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This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

Your Role at Baxter

This multifaceted role within the healthcare software industry is pivotal within Baxter Connected Care Group. The Associate Project Manager is a remote-based role, responsible for the planning, coordination, documentation, and execution of customer-awarded projects according to Baxter Standards. Connected Care project managers lead all aspects of the client project engagement from the sales handoff to a transition to ongoing support. Key activities include project planning, resource prioritization, project risk assessment and mitigation, revenue forecasting, customer communication and internal partner management. This role is an entry level role in our PMO and primarily responsible for smaller, fast paced projects and success is partially measured by speed of project completion.

This role requires the new hire to work in the Pacific (PT) Time Zone. Candidates must reside in the West Coast OR be able to commit to working PT hours.

What you'll be doing:

Provide strong and proactive project leadership.
Act with autonomy as the primary point of contact for all client project related needs.
Develop and distribute project plans detailing resource engagement and product delivery timelines.
Host remote and in-person recurring meetings, providing agendas and meeting minutes.
Build internal and external customer relationships and manage expectations.
Accurately forecast project completion and revenue delivery Develop applicable product expertise
Continuously reassess and prioritize defined sequence tasks, through individual effort and the coordination of the work of others.

What you'll bring:

Bachelor’s degree in healthcare, IT, business or related background
2+ years of professional, customer facing work experience
Experience using MS Dynamics, Kanata and/or Power BI is preferred
Comfortable working and learning in an IT-focused environment with complex products and requirements
Knowledge of Microsoft Suite including Outlook, Teams, PowerPoint, and Excel
Travel: 10– 20% depending on geographic location.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, 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 $88,000 to $121,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of 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. This position may also be eligible for discretionary bonuses. 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.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.US Benefits at Baxter (except for Puerto Rico)

US Benefits at Baxter (except for Puerto Rico)

This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees. For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter

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.

Know Your Rights: Workplace Discrimination is Illegal

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.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

19:T1b95,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Your role at Baxter

The Sr. Project Specialist is responsible for the site planning and implementation of Baxter's very sophisticated product line at medical and healthcare facilities throughout a dedicated region. Baxter's surgical portfolio of products within this position consists of surgical and examination lights, equipment management systems (booms), video integration, and overhead patient lifts.

This is a remote role that requires overnight travel throughout the Southeast (75%).

What you will be doing

Responsible for delivering construction projects on time, on budget, with high customer satisfaction
Attends coordination meetings as needed to ensure site readiness progresses appropriately
Coordinates in house and third-party equipment integration (i.e., video cables, custom monitor mounts, etc.)
Maintains pre-installation and rough-in information for 3rd party contractors
Proactively identifies, communicates, and resolves customer issues that threaten the success of the project both internally and at the customer site.
Regularly communicates the status of multiple projects to customer project and ‘C’ level management, Baxter senior management, and internal project team members.
Utilize effective change management best practices in leading product implementation projects.
Proactively identifies out of scope opportunities during the execution of implementation projects and pursues them in concert with the appropriate team members.
Focuses on meeting or exceeding established project metrics, including pre-install planning, risks/potential issues and risk mitigation strategies, project delivery and closeout.

What you will bring

Bachelor’s degree required
Overnight travel up to 75%
Experience managing capital equipment projects is preferred
5+ years of relevant experience
An understanding of construction and previous experience with medical equipment is a plus
Ability to proactively seek out future pitfalls and develop strategies to mitigate or avoid setbacks
Must live within 35 miles of an airport
PMP, PMI, IPMA, or equivalent project management certification preferred.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all our employees, and we strive to be more transparent with our pay practices. To that end, this position has a base salary range of $80,000 to $110,000 plus an annual incentive bonus. The above range represents the expected base salary range for this position. The actual salary may vary based upon several factors including, but not limited to, relevant skills/experience, time in the role, business line, and geographic/office location.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

1a:T2124,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Your role at Baxter

Join Baxter's Medical Affairs team as a trusted scientific leader at the forefront of advancing patient care and innovation. In this senior individual contributor role, you'll build influential partnerships with healthcare leaders, academic institutions, and key opinion leaders to drive meaningful scientific exchange, generate actionable insights, and shape evidence-based strategies. Leveraging deep clinical expertise and strategic influence, you'll lead high-impact initiatives that strengthen Baxter's scientific leadership, support evidence generation, and connect external perspectives to organizational priorities.

What you'll be doing

Build and maintain strategic scientific relationships with healthcare professionals, KOLs, investigators, health systems, academic institutions, and professional societies.
Deliver credible, evidence-based scientific exchange through presentations, educational programs, and peer-to-peer discussions while responding compliantly to scientific inquiries.
Gather and communicate clinical insights, emerging trends, unmet needs, and evidence gaps to inform Medical Affairs strategy and decision-making.
Lead external engagement strategies, including KOL development, advisory boards, investigator collaborations, executive scientific interactions, and research initiatives.
Support scientific congresses and professional meetings by facilitating engagement, sharing insights, and identifying collaboration opportunities.
Partner with Medical Affairs, R&D, Regulatory, Quality, Marketing, and Commercial teams to address evidence needs and enhance scientific understanding across the organization.
Serve as a subject matter expert in infusion therapy, smart pump technology, and related clinical practice areas.
Independently lead complex Medical Affairs initiatives, strategic projects, and process improvements from planning through execution, driving measurable organizational impact.

What you'll bring

Strong ability to analyze, interpret, and communicate complex scientific and clinical information to diverse audiences.
Proven success building trusted relationships with healthcare professionals, KOLs, and senior clinical stakeholders.
Exceptional presentation, communication, and scientific engagement skills.
Advanced understanding of Medical Affairs compliance requirements and scientific exchange principles.
Demonstrated ability to translate customer insights into actionable strategies and recommendations.
Strong cross-functional collaboration, project leadership, and organizational skills.
Self-directed, adaptable, and effective at managing multiple priorities in a fast-paced environment.
Proven experience leading complex initiatives and influencing stakeholders without direct authority.

