Global Marketing Management (Onsite) - Req Exp in Regulated Industry

Job Title:

Global Marketing Management

Job Location:

17200 Laguna Canyon Road, Irvine, California, United States of America, 92618

Duration:

12 Months

Key Responsibilities

Partner with regional marketing teams to understand market needs, collect insights, and ensure consistent global messaging and positioning. Assist in coordinating product availability, demand planning, and cross‑regional alignment to support commercial success. Track and report global product adoption, customer usage trends, and key commercial metrics.

Develop and update marketing collateral, product presentations, sales enablement tools, and training materials. Support campaign execution, product launches, and promotional activities across regions. Conduct competitive analysis and market research to inform product strategy and positioning.

Support end‑to‑end product lifecycle activities, including product introductions, updates, discontinuations, and quality/improvement initiatives. Monitor product performance, competitive activity, and customer feedback to identify enhancement opportunities and risks. Maintain product documentation, forecasts, and SKU management to ensure global accuracy and continuity.

Work closely with engineering, clinical, regulatory, and operations teams to support product updates, quality improvements, and compliance activities. Participate in field visits, customer feedback cycles, and VOC activities to deepen understanding of user needs. Support project teams with timelines, documentation, and communications to ensure aligned, on‑time delivery of initiatives.

Qualifications

Bachelor’s degree in Marketing, Business, Engineering, Life Sciences, or related field.

1-3 years of experience in product management, marketing, or related healthcare/technology field (medical device experience preferred).

Strong analytical, communication, and organizational skills.

Ability to collaborate in a cross‑functional, fast‑paced environment.

Proficiency in PowerPoint, Excel, and project management tools; familiarity with medical device regulations is a plus.

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