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Mirion

Product Line Director - Nuclear Medicine

Mirion, Florham Park, New Jersey, us, 07932

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Product Line Director - Nuclear Medicine

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Mirion

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.

Responsibilities

Overall business management of assigned product lines through full product lifecycle from launch through rationalization.

Define global product line vision aligned with global market needs and opportunities (as defined by Market Driven Strategy (MDS)).

Contribute to the MDS and Innovation Driven Strategy (IDS) processes within the Mirion Business System (MBS).

Engage customers, support, and sales in key regions, as well as technology owners, to maintain ongoing capture of market needs and technology feedback to drive innovation and business value.

Create business cases to support the development of high-value new products, features and functionality.

Track performance of product lines (orders, sales, gross margin) and drive prompt and appropriate action as needed (sales improvement through promotional activities, quality improvement, lifecycle extension or rationalization).

Use the Product Development Process (with cross-functional teams) to deliver winning products; collaborate with global R&D 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.

D emonstrated 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.

Seniority level

Director

Employment type

Full-time

Job function

Health Care Provider

Industries

Manufacturing

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