Education & Experience

Bachelor's degree in a scientific, clinical, or healthcare discipline required; advanced degree, relevant licensure, or certification preferred.
Significant experience in infusion therapy, smart pump technology, Medical Affairs, clinical practice, or related healthcare fields.
Prior Medical Science Liaison, field medical, scientific affairs, or comparable external scientific engagement experience preferred.
Demonstrated success presenting scientific or clinical information to healthcare professionals and expert audiences.
Experience in medical devices, pharmacy, nursing, pharmaceuticals, nutrition, or related therapeutic areas preferred.
Ability to travel approximately 50-70%.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

#LI-Remote1b:T1b95,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Your role at Baxter

This is a remote role that requires overnight travel throughout the Southeast (75%).

What you will be doing

Responsible for delivering construction projects on time, on budget, with high customer satisfaction
Attends coordination meetings as needed to ensure site readiness progresses appropriately
Coordinates in house and third-party equipment integration (i.e., video cables, custom monitor mounts, etc.)
Maintains pre-installation and rough-in information for 3rd party contractors
Proactively identifies, communicates, and resolves customer issues that threaten the success of the project both internally and at the customer site.
Regularly communicates the status of multiple projects to customer project and ‘C’ level management, Baxter senior management, and internal project team members.
Utilize effective change management best practices in leading product implementation projects.
Proactively identifies out of scope opportunities during the execution of implementation projects and pursues them in concert with the appropriate team members.
Focuses on meeting or exceeding established project metrics, including pre-install planning, risks/potential issues and risk mitigation strategies, project delivery and closeout.

What you will bring

Bachelor’s degree required
Overnight travel up to 75%
Experience managing capital equipment projects is preferred
5+ years of relevant experience
An understanding of construction and previous experience with medical equipment is a plus
Ability to proactively seek out future pitfalls and develop strategies to mitigate or avoid setbacks
Must live within 35 miles of an airport
PMP, PMI, IPMA, or equivalent project management certification preferred.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

1c:T2124,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Your role at Baxter

What you'll be doing

Build and maintain strategic scientific relationships with healthcare professionals, KOLs, investigators, health systems, academic institutions, and professional societies.
Deliver credible, evidence-based scientific exchange through presentations, educational programs, and peer-to-peer discussions while responding compliantly to scientific inquiries.
Gather and communicate clinical insights, emerging trends, unmet needs, and evidence gaps to inform Medical Affairs strategy and decision-making.
Lead external engagement strategies, including KOL development, advisory boards, investigator collaborations, executive scientific interactions, and research initiatives.
Support scientific congresses and professional meetings by facilitating engagement, sharing insights, and identifying collaboration opportunities.
Partner with Medical Affairs, R&D, Regulatory, Quality, Marketing, and Commercial teams to address evidence needs and enhance scientific understanding across the organization.
Serve as a subject matter expert in infusion therapy, smart pump technology, and related clinical practice areas.
Independently lead complex Medical Affairs initiatives, strategic projects, and process improvements from planning through execution, driving measurable organizational impact.

What you'll bring

Strong ability to analyze, interpret, and communicate complex scientific and clinical information to diverse audiences.
Proven success building trusted relationships with healthcare professionals, KOLs, and senior clinical stakeholders.
Exceptional presentation, communication, and scientific engagement skills.
Advanced understanding of Medical Affairs compliance requirements and scientific exchange principles.
Demonstrated ability to translate customer insights into actionable strategies and recommendations.
Strong cross-functional collaboration, project leadership, and organizational skills.
Self-directed, adaptable, and effective at managing multiple priorities in a fast-paced environment.
Proven experience leading complex initiatives and influencing stakeholders without direct authority.

Education & Experience

Bachelor's degree in a scientific, clinical, or healthcare discipline required; advanced degree, relevant licensure, or certification preferred.
Significant experience in infusion therapy, smart pump technology, Medical Affairs, clinical practice, or related healthcare fields.
Prior Medical Science Liaison, field medical, scientific affairs, or comparable external scientific engagement experience preferred.
Demonstrated success presenting scientific or clinical information to healthcare professionals and expert audiences.
Experience in medical devices, pharmacy, nursing, pharmaceuticals, nutrition, or related therapeutic areas preferred.
Ability to travel approximately 50-70%.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

#LI-Remote1d:T1f72,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Your Role at Baxter

THIS IS WHERE you build trust to achieve results

As an Associate Sales Representative for our full operating room capital equipment product portfolio, you take pride in representing Baxter and our products. Your keen understanding of our deep portfolio of products and belief in the value and quality they provide to patients fuels your confidence. Our customers trust you and appreciate your knowledge and curiosity when finding solutions to meet their needs. You enjoy being on location, building relationships, and establishing trust with the doctors and nurses who use Baxter solutions every day.

As a member of Baxter’s sales team, aligned to the Southern California region in our Surgical Business unit, you'll promote our Surgical Portfolio focusing on surgical professionals such as surgeons, nurses, and operating room staff, ensuring patient-centric approach in all your dealings. You’ll work with a team of Sales Consultants in your region to achieve or exceed personal and business goals, all in pursuit of our mission to save and sustain lives. In the sales role, you’ll have the opportunity to provide input on new markets and products, handle customer concerns, and collaborate with other teams

What you'll be doing:

Supporting and promoting our Surgical Portfolio in your territory to meet customer’s clinical and economic needs
Independently formulating and implementing selling strategies to sell products of intermediate complexity directly to customers by phone and on site.
Engaging with the install base and existing customers for incremental purchases, pricing/delivery issues, and overall support to improve their experience
Ensuring clinical adoption across the product portfolio through product trialing, demonstrations, and in-servicing to improve customers’ adoption of their portfolio
Scheduling and completing customer sales calls quotas and following up on opportunities to develop the business
Assisting with set up of product demonstrations for customers as requested
Supporting site visits, product fairs, and mock rooms, as necessary

