Quality Project Manager - 30424

OLSA Resources, Inc.; Princeton (NJ); On-site; USD 100,000 - 120,000; Full time

Job summary

A leading medical device company located in New Jersey is seeking a qualified professional to drive product development and manage quality initiatives. This role demands 6-10 years of quality-related experience in medical device or pharmaceutical manufacturing, alongside a 4-year degree in Engineering or Science. The ideal candidate will demonstrate strong project management skills and familiarity with programming languages. A PMI certification is a plus. Competitive compensation and benefits offered.

Qualifications

• 6-10 years of quality-related experience in medical device, diagnostics, or pharmaceutical manufacturing.
• Demonstrated success navigating a full software project life cycle.
• PMI certification desired.

Responsibilities

• Develop and manage project objectives and timelines for quality initiatives.
• Collaborate with project team to execute development plans for software.
• Accountable for driving product development design control.

Skills

Project management

Quality assurance

Risk assessment

Team leadership

Education

4-year degree in Engineering or Science

Tools

MS Project

Visio

C++

Java

C#

Job description

Overview

• Develop and manage project objectives, strategies, timelines and milestones for Quality related initiatives. Translate project goals into project tasks. Identify resource requirements, costs, and time schedules. Develop relationships with contractors, vendors and/or consultants. Develop an implementation plan, conduct risk assessments and develop contingency plans to accommodate unforeseen events. Manage the Management Review process. Identify gaps in Quality Processes and manage the development and implementation of improvements.
• Collaborate with the project team and technical leader to establish and execute development plans for medical device software. Lead the team in defining the product design control strategy as well as the overall scope, timeline and budget of the project. Drive for results and ensure the team remains focused on project objectives.
• Translate project goals into actionable project tasks. Identify resources, costs, schedules and relationships with contractors, vendors and/or consultants. Develop implementation plans, conduct risk assessments and contingency plans as needed.
• Position Accountability: accountable for driving product development design control from initiation through design transfer, including planning and interactions across R&D, Manufacturing, and Quality/Regulatory. Ensure that Design Control and compliance requirements are met. Ensure the successful completion of project tasks on time and within budget.

Qualifications

Must have a 4-year degree in Engineering, Science or related area or possess equivalent, relevant experience. Relevant experience would consist of 6-10 years quality-related experience in medical device, diagnostics or pharmaceutical manufacturing. Demonstrated success in navigating a full software project life cycle. PMI certification desired. MS Project, Visio. Familiar with programming languages such as C++, Java, C#. Familiar with platforms such as J2EE, Web Services. Working knowledge of current Internet technologies.