Senior Program Manager - PFAS

December 4

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Logo of Integer Holdings Corporation

Integer Holdings Corporation

Medical device outsource (MDO) manufacturer • R&D Capabilities • Transfer to Manufacturing • Manufacturing Process Oversight • Quality/Regulatory

10,000+ employees

Founded 1970

⚕️ Healthcare Insurance

💊 Pharmaceuticals

🧬 Biotechnology

💰 Post-IPO Debt on 2023-01

Description

• Lead the management and execution of multiple concurrent complex projects across functions and technologies. • Mentor and support the career development of direct reports. • Ensure compliance with customer agreements and manage project budgets and timelines. • Collaborate with executives on resource allocation for engineering projects. • Establish project portfolio reviews and governance for all projects. • Enhance internal project management processes and train teams accordingly. • Identify continuous improvement opportunities within product development and manufacturing processes.

Requirements

• Minimum Education: Bachelor’s degree in Engineering or related technical field. • Master’s degree in business or technical field preferred. • Certification from an accredited institution in Project/Program Management preferred. • Minimum Experience: Minimum of 10 years of experience, at least 5 in the medical products industry in addition to 4 in a project management capacity. • 2 to 5 years of previous direct supervision of professionals preferred. • Special Skills: Demonstrated ability to lead team activities. • Strong ability to coach. • Advanced critical thinking & problem-solving skills. • Strong communication, presentation, follow-through, and organizational skills. • Ability to effectively work both vertically and horizontally across the organization and cross functionally. • Collaboration and conflict resolution skills. • Recognized competence in both fundamental and advanced Project Management skills--ability and capability to share key learnings with internal and external audiences. • Specialized Knowledge: Knowledge of current FDA, ISO, MDD, and other related quality and regulatory system requirements that intersect with design control and product development activities. • Comprehension of product & process development engineering principles sufficient to allow participation in product and technology development program ideation, scoping, initiation, and execution. • Broad experience base with manufacturing processes across multiple products and processes, preferably inclusive of medical components, subassemblies and finished medical devices. • Well versed and cognizant of various schools of thought on Project Management techniques as evidenced by working knowledge of the Project Management Book of Knowledge (PMBOK) and likely a follower of Project Management forums and/or conferences. • Able to travel domestically and internationally, as required (up to 30% at times).

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