Urwah Admin

Zimmer Biomet

<div>At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient&rsquo;s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.<br>
<div><div><div><h2 class="jobSectionHeader"><b>
What You Can Expect</b></h2>
</div><div><p>
The Systems Engineer &ndash; Complaint &amp; Event Investigation is responsible for conducting rigorous, compliant investigations of product complaints, nonconformances, and adverse events to determine root cause, assess device and patient impact, and support regulatory decision-making. This role plays a critical role in post-market surveillance, MDR assessment, risk management linkage, and inspection readiness.<br>
The position partners closely with Quality, Regulatory Affairs, Manufacturing, R&amp;D, and Clinical teams and is especially suited to complex electromechanical or robotic medical devices.</p><p></p><p><b><br>
Work Location: Bangalore</b><br>
<b>Work Mode: Hybrid (3 Days in office)</b><b>
</b></p></div></div><div><div><h2 class="jobSectionHeader"><b>How You'll Create Impact</b></h2>
</div><div><p><b>
Complaint &amp; Event Investigation</b></p><ul><li>
Conduct thorough investigations of complaints, nonconformances, and adverse events</li><li>
Determine root cause, contributing factors, and device performance impact</li><li>
Evaluate investigation data including complaint records, service data, manufacturing history, and design documentation</li><li>
Ensure investigations are completed accurately, thoroughly, and within required timelines</li></ul><p><b>
FDA Regulatory Compliance</b></p><ul><li>
Perform investigations in accordance with 21 CFR Part 820 (Quality System Regulation)</li><li>
Support 21 CFR Part 803 (Medical Device Reporting &ndash; MDR) reportability assessments</li><li>
Provide investigation outputs that support regulatory submissions and health authority inquiries</li><li>
Ensure documentation meets FDA and internal quality expectations</li></ul><p><b>
Risk &amp; Patient Safety Evaluation</b></p><ul><li>
Assess patient safety, clinical risk, and device performance impact of reported events</li><li>
Link investigation outcomes to risk management activities per ISO 14971</li><li>
Support updates to risk files, hazard analyses, and risk controls based on post-market findings</li></ul><p><b>
Cross-Functional Coordination</b></p><ul><li>
Collaborate with Quality, Regulatory Affairs, Manufacturing, R&amp;D, Clinical, and Supplier Quality teams</li><li>
Facilitate cross-functional reviews to align on investigation conclusions and next steps</li><li>
Support escalation to CAPA, design changes, process improvements, or MDR reporting as required</li></ul><p><b>
Documentation &amp; Inspection Readiness</b></p><ul><li>
Produce clear, complete, and traceable investigation records</li><li>
Ensure documentation supports FDA inspections, internal audits, and management review</li><li>
Clearly document conclusions, rationale, and decision-making related to safety and compliance</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
What Makes You Stand Out</b></h2>
</div><div><p><b>
Preferred Qualifications</b></p><ul><li>
4 to 6 years total experience in regulated medical device environments</li><li>
Experience investigating serious injuries, malfunctions, or death-related events</li><li>
Experience with robotic, software-driven, or capital medical equipment</li><li>
Experience collaborating with Clinical or Medical Affairs teams</li><li>
Quality or regulatory certifications (CQE, RAC, Six Sigma &ndash; preferred)</li></ul><p><b>
Core Competencies</b></p><ul><li>
Strong analytical and systems-thinking skills</li><li>
High attention to detail and documentation rigor</li><li>
Ability to make defensible, risk-based decisions</li><li>
Clear communication with technical, clinical, and regulatory stakeholders</li><li>
Strong ownership for patient safety and compliance outcomes</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Your Background</b></h2>
</div><div><p><b>
Required Technical Skills</b><b>
</b></p><ul><li>Experience in medical device systems engineering, quality engineering, or post-market surveillance</li><li>
3+ years conducting complaint investigations or adverse event investigations in FDA-regulated environments</li><li>
Demonstrated experience supporting FDA inspections or regulatory audits</li><li>
Experience with complex electromechanical devices; robotic medical device experience preferred</li></ul><p></p><p><b><br>
Technologies &amp; Tools</b></p><p><b>
Quality &amp; Investigation Systems</b></p><ul><li>
Electronic Quality Management Systems (eQMS) (e.g., TrackWise, ETQ, MasterControl)</li><li>
Complaint handling and investigation workflows</li><li>
NCR, CAPA, and deviation management systems</li></ul><p><b>
Risk Management &amp; Analysis</b></p><ul><li>
ISO 14971 risk management frameworks</li><li>
Hazard analysis, FMEA/FMECA, fault tree analysis (support level)</li><li>
Root cause analysis tools (5 Whys, Fishbone/Ishikawa)</li></ul><p><b>
Regulatory &amp; Standards</b></p><ul><li>
21 CFR Part 820 (QSR)</li><li>
21 CFR Part 803 (Medical Device Reporting)</li><li>
ISO 13485 (preferred)</li><li>
Post-market surveillance and vigilance processes</li></ul><p><b>
Data &amp; Documentation</b></p><ul><li>
Technical documentation systems (PLM, document control systems)</li><li>
Data analysis tools (Excel &ndash; advanced; statistical tools preferred)</li></ul></div></div></div><br>
<p></p>
EOE/M/F/Vet/Disability</div>

