Senior Program Manager

Cryoport Systems is the life science industry's most trusted provider of supply chain solutions for temperature-sensitive materials, serving biopharmaceutical, IVF and surrogacy and animal health organizations around the world. Cryoport Systems' proprietary Cryoport Express shippers, Cryoportal Logistics Management Platform, leading-edge Smartpak Condition Monitoring System and geo-sensing technology paired with unparalleled logistics expertise and 24/7/365 customer support, make Cryoport Systems the end-to-end temperature controlled supply chain partner that you can trust.

Position Summary:

This position is responsible for managing engineering product development projects from inception

through successful commercial launch which includes the full range of solutions in the Cryoport product

Portfolio. This role will focus on driving multiple and complex product development projects, including

design, manufacturing, and integration. Role may also lead some sustaining projects, as required.

Responsibilities include but are not limited to:

• Lead Product Development (PD) cross-functional teams in the execution of PD projects and

programs from initiation through to transfer to mature product support.

• Engage in lead discovery/scoping meetings with support from Product Marketing, Product

Management & Business Development to qualify New Product Development projects and identify

scope of work, budget, and timelines ñ including internal and external team scheduling and

coordination and capture sufficient information to create a formal project plan.

• Creation and active management of comprehensive, accurate and multi-stakeholder PD project

plans which align to PD PMO standards, templates and processes.

• Lead schedule and budget and scope activities for PD projects and programs constituting the

strategic initiatives for the business Portfolio.

• Use of consistent project management and product development methodologies to maintain

accountability of all team members, project budgets and timelines.

• Develop Key Performance Indicators and project health metrics and maintain these metrics at a

project and portfolio basis.

• Lead product requirements gathering sessions with key stakeholders and ensure core

requirements are captured to meet product-specific objectives.

• Identify major milestones and delivery dates, manage project scope, track progress to detailed

schedules including identifying critical path, constraints, contingencies, and mitigations to achieve

project objectives.

• Manage and identify key resource needs across projects and across the product portfolio to

ensure project deliverables can be delivered on time and budget with existing resources (or

identify need for additional resources or key business leader commitment to have resources

needed when required). Deliver regular reports on project and portfolio resource utilization,

blockers and insufficiency.

• Quantify project deliverables and track progress, managing to prevent roadblocks rather than

reacting to them.

• Coordinate resources to ensure established time to market target date is achieved.
• Develop and maintain initial, monthly, and quarterly operating budgets for each project.
• Develop and maintain initial, monthly and quarterly project summaries, highlighting mitigation

options for key issues and risks with team proposed recovery plans.

• Conduct post project analysis to identify potential improvement in processes, ensure project goals

were met, evaluate cost variances, analyze actual versus projected metrics, and determine the

overall efficiency of the project.

• Escalate threats to project plan as required to functional management and senior leadership.
• Ability to lead/guide/mentor junior level project managers.
• Present project updates in global recurring meetings, providing cost/benefit analysis summaries

and forecasting models for project resources, budget vs. actual costs, key risks/issues and

team asks.

• Responsible for timely communication of project status updates, with mitigations to any gaps.

Competencies:

• Analytical & Management Skills: Capable of quantifying project deliverables into a clear and

concise plan.

• Excellent organizational and problem-solving skills to coordinate product validation activities with

in-house Value Engineering team.

• Excellent communication skills; including interpersonal communication across all levels (team

members, team leaders and executive management) and ability to tailor communications to the

objective, stakeholder and project.

• Quality Systems: Understanding of the design control deliverables required of a highly regulated

industry.

• Strong decision making, negotiating and change management skills.
• Knowledge and experience in the implementation of regulatory requirements for medical device

development such as FDAís Design Controls.

• Strong teamwork/collaboration and influencing skills at levels below, on par and above status.
• Experience in analyzing tradeoffs between product features, customer needs/requirements,

manufacturability, and cost.

• Experience with schedule, budget, cost, resource, and risk management tracking tools.
• Ability to facilitate meetings, including creating clear agendas and documenting meeting minutes.
• Ability to make independent decisions (within established guidelines).
• Strong working knowledge of commonly used project management software programs.
• Experience in Stage gate implementations in product development process.
• Experience with PPM Tools (e.g. Clarizen/Planview) is advantageous.

Qualifications and Education Requirements:

• Bachelorís degree experience in an engineering or technical field. Advanced degree is a plus.
• Business degree preferred.
• Certificate in Project Management (PMP) required.
• Certificate in Program Management (PgMP) or Portfolio Management (PfMP) preferred.
• Minimum 8-10 years of experience in the development and commercialization of

technical/engineering/industrial/wireless consumer products.

• Experience in managing projects in FDA-regulated industry or comparable experience in other

regulated environments.

• Experience in the medical device industry and compliance with internal Quality Systems.

Compensation: up to $140,000 depending on experience + bonus + stock + benefits including 401k match