What you'll bring:

High school degree/GED required. Bachelor’s degree preferred with 2+ years experience or at least 4+ years related experience. Inside or field sales role in the healthcare or similar industry preferred. Medical device experience preferred
Effective influencing skills –ability to understand the needs of, and influence, personnel ranging from nurses to key decision makers
Outstanding communication, negotiation, organizational, problem solving, facilitation, and presentation skills are essential for success
Flexible, autonomous, and the ability to collaborate with multiple team members to ensure customer satisfaction
Must be willing/able to travel at least 75% and may involve visits to remote or urban areas either individually or with other personnel. Position will have an assigned geographic territory which may span several states

Territory: State of Arkansas/ State of Louisiana

The estimated base pay range for this position is $64,000 - $72,000 annually, with additional opportunity to earn sales incentive compensation for achieving or exceeding your goals. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less within the anticipated range based upon market data and other factors, all of which are subject to change.

Individual pay is based 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.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

#LI-Remote1e:T1e09,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Your Role at Baxter

As a Critical Account Lead, you will serve as the single point of accountability for Baxter's most complex customer escalations within the Care Communications Solutions business. This newly created role was designed to improve the customer experience when issues span multiple products, teams, or technologies.

You'll partner closely with Technical Support, Product Management, R&D, Customer Success, Sales, and leadership teams to coordinate resolution efforts and ensure customers have a clear path forward. This is an opportunity to help build a new function, influence how critical customer situations are managed, and play a direct role in strengthening Baxter's relationships with healthcare customers.

What You'll Do

Own critical customer escalations from intake through customer stabilization, serving as the single point of accountability throughout the lifecycle.
Triage incoming escalations, assess severity levels, and determine appropriate engagement and response plans.
Lead cross-functional resolution teams across Technical Support, Product Management, R&D, Customer Success, Services, and Sales.
Coordinate resolution activities for complex customer issues, including incidents that span multiple products, technologies, business units, and support organizations.
Deliver executive-level status updates and escalation communications to internal stakeholders and customer leadership.
Maintain escalation records, action plans, and status reporting within established systems and processes.
Conduct post-incident reviews, document root causes, and identify opportunities to improve products, processes, and customer outcomes.
Support the development of escalation criteria, critical account pathways, performance metrics, and scalable operational processes for the Critical Account Lead program.

What You'll Bring

Bachelor's degree in Healthcare, Information Technology, Business, Engineering, or a related field.
8+ years of experience in technical support, escalation management, technical account management, customer success, program management, or related customer-facing technical roles.
Experience managing high-severity customer issues that require coordination across multiple teams, products, or business functions.
Knowledge of healthcare technology environments, hospital IT operations, or medical device technologies.
Experience working with networking technologies and HL7 integrations.
Proficiency with program and case management tools such as ServiceNow, Salesforce, Smartsheet, Microsoft Project, or similar platforms.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, 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 $96,000 - $132,000.The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of 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.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

#LI-Remote1f:T2e7a,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Your Role at Baxter

This is where your work saves lives

Your role at Baxter

The Senior Manager role demonstrates advanced functional and organizational acumen, deep integration across Medical Affairs priorities, and accountability for independently leading significant special initiatives and projects from strategy through execution, as well as potential to lead direct reports. The senior manager is a subject matter resource across the Medical Affairs organization, anticipating dependencies and risks, advising colleagues and leadership, facilitating cross-pillar alignment, and helping translate strategic priorities into coordinated action. The role provides leadership through expertise, judgment, collaboration, and influence rather than formal supervisory authority. The Medical Information role is responsible for delivering accurate, balanced, timely, and evidence-based scientific information that supports informed clinical and business decisions. The role applies rigorous literature evaluation and clinical judgment to ensure scientific accuracy and consistency in accordance with applicable laws, regulations, company policies, and established review processes. Although aligned to Medical Information & Scientific Responses, the role operates as part of one integrated Medical Affairs organization and is expected to contribute expertise and work across the department as organizational priorities require.

What you'll be doing

Research, develop, communicate, and document accurate, balanced, and timely responses to unsolicited medical, clinical, and scientific inquiries from healthcare professionals, customers, and appropriate internal stakeholders, including escalated and off-label inquiries, in accordance with local applicable requirements and company policy.
Independently lead significant Medical Affairs initiatives, special projects, or complex workstreams from scoping and strategy through execution, stakeholder alignment, risk management, delivery, and evaluation of outcomes. Assess and identify operational gaps, implement solutions to drive initiatives that improve and streamline current processes within Medical Information to improve medical communication services to internal and external customers.
Develop, maintain, and periodically refresh standard response documents, frequently asked questions, scientific slide decks, clinical summaries, medical content, bibliographies, and other approved scientific resources used to support consistent Medical Affairs communication within the approved Content Management repository.
Maintain current familiarity of published medical literature. Conduct structured literature searches and critically evaluate published evidence, clinical practice guidelines, product information, and relevant scientific data to support medical responses and scientific content. Independently design and lead significant Medical Information initiatives such as scientific response strategy.
Provide medical and scientific review of promotional and non-promotional materials through established governance processes, evaluating scientific accuracy, substantiation, balance, clinical relevance, and consistency with approved labeling and applicable requirements.
Identify, assess, and communicate VOC trends in medical information requests, evidence gaps, clinical practice, and emerging literature to External Scientific Engagement, Medical Excellence & Strategy, and other appropriate stakeholders.
Develop and deliver internal and external scientific education, as appropriate, including disease-state, product, clinical, and evidence-based training in partnership with Medical Affairs colleagues and relevant functional experts.
Provide clinical and scientific input to Regulatory, Quality, Patient Safety, R&D, Marketing, Commercial, and other functions when appropriate, including support related to product complaints, safety questions, launches, and customer needs within established Medical Affairs boundaries.
Lead and support medical information activities associated with product launches, congresses, scientific booths, and other Medical Affairs initiatives, ensuring readiness of scientific content and response materials.
Perform other duties and responsibilities consistent with the scope, purpose, and level of the role, as assigned, to support evolving Medical Affairs and organizational priorities.