System Engineer

<div>At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient&rsquo;s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.<br>
<div><div><div><h2 class="jobSectionHeader"><b>
What You Can Expect</b></h2>
</div><div><p>
The Senior Systems Engineer &ndash; Complaint Investigation &amp; Regulatory Compliance leads complex, high-risk investigations of medical device complaints to ensure timely, thorough, and compliant evaluations in accordance with 21 CFR Part 820.198. This role performs deep technical and clinical analyses to identify root causes and systemic issues, supports Medical Device Reporting (MDR) determinations under 21 CFR Part 803, and ensures alignment with ISO 14971 risk management.<br>
The role partners closely with Quality, Regulatory Affairs, R&amp;D, Manufacturing, Clinical, and Field Service teams and is especially suited to complex electromechanical or robotic medical devices.</p><p></p><p><b><br>
Work Location: Bangalore</b><br>
<b>Work Mode: Hybrid (3 Days in office)</b><b>
</b></p></div></div><div><div><h2 class="jobSectionHeader"><b>How You'll Create Impact</b></h2>
</div><div><p><b>
Regulatory-Compliant Investigation</b></p><ul><li>
Lead and execute complaint investigations in compliance with 21 CFR Part 820.198</li><li>
Ensure investigations are timely, complete, and well-documented, meeting internal and regulatory timelines</li><li>
Synthesize evidence from complaints, service data, manufacturing history, design documentation, and clinical inputs</li></ul><p><b>
Root Cause Determination</b></p><ul><li>
Perform advanced technical and clinical analyses to identify failure modes, contributing factors, and potential systemic issues</li><li>
Apply structured root cause methodologies (e.g., 5 Whys, Fishbone, Fault Tree)</li><li>
Differentiate between isolated events and trends requiring escalation (e.g., CAPA, design changes)</li></ul><p><b>
MDR Reportability Assessment</b></p><ul><li>
Support evaluation of complaints for MDR reportability in accordance with 21 CFR Part 803</li><li>
Document clear, defensible reportability decisions and rationale</li><li>
Partner with Regulatory Affairs to ensure consistent interpretation and timely submissions when required</li></ul><p><b>
Risk &amp; Patient Safety Assessment</b></p><ul><li>
Assess patient safety, clinical risk, and device performance impact of reported events</li><li>
Link investigation outcomes to risk management activities per ISO 14971</li><li>
Support updates to risk files, hazard analyses, and risk controls based on post-market findings</li></ul><p><b>
Documentation &amp; Audit Readiness</b></p><ul><li>
Maintain complete, accurate, and traceable investigation records</li><li>
Ensure documentation is inspection-ready for FDA inspections, internal audits, and management review</li><li>
