Sr. Program Manager - Medical Device at RESOLUTION MEDICAL LLC

Minneapolis, Minnesota, United States -

Full Time

Start Date

Immediate

Expiry Date

24 Jun, 26

Salary

180000.0

Posted On

27 Mar, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Program Management, Product Development, Project Planning, Team Leadership, Cross-functional Team Management, Product Commercialization, Scope Management, Risk Management, Budget Management, Quality Control, Vendor Management, Status Reporting, Problem Solving, Innovation, Process Improvement, Regulatory Compliance

Industry

Medical Device

Description

Description Job Summary The Sr Program Manager is responsible for the successful planning, management and execution of complex, usually multi-device product development projects and all applicable standard operating procedures. The Sr Program Manager will lead a cross-functional team consisting of product development, quality, manufacturing, and procurement personnel, through the Product Development cycle from concept to commercialization, as defined by customer development agreements. Essential Functions Manage a portfolio of complex initiatives that span one or multiple lines of business Provide on-site leadership for project team by building and motivating team members to meet project goals, adhering to their responsibilities and project milestones Full project life cycle ownership: successful project delivery will include meeting or exceeding customer expectations with respect to project deliverables Report on project success criteria results, metrics, test and deployment management activities Work creatively and analytically within Resolution Medical’s problem-solving environment demonstrating teamwork, innovation and excellence Participate in establishing practices, templates, policies, tools and partnerships to expand and mature these capabilities for the organization Support preparation of estimates and develop detailed project plans for all phases of the project Procure adequate resources to achieve project objectives in planned timeframes Provide status reporting regarding project milestones, deliverable, dependencies, risks and issues, communicating across leadership Demonstrate a functional acumen to support how solutions will address customer goals while maintaining alignment with Resolution Medical and industry best practices Manage project scope and changes Manage ongoing quality control and participate in quality issue resolution Define the Statement of Work and Specifications for the requested goods and services Develop and manage all aspects of project and program engagement from planning, external vendor relationships, communications, resources, budget, change, risks and issues Provide progress reports as requested by key stakeholders Coach, mentor, motivate and supervise project team Ensure that projects and programs are proceeding according to scope, schedule, budget and quality standards Support continued development of best practices, templates, policies, tools and partnerships to expand and mature these capabilities for the organization Support company finance, accounting, human resources, and quality as necessary to ensure compliance with requirements Requirements Education, Experience, Required Skills Minimum of a Bachelor level degree in a Scientific or Technical Field and 15+ years or more experience in regulated industry, such as Pharmaceuticals or Medical Devices Minimum of 10 years Project Management experience within a Regulated Industry such as Pharmaceuticals or Medical Devices. Ability to handle and be trusted with confidential and/or sensitive information Able to work in a fast-paced, constantly changing environment Ability to be flexible and to handle multiple projects in an organized, timely manner Able to problem-solve, work under pressure, and to effectively manage stress Physical Requirements Prolonged periods of sitting at a desk and working on a computer Must be able to lift up to 25 pounds at times Must have excellent hand-eye coordination Ability to differentiate between colored wires, tabs, and electronic components preferred Must wear gown, gloves, ear protection and other personal protective equipment as applicable Summary of Benefits Group health & welfare benefits: Options for Medical, Dental and Vision insurance, Health Savings Account (requires participation in eligible medical plan), and Flexible Spending Accounts. Company-paid benefits: Employee Life Insurance & Accidental Death & Dismemberment (AD&D), Long Term Disability (LTD), Kavira (requires participation in medical plan). Voluntary, employee-paid benefits: Employee Supplemental Life & AD&D, Spouse and Dependent Life & AD&D, Short Term Disability (STD), Accident, Critical Illness, and Hospital Indemnity, Employee Assistance Program. Flexible Time Off Programq Paid Parental Leave Paid Holidays Benefits and incentive compensation may be subject to generally applicable eligibility, waiting period, contribution, and other requirements and conditions. Compensation The typical base pay range for this role is between $150,000-180,000/year. Compensation may vary based on individual job-related knowledge, skills, expertise, and experience. This position is eligible for a discretionary annual incentive program driven by organization and individual performance. 401(k) Plan: Company-provided Safe Harbor Contribution of 3% of eligible earnings.

Responsibilities

The Senior Program Manager is tasked with the successful planning, management, and execution of complex, multi-device product development projects from concept through commercialization, adhering to standard operating procedures. This role involves leading cross-functional teams and maintaining full ownership of the project life cycle, ensuring deliverables meet or exceed customer expectations.