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Engineering Program Manager

Company:
Planet Pharma
Location:
Spring Lake Park, MN, 55432
Posted:
April 07, 2026
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Description:

Additional position details from the manager below:

Can you please confirm your top 3 skills sets required?

Portfolio-wide strategy/planning for post-market product maintenance. We receive inputs on product changes from across the org, and we need to plan the timing/order of incorporating these changes into the finished goods/eManuals to support global distribution while avoiding stockouts, meeting regulatory and compliance deadlines, expediting safety-related changes, etc. Strategic thinking and planning is important.

Effective program leadership in a regulated environment plus a matrixed organization. We lead teams that are dispersed across multiple sites, working in different environments. Need to be effective at planning schedules, leading teams, meeting facilitation, risk management, project management, partnering with other project managers across the org, etc.

Communications, progress monitoring, and reporting. Ownership of project budgets (financial planning, monitoring, and reporting), product release roadmaps (timelines for changes and new product releases across the portfolio), monthly progress reporting (to leadership, with peers / cross-functional leaders, etc.)

Can you please confirm the 3 main responsibilities/day to day activities required for this role?

Project intake & Release Planning (gathering inputs on detailed changes, thinking through and documenting the strategy for implementing changes in final pack / eManuals to meet deadlines and minimize frequency of changes)

Monitoring and controlling in-process release projects (leading the core release team, manufacturing site team, translations team, etc.)

Maintaining effective communication (release roadmaps, schedules, release plans, proforma/budget tracker, etc.)

What products (if any) will this role support?

This position will support across all Neuromodulation and Pelvic Health products, but with a focus on TDD.

What is your target years of experience?

Four years of work experience plus Bachelor's degree, at least two years of Project Management experience

When do you plan to start interviewing?

Within the next two weeks

Will you be looking to hire and start ASAP or will the start date be delayed?

Start beginning of May, if we can make that happen.

Will the contingent worker be working remotely or onsite, or both (if both, please confirm possible schedule)?

On site 4 days per week. Can work remotely on Fridays.

The Product Release Program Lead is responsible for leading, establishing, and driving execution of product release cadences for the Neuromodulation and Pelvic Health (NMPH) portfolio of products. Projects within scope will include but are not limited to: Release Product Engineering (RPE), CAPAs, Sustaining Engineering, and New Product Introduction. This position requires broad cross-functional knowledge and comprehensive business management skills.

A Day in the Life

• Accountable for overall project execution. Including: project planning, budgeting, schedule creation, and execution.

• Establishes product release strategy through multiple project inputs, establishing operational plans and execution.

• Leads and manages site-specific and cross-functional teams established with the purpose of successfully accomplishing the objectives of the product release program.

• Monitors progress toward pre-established objectives, assesses risks, and implements strategies to ensure successful program execution.

• Directs the work of site-specific and cross-functions through a matrix organization.

• Secures site-specific and cross-functional commitments, maintaining milestones and budget. Deploys team resources to meet project/program objectives.

• Maintains effective communication and interface with various leadership teams.

• Ensure effective project transition relevant to development, quality, manufacturing, distribution, regulatory, and commercial entities.

• Provides input to Functional Managers on team member performance, as needed.

• Assesses project issues and develops resolutions to meet productivity, quality, and client-satisfaction goals and objectives.

• Develops mechanisms for monitoring and reporting project progress and for intervention and problem solving with project managers, line managers, and clients.

• Ensures the project/program complies with all aspects of the quality policy/system.

• Ensure appropriate departmental resources are assigned to the program/project and are available to effectively maintain the quality system (people, facilities, tools, and training).

• Problems and issues faced can be complex, difficult and undefined, requiring detailed information gathering, analysis and investigation to understand the problem.

• Other responsibilities, as required and assigned.

Must Haves

• Bachelor's degree with 4+ years of job-related experience -OR- Master's degree with 2+ years of job-related experience

• 2+ years of project management experience

Nice to Haves

• 2+ years coordinating manufacturing site activities.

• 5+ years in medical device product development, or other highly regulated environment.

• Project Management Professional (PMP) certified.

• Experience working with FDA, ISO, EN, and/or GMP standards.

• Highly developed skill set in project leadership practices including ability to balance risk, effectively influence diverse teams, and ownership of responsibility for outcomes.

• Excellent downward, lateral, and upward communication skills.

• Good balance of high level strategic and detailed tactical thought processes.

• Demonstrated track record of successfully leading projects/programs to completion.

Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.

Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it's from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.

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