Present investigation conclusions, trends, and recommendations to cross-functional and leadership audiences</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
What Makes You Stand Out</b></h2>
</div><div><p><b>
Preferred Qualifications</b></p><ul><li>
7 to 10 years total experience in regulated medical device environments</li><li>
Experience investigating serious injuries, malfunctions, or death-related events</li><li>
Experience collaborating with Clinical/Medical Affairs on safety assessments</li><li>
Experience with robotic, software-driven, or capital equipment</li><li>
Quality or regulatory certifications (CQE, RAC, Six Sigma &ndash; preferred)</li></ul><p><b>
Core Competencies</b></p><ul><li>
Strong systems thinking and analytical rigor</li><li>
High documentation discipline and audit readiness</li><li>
Ability to make defensible, risk-based decisions</li><li>
Clear communication with technical, clinical, and regulatory stakeholders</li><li>
Ownership mindset for patient safety and compliance outcomes</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Your Background</b></h2>
</div><div><p><b>
Required Technical Skills</b><b>
</b></p><ul><li>7&ndash;10 years of experience in medical device systems engineering, quality engineering, or post-market surveillance</li><li>
4+ years leading complaint investigations in FDA-regulated environments</li><li>
Demonstrated experience supporting FDA inspections or regulatory audits</li><li>
Experience with complex electromechanical devices; robotic medical device experience preferred</li></ul><p></p><p><b><br>
Technologies &amp; Tools</b></p><p><b>
Quality &amp; Investigation Systems</b><br>
Electronic Quality Management Systems (eQMS) (e.g., TrackWise, ETQ, MasterControl)<br>
Complaint handling, investigation, NCR, and CAPA workflows<br>
Service and manufacturing data systems (traceability, DHR/DHF access)</p><p><b>
Risk Management &amp; Analysis</b><br>
ISO 14971 risk management frameworks<br>
Hazard analysis, FMEA/FMECA, fault tree analysis<br>
Root cause analysis tools (5 Whys, Fishbone/Ishikawa)</p><p><b>
Regulatory &amp; Standards</b><br>
21 CFR Part 820.198 (Complaint Handling)<br>
21 CFR Part 803 (Medical Device Reporting)<br>
ISO 13485 (preferred)<br>
Post-market surveillance and vigilance processes</p><p><b>
Data, Reporting &amp; Documentation</b><br>
Advanced Excel; statistical or BI tools (Power BI/Tableau preferred)<br>
Document control and PLM systems<br>
Technical documentation and controlled records management<br>
<br>
<b>Education and Experience Requirements</b></p><p>
Bachelor&rsquo;s degree in systems engineering, Biomedical Engineering, Mechanical Engineering, Electrical Engineering, or related technical field (or equivalent experience)</p></div></div></div><br>
EOE/M/F/Vet/Disability</div>

