Principal Enterprise Solutions Project Manager

Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for Principal Enterprise Solutions Project Manager (ESPM) to work within our Bioprocess Enterprise Solutions business. Do you have a passion for project management? Then we would love to hear from you.
The Enterprise Solutions Project Manager (ESPM) reports to the Global Project Director, Enterprise Solutions. Enterprise Solutions provides integrated end-to-end single use or hybrid platforms for bioprocessing facilities designed to customer specifications.
What you’ll do
The ESPM is a senior project management position, which will lead and manage global project teams from project conception through biopharmaceutical facility and operation design, delivery and plant start-up. He/she is the main point of contact with the client and is instrumental for bridging functions and operating cross-functionally with the commercial and technical teams for successful execution. In addition, this position is accountable for achieving quality objectives, creating/meeting development schedules and project budgets, as well as communicating project status and escalating issues when appropriate to facilitate transparency
Maintaining excellent customer relationships, communication, and exchange of information as required by the contract and to support timely and efficient project execution
Coordination, motivating and driving objectives across cross-functional groups including sub-contractors to deliver effective results
Ensuring compliance with Finance, Accounting, Legal, Sourcing, EHS and other internal functional support processes
Managing global program resources, quality objectives, regulatory requirements, schedules, change management, program risk management and making decisions based on business objectives
Managing/ executing all customer, vendor/supplier and consulting contracts coordinating efforts with facility and construction engineering personnel
Chairing internal and customer Project Team meetings on a regular basis and reporting out to stakeholders
Preparing project plans, schedules, budgets, monthly reports, meeting minutes, and maintaining high quality project files
Travel as needed to support portfolio of projects; ~ 15-50%

Who you are


BS/MS Degree in Engineering discipline or equivalent; MBA preferred
Minimum of ten (10) years relevant project leadership experience with greater than 7 years multi-disciplinary knowledge of the life sciences or biomedical industry
Demonstrated leadership of cross-functional project teams and an ability to drive project design plans to completion
Demonstrated success in building and leading collaborative global and cross-functional teams and relationships
Demonstrated facilitation and negotiation skills in driving closure on project/product/program-related decisions/issues
Exceptional leadership, time management, facilitation, and organizational skills
Excellent analytical and problem-solving skills - communicates in a clear and succinct manner and effectively evaluates information / data to make decisions, anticipates obstacles and develops plans to resolve, creates actionable strategies and operational plans
Proficient with project management principles (e.g., resource allocation, cost estimation, risks analysis) & project management tools and applications software to manage complex project timelines and resources.
Familiar with FDA, cGMP and other regulatory and guidelines applicable to biomanufacturing facility design and operation
Professional Project Management (e.g. certified by PMI®, Program Management Institute) preferred.

Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Cytiva is a global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to advance and accelerate therapeutics. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of life sciences companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world. As part of a greater Life Sciences platform, you’ll redefine what it means to innovate every day. Pioneering the future of science, research, and medicine gives you unlimited opportunities to find the next breakthrough that will best serve scientists and medical professionals in the fight to save lives.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.