- Location: Tennessee, United States
- Type: Contract
- Job ID: 10607
- Work Setting: On-Site
- Posted: September 16, 2026
- Closing Date: June 27, 2027
- Tax Status: W2
Project Manager
9 month contract
Must be able to work on a W2
On-site in Arlington, TN
SUMMARY
Our 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
MANDATORY REQUIREMENTS
NICE TO HAVE
9 month contract
Must be able to work on a W2
On-site in Arlington, TN
SUMMARY
Our 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.