Senior System Engineer

<div>At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient&rsquo;s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.<br>
<div><div><div><h2 class="jobSectionHeader"><b>
What You Can Expect</b></h2>
</div><div><p>
The SAP Senior FICO Analyst is a senior functional expert responsible for the design, configuration, integration, and support of SAP Finance and Controlling (FI/CO) solutions. This role partners closely with Finance, Accounting, FP&amp;A, and IT teams to deliver scalable, compliant, and high-performing financial systems aligned with enterprise financial processes and regulatory requirements.<br>
The role focuses on solution quality, financial process optimization, and production stability and operates without direct people-management responsibility.<br>
<br>
<b>Work Location: Bangalore</b><br>
<b>Work Mode: Hybrid (3 Days in office)</b></p></div></div><div><div><h2 class="jobSectionHeader"><b>
How You'll Create Impact</b></h2>
</div><div><p><b>
FI/CO Solution Design &amp; Configuration</b></p><ul><li>
Design, configure, and support SAP FI and CO modules to meet enterprise financial requirements</li><li>
Lead functional design workshops and translate business requirements into SAP configurations</li><li>
Configure and support financial processes including GL, AP, AR, Treasury, Asset Accounting, Cost Center Accounting, Profitability Analysis, and Product Costing</li><li>
Third party application or SAP bolt on knowledge of; High Radius, Vertex, MBC, AFC</li><li>
Ensure alignment with SAP best practices and enterprise architecture standards</li></ul><p><b>
Integration &amp; Financial Data Enablement</b></p><ul><li>
Lead and support integrations between SAP FI/CO and upstream/downstream systems (e.g., Sales, Procurement, Manufacturing, Banking)</li><li>
Support interfaces with external financial systems, banks, and reporting platforms</li><li>
Ensure financial data integrity, reconciliation, and auditability</li></ul><p><b>
Testing, Deployment &amp; Production Support</b></p><ul><li>
Lead functional testing, support UAT, and validate financial controls prior to production releases</li><li>
Act as a senior escalation point for complex FI/CO defects and production issues</li><li>
Perform root-cause analysis and implement long-term corrective actions</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
What Makes You Stand Out</b></h2>
</div><div><p><b>
Governance, Compliance &amp; Controls</b></p><ul><li>
Support SOX ITGC and business process controls related to financial systems</li><li>
Partner with Internal Audit, Compliance, and GRC teams on audits and control remediation</li><li>
Ensure configurations comply with accounting standards and regulatory requirements</li></ul><p><b>
Process Optimization &amp; Collaboration</b></p><ul><li>
Identify opportunities to improve financial processes, automation, and reporting</li><li>
Partner with Finance, FP&amp;A, Treasury, and Controlling stakeholders</li><li>
Provide guidance and informal mentoring to junior FI/CO analysts</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Your Background</b></h2>
</div><div><p><b>
Required Technical Skills</b></p><ul><li>
Design, configure, and support SAP FI and CO modules to meet enterprise financial requirements</li><li>
Configure and support financial processes including GL, AP, AR, Asset Accounting, Cost Center Accounting, Profitability Analysis, and Product Costing</li><li>
Integration &amp; Financial Data Enablement</li><li>
Lead functional testing, support UAT, and validate financial controls prior to production releases</li></ul><p><b>
Education and Experience Requirements</b></p><ul><li>
7&ndash;10+ years of experience supporting SAP FI/CO in enterprise environments</li><li>
6+ years in a senior functional analyst role</li><li>
10+ years supporting production SAP financial systems</li><li>
Experience delivering complex, cross-functional finance system initiatives</li><li>
8+ years total SAP finance experience</li><li>
Experience with S/4HANA Finance</li><li>
Experience supporting global or multi-country financial operations</li><li>
Experience in regulated or SOX-controlled environments</li><li>
SAP FI/CO certifications (preferred)</li></ul></div></div><p></p><div><div><h2 class="jobSectionHeader"><b><br>
Physical Requirements</b></h2>
</div></div><div></div><div><div><h2 class="jobSectionHeader"><b>Travel Expectations</b></h2>
</div></div></div><br>
<div></div>
EOE/M/F/Vet/Disability</div>

