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Capintec

Product Line Director

Capintec, Trenton, New Jersey, United States

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Recruiting professionals to join high-performing teams in the medical device field. Overview

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 acts 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 actions to improve sales, quality, or lifecycle management as needed. Utilize the Product Development Process with cross-functional teams to deliver winning products, partnering with global R&D to ensure on-time, on-budget launches to specification (embodies the classic “4 Ps” of marketing). Additional tasks and projects as assigned. Qualifications

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. Ability to manage complex initiatives with limited supervision. Experience navigating the regulatory submission landscape. Strong leadership with excellent organizational, verbal and written communication skills. Ability to prioritize effectively and manage multiple assignments concurrently. Proven analytical and problem-solving skills. Ability to work effectively both independently and as part of a team. Seniority level

Director Employment type

Full-time Job function

Product Management, Project Management, and General Business Industries

Appliances, Electrical, and Electronics Manufacturing, Medical Equipment Manufacturing, and Pharmaceutical Manufacturing

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