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We are seeking a strategic Senior Product Manager to join our TrackWise Manufacturing offering team. In this individual contributor role, you will drive product strategy for our innovative medical device manufacturing solutions with a focus on reducing the cost of compliance through tight integration with TrackWise Digital. Reporting to the Offering Management Director, you will focus on optimizing Device History Records (DHR), Device Master Records (DMR), and quality management processes across the medical device manufacturing lifecycle. Your expertise in medical device manufacturing and quality documentation will be instrumental in developing solutions that streamline compliance activities, reduce overhead costs, and improve operational efficiency for our customers.

Key Responsibilities

•Drive market research to identify key segments and opportunities within medical device manufacturing for integrated compliance solutions

•Build compelling business cases and ROI models for offerings that reduce the cost of compliance through TrackWise Digital integration

•Develop and execute Voice of Customer (VOC) plans to gather deep insights on DHR, DMR, and quality management pain points

•Analyze VOC data to prioritize feature requirements and market opportunities

•Create product epics, user stories, and roadmaps in collaboration with Product Owners and development teams

•Develop go-to-market strategies that clearly articulate value proposition and competitive differentiation

•Partner with customer marketing to create targeted content, case studies, and messaging that highlight compliance cost reduction

•Create and deliver compelling product demonstrations showcasing the integration between manufacturing operations and quality systems

•Represent the voice of the customer throughout the product development process

•Monitor regulatory landscape, industry trends, and competition to ensure offering positioning remains relevant

•Work with cross-functional teams to ensure successful product launches and adoption

Focus Areas

•Streamlining DHR and DMR processes through digital transformation

•Integration between manufacturing execution and quality management systems

•Reducing compliance overhead through automated data transfer between systems

•Optimizing audit readiness and traceability across the product lifecycle

•Enhancing non-conformance, CAPA, and deviation management through system integration

•Designing user experiences that simplify compliance activities for manufacturing personnel

YOU MUST HAVE

•Bachelor's degree required; Master's degree preferred in Engineering, Life Sciences, or related field

•7+ years of relevant experience in medical device manufacturing, quality systems, or product-related roles

•Required: Hands-on experience with DHR, DMR, and quality documentation in regulated medical device environments

•Strong understanding of medical device manufacturing processes and compliance requirements

•Entrepreneurial mindset with ability to identify market opportunities and drive innovation

•Experience working with Agile development methodologies

•Proven track record in gathering and analyzing customer requirements to build successful solutions

•Excellent communication and presentation skills, with the ability to translate complex technical and regulatory concepts into clear business value

•Strong analytical skills for business case development and ROI modeling

WE VALUE

•Experience with TrackWise Digital or other quality management systems

•Experience with manufacturing execution systems (MES) in medical device environments

•Knowledge of 21 CFR Part 820, ISO 13485, EU MDR, and other medical device regulations

•Background in manufacturing quality or regulatory affairs

•Experience with product management or offering management methodologies

•Experience with digital transformation initiatives in manufacturing operations

•History of successfully bringing new solutions to market

•Understanding of UDI (Unique Device Identification) implementation and tracking

Travel Requirements

This position requires moderate travel for customer visits, industry events, and internal collaboration meetings.

What We Offer

•Opportunity to shape the future of integrated manufacturing and quality solutions in the medical device industry

•Collaborative environment working with cutting-edge manufacturing and compliance technologies

•Career growth in a rapidly evolving and high-impact domain

•Competitive compensation and benefits package

•Professional development opportunities and training on emerging technologies and regulations

We are an equal opportunity employer committed to diversity in the workplace.

Compensation & Benefits:

Incentive Eligible

Salary Range: $181,000-225,000

For benefits information please visit https://benefits.honeywell.com/.

Current employees may visit HR Direct.

Honeywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status.