Jobs at Trouva

As the Lead Cloud DevOps Platform Engineer, you will design and maintain the internal developer platform, ensure compliance, guide teams, and optimize cloud resources to advance health technology.

Design, develop, and implement test methods for diagnostic systems, ensuring quality and reliability through testing, validation, and cross-functional collaboration.

As a SQA Test Automation Intern, you'll design automated test scripts, maintain test frameworks, execute test cases, and help integrate tests into CI/CD pipelines.

The Diagnostic Account Executive promotes diagnostic technology, manages sales accounts, blocks competition, builds sales forecasts, and represents the company at trade shows.

The Manager of Regulatory Clinical Services develops and oversees clinical evaluations, post-market follow-ups, and safety reports for medical devices, ensuring compliance with EU MDR and global regulations.

The Associate Director drives operational planning and communication across teams, enhancing product availability strategies and improving processes for effective execution.

The Program Manager oversees complex software programs, leading cross-functional teams, ensuring compliance, managing risks, and driving process improvements throughout the software development lifecycle for medical devices.

The Principal Regulatory Intelligence & Strategy Specialist monitors global regulatory changes, advises on regulatory strategy, ensures compliance, and supports product development across the Surgical Division.

The Sales Education and Development Manager will lead training programs for Oncology sales teams, enhancing product knowledge and sales skills through effective curriculum design, delivery, and collaboration with cross-functional teams.

Lead cross-functional teams to drive new product development for medical devices, ensuring compliance with ISO and FDA regulations.

Lead strategic programs in medical device innovation, manage global cross-functional teams, oversee budgets, ensure project readiness, and mentor junior members.

The Clinical Operations Quality Manager oversees clinical trials, ensuring quality and compliance, and collaborates with cross-functional teams. Responsibilities include managing CROs, quality assurance, regulatory support, and developing operational processes.

The Recall Coordinator will manage global field actions, develop recall strategies, conduct health risk evaluations, and communicate with stakeholders and regulatory bodies to ensure compliance in the medical device industry.