Strategic PM, Upstream Imaging | Lifecycle & Software

Philips; Plymouth (MN); On-site; USD 103,000 - 174,000; Full time

Benefits offered by this job

PTO

401k match

HSA with company contribution

Stock purchase plan

Education reimbursement

Job summary

Philips is seeking a Product Manager, Upstream Marketing for Advanced Imaging based in Plymouth, MN or Bedford, MA. You will manage lifecycle changes across the sustaining portfolio and coordinate software releases for the HyperVue platform.

You will translate customer feedback into product requirements, support next-generation programs with market insights, and collaborate with cross-functional teams in a regulated medical-device environment. This is an onsite role requiring in-office presence.

Qualifications

• Translate customer feedback, complaints and post-market data into product requirements and business cases.
• Experience with UI/UX design, user stories, backlog priorities, risk mitigations.
• Familiarity with agile development, software testing, verification/validation.

Responsibilities

• Manage product lifecycle changes across sustaining portfolio, including obsolescence and cost-reduction initiatives.
• Oversee software sustaining backlog and release roadmap for Advanced Imaging on HyperVue, coordinating releases.
• Support next-generation programs with customer, market and competitive insights to inform strategy.

Skills

Translating customer feedback

UI/UX design

Backlog prioritization

Agile development

Cross-functional collaboration

Regulated medical-device environment

Product lifecycle management

Education

Bachelor's degree in business/marketing/engineering

MBA or advanced technical degree preferred

Tools

HyperVue platform

Job description

Philips is seeking a Product Manager, Upstream Marketing for Advanced Imaging based in Plymouth, MN or Bedford, MA. You will manage lifecycle changes across the sustaining portfolio and coordinate software releases for the HyperVue platform.

You will translate customer feedback into product requirements, support next-generation programs with market insights, and collaborate with cross-functional teams in a regulated medical-device environment. This is an onsite role requiring in-office presence.