By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success.
At Integer, our values are embedded in everything we do.
Customer
We focus on our customers’ success
Innovation
We create better solutions
Collaboration
We create success together
Inclusion
We always interact with others respectfully
Candor
We are open and honest with one another
Integrity
We do the right things and do things right
Job Summary
The primary purpose of this position is to lead the strategic direction and execution of all product development and engineering initiatives and programs across product lines. This position will lead the deployment of enterprise wide portfolio and program management processes. This position will also be a direct liaison to the Sales and Marketing organization as they identify new business opportunities in this category.
Key Accountabilities and Responsibilities
1. Adheres to GB Core Beliefs and all safety and quality requirements.2. Directs new product development programs by establishing strategy, providing leadership and an organizationnecessary for successful implementation. Works closely with other departments to ensure proper implementation.3. Manages a team of Project Managers, Engineers and Technicians as they design, develop, and introduce new products and systems to production, both technically and economically.4. Ensures the timely completion and proper prioritization of product development projects on budget and per delivery milestones.5. Leads creation, deployment and maintenance of enterprise-wide portfolio and program management processes working in coordination with Business Category and R&D leaders6. Establishes and supports the Product Development Engineering team components and systems necessary to successfully complete critical company objectives and long range plans.7. Partners with Sales and Marketing team to identify new business opportunities. Participates in the development and analysis of new business and market opportunities.8. Stays informed of innovations in technology. Utilize this knowledge to proactively propose initiatives that drive value based on key strategic mandates.9. Monitor technologies being used within relevant industries, by both direct and indirect competitors, to help Greatbatch maintain its competitive advantage.10. Responsible for championing continuous improvement initiatives in engineering technology, skills, and tools.11. Coordinates product approval trials in collaboration with Greatbatch Clinical Regulatory resources as required, analyzes the outcomes, and makes appropriates modifications.12. Develops and utilizes Six Sigma and DMAIC techniques.13. Participates in succession planning for management positions and in the recruitment and/or development of new talent for positions.14. Directs and controls all budgets related to department.15. Performs other functions as required.Job RequirementsMinimum Education:15+ years of experience in engineering or related technical position with at least 10 years of experience in a managerial capacity.Minimum of 10 years of industry experience in one of the following areas: cardiovascular products including coronary balloons, stents, catheters, introducers and supporting accessoriesMinimum Experience:Ability to work in a company environment experiencing rapid growth and change.Established reputation as a professional leader from previous assignments and companies including strong relationships in the interventional community.Proven ability to assess business needs, identify key vendors and negotiate productive working relationships with suppliers.Proven management track record of success in leading groups in development of medical devices including navigation of regulatory and quality system compliance.Excellent problem-solving skills.Demonstrated ability in building program management processes and portfolio and pipeline planning tools.Excellent presentation, verbal and written communication skills required.Specialized Knowledge:A strong background in the management and technical development of complexprojects and products, including deep understanding of product design and process validation and verification of medical devicesExperience in working with quality management systems, ISO, and FDA (510K, PMA, CE).Ability to perform effectively under stressful conditions such as directional changes, tightdeadlines, and limited resources.Special Skills:Demonstrated ability to take a concept to production on time and on budget.Effective communication skills.Other: Some travel required.Salary: $114,000-167,200U.S. Applicants: EOE/AA Disability/Veteran