Project Manager

LSP Recruitment; San Francisco (CA); On-site; USD 100,000 - 130,000; Full time

Job summary

A leading medical technology firm is seeking an experienced Project Manager to supervise the development of life-saving medical devices. The role involves overseeing projects from initiation to completion, coordinating cross-functional teams, and ensuring compliance with FDA and ISO regulations. Candidates should hold a Bachelor's degree in engineering or a related field and possess over 8 years of relevant industry experience. This position is based in San Francisco, California.

Qualifications

• 8+ years of industry experience in coordinating the development of medical devices.
• Knowledge of FDA and ISO regulations for medical devices.

Responsibilities

• Overseeing projects from initiation to completion.
• Coordinating cross-functional teams, including engineering, production, quality, and regulatory affairs.
• Ensuring compliance with all regulatory standards throughout the product lifecycle.

Skills

Project management

Cross-functional team coordination

Risk assessment

Education

Bachelor's degree in engineering or related field

Job description

Representing a pioneering medical device company that specializes in the development of unique life-saving Medical Technologies.

They are currently seeking an experienced Project Manager to join their dynamic team. The successful candidate will have a robust background in the medical device industry, with specific experience in managing the development of medical devices from concept to completion.

Key responsibilities:

• Overseeing projects from initiation to completion, ensuring they are completed on time, and within scope and budget.
• Coordinating cross-functional teams, including engineering, production, quality, and regulatory affairs.
• Establishing and maintaining processes for managing project scope throughout the lifecycle, setting performance standards, and assessing risks.
• Ensuring compliance with all regulatory standards throughout the product lifecycle.
• Communicating effectively with all stakeholders to ensure alignment and meet project objectives.

Qualifications:

• Bachelor's degree in engineering, or related field.
• 8+ years of industry experience in coordinating the development of medical devices.
• Knowledge of FDA and ISO regulations for medical devices.