What you'll bring

Excellent medical and scientific writing, oral communication, and literature-search skills, with demonstrated ability to synthesize complex evidence into accurate, balanced, and audience-appropriate scientific responses.
Strong critical thinking skills with attention to detail. The ability to evaluate study design, data quality, clinical relevance, limitations, and the strength of supporting evidence.
Working knowledge of regulatory and compliance requirements applicable to medical communications, unsolicited requests, scientific exchange, promotional review, and approved product information.
Excellent presentation, teaching, and interpersonal skills, including the ability to communicate effectively with healthcare professionals and cross-functional stakeholders.
Ability to work collaboratively across Medical Affairs pillars and in cross-functional teams, manage conflict, competing priorities, and contribute effectively in a changing environment.
Advanced functional expertise, strategic judgment, and organizational acumen, with demonstrated ability to independently lead complex cross-functional initiatives, influence senior stakeholders, navigate ambiguity, and deliver results without formal authority.

Education and/or Experience

Bachelor's degree in a clinical, scientific, or healthcare discipline required; advanced clinical or scientific degree and/or relevant professional licensure or certification preferred.
Substantial progressively responsible relevant experience demonstrating advanced proficiency in Medical Information and broader Medical Affairs organization, including independent ownership and successful delivery of complex initiatives or special projects; level placement should reflect significant depth and years of applicable experience.
Experience responding to medical or scientific inquiries, conducting literature evaluation, developing scientific content, or performing medical/scientific review is preferred.
Experience in infusion therapy, pharmacy, nursing, nutrition, medical devices, pharmaceuticals, or other relevant therapeutic/technology areas is preferred, depending on assigned portfolio.
Experience working within regulated healthcare or life sciences environments and with cross-functional review processes is preferred.
Ability and willingness to travel up to 20% to support business meetings, scientific activities, team collaboration, and other Medical Affairs priorities.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

#LI-MS1

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

#LI-Remote20:T2389,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Your role at Baxter

As a Principal Specialist, Global Regulatory Affairs, you will manage regulatory activities for an assigned portfolio of medical device products across the U.S., EU, and other global markets. You will develop regulatory strategies, assess product and process changes, and support submissions that maintain market access and compliance throughout the product lifecycle.

This is where you will apply your knowledge of global medical device regulations to guide product changes, support regulatory submissions, and help bring new and updated products to market. Working closely with Regulatory Affairs, R&D, Quality, Marketing, and Operations, you will provide regulatory input that supports sound business and compliance decisions.

In this role, you will contribute to global regulatory planning and execution for Baxter products. Success will be measured through effective lifecycle management, timely regulatory submissions and approvals, and the ability to support product changes while meeting regulatory requirements.

What you'll be doing

Manage regulatory approvals, registrations, and change assessments to support the ongoing compliance and market availability of medical device products.
Develop regulatory strategies and submission plans to support product changes, process changes, and new market introductions.
Evaluate regulatory impact and determine submission requirements for the U.S., EU, and other international markets.
Prepare and submit U.S. regulatory filings, including 510(k) submissions, pre-submissions, and responses to FDA requests.
Maintain EU MDR regulatory documentation and support updates to technical documentation.
Support interactions with Notified Bodies and regulatory authorities for assigned products.
Review technical, scientific, and quality information to assess regulatory impact and support implementation of product lifecycle changes.
Monitor changes in regulatory requirements and assess potential impact to products, processes, and regulatory strategies.
Partner with cross-functional teams and international regulatory colleagues to support global submission planning, execution, and compliance activities.

What you'll bring

Bachelor’s degree in scientific or engineering subject area.
5 years regulatory experience in the medical device industry.
Experience with electromechanical medical devices is desirable.
Experience with FDA change assessment guidance and EU MDR technical documentation expectations.
Ability to document regulatory decisions and defend submission strategy.
Successful preparation and submission of 510(k)s
Familiarity with global registrations beyond the US and EU.
Strong regulatory knowledge and ability to interpret scientific information to support regulatory submissions.
Ability to influence cross-functional partners and drive regulatory alignment in a matrixed, global organization
Ability to manage multiple projects and timelines in a multinational/multicultural team environment.
Strong oral and written communication and presentation skills.
Strong negotiation skills.
Identify, prioritize and communicate regulatory risks and raise issues when appropriate.

$5,000 sign‑on bonus offered for this role.

The $5,000 sign‑on bonus will be paid to external applicants successfully hired after completion of your first 30 days at Baxter.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, 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 $104,000 - $143,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of 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. This position may also be eligible for discretionary bonuses. 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.

Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a required minimum number of days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission. The flexible workplace policy is subject to local laws and legal requirements. At its discretion, Baxter may decide to adjust, suspend, or discontinue as business needs change.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

#LI-Remote21:T21be,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Your Role at Baxter

THIS IS WHERE you build trust to achieve results!

As a Clinical Sales Account Manager, you take pride in representing Baxter and our products. Your keen understanding of our deep portfolio of products and believe in the value and quality they provide to patients fuels your confidence. Our customers trust you and appreciate your knowledge and curiosity when finding solutions to meet their needs. You enjoy being on location, forming relationships, and establishing trust with the doctors and nurses who use Baxter solutions every day.

As our primary connection to the healthcare professionals who rely on our products to save and sustain lives, you are the face and voice of our solutions. You enjoy seeing the connections between teams and how they work together to drive business results. The insights and feedback you share with your team and to cross-functional partners help validate and inform priorities and changes.

We accept opportunities to connect with the doctors and nurses that use our products every day to save and sustain lives. Observing their work, understanding their needs, and building positive relationships are integral to our success.

