Medasource
Project Manager, R&D Orthopedics (Contract)
Location:
Warsaw, IN; onsite 3 days/week
Engagement:
Long term contractor
Pharmaceutical Recruiter & Premier Delivery Lead at Medasource Role Summary:
The Project Manager will lead the coordination, scheduling, risk management, and cross‑functional alignment of a multi‑year medical device development program. This includes managing two major program schedules in 2026, partnering closely with the DRI, and providing ongoing visibility to senior leadership. The PM will operate fluidly across R&D, Regulatory, Quality, Supply Chain, HEMA, and Clinical organizations to ensure that all activities and deliverables meet stringent global regulatory standards.
Core Responsibilities: Project Management
Own and manage two major project schedules spanning three program waves/pillars.
Drive alignment across a large cross‑functional core team (~20 members).
Serve as the central hub for project communication, issue escalation, and decision‑driving.
Facilitate program meetings, action tracking, and formal risk reviews.
Utilize Smartsheet and “At Risk” tools for schedule analytics and risk‑adjusted planning.
Leadership & Communication
Communicate effectively with senior stakeholders, including the:
Head of R&D
President of Joint Recon Marketing & Commercial
Foster an accountable, engaged culture within the project team.
Partner directly with the DRI (Jamie), ensuring full transparency and alignment.
Technical / Engineering Contribution
Apply engineering judgment to interpret requirements and understand cross‑functional interdependencies.
Support technical tasks that fall within the PM’s scope and require an engineering mindset.
Assess cross‑functional risks and the integration of technical deliverables.
Compliance & Regulatory Alignment
Ensure project activities meet global regulatory expectations.
Operate effectively in a highly regulated medical device environment with strict process rigor.
Requirements: Experience
2–5 years of project management experience.
Background managing projects in highly regulated industries.
Medical device experience strongly preferred due to complex regulatory deliverables.
Experience working with cross‑functional teams and coordinating 15–25 stakeholders.
Comfortable presenting during 2–3 monthly leadership forums.
Technical & Industry Skills
Engineering background required (degree preferred but not mandatory).
Ability to understand and interpret technical deliverables.
Proficiency in schedule management, risk management, and cross‑functional orchestration.
Tools
Smartsheet (proficiency expected; easy to learn).
“At Risk” tools for risk‑adjusted schedule modeling.
Soft Skills
Outstanding written and verbal communication, with strong executive presence.
Ability to influence without authority and shape the team’s culture.
Strong personality fit — must collaborate effectively with the DRI and broader team.
Skilled in motivating teams, driving engagement, and addressing performance gaps.
Seniority level
Associate
Employment type
Contract
Job function
Project Management and Engineering
Industries
Hospitals and Health Care, Pharmaceutical Manufacturing, and Biotechnology Research
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Location:
Warsaw, IN; onsite 3 days/week
Engagement:
Long term contractor
Pharmaceutical Recruiter & Premier Delivery Lead at Medasource Role Summary:
The Project Manager will lead the coordination, scheduling, risk management, and cross‑functional alignment of a multi‑year medical device development program. This includes managing two major program schedules in 2026, partnering closely with the DRI, and providing ongoing visibility to senior leadership. The PM will operate fluidly across R&D, Regulatory, Quality, Supply Chain, HEMA, and Clinical organizations to ensure that all activities and deliverables meet stringent global regulatory standards.
Core Responsibilities: Project Management
Own and manage two major project schedules spanning three program waves/pillars.
Drive alignment across a large cross‑functional core team (~20 members).
Serve as the central hub for project communication, issue escalation, and decision‑driving.
Facilitate program meetings, action tracking, and formal risk reviews.
Utilize Smartsheet and “At Risk” tools for schedule analytics and risk‑adjusted planning.
Leadership & Communication
Communicate effectively with senior stakeholders, including the:
Head of R&D
President of Joint Recon Marketing & Commercial
Foster an accountable, engaged culture within the project team.
Partner directly with the DRI (Jamie), ensuring full transparency and alignment.
Technical / Engineering Contribution
Apply engineering judgment to interpret requirements and understand cross‑functional interdependencies.
Support technical tasks that fall within the PM’s scope and require an engineering mindset.
Assess cross‑functional risks and the integration of technical deliverables.
Compliance & Regulatory Alignment
Ensure project activities meet global regulatory expectations.
Operate effectively in a highly regulated medical device environment with strict process rigor.
Requirements: Experience
2–5 years of project management experience.
Background managing projects in highly regulated industries.
Medical device experience strongly preferred due to complex regulatory deliverables.
Experience working with cross‑functional teams and coordinating 15–25 stakeholders.
Comfortable presenting during 2–3 monthly leadership forums.
Technical & Industry Skills
Engineering background required (degree preferred but not mandatory).
Ability to understand and interpret technical deliverables.
Proficiency in schedule management, risk management, and cross‑functional orchestration.
Tools
Smartsheet (proficiency expected; easy to learn).
“At Risk” tools for risk‑adjusted schedule modeling.
Soft Skills
Outstanding written and verbal communication, with strong executive presence.
Ability to influence without authority and shape the team’s culture.
Strong personality fit — must collaborate effectively with the DRI and broader team.
Skilled in motivating teams, driving engagement, and addressing performance gaps.
Seniority level
Associate
Employment type
Contract
Job function
Project Management and Engineering
Industries
Hospitals and Health Care, Pharmaceutical Manufacturing, and Biotechnology Research
#J-18808-Ljbffr