Vantive: A New Company Built On Our Legacy

 

Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.

 

At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us are driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support.

 

*Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions.

Summary:

The Lead System Integrator (LSI) team is a part of the R&D organization that supports the Kidney Care business segment. Within the team, we provide R&D focused, project management support for all product phases, innovation initiatives, new product development and improvement programs for existing therapy systems. This collaborative role gives you the direct opportunity to define solutions to new products challenges and services to patients and continue Baxter’s mission to save and sustain lives.

Baxter is a global company with R&D sites at multiple locations in the world; competences and capabilities are spread over the different R&D sites, and you will commonly collaborate with colleagues across several of these R&D sites and with other functional representatives. Work assignments within the team are highly variable and we can promise you a work environment with exciting project management challenges and variability in your day-to-day activities.

The Director role is responsible for establishing and leading the Lead System Integrator team and supporting the projects within the Kidney Care portfolio. This team will be focused on supporting Kidney Care drug products (dialysis solutions, concentrates, etc) and related sciences (Sterility Assurance, Analytical Chemistry, materials compliance, Extractables & Leachables, Toxicology) projects and initiatives.

Essential Duties and Responsibilities.  This section contains a list of five to eight primary responsibilities of the work.  The incumbent will perform other duties as assigned.

Establish and lead a team of Lead System Integrators (LSIs) supporting research and development (R&D) project management work and facilitates technical decision making for pharmaceutical products, medical devices, and other regulated healthcare productsEstablish and continuously improve relevant operating mechanisms to drive organizational accountability, aggressive project execution, and diligent technical rigorEnsure LSI organization accountability for R&D focused program schedule creation, tracking, and executionResponsible for strategic portfolio management for all projects supported by the Drug Products and Sciences organizationEstablish and drive maintenance of on-market product roadmaps in collaboration with R&D product design owners (PDOs) and cross-functional interfacesAccountable for R&D team project performance, program schedule commitments, budget commitments and spendLeads team in defining program strategies, developing goals, and facilitates cross-functional decision making through structured, best-practice processesProvides clear direction on product lifecycle management requirements to meet expectations of external customers and business stakeholdersInteracts through program updates and reviews with all functions and levels of management ensuring effective ongoing communications across teams and stakeholdersEnsures identification, escalation, and communication of project risks, development of risk assessment/mitigation plans and proactive management of risk response strategiesAnticipates potential conflict situations for proactive solutions and manages conflict situations to result in win-win outcomesMaximizes business results through continuous improvement in organization's ability to execute programs from identification through implementationParticipates as a member of cross functional teams and/or integrates cross functional inputs into project deliveryDemonstrates understanding of and adherence to FDA, ISO and IEC design control procedures, regulations, and standards

Qualifications.  To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.  List knowledge, skills, and/or abilities required. 

Significant technical product lifecycle management experience (as an engineer or scientist on a project team) preferredDemonstrated experience developing and implementing project/portfolio management focused operating mechanismsStrong interpersonal and communication skills in written and verbal form.Demonstrated ability to communicate complex technical subjects to executive level audiences of varying technical backgroundsFunctional management experience; global team management experience preferredAbility to manage multiple cross-functional teams simultaneously in a matrix environmentDetailed understanding of project management principles and methodologiesDemonstrated ability to draw conclusions and make recommendations based on technical inputs from multiple and varied functions (Marketing, Quality, Regulatory, etc.).Ability to provide technical leadership for medical product projects with substantial complexity and scopeAbility to decompose complex problems into actionable plans/tasksUnderstanding of design requirements for development, validation, and verification of medical products

Education and/or Experience.  Include the education and/or experience that is necessary to perform the job satisfactorily.

Bachelor’s degree in engineering, Sciences or equivalent field7+ years of R&D experience; 5+ years project management experienceExperience in pharmaceuticals or medical device industry preferred

We understand compensation is an important factor as you consider the next step in your career. At Vantive, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $184,000 - $253,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.  

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
                                                                                                                                                               
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Pay Transparency Policy

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

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