We're a friendly, collaborative group of people who push each other to do better every day. We find outstanding strategies to close deals and expand our skills by challenging ourselves and others. Whether out in the field with a partner or seeking challenges with your territory team, you always have camaraderie and support to help accomplish your goals.

The Clinical Sales Account Manager drives the generation of Baxter's Rental Therapy. In collaboration with the Account Executive and specialty sales partners, you will develop and implement sales strategies that deliver comprehensive solutions to customers within the assigned territory or account base.

What you'll be doing

Drive overall revenue attainment across assigned accounts by developing and implementing sales strategies that deliver comprehensive solutions to customers. Conduct negotiations with customers to finalize sales and achieve product revenue goals by ensuring new product success
Collaborate with internal sales and service partners to seamlessly serve shared accounts
Coordinate customer sales support activities across assigned accounts by leading customer business reviews and collecting evidence-based outcomes data associated with the assigned portfolio
Ensure post-sales customer happiness and improve perceived return on investment
Travel as required to lead assigned territory and to attend regional/national meetings

What you'll bring

Bachelors Degree with 4+ years experience or 8+ years of relevant sales experience
Preferred 4+ years of validated experience selling products in the healthcare field. Capital/durable medical equipment solutions selling is preferred or 3 years of hospital leadership experience to include handling staff, leading budgets, and communicating innovative ideas to executive-level healthcare customers

Travel Requirements:

Travel up to 75%, with overnight travel expected, occasional Regional and National travel
Must have a valid driver’s license, a clean driving record, and be able to drive an automobile

Territory: All of Minnesota, Eastern North Dakota, Eastern South Dakota, Northeast corner of Nebraska

The estimated pay range for this position is $80,000 - $85,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less within the anticipated range based upon market data and other factors, all of which are subject to change.

Individual pay is based upon location, skills and expertise, experience, and other relevant factors. This position is also eligible for a Sales Incentive Plan (SIP), which provides the opportunity to earn incentive compensation for achieving or exceeding your goals. 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.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

#LI-Remote22:T1db6,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Job Description

Your Role at Baxter

As a Technical Support Specialist, you will provide front-line support for Baxter's infusion systems, software applications, and connected technologies used in healthcare environments. This is where you can make an impact by helping hospitals, clinicians, biomedical technicians, and IT teams quickly resolve technical issues involving equipment that supports patient care. In this role, you'll balance technical support activities with case management and ticket processing while partnering with customers to maintain system performance and uptime.

What You'll Do

Provide Level 1 technical support via phone, email, and future chat channels for Baxter infusion pumps, associated software, and connected digital products.
Troubleshoot hardware, software, connectivity, and system-related issues using established troubleshooting guides, technical documentation, and standard operating procedures.
Process, document, and manage customer cases, ensuring accurate updates, issue tracking, and timely resolution of support requests.
Support Return Material Authorization (RMA) activities for devices requiring repair, replacement, or depot service.
Guide customers through product setup, configuration, and operational issues related to Baxter infusion systems and software applications.
Escalate complex technical issues to advanced support teams and collaborate with internal partners to drive resolution.
Utilize support systems, Microsoft applications, knowledge management tools, laptops, tablets, and mobile devices to manage daily work activities.
Maintain compliance with HIPAA, GDPR, and all applicable environmental, health, and safety requirements.

What You'll Bring

High school diploma or GED.
1+ years of technical support, help desk, desktop support, service desk, or technical call center experience.
Experience troubleshooting computer hardware, software applications, operating systems, and connected devices.
Working knowledge of Microsoft Windows operating systems and general computer networking concepts.
Experience using case management, ticketing, CRM, or knowledge management systems.
Experience utilizing Microsoft Office applications, including Outlook, Excel, and Word, to support daily work activities.
Experience supporting customers via phone, email, or other service channels.
Ability to work the scheduled 10:00 AM - 7:00 PM EST shift and participate in a rotating on-call schedule approximately every six weeks.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, 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 $44,800 - $61,600. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of 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.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

#LI-Remote23:T1db6,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Job Description

Your Role at Baxter

What You'll Do

Provide Level 1 technical support via phone, email, and future chat channels for Baxter infusion pumps, associated software, and connected digital products.
Troubleshoot hardware, software, connectivity, and system-related issues using established troubleshooting guides, technical documentation, and standard operating procedures.
Process, document, and manage customer cases, ensuring accurate updates, issue tracking, and timely resolution of support requests.
Support Return Material Authorization (RMA) activities for devices requiring repair, replacement, or depot service.
Guide customers through product setup, configuration, and operational issues related to Baxter infusion systems and software applications.
Escalate complex technical issues to advanced support teams and collaborate with internal partners to drive resolution.
Utilize support systems, Microsoft applications, knowledge management tools, laptops, tablets, and mobile devices to manage daily work activities.
Maintain compliance with HIPAA, GDPR, and all applicable environmental, health, and safety requirements.

What You'll Bring

High school diploma or GED.
1+ years of technical support, help desk, desktop support, service desk, or technical call center experience.
Experience troubleshooting computer hardware, software applications, operating systems, and connected devices.
Working knowledge of Microsoft Windows operating systems and general computer networking concepts.
Experience using case management, ticketing, CRM, or knowledge management systems.
Experience utilizing Microsoft Office applications, including Outlook, Excel, and Word, to support daily work activities.
Experience supporting customers via phone, email, or other service channels.
Ability to work the scheduled 10:00 AM - 7:00 PM EST shift and participate in a rotating on-call schedule approximately every six weeks.

We understand compensation is an important factor as you consider the next step in your career. At Baxter, 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 $44,800 - $61,600. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of 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.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

#LI-Remote24:T270d,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

This is where my hands make life-sustaining products

You are driven by the knowledge that the products you help make saves and sustain lives. You can move quickly, address questions, and encourage teammates, all while getting quality products out on time. You are calm, positive, and a key part of a fast-paced environment that emphasizes camaraderie and teamwork. As a Operator III - Machine L-5, you are happiest when you are moving, and we will not disappoint!

