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Job Requirements of Program Manager III:
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Employment Type:
Contractor
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Location:
Mansfield, MA (Onsite)
Do you meet the requirements for this job?
Program Manager III
Location: On-Site | Schedule: M-F | Type: Temp-to-Perm
Job Overview:
The Program Manager II will lead FDA remediation efforts and assist in other audit-related programs while managing multiple project managers. This role requires strong leadership, strategic oversight, and hands-on problem-solving skills to drive large-scale projects in a medical device manufacturing environment.
Key Responsibilities:
- Lead FDA Remediation Efforts: Oversee and execute strategies for compliance and remediation initiatives.
- Program & Project Oversight: Manage multiple projects/programs related to mergers, capacity expansions, manufacturing transfers, and process improvements.
- Stakeholder Management: Influence and collaborate with cross-functional teams, senior leaders, and regulatory bodies.
- Process Optimization: Implement Lean Six Sigma principles to improve operational efficiency and quality.
- Risk & Change Management: Develop and execute risk mitigation plans while ensuring smooth transitions during change initiatives.
- Budget & Resource Allocation: Manage program funding, budget, and resource distribution for maximum efficiency.
Required Qualifications:
Bachelor’s degree in Health Sciences, Business, or Financial Management (Advanced degree preferred) or High School Diploma/GED with equivalent experience.
10+ years of professional experience, with 5+ years in program management
Experience leading large-scale programs/projects with proven success
Strong leadership & stakeholder management skills
Expertise in program/project management methodologies (PMP preferred)
Excellent business, analytical, and planning skills
Tech-savvy with experience handling multiple projects
Preferred Qualifications:
Medical device industry experience
Lean Six Sigma knowledge/training
Experience with mergers, site expansions, and regulatory programs