SAP Senior FICO Analyst

<div>At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient&rsquo;s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.<br>
<div><div><div><h2 class="jobSectionHeader"><b>
What You Can Expect</b></h2>
</div><div><p>
The Senior Risk Assessment &amp; Management Analyst supports global enterprise cyber and technology risk programs by independently executing complex risk assessments, maintaining risk data quality, and providing actionable risk insights to global stakeholders. This role operates with limited supervision and serves as a subject matter expert for risk methodology and assessment execution within the Bangalore GCC.</p><p></p><p><b><br>
Work Location: Bangalore</b><br>
<b>Work Mode: Hybrid (3 Days in office)</b><b>
</b></p></div></div><div><div><h2 class="jobSectionHeader"><b>How You'll Create Impact</b></h2>
</div><div><ul><li>Lead execution of enterprise cyber and technology risk assessments aligned to NIST CSF, ISO 27001, and internal risk frameworks.</li><li>
Perform inherent and residual risk analysis, control effectiveness assessments, and risk scoring.</li><li>
Maintain and update the enterprise risk register, ensuring accuracy, consistency, and timely remediation tracking.</li><li>
Conduct third-party, cloud, and application risk assessments in coordination with global security teams.</li><li>
Support business impact analyses (BIA) and risk scenario modeling.</li><li>
Prepare executive-ready risk reports, dashboards, and summaries for global leadership.</li><li>
Partner with Internal Audit and Compliance on control testing, evidence collection, and remediation validation.</li><li>
Identify risk trends and emerging threats and escalate insights to management.</li><li>
Mentor Risk Analysts and support onboarding and knowledge transfer within the GCC.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
What Makes You Stand Out</b></h2>
</div><div><p><b>
Technical Skills:</b></p><ul><li><b>
Experience:</b> 5+ years in GRC/Risk Management</li><li><b>
Core Competency: </b>Strong experience in end-to-end <b>Vendor/Third-Party Risk Assessment</b> (TPRM).</li><li><b>
Tools:</b> Proficiency in configuring/operating workflows in <b>any GRC platform</b> (<b>ServiceNow is preferred</b>/ Archer/ One Trust).</li><li><b>
Frameworks:</b> Experience with <b>ISO 27001</b> (critical as org is migrating) and <b>NIST</b> Cybersecurity Framework (CSF).</li><li><b>
Technical/Audit:</b> Ability to interpret SOC 1/SOC 2 reports and identify control gaps; experience <b>supporting SOX/HIPAA audits.</b></li><li><b>
Reporting:</b> High proficiency in Excel for reporting and analytics.</li></ul><p></p><p><b><br>
Soft Skills</b>:</p><ul><li>
Ability to translate complex technical risks into business language for stakeholders.</li><li>
Strong Communication skills</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Your Background</b></h2>
</div><div><p><b>
Educational Qualification &amp; Experience</b></p><ul><li>
Bachelor&rsquo;s degree in Information Security, Risk Management, IT, or related field.</li><li>
5+ years of experience in cybersecurity risk, IT risk, or GRC.</li><li>
Demonstrated experience supporting global enterprise risk programs.</li><li>
Strong analytical, documentation, and stakeholder communication skills.</li><li>
Ability to work independently and manage multiple concurrent assessments.</li></ul><p><b>
Technologies &amp; Tools</b></p><ul><li>
GRC Platforms: ServiceNow GRC, Archer, OneTrust</li><li>
Risk Frameworks: NIST CSF, ISO 27001, COBIT</li><li>
Third-Party Risk: SecurityScorecard, BitSight, OneTrust TPRM</li><li>
Cloud Risk &amp; Posture: AWS Security Hub, Azure Security Center</li><li>
Reporting &amp; Analytics: Power BI, Tableau, Excel</li><li>
Collaboration &amp; Workflow: Jira, Confluence, MS Teams</li></ul><p><b>
Preferred Certifications</b></p><ul><li>
CRISC, CISM, ISO 27001 Lead Implementer or Lead Auditor, CISSP (or in progress)</li></ul></div></div></div><br>
EOE/M/F/Vet/Disability</div>

