Senior Engineering Project Manager

Technical background: Bachelor’s or Master’s degree in Engineering, Computer Science, or a related field.
Experience in program/project management: 5+ years managing complex technical projects, preferably in hardware, semiconductors, or deep tech.
Highly organized and efficient: Proven track record of handling multiple projects and priorities.
Strong communication skills: Ability to translate technical challenges into actionable program management plans.
Experience with regulated industries: Familiarity with ISO 13485, FDA QSR, IEC 60601, or similar standards.
Data-driven decision-making: Proficient in project tracking, reporting, and analytics tools.
Ability to work across disciplines: Experience coordinating work across hardware, software, and regulatory teams.

Own the planning and execution of technical projects across the R&D, product development, new product introduction, and regulatory compliance.
Work closely with engineering, regulatory, quality, legal, and supply chain teams to ensure projects remain on track.
Track and manage project budgets, forecasts, and internal time tracking for accurate financial reporting.
Maintain alignment between Octiv’s technical priorities and those of its partners, ensuring deliverables meet strategic goals.
Keep detailed records of project milestones, technical dependencies, and risk management plans.
Work with internal and external teams to ensure medical device compliance, including FDA, ISO, and other regulatory standards.
Oversee procurement, production scheduling, and logistics to ensure timely delivery of products and components.
Identify bottlenecks in project execution and improve processes to enhance efficiency.