Baxter is known for its speed and high-quality product. Our manufacturing operations are around-the-clock to meet the needs of our customers. Our high-caliber talent works through the challenges at hand while pushing toward meeting client order needs. Different shift assignments allow for flexibility and safety.

Your team

Baxter is focused on saving and sustaining lives by manufacturing high-quality products. We strive to create quality products for our customers each day.

Delivering life-saving products is about getting them right, and attention to detail is how we make sure we meet that challenge. We are a team that supports each other throughout each shift. Working together in a supportive and open culture makes our processes evolve for the better and engages our workforce.

You'll be offered extensive training, and the tight-knit working environment within the Manufacturing team means employees get additional training from their direct manager and peers when needed.

What You'll Be Doing

Operar maquinaria automática y/o semiautomática en los procesos de manufactura y realizar ajustes y reparaciones según sean necesarios para lograr su óptimo rendimiento y productividad.
Operar maquinaria automática y / o semiautomática de manufactura controlando su funcionamiento dentro de los parámetros de operación establecidos por procedimientos, especificaciones y regulaciones de seguridad y ambiental.
Observar el proceso de manufacturas y los paneles de controles electromecánicos del equipo y realizar ajustes a los controles o reparaciones cuando sean necesarias. Notificar de condiciones de la máquina o equipo que pudieran afectar su buen funcionamiento.
Suplir materiales a las maquinas asignadas. Inspeccionar, empacar y documentar el material según los procedimientos de la Planta. Coordinar y monitorear el uso de materiales en las áreas del departamento.
Realizar los “set-up” de los cambios de código siguiendo los manuales correspondientes del equipo y las especificaciones y procedimientos del producto.
Cumplir con los estandares de la operación tales como pero no limitados a producción, “scrap”, “down time”, tiempo de cambios de código u otros establecidos por el departamento.
Realizar trabajos de mantenimiento rutinario, preventivo y correctivo tales como limpieza, engrase y lubricación de la maquinaria.
Realizar los mantenimientos preventivos (PM) en el tiempo establecido siguiendo el procedimiento SOP aplicable.
Responsable de mantener y asegurar las herramientas que se le proveen.
Consultar y participar activamente junto con el personal de Automation, de Ingeniería de Proceso (Process and Products) y/o del Departamento de Calidad en el análisis del proceso de manufactura para identificar áreas de oportunidad de mejoras al mismo. Esto incluye pero no se limita a : Asistencia a las reuniones, participar de las actividades de mejoras al proceso y documentar información requerida por el proyecto.
Documentar por medios manuales (ej. Checker Chart) y/o electrónicos (ej. POMS, MMS 3) la información requerida por especificaciones y procedimientos. Esto incluye pero no se limita a parámetros, lotes, producciones y otras.
Mantener información escrita o graficas de producción, “down time”, “setup time” o cualquier otro indicador que sea establecido por máquina con el propósito de monitorear su productividad o establecer tendencias en el mismo.
Inspeccionar y evaluar los materiales y el producto para detectar o prevenir posibles defectos antes de usar los materiales o de retirar el producto terminado.
Mantener limpia, organizada y libre de riesgos su área de trabajo. Participar activamente de iniciativas dirigidas a ese propósito como por ejemplo SOL 5’s (Seguridad Orden y Limpieza).
Cumplir en todo momento con las reglas de la Compañía, de ambiental, salud y seguridad (EHS). Utilizar los equipos de seguridad: gafas, guantes u otro equipo de protección requeridos para realizar sus funciones.

What You'll Bring

Grado Asociado o su equivalente en estudios de mecánica, electrónica, troquelaría y 0 - 1 años de experiencia en mecánica, electrónica, troquelaría u otra actividad relacionada con el funcionamiento de equipos automáticos o semiautomáticos. Conocimientos en Medición (Caliper, Micrómetro, Regla, etc.).
Establece prioridad de trabajos. Capacidad para analizar y distinguir situaciones de mal funcionamiento para identificar posibles causas y soluciones. Identificar desviaciones en los parámetros de procesos, parar la maquinaria si es necesario, hacer las correcciones o gestionar ayuda necesaria para sus correcciones. Disponibilidad para trabajar en otros turnos y tiempo extras cuando sea requerido por el supervisor del departamento. Seguir instrucciones y procedimientos requeridos. Trabajar con un mínimo de supervisión.
Buenas destrezas de comunicación en Inglés y Español.
Trabajo Mediano: Ejerce de 20 lbs hasta 50 lbs. de fuerza ocasionalmente, y/o de 10 lbs. hasta 25lbs. de fuerza frecuentemente, y/o una cantidad insignificante mayor 10 lbs. de fuerza constantemente para levantar, cargar, empujar, halar y mover objetos. Las demandas de los requerimientos físicos exceden los del Trabajo Liviano.

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

25:T21a4,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Your Role at Baxter

THIS IS WHERE you build trust to achieve results!

What you'll be doing

Drive overall revenue attainment across assigned accounts by developing and implementing sales strategies that deliver comprehensive solutions to customers. Conduct negotiations with customers to finalize sales and achieve product revenue goals by ensuring new product success
Collaborate with internal sales and service partners to seamlessly serve shared accounts
Coordinate customer sales support activities across assigned accounts by leading customer business reviews and collecting evidence-based outcomes data associated with the assigned portfolio
Ensure post-sales customer happiness and improve perceived return on investment
Travel as required to lead assigned territory and to attend regional/national meetings

What you'll bring

Bachelors Degree with 4+ years experience or 8+ years of relevant sales experience
Preferred 4+ years of validated experience selling products in the healthcare field. Capital/durable medical equipment solutions selling is preferred or 3 years of hospital leadership experience to include handling staff, leading budgets, and communicating innovative ideas to executive-level healthcare customers

Travel Requirements:

Travel up to 75%, with overnight travel expected, occasional Regional and National travel
Must have a valid driver’s license, a clean driving record, and be able to drive an automobile

Territory: All of Wisconsin and Iowa, Chicago, and the UP of Michigan

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

#LI-Remote26:T21b9,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Your Role at Baxter

THIS IS WHERE you build trust to achieve results

As a Territory Business Manager, you take pride in representing our Advanced Surgery division at Baxter. Your keen understanding of our deep portfolio of surgical products and belief in the value and quality they provide to patients fuels your confidence. Our customers trust you and appreciate your knowledge and curiosity when finding solutions to meet their needs. You enjoy being on location, building relationships, and establishing trust with the doctors and nurses who use Baxter solutions every day.