Risk Assessment and Management Senior Analyst

<div>At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient&rsquo;s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.<br>
<div><div><div><h2 class="jobSectionHeader"><b>
What You Can Expect</b></h2>
</div><div><p>
The primary responsibilities of the Procurement Category Manager are to manage end-to-end procurement activities for their category and lead cross-functional collaboration for Utilities category. They will be responsible for securing total cost of ownership reductions for their assigned category, define global strategy, and work with other counterparts globally to execute the regional strategies.</p><p><b>
Work Location: Bangalore</b><br>
<b>Work Mode: Hybrid (3 Days in office)</b></p></div></div><div><div><h2 class="jobSectionHeader"><b>
How You'll Create Impact</b></h2>
</div><div><ul><li>End-to-end accountability for defining the category and supplier strategy with stakeholders and delivering year-over-year cost reduction within their category</li><li>
Strategic interface with suppliers and accountable for building strong and strategic supplier relationships</li><li>
Understand supplier market dynamics/intelligence and use it as input into the strategy</li><li>
Monitor and report compliance to Source-to-Pay process for their category/suppliers</li><li>
Drive supplier selection according to strategy, develop supplier base, and identify new suppliers</li><li>
Ensure alignment, anticipate changes, and drive activities based on supply market changes and broader company/functional strategy</li><li>
Lead contract and price negotiations withs suppliers</li><li>
Create and update supplier list according to category strategy</li><li>
Work closely with key stakeholders, member organizations and corporate functions to develop effective cost reduction strategies and implementation plans.</li><li>
Identify and define procurement best practices both within and external to Zimmer Biomet and ensure that those best practices are implemented in their category</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
What Makes You Stand Out</b></h2>
</div><div><ul><li>8+ years of track record in Strategic Procurement, specifically in Travel category.</li><li>
Ability to develop high impact procurement strategies.</li><li>
Previous experience with assigned category preferred.</li><li>
Cost analysis and management, negotiation and project management skills.</li><li>
Strategic thinking and leadership skills.</li><li>
Internal stakeholder and supplier relationship management.</li><li>
Excellent market information analysis skills and supply market knowledge.</li><li>
Good conflict resolution skills.</li><li>
Ability to work independently.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Your Background</b></h2>
</div><div><p><b>
Required Skills</b></p><ul><li>
Experience managing the full spend responsibility for an utilities category.</li><li>
Hands‑on experience in global procurement of utilities, with primary focus on natural gas and electricity.</li><li>
Strong capability in developing and executing procurement strategies, owning supplier relationships, conducting negotiations, performing cost analysis, and managing the RFP process.</li><li>
Ability to act as a change agent within the organization and drive continuous improvement.</li><li>
Solid understanding of different market types with foundational knowledge that can be applied across new geographies.</li><li>
Experience working with internal and external stakeholders.</li><li>
Expertise across the full sourcing lifecycle, including contract and vendor management.</li><li>
Strong proficiency in MS Office, particularly Excel for analytics and reporting.</li></ul><p><b>
Desired Skills</b></p><ul><li>
Specialized Procurement or related certification or training preferred.</li><li>
Lean and/or Six Sigma certification or training preferred.</li></ul><p><b>
Education and Experience Requirements</b></p><ul><li>
Experience Range: 10+ Years.</li><li>
Bachelor&rsquo;s Degree in any related discipline is required.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Travel Expectations</b></h2>
</div><div><p>
Upto 10%</p></div></div></div><br>
EOE/M/F/Vet/Disability</div>

