Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Convatec

PLM Application Engineer – Teamcenter

Convatec

Teamcenter Application Engineer providing in-house support for Siemens Teamcenter PLM platform. Involves debugging, customization, and compliance documentation in a regulated medical device environment.

Posted 7/2/2026full-timeRemote • 🇮🇳 IndiaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Teamcenter application management, including incident resolution, custom solution development, and compliance with medical device regulatory standards. Proficient in technical documentation and user training within a validated environment.

Highest-signal resume keywords
Teamcenter Incident ResolutionTeamcenter ITK DevelopmentComputer System Validation (CSV)Regulatory Compliance (FDA 21 CFR Part 11, ISO 13485)Technical Documentation Authoring

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Teamcenter Core ModulesITK APIsBMIDE Business ModellerJavaC++Workflow Handler DevelopmentData Model ConfigurationDebugging SkillsChange ManagementEnvironment Health Monitoring
Soft Skills
Analytical SkillsWritten CommunicationVerbal CommunicationTraining DeliveryStakeholder Presentation
Tools & Technologies
Active WorkspacePolarionAWSAzure
Industry Keywords
GxP SDLCISO 13485EU MDR 2017/745IEC 62304ISO 14971

Tech Stack

Tools & technologies
AWSAzureJavaSDLC

About the role

Key responsibilities & impact
  • Resolve L1/L2/L3 Teamcenter incidents and service requests within SLA
  • Investigate, diagnose, and resolve Teamcenter application defects, server errors, workflow failures, and data issues, applying structured root-cause analysis and providing permanent fixes with full traceability
  • Develop custom Teamcenter solutions using ITK APIs, BMIDE business modeller, Active Workspace client-side customization, Java or C++ extensions, and workflow handler development, all under a controlled GxP SDLC
  • Author and maintain controlled technical documents including System Design Specifications (SDS), Validation Plans, IQ/OQ/PQ protocols, SOPs, change control records, and user guides in compliance with ISO 13485 and 21 CFR Part 11 document control requirements
  • Support Computer System Validation (CSV) activities – including installation qualification, operational qualification, and performance qualification – to keep Teamcenter in a validated state aligned with EU MDR 2017/745, ISO 13485, and FDA 21 CFR Part 11
  • Manage day-to-day Teamcenter server administration: environment health monitoring, patch and upgrade planning, data model migrations
  • Participate in internal and external audits (FDA, Notified Body, ISO) as the Teamcenter SME, providing evidence of system validation, data integrity controls, and audit trail completeness
  • Manage change requests through the formal change control process, including impact assessments, regression testing, and updating validation documentation prior to deployment in the production environment
  • Deliver end-user training, create user guides and quick-reference materials, and provide ongoing helpdesk-level support to Teamcenter users across engineering, quality, and regulatory functions

Requirements

What you’ll need
  • Minimum of 3–5 years of hands-on Teamcenter experience in a production environment
  • Proficiency in Teamcenter core modules (BOM Management, Workflow, Classification, Change Management, Dispatcher) and Active Workspace; experience with Polarion
  • Hands-on development experience with Teamcenter ITK (C/C++ or Java), BMIDE data model configuration, workflow handler programming, and Active Workspace (AWC) client-side customization
  • Understanding of medical device regulatory requirements: FDA 21 CFR Part 11 (electronic records/signatures), ISO 13485 (QMS), EU MDR 2017/745, IEC 62304 (medical device software lifecycle), and ISO 14971 (risk management)
  • Strong analytical and debugging skills with the ability to trace complex multi-tier Teamcenter issues across server logs, database queries, and client-side behavior
  • Excellent written and verbal communication skills; able to produce clear technical documentation and present solutions to non-technical stakeholders including QA, Regulatory Affairs, and senior management
  • Experience with Teamcenter deployment on on-premise or hybrid infrastructure (AWS, Azure) is a plus
  • Ability to deliver end-user training, create user guides and quick-reference materials, and provide ongoing helpdesk support in a regulated medical device environment.

Benefits

Comp & perks
  • Health insurance
  • Flexible work arrangements
  • Professional development opportunities