Senior PM Global Medical Devices Regulatory & Integration

Real Staffing Group; Milpitas (CA); On-site; USD 89,000 - 126,000; Part time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

Job summary

Medical Device Company in Milpitas, CA seeks a Senior Project/Program Manager to drive a global regulatory registration and product transition initiative on a 1-year, W2 contract. Onsite in Milpitas with possible remote consideration for exceptional candidates operating on Pacific Time.

The role requires 10+ years in program management within regulated life sciences, a Bachelor's degree, and PMP certification.

Qualifications

• Bachelor's degree in business, science, engineering, operations, information systems or related discipline is required.
• PMP certification is essential.
• At least ten years of progressive project or program management experience, preferably in a regulated life sciences environment.
• Expertise in integrated project planning, regulatory submissions, technical dossier management, quality and design controls, labeling transitions, and RAID management.
• Advanced proficiency in Excel with strong skills in Power BI or comparable dashboard tools; experience using PowerPoint, Teams, SharePoint, and project-planning platforms.

Responsibilities

• Drive a major global regulatory registration and product transition initiative.
• Integrate activities across regulatory, quality, technical, labeling, operational, commercial, and IT functions.
• Translate program objectives into actionable plans and manage dependencies and risks.
• Maintain reliable program data, reporting, and dashboards; consolidate information from multiple workstreams to identify trends and risks.

Skills

Integrated project planning

Regulated life sciences

Regulatory submission

Technical dossier management

Quality

Design controls

Labeling

Artwork management

Education

Bachelor's degree in business/science/engineering

Tools

Microsoft Excel

Power BI

PowerPoint

Microsoft Teams

SharePoint

Project-planning platforms

Job description

Medical Device Company in Milpitas, CA seeks a Senior Project/Program Manager to drive a global regulatory registration and product transition initiative on a 1-year, W2 contract. Onsite in Milpitas with possible remote consideration for exceptional candidates operating on Pacific Time.

The role requires 10+ years in program management within regulated life sciences, a Bachelor's degree, and PMP certification.