As our primary connection to the healthcare professionals who rely on our products to save and sustain lives, you are the face and voice of our solutions. You promote our hemostats, sealing, and tissue products in an assigned geography to meet customer's clinical and economic needs. You enjoy allowing surgical teams across a multitude of specialties, the freedom to innovate and think creatively without restraint in the operating room.

We are seeking individuals who take personal accountability for achieving results and has the ability to “win” at each stage of the customer's buying process! Are you ready to become a subject matter authority in our surgical portfolio?

What you'll be doing:

Achieving sales quotas through the direct sale of all products and services
Growing awareness and educating physicians on the accurate use of our products in on label surgical procedures, as well as the features and benefits of our products
Calling on prospective customers, providing technical and administrative product information and/or demonstrations
Maintaining effective relationships with customers and can gain their trust and respect; Is dedicated to meeting the expectations and requirements of internal and external customers
Monitoring sales against forecasts and participating in the determination of market potential for the territory. Is aware of how sales strategies and tactics work in the marketplace; knows the competition
Coordinating with hospital administration, supply chain management, materials management, and purchasing
Demonstrating support for other people and teams and is willing to participate & contribute to efforts beyond own scope of responsibilities
Providing feedback to immediate supervisor and marketing personnel for the development of marketing programs, recommended products and product line revisions as well as pricing changes
Able to work autonomously to achieve established goals while proactively remotely communicating with management

What you'll bring:

Bachelor’s degree with 3+ years of relevant experience OR 8+ years of operating room sales experience. High School degree required
The successful candidate must have shown experience with hospital based selling in the operating room as well as experience leading a large territory
Excellent written and verbal communication skills, as well as strong analytical and social skills
At least 50% travel is required and may involve visits to remote or urban areas either individually or with other personnel as the position will have a geography which may span several states
Individuals must live within the current geography or be willing to relocate to it. Familiarity with posted territory is strongly desired
Must have a valid driver’s license

The estimated pay range for this position is 80,000 to 110,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less within the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based upon location, skills and expertise, experience, and other relevant factors. This position is also eligible for a Sales Incentive Plan (SIP), which provides the opportunity to earn incentive compensation for achieving or exceeding your goals. 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.

#LI-CH1

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

27:T2e7a,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Your Role at Baxter

This is where your work saves lives

Your role at Baxter

What you'll be doing

Research, develop, communicate, and document accurate, balanced, and timely responses to unsolicited medical, clinical, and scientific inquiries from healthcare professionals, customers, and appropriate internal stakeholders, including escalated and off-label inquiries, in accordance with local applicable requirements and company policy.
Independently lead significant Medical Affairs initiatives, special projects, or complex workstreams from scoping and strategy through execution, stakeholder alignment, risk management, delivery, and evaluation of outcomes. Assess and identify operational gaps, implement solutions to drive initiatives that improve and streamline current processes within Medical Information to improve medical communication services to internal and external customers.
Develop, maintain, and periodically refresh standard response documents, frequently asked questions, scientific slide decks, clinical summaries, medical content, bibliographies, and other approved scientific resources used to support consistent Medical Affairs communication within the approved Content Management repository.
Maintain current familiarity of published medical literature. Conduct structured literature searches and critically evaluate published evidence, clinical practice guidelines, product information, and relevant scientific data to support medical responses and scientific content. Independently design and lead significant Medical Information initiatives such as scientific response strategy.
Provide medical and scientific review of promotional and non-promotional materials through established governance processes, evaluating scientific accuracy, substantiation, balance, clinical relevance, and consistency with approved labeling and applicable requirements.
Identify, assess, and communicate VOC trends in medical information requests, evidence gaps, clinical practice, and emerging literature to External Scientific Engagement, Medical Excellence & Strategy, and other appropriate stakeholders.
Develop and deliver internal and external scientific education, as appropriate, including disease-state, product, clinical, and evidence-based training in partnership with Medical Affairs colleagues and relevant functional experts.
Provide clinical and scientific input to Regulatory, Quality, Patient Safety, R&D, Marketing, Commercial, and other functions when appropriate, including support related to product complaints, safety questions, launches, and customer needs within established Medical Affairs boundaries.
Lead and support medical information activities associated with product launches, congresses, scientific booths, and other Medical Affairs initiatives, ensuring readiness of scientific content and response materials.
Perform other duties and responsibilities consistent with the scope, purpose, and level of the role, as assigned, to support evolving Medical Affairs and organizational priorities.

What you'll bring

Excellent medical and scientific writing, oral communication, and literature-search skills, with demonstrated ability to synthesize complex evidence into accurate, balanced, and audience-appropriate scientific responses.
Strong critical thinking skills with attention to detail. The ability to evaluate study design, data quality, clinical relevance, limitations, and the strength of supporting evidence.
Working knowledge of regulatory and compliance requirements applicable to medical communications, unsolicited requests, scientific exchange, promotional review, and approved product information.
Excellent presentation, teaching, and interpersonal skills, including the ability to communicate effectively with healthcare professionals and cross-functional stakeholders.
Ability to work collaboratively across Medical Affairs pillars and in cross-functional teams, manage conflict, competing priorities, and contribute effectively in a changing environment.
Advanced functional expertise, strategic judgment, and organizational acumen, with demonstrated ability to independently lead complex cross-functional initiatives, influence senior stakeholders, navigate ambiguity, and deliver results without formal authority.

