of US GAAP, IFRS, and SOX requirements.
• Familiarity with SAP FI/CO integration with other SAP modules such as MM, SD, and PP.
• Knowledge of manufacturing processes and cost management.
• Strong leadership and team management abilities.

India-Haryana, Gurgaon

Purpose Statement:

Develops, establishes, and maintains quality engineering methodologies, systems, and practices which meet BSC, customer, and regulatory requirements. Serves as a Quality representative to improve awareness, visibility, communication on quality initiative.

Key Responsibilities:

• Be a part of core project team and lead the quality engineering across the entire development cycle.
• Support the development of CTQ’s, design input and output documents.
• Support the fixture qualification and test method validation.
• Support the development and implementation of design verification and validation plans with project design lead.
• Support product risk management, usability, reliability and design validation efforts for new product development and design change projects.
• Participate and implement tools like Design of Experiments (DOE’s), FMEA sessions, Risk Management and ensure compliance to CTQ’s and safety requirements.
• Responsible for co-leading stage gate reviews and signatory on all PDP document approvals
• Manage electronic document control and version control on all project related documents.
• Ensure adherence to the quality systems and design assurance SOPs and Boston Scientific’s PLCP.
• Support usability, reliability, testing, verification and validation testing – internal and local vendors.
• Provide statistical testing and reliability plans.
• Work closely with regulatory team to drive alignment of project documentation and regulatory requirements.
• Provide quality and regulatory compliance guidance as needed to product development or design change project teams to assure country specific compliance to the laws and regulations of the targeted market for distribution.
• Ensure appropriate Project/Sustaining Quality Deliverables are created and properly executed (e.g. Project Design & Development Plan, Risk Management Plan, Hazard Analysis, Use and Design FMEA, Field Assessment Plan, and Software Validation Plan if applic
• Co-Lead CAPA efforts, and apply sound, systematic problem-solving methodologies identifying, prioritizing, communicating, and driving resolution of quality issues (e.g., 5 why’s analysis, Is-Is Not analysis, and Six Sigma problem solving methodologies).
• Devise and support the implementation of effective quality assurance, process controls, statistical analyses, and metrics that assure products meet or exceed internal quality as well as statutory requirements.
• Participate in ISO13485 site certification for the R&D center.

Requirements:

• Bachelors (or higher) degree in engineering with preference mechanical engineering.
• 5-7+ years of experience in medical device R&D quality engineering, systems and / or quality engineering supporting R&D projects, design assurance and documentation.
• Professional training and certification in in Quality Management Systems including ISO 13485, Risk management ISO 14971, design assurance / control, verification and validation.
• Sound understanding of medical device regulatory requirements for Class II and III medical devices.
• Project planning – resourcing, timelines, quality and budgets.
• Skilled in implementing Quality tools like design of six sigma, risk management, FMEA, FTA (Fault Tree Analysis).
• Preference for candidates with CQE certification or similar training and experience
• Proficient in project management tools like MS project.
• Experience in GD&T
• Well versed with statistical analytical techniques and s/w tools like MATLAB, MINITAB.

India-Haryana, Gurgaon

Purpose Statement:

Provide Software Quality Assurance support, to corporate software policies and regulations, at the Penang site. Provides support on software validation requirements to project teams that are implementing software systems and provides an independent review to teams.

Key Responsibilities:

• Develop an in-depth knowledge of BSC’s policies and procedures, especially those that apply to BSC's software. Understand and be able to explain how these policies achieve compliance with appropriate regulations and standards.
• Be able to interpret policies and regulations in support of a wide variety of software such as Custom, Off-The-Shelf, as well as everything from equipment controllers to database-driven solutions.
• Apply these policies and procedures to the site’s software systems and computer-driven equipment.
• Be able to explain software validation deliverables to business owners of the applications.
• Ability to perform risk analysis on multiple systems.
• Create validation documentation for a wide range of software applications including equipment software.
• Provide guidance and direction on the acceptability of Software Quality deliverables, based on requirements and templates given.

Requirements:

• Bachelors (or higher) degree in engineering with preference Computer Science.
• 5-7+ years of experience in medical device R&D quality engineering, systems and / or quality engineering supporting R&D projects, design assurance and documentation.
• Professional training and certification in in Quality Management Systems including ISO 13485, Risk management ISO 14971, design assurance / control, verification and validation.
• Sound understanding of medical device regulatory requirements for Class II and III medical devices.
• Project planning – resourcing, timelines, quality and budgets.
• Skilled in implementing Quality tools like design of six sigma, risk management, FMEA, FTA (Fault Tree Analysis).
• Preference for candidates with CQE certification or similar training and experience
• Proficient in project management tools like MS project.
• Experience in ISO 62304

India-Haryana, Gurgaon

Responsible for providing mechanical engineering support in the maintenance of project DHF deliverables in Requirements Management (RM) tool for new and sustaining medical device products (invasive and non-invasive).

Key Responsibilities:

• Read and interpret technical drawings, procedures, and protocols.

• Import and maintains the project documentation in online RM tool throughout all phases of NPD and Sustaining.

• Investigates and evaluates the compliance requirements driven from organization’s QMS/Work Instructions and validate the same in templates developed in RM tool.

• Investigates and evaluates existing RM tools/technologies – JAMA, Polarion etc.

• Investigates compliance gaps in project documents and resolve them with project stake holders. Collaborate with cross-functional process, method, and teams to understand and implement solutions to resolve compliance gap issues in documents.

• Performs validation of patches and versions of RM tool as and when available.

• Support multiple projects across different time zones - Asia, Ireland, and North America

Qualifications:

• Mechanical Engineering ( B.E./B.Tech) with 8-10 years of experience.

• Preferred experience in management of DHF documentation during full life cycle of medical device as per ISO 13485, and ISO 14971

• Preferred experience in RM tools like JAMA, Polarion, DOORS, Cockpit.

• Knowledge of MS Office Tools – Word, Excel, PowerPoint.

• Strong attention to detail with good communication skills.

• Strong strategic / analytical thinking and problem-solving abilities, with a data-driven approach to decision-making.

• Ability to collaborate and work as a team player.

• Nice to have experience in product lifecycle management software and tools.

• Willingness to work in an agile environment.