Product Line Director - Nuclear Medicine

The Product Line Director will be a key driver with overall responsibility for the vision and strategy, and will lead a team to design, build, and launch a new suite of Nuclear Medicine products from the ground up. Demonstrates strong leadership and act as General Manager of their product lines, taking necessary actions to drive sustained success. Works collaboratively with different business functions including Engineering, Sales, Sales Operations, Service and Operations in order to deliver this mission.

Key Areas of Responsibilities:

• Overall business management of assigned product lines through full product lifecycle from launch through rationalization.
• Works with manager to define global product line vision that is fully aligned with global market needs and opportunities (as defined by Market Driven Strategy (MDS).
• Serves as a key contributor to the MDS and Innovation Driven Strategy (IDS) processes within the Mirion Business System (MBS).
• Ensures the regular engagement of customers, support, and sales in key regions, as well as technology owners, to maintain the ongoing capture of market needs and technology feedback, in order to drive innovation and business value.
• Creates Business Cases to support the development of high-value new products, features and functionality.
• Tracks performance of product lines (orders, sales, gross margin) and drives prompt and appropriate action as needed (sales improvement through promotional activities, quality improvement, lifecycle extension or rationalization).
• Uses the Product Development Process (working closely with cross functional teams) to deliver winning products (includes partnering with global R&D through the development cycle to ensure products are launched on time, on budget and to specification (embodies the classic "4 Ps" of marketing).
• Additional tasks and projects as assigned.

Knowledge, Skills and Abilities:

• 10+ years of product management, upstream/inbound marketing, or development experience, preferably in Nuclear Medicine or in a similar/related medical device industry.
• MS in Nuclear Technology (or related) with at least 8 years of relevant work experience, and at least 5 years in the direct field.
• Clinical knowledge in pharma/medical device development preferred.
• Experience with phased product development methodologies and tools needed.
• Ability to manage complex initiatives with limited supervision necessary.
• Must possess experience with navigating the regulatory submission landscape.
• Strong leadership with excellent organizational, verbal and written communication skills a must.
• Demonstrated ability to prioritize effectively and must be able to work on multiple assignments concurrently.
• Proven analytical skills and problem-solving techniques.
• Ability to work effectively both individually and as part of a team required.