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ct Manager with Medical Device Exp. :: Local to MA :: USC & GC at Remote, Remote, USA
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ription
USC/GC
need LinkedIn, VISA DL
Local to MA 
in Raynham, MAthis is HYBRID, 3x onsite a week, Tues, Wed, and Thurs.  This contract goes to at least the end of 2025, most likely to extend
We are seeking a detail-oriented and proactive Project Manager to support a cross-functional initiative related to MDR regulations and the EUDAMED database. This role will be instrumental in ensuring timely and accurate data submissions for the UDI data module, working across both Regulatory and Supply Chain teams. This position will coordinate efforts between Supply Chain and Labeling, ensuring project milestones are met, stakeholders are engaged, and any challenges are addressed.
Principal Roles and Responsibilities  
Lead and manage all aspects of project planning, execution, and delivery.
Define project scope, goals, and deliverables in collaboration with stakeholders.
Develop detailed project plans and schedules, ensuring resource allocation and task prioritization.
Coordinate with cross-functional teams to ensure project milestones are achieved.
Monitor and track project progress, adjusting plans as necessary to stay on track.
Manage project risks, issues, and changes to mitigate negative impacts.
Ensure clear and consistent communication with team members and stakeholders.
Conduct regular project meetings to review progress, resolve issues, and provide updates.

Qualifications
Proven experience as a Project Manager or similar role.
Strong leadership, communication, and organizational skills.
Proficiency in Microsoft applications
Working knowledge of Medical Device Regulations Legal Manufacturing requirements
Demonstrated knowledge and expertise in bridging technical and business disciplines, evaluating and determining appropriate risks required

Skills:
Excellent problem-solving and decision-making abilities.
Strong interpersonal and team management skills.
Ability to work effectively with clients and other stakeholders.
ription
USC/GC
need LinkedIn, VISA DL
Local to MA 
in Raynham, MAthis is HYBRID, 3x onsite a week, Tues, Wed, and Thurs.  This contract goes to at least the end of 2025, most likely to extend
We are seeking a detail-oriented and proactive Project Manager to support a cross-functional initiative related to MDR regulations and the EUDAMED database. This role will be instrumental in ensuring timely and accurate data submissions for the UDI data module, working across both Regulatory and Supply Chain teams. This position will coordinate efforts between Supply Chain and Labeling, ensuring project milestones are met, stakeholders are engaged, and any challenges are addressed.
Principal Roles and Responsibilities  
Lead and manage all aspects of project planning, execution, and delivery.
Define project scope, goals, and deliverables in collaboration with stakeholders.
Develop detailed project plans and schedules, ensuring resource allocation and task prioritization.
Coordinate with cross-functional teams to ensure project milestones are achieved.
Monitor and track project progress, adjusting plans as necessary to stay on track.
Manage project risks, issues, and changes to mitigate negative impacts.
Ensure clear and consistent communication with team members and stakeholders.
Conduct regular project meetings to review progress, resolve issues, and provide updates.

Qualifications
Proven experience as a Project Manager or similar role.
Strong leadership, communication, and organizational skills.
Proficiency in Microsoft applications
Working knowledge of Medical Device Regulations Legal Manufacturing requirements
Demonstrated knowledge and expertise in bridging technical and business disciplines, evaluating and determining appropriate risks required

Skills:
Excellent problem-solving and decision-making abilities.
Strong interpersonal and team management skills.
Ability to work effectively with clients and other stakeholders.
ription
USC/GC
need LinkedIn, VISA DL
Local to MA 
in Raynham, MAthis is HYBRID, 3x onsite a week, Tues, Wed, and Thurs.  This contract goes to at least the end of 2025, most likely to extend
We are seeking a detail-oriented and proactive Project Manager to support a cross-functional initiative related to MDR regulations and the EUDAMED database. This role will be instrumental in ensuring timely and accurate data submissions for the UDI data module, working across both Regulatory and Supply Chain teams. This position will coordinate efforts between Supply Chain and Labeling, ensuring project milestones are met, stakeholders are engaged, and any challenges are addressed.
Principal Roles and Responsibilities  
Lead and manage all aspects of project planning, execution, and delivery.
Define project scope, goals, and deliverables in collaboration with stakeholders.
Develop detailed project plans and schedules, ensuring resource allocation and task prioritization.
Coordinate with cross-functional teams to ensure project milestones are achieved.
Monitor and track project progress, adjusting plans as necessary to stay on track.
Manage project risks, issues, and changes to mitigate negative impacts.
Ensure clear and consistent communication with team members and stakeholders.
Conduct regular project meetings to review progress, resolve issues, and provide updates.

Qualifications
Proven experience as a Project Manager or similar role.
Strong leadership, communication, and organizational skills.
Proficiency in Microsoft applications
Working knowledge of Medical Device Regulations Legal Manufacturing requirements
Demonstrated knowledge and expertise in bridging technical and business disciplines, evaluating and determining appropriate risks required

Skills:
Excellent problem-solving and decision-making abilities.
Strong interpersonal and team management skills.
Ability to work effectively with clients and other stakeholders.

Keywords: green card Massachusetts
ct Manager with Medical Device Exp. :: Local to MA :: USC & GC
[email protected]
[email protected]
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04:03 AM 05-Feb-25


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