Global Indirect Category Manager - Utilities

<div>At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient&rsquo;s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.<br>
<div><div><div><h2 class="jobSectionHeader"><b>
What You Can Expect</b></h2>
</div><div><p>
The Data Engineer is responsible for designing, developing, and maintaining scalable data pipelines and models within Snowflake and cloud environments, with a strong focus on enabling analytics through Power BI datasets/semantic models and DAX-based metrics. This role combines strong SQL and Python development with hands-on data engineering in Agile teams. The engineer will partner with architects, analysts, and business teams to deliver secure, reliable, high-quality data solutions that power analytics, reporting, and operational workflows</p><p></p><p><b><br>
Work Location: Bangalore</b><br>
<b>Work Mode: Hybrid (3 Days in office)</b></p></div></div><div><div><h2 class="jobSectionHeader"><b>
How You'll Create Impact</b></h2>
</div><div><ul><li>Design, build, and optimize SQL pipelines, transformations, and data models within Snowflake.</li><li>
Design and maintain reporting-ready data models that support Power BI datasets/semantic models and enterprise KPIs.</li><li>
Develop, standardise, and support DAX measures and KPI definitions in partnership with BI/Analytics stakeholders.</li><li>
Support and troubleshoot Power BI dataset refresh, performance, and reconciliation of key metrics back to source-of-truth tables.</li><li>
Develop Python-based data processing, automation, and integration workflows.</li><li>
Ingest and process structured, semi-structured, and unstructured data from databases, APIs, files, SaaS applications, and cloud storage.</li><li>
Implement ETL/ELT processes using SQL, Python, dbt, Snowflake features, or orchestration tools such as Airflow/Dagster.</li><li>
Contribute to Agile ceremonies and deliverables, ensuring timely and high-quality sprint outcomes.</li><li>
Implement CI/CD workflows and maintain version-controlled repositories (GitHub or equivalent).</li><li>
Support data governance, data quality, and secure data handling practices.</li><li>
Troubleshoot pipeline issues and proactively drive performance improvements.</li><li>
Maintain documentation, monitoring, alerting, and operational playbooks for pipelines.</li><li>
Collaborate with cross-functional teams (Data Engineering, Architecture, Data Science, Business) to translate requirements into technical solutions.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
What Makes You Stand Out</b></h2>
</div><div><ul><li>Ability to work effectively within cross-functional and Agile teams.</li><li>
Ability to define, validate, and explain BI metrics/KPIs and their implementation in DAX and Power BI models.</li><li>
Strong analytical, problem-solving, and critical-thinking skills.</li><li>
Clear written and verbal communication skills, including the ability to translate technical information for non-technical partners.</li><li>
Strong organizational skills with attention to detail and documentation.</li><li>
Ability to influence and collaborate across teams and geographies.</li><li>
Demonstrated ownership, adaptability, and willingness to embrace new technologies.</li><li>
Ability to understand and work across multiple technology stacks.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Your Background</b></h2>
</div><div><ul><li>4 + years of experience designing and developing SQL-based pipelines and data models.</li><li>
Power BI (Desktop/Service) and DAX (measures, KPI logic, performance basics)</li><li>
SQL (strong expertise), Snowflake, and data modeling</li><li>
Hands-on experience delivering or supporting Power BI datasets/semantic models and implementing DAX measures for enterprise KPIs.</li><li>
Hands-on experience with Python for ETL/ELT development and automation.</li><li>
Experience with Snowflake or other cloud data warehouses.</li><li>
Experience with orchestration platforms such as Airflow, Dagster, or Prefect.</li><li>
Experience with ingestion tools (Fivetran, Nifi, Airbyte) is a plus.</li><li>
Familiarity with APIs, JSON/CSV/XML/Parquet data formats, and cloud storage environments.</li><li>
Understanding of CDC mechanisms, data governance, and security best practices.</li><li>
Exposure to real-time or streaming ingestion (Kafka, EventHub) is beneficial.</li><li>
Experience working in Agile environments and delivering iterative outcomes.</li><li>
Ability to participate in and lead technical discussions.</li><li>
Interest or exposure to AI/ML workflows is a plus.</li></ul><p><b>
Preferred:</b></p><ul><li>
Python for data pipelines and automation</li><li>
dbt / SQL-based transformation frameworks</li><li>
Airflow, Dagster, or similar orchestration tools</li><li>
CI/CD tools (GitHub, GitLab, Azure DevOps)</li><li>
ETL/ELT tools such as Fivetran, Airbyte, Apache Nifi (preferred)</li><li>
Cloud services (AWS, Azure, GCP) and cloud storage<br>
<ul><li>Git-based version control.</li></ul></li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Physical Requirements</b></h2>
</div></div><div></div><div><div><h2 class="jobSectionHeader"><b>Travel Expectations</b></h2>
</div><div><p>
Up to 5%</p></div></div></div><br>
EOE/M/F/Vet/Disability</div>