Education and/or Experience

Bachelor's degree in a clinical, scientific, or healthcare discipline required; advanced clinical or scientific degree and/or relevant professional licensure or certification preferred.
Substantial progressively responsible relevant experience demonstrating advanced proficiency in Medical Information and broader Medical Affairs organization, including independent ownership and successful delivery of complex initiatives or special projects; level placement should reflect significant depth and years of applicable experience.
Experience responding to medical or scientific inquiries, conducting literature evaluation, developing scientific content, or performing medical/scientific review is preferred.
Experience in infusion therapy, pharmacy, nursing, nutrition, medical devices, pharmaceuticals, or other relevant therapeutic/technology areas is preferred, depending on assigned portfolio.
Experience working within regulated healthcare or life sciences environments and with cross-functional review processes is preferred.
Ability and willingness to travel up to 20% to support business meetings, scientific activities, team collaboration, and other Medical Affairs priorities.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

#LI-MS1

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

#LI-Remote28:T220e,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Your Role at Baxter

The Manager, Medical Affairs serves as a clinical, scientific, and operational leader responsible for supporting the development, commercialization, and lifecycle management of medical devices and healthcare solutions. This role combines clinical expertise, Medical Affairs strategy, evidence generation, product support, and operational execution to ensure the organization delivers clinically relevant, evidence-based solutions that improve patient care and healthcare outcomes.

The Manager, Medical Affairs provides medical and device subject matter expertise across product development, clinical evaluation, risk management, evidence generation, medical education, and post-market activities. In addition, this role supports key Medical Affairs operations including project management, budget oversight, vendor management, strategic planning, and cross-functional collaboration.

Success in this role requires the ability to translate clinical insights into actionable business and product strategies while effectively managing multiple projects and stakeholders in a highly collaborative environment.

What you'll be doing

Serve as the clinical and medical device subject matter expert supporting product development, implementation, risk assessment, training, and lifecycle management.
Provide clinical guidance and collaborate with cross-functional teams including R&D, Clinical Research, Regulatory, Quality, Marketing, and Commercial organizations.
Evaluate clinical evidence, literature, healthcare trends, and customer insights to inform product strategy and identify unmet clinical needs.
Support Medical Affairs strategy, evidence generation initiatives, research collaborations, publications, and scientific congress activities.
Develop and deliver clinical and scientific education programs for internal teams and customers to support product adoption and best practices.
Lead Medical Affairs projects, timelines, governance activities, strategic planning, and operational process improvements.
Manage budgets, forecasts, vendor relationships, contracts, purchase orders, and financial reporting in partnership with Finance and Procurement.
Ensure compliance with regulatory and company standards while driving cross-functional collaboration, reporting, analytics, and continuous improvement initiatives.

What you'll bring:

Required Qualifications

Bachelor's degree in a clinical, scientific, healthcare, or related discipline.
Minimum of 5 years of experience in Medical Affairs, Clinical Research, healthcare, medical devices, pharmaceuticals, or related healthcare industries.
Demonstrated experience managing complex projects with multiple stakeholders.
Strong communication, presentation, organizational, and interpersonal skills.
Experience supporting budgets, contracts, vendors, and operational processes.
Ability to effectively manage multiple priorities and work independently in a fast-paced environment.
Proficiency with Microsoft Office applications and project management tools.
Ability to travel domestically and internationally as business needs require (up to 30-50%).

Preferred Qualifications

Advanced clinical or scientific degree (NP, PA, MD/DO, DNP, or equivalent).
Active clinical licensure in good standing preferred.
Prior Medical Affairs experience in the medical device, diagnostics, digital health, or healthcare technology industry.
Experience supporting evidence generation, publications, investigator-sponsored research, and scientific communications.
Experience with financial management systems, procurement platforms, and vendor oversight.
PMP certification or comparable project management training preferred.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

#LI-MS1

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

#LI-Remote29:T2e7a,

This is where your work makes a difference.

Here, you will find more than just a job—you will find purpose and pride.

Your Role at Baxter

This is where your work saves lives

Your role at Baxter

What you'll be doing

Research, develop, communicate, and document accurate, balanced, and timely responses to unsolicited medical, clinical, and scientific inquiries from healthcare professionals, customers, and appropriate internal stakeholders, including escalated and off-label inquiries, in accordance with local applicable requirements and company policy.
Independently lead significant Medical Affairs initiatives, special projects, or complex workstreams from scoping and strategy through execution, stakeholder alignment, risk management, delivery, and evaluation of outcomes. Assess and identify operational gaps, implement solutions to drive initiatives that improve and streamline current processes within Medical Information to improve medical communication services to internal and external customers.
Develop, maintain, and periodically refresh standard response documents, frequently asked questions, scientific slide decks, clinical summaries, medical content, bibliographies, and other approved scientific resources used to support consistent Medical Affairs communication within the approved Content Management repository.
Maintain current familiarity of published medical literature. Conduct structured literature searches and critically evaluate published evidence, clinical practice guidelines, product information, and relevant scientific data to support medical responses and scientific content. Independently design and lead significant Medical Information initiatives such as scientific response strategy.
Provide medical and scientific review of promotional and non-promotional materials through established governance processes, evaluating scientific accuracy, substantiation, balance, clinical relevance, and consistency with approved labeling and applicable requirements.
Identify, assess, and communicate VOC trends in medical information requests, evidence gaps, clinical practice, and emerging literature to External Scientific Engagement, Medical Excellence & Strategy, and other appropriate stakeholders.
Develop and deliver internal and external scientific education, as appropriate, including disease-state, product, clinical, and evidence-based training in partnership with Medical Affairs colleagues and relevant functional experts.
Provide clinical and scientific input to Regulