Project Manager

GForce Life Sciences; Arlington (TN); On-site; USD 76,000 - 124,000; Full time

Job summary

GForce Life Sciences seeks a Project Manager - Individual Contributor to support EU MDR compliance efforts at the Arlington, TN site. This 9-month, on-site role requires coordinating cross-functional teams to deliver compliant project plans on time and within budget.

The candidate will identify risks, manage schedules and budgets, and communicate with internal stakeholders to ensure successful delivery. A strong PM background and ability to work independently are essential.

Qualifications

• Minimum of 4 or more years of relevant project management experience.
• Bachelor’s degree or equivalent in a related field.
• Demonstrated ability to lead cross-functional teams in project execution.
• Strong organizational skills with attention to detail in managing schedules, budgets, and risks.
• Professional mastery of project management principles, with the ability to work independently with minimal supervision.

Responsibilities

• Lead a cross-functional team in development and execution of project management plans for EU MDR compliance.
• Identify risks and implement mitigation strategies to ensure project success.
• Coordinate project activities, schedules, and budgets to facilitate on-time and within-budget delivery.
• Monitor progress from initiation through delivery, interfacing with internal stakeholders.
• Organize interdepartmental meetings and ensure communication facilitates project completion.
• Apply professional expertise independently, making evaluative judgments based on factual analysis.

Skills

Project management

Cross-functional leadership

Risk management

Budget management

Communication

Education

Bachelor’s degree or equivalent

Job description

SummaryOur client, a manufacturing organization, has engaged GForce Life Sciences to provide a Project Manager - Individual Contributor. This position will support the implementation of the EU Medical Device Regulation (EU MDR) requirements at the Arlington manufacturing site.

9 month contract

Must be able to work on a W2

On-site in Arlington, TN

SummaryOur client, a manufacturing organization, has engaged GForce Life Sciences to provide a Project Manager - Individual Contributor. This position will support the implementation of the EU Medical Device Regulation (EU MDR) requirements at the Arlington manufacturing site.

DUTIES / EXPECTATIONS OF ROLE

• Lead a cross-functional team in development and execution of project management plans for EU MDR compliance.
• Identify risks and implement mitigation strategies to ensure project success.
• Coordinate project activities, schedules, and budgets to facilitate on-time and within-budget delivery.
• Monitor progress from initiation through delivery, interfacing with internal stakeholders.
• Organize interdepartmental meetings and ensure communication facilitates project completion.
• Apply professional expertise independently, making evaluative judgments based on factual analysis.

Mandatory Requirements

• Minimum of 4 or more years of relevant project management experience.
• Bachelor’s degree or equivalent in a related field.
• Demonstrated ability to lead cross-functional teams in project execution.
• Strong organizational skills with attention to detail in managing schedules, budgets, and risks.
• Professional mastery of project management principles, with the ability to work independently with minimal supervision.

NICE TO HAVE

• Experience in the manufacturing industry.
• Familiarity with EU MDR regulations and compliance efforts.
• Previous work on regulatory or quality projects related to medical devices.