<![CDATA[JBL Resources: jobboards]]>

<![CDATA[JBL Resources: jobboards]]> https://JOBS.JBLRESOURCES.COM/ en-us <![CDATA[Engineering Project Manager]]> Engineering Project Manager
Location: Salt Lake City, Utah
About Our Client:
Our client is a highly sought after Fortune 500 Medical Device organization looking for results driven professionals like you! This facility focuses on Class III electromechanical ALS & BLS devices used around the world. Offering an environment where collaboration and results are equally important, this highly sought after company has a global reputation for growth and company culture.
Key Responsibilities:

Assisting in the management of multiple engineering projects to ensure efficient use of resources and timely completion of deadlines.
Prioritizing tasks and assigning team members to support project goals and streamline workflows.
Evaluating and authorizing changes that significantly impact the scope, budget, or timeline of a project, maintaining project integrity.
Leading engineering projects by monitoring progress and performance against the project plan, ensuring milestones are met.
Identifying and resolving operational problems promptly to minimize delays and keep projects on track.
Managing ongoing relationships with external contractors to ensure satisfactory standards of service and collaboration.

Qualifications:

Bachelorâs degree in Engineering, Industrial Management, or a related field.
Minimum of 6+ years of manufacturing experience in a regulated industry, with a strong understanding of quality systems.
Prior experience with companies like Philips, GE Healthcare, Boston Scientific, or similar organizations.
Proven track record leading engineering projects within a manufacturing setting.
Exceptional stakeholder management and communication skills.
Ability to navigate multiple priorities and adjust project plans accordingly.
Experience evaluating and implementing operational improvements.
Experience leading change initiatives in a factory environment.
PMP certification or other project management credentials.
Previous experience in medical manufacturing or related sectors such as healthcare devices or pharmaceuticals.
NO C2C CANDIDATES

Interested Candidates please apply on our website at https://jobs.jblresources.com.
For more information about our services and great opportunities at JBL Resources, please visit our website: https://www.jblresources.com.
JBL Resources is proud to have earned the reputation of being a premier provider of top talent professionals in the fields of engineering, human resources, logistics, operations, and supply chain management. As specialists in both permanent placement and contract services, our mission is to help companies and individuals become all they were created to be.
**JBL is an Equal Opportunity Employer and E-Verify Company]]> Tue, 08 Sep 2026 00:00:00 EDT 0 <![CDATA[EU MDR Project Manager]]> EU MDR Project Manager
Location: Greater Memphis, Tennessee Area
About Our Client:
Our client has recently merged with another highly sought after Medical Device company! They are focused on creating quality Class III implantables that will improve the lives and mobility of patients. This Fortune 500 Company is known for the culture and growth opportunity they provide their employees. Are you a top performer who is driven to be the best at what they do? This position may be just what youâre looking for!
Key Responsibilities:

Leading a cross-functional team to implement EU MDR requirements.
Developing and executing the project management plan.
Identifying risks and mitigation strategies to address potential project challenges.
Keeping stakeholders updated on project progress through regular communication.
Directing, managing, and monitoring project activities to ensure alignment with objectives.
Evaluating tradeoffs within the project to optimize outcomes.
Meeting with project stakeholders to understand and refine the project scope.
Reviewing project scope with the manager for approval and alignment.
Creating a detailed Work Breakdown Structure to organize project tasks.
Developing and managing the detailed project schedule.
Analyzing the critical path and major workstreams to identify potential delays.
Developing a risk management plan to proactively address project risks.
Identifying, analyzing, and understanding potential project risks.
Developing and monitoring a risk response plan to mitigate identified risks.
Estimating, acquiring, and assigning resources for the project team.
Defining roles, responsibilities, and deliverables for each team member.

Qualifications:

Bachelorâs degree in Engineering, Life Sciences, or related field (advanced degrees preferred).
Minimum of 5 years of project management experience in the medical device industry, with a focus on EU MDR or similar regulations.
Strong understanding of regulatory requirements, risk analysis, and mitigation strategies under EU MDR.
Expertise in developing and managing project schedules, Work Breakdown Structures (WBS), critical path analysis, and project risk plans.
Demonstrated ability to lead cross-functional teams, facilitate stakeholder communications, and drive project execution.
Excellent problem-solving, organizational, and communication skills.
Familiarity with regulatory compliance tools and project management software.
Knowledge of manufacturing processes and quality systems in a regulated environment.
Previous success in managing on-site projects and coordinating cross-departmental efforts.
NO C2C CANDIDATES