Senior Program Manager at Jobot
Andover, MA 01812
About the Job
Leading Medical Device Company Seeking Senior Program Manager - Strong Pay, Excellent Benefits, 401k match!
This Jobot Job is hosted by: Matt Gennari
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $170,000 - $200,000 per year
A bit about us:
We're a Medical Device Manufacturer that is hiring a Senior Program Manager to take ownership of a flagship product!
Why join us?
Competitive salary & bonus
Generous 401 (K) match
Excellent Health & Dental
Flexible spending accounts
Life & Disability insurance
Hybrid schedule
Job Details
This position is responsible for managing programs consisting of product development and/or sustaining projects within the Program Management Office.
Responsible for overall project planning, execution, to insure meets objectives (scope, schedule, cost, quality).
Leads the cross functional teams throughout the product development lifecycle, from conceptualization, through definition, design, realization, validation, to production release
Responsible for tracking and communicating project details as it relates to performance metrics, status, key decisions, risks, issues, and mitigation strategies to senior management.
Works closely with department heads regarding resource planning, schedules, budgets, and quality of deliverables
Contributes to program planning, strategic planning, budgeting, and process improvement initiatives.
Applies project management best practices while ensuring compliance to internal SOPs, QMS and FDA and other industry regulations.
Related Experience:
10+ years in the development of embedded systems, PC-based products, electro-mechanical systems, or medical devices.
5+ years project management in a cross-functional environment including multi-locational teams.
Thorough understanding of developing products using a structured new product development process.
Ability to work successfully across functional lines.
Knowledge of GMPs as defined by the FDA.
Experience with regulators and regulatory audits preferred.
Proficiency with project management tools, including MS Project, Excel, SharePoint and PowerPoint.
Skilled in leading multi-disciplinary teams including Engineering, Regulatory, Quality, Purchasing, Service, Production, in an FDA regulated environment.
Education:
BS in engineering discipline
Medical devices background is preferred
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
This Jobot Job is hosted by: Matt Gennari
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $170,000 - $200,000 per year
A bit about us:
We're a Medical Device Manufacturer that is hiring a Senior Program Manager to take ownership of a flagship product!
Why join us?
Competitive salary & bonus
Generous 401 (K) match
Excellent Health & Dental
Flexible spending accounts
Life & Disability insurance
Hybrid schedule
Job Details
This position is responsible for managing programs consisting of product development and/or sustaining projects within the Program Management Office.
Responsible for overall project planning, execution, to insure meets objectives (scope, schedule, cost, quality).
Leads the cross functional teams throughout the product development lifecycle, from conceptualization, through definition, design, realization, validation, to production release
Responsible for tracking and communicating project details as it relates to performance metrics, status, key decisions, risks, issues, and mitigation strategies to senior management.
Works closely with department heads regarding resource planning, schedules, budgets, and quality of deliverables
Contributes to program planning, strategic planning, budgeting, and process improvement initiatives.
Applies project management best practices while ensuring compliance to internal SOPs, QMS and FDA and other industry regulations.
Related Experience:
10+ years in the development of embedded systems, PC-based products, electro-mechanical systems, or medical devices.
5+ years project management in a cross-functional environment including multi-locational teams.
Thorough understanding of developing products using a structured new product development process.
Ability to work successfully across functional lines.
Knowledge of GMPs as defined by the FDA.
Experience with regulators and regulatory audits preferred.
Proficiency with project management tools, including MS Project, Excel, SharePoint and PowerPoint.
Skilled in leading multi-disciplinary teams including Engineering, Regulatory, Quality, Purchasing, Service, Production, in an FDA regulated environment.
Education:
BS in engineering discipline
Medical devices background is preferred
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
Salary
170,000 - 200,000 /year