Data BI Engineer

<div>At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient&rsquo;s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.<br>
<div><div><div><h2 class="jobSectionHeader"><b>
What You Can Expect</b></h2>
</div><div><p>
The primary responsibilities of the Procurement Category Manager are to manage end-to-end procurement activities for their category and lead cross-functional supplier qualifications for their assigned category. They will be responsible for securing total cost of ownership reductions for their assigned category, define global strategy, and work with other counterparts globally to execute the regional strategies.</p><p><b>
Work Location: Bangalore</b><br>
<b>Work Mode: Hybrid (3 Days in office)</b></p></div></div><div><div><h2 class="jobSectionHeader"><b>
How You'll Create Impact</b></h2>
</div><div><ul><li>End-to-end accountability for defining the category and supplier strategy with stakeholders and delivering year-over-year cost reduction within their category</li><li>
Responsible for the development and execution of global category strategies for IT Services, Hardware, Software, and Telecom. This role may be for one or several of the IT sub categories listed.</li><li>
Strategic interface with suppliers and accountable for building strong and strategic supplier relationships</li><li>
Understand supplier market dynamics/intelligence and use it as input into the strategy</li><li>
Monitor and report compliance to Source-to-Pay process for their category/suppliers</li><li>
Drive supplier selection according to strategy, develop supplier base, and identify new suppliers</li><li>
Ensure alignment, anticipate changes, and drive activities based on supply market changes and broader company/functional strategy</li><li>
Lead contract and price negotiations withs suppliers</li><li>
Create and update supplier list according to category strategy</li><li>
Work closely with key stakeholders, member organizations and corporate functions to develop effective cost reduction strategies and implementation plans.</li><li>
Identify and define procurement best practices both within and external to Zimmer Biomet and ensure that those best practices are implemented in their category</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
What Makes You Stand Out</b></h2>
</div><div><ul><li>5+ years of track record in Strategic IT Procurement</li><li>
Ability to develop high impact procurement strategies</li><li>
Previous experience with IT Category Management required</li><li>
Experience negotiating large and complex technology agreements</li><li>
Cost analysis and management</li><li>
Strategic thinking</li><li>
Negotiation skills</li><li>
Project management skills</li><li>
Leadership skills</li><li>
Internal stakeholder management</li><li>
Supplier relationship and management skills</li><li>
Excellent market information analysis skills and supply market knowledge</li><li>
Good conflict resolution skills</li><li>
Ability to work independently</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Your Background</b></h2>
</div><div><p><b>
Required Skills</b></p><ul><li>
End-to-end Strategic Procurement experience in IT category or sub-category</li><li>
Contract Management &ndash; Negotiations, signing contract agreements, driving RFP process.</li><li>
Cost Management - Cost analysis/ Expense analysis/ Spend analysis</li><li>
Internal (IT Leadership, Legal and finance for privacy) and External (Supplier/Vendor) stakeholder Management</li></ul><p><b>
Desired Skills</b></p><ul><li>
Proficiency in MS Office Suite, especially Excel for analytics, is required.</li><li>
Excellent Communication skills.</li><li>
Prior experience working in US/North America/European markets or Multinational organizations is preferred</li><li>
Open for both IT (Hardware or Software or both). Non-IT category with strong global procurement experience</li><li>
Power Bi/Tableau for analytics are plus</li><li>
SAP Ariba is nice to have</li></ul><p><b>
Education and Experience Requirements</b></p><ul><li>
Experience Range: 10+ Years</li><li>
Bachelor&rsquo;s Degree in a related discipline required</li><li>
Experience in a regulated environment preferred</li><li>
Specialized Procurement or related certification or training strongly preferred.</li><li>
Lean and/or Six Sigma certification or training preferred.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Travel Expectations</b></h2>
</div><div><p>
Must possess the ability to travel on a regular basis with overnight stays up to 25%. Occasional regional travel and global travel may be required.</p></div></div></div><br>
EOE/M/F/Vet/Disability</div>

Category Manager - IT

Join Zimmer Biomet and explore 7   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.