Remote Technical Program Manager — Medical Device Development

Plutus21 Capital, L.L.C.; Bogotá ciudad; À distance; COP 415 747 000 - 543 669 000; Plein temps

Résumé du poste

Plutus21 Capital, L.L.C. is seeking a Technical Program Manager to drive the development of a medical device across hardware, optics, software, imaging, systems engineering and manufacturing workstreams.

You will own the integrated plan, maintain records, and coordinate reviews and approvals to keep the program on track for testing and early production. You will lead cross-functional teams, track milestones, manage changes and maintain traceability from requirements through test evidence, with

Qualifications

• 5-10 years of experience in technical program management, engineering operations, systems engineering, product development or a related role.
• A degree in engineering, science or another technical field is preferred.
• Experience managing multidisciplinary hardware and software products and integrated schedules involving technical dependencies, suppliers, contractors and testing.
• Hands-on experience with bills of materials, configuration and change control, inventory tracking, purchasing coordination and material planning for prototype or early-production builds.
• Strong technical fluency and communication skills, with the ability to lead technical discussions, document decisions clearly, challenge assumptions, identify risks and hold contributors accountable while respecting technical ownership.

Responsabilités

• Maintain the integrated development plan and translate objectives into milestones, deliverables, owners, dependencies, resource needs and target dates through verification, regulatory submission and manufacturing transfer.
• Lead recurring meetings and milestone reviews, document decisions, maintain risk and action logs, and drive cross-functional blockers and open items to closure.
• Coordinate prototype builds, integration, software releases, test campaigns, and laboratory, cadaver or clinical activities, including materials, configurations, contractor deliverables, external bookings and readiness reviews.
• Maintain development and released bills of materials, including part numbers, revisions, quantities, supplier information and links to specifications and drawings, in partnership with engineering leads.
• Coordinate approved engineering changes and assess their impact on schedules, suppliers, inventory, testing, risks and documentation.
• Maintain records of build configurations, software versions and approved deviations.
• Track stock quantities, locations, allocations, open orders, shortages and replenishment needs, and work with on-site staff to record receiving, consumption, stock movements and inventory checks.
• Coordinate quotations, purchase requests, orders and supplier follow-up within approved budgets, monitor lead times and delivery commitments, and elevate material risks.
• Partner with engineering, quality and regulatory leads to maintain design and development records, coordinate design reviews, track missing documentation, and maintain traceability from requirements and risk controls to test evidence.
• Support controlled-document and approval workflows, training records, and follow-up on assigned quality actions under the direction of quality and regulatory leads.
• Maintain practical dashboards and processes, and provide concise leadership updates on progress, critical-path activities, resource constraints, risks, material readiness and decisions needed.
• Coordinate closely with on-site staff on inventory and build records.

Connaissances

Program management

Engineering operations

Systems engineering

Cross-functional leadership

Technical communication

Remote coordination

Formation

Engineering degree

Outils

Jira

Confluence

Smartsheet

Asana

Arena

OpenBOM

Description du poste

Plutus21 Capital, L.L.C. is seeking a Technical Program Manager to drive the development of a medical device across hardware, optics, software, imaging, systems engineering and manufacturing workstreams.

You will own the integrated plan, maintain records, and coordinate reviews and approvals to keep the program on track for testing and early production. You will lead cross-functional teams, track milestones, manage changes and maintain traceability from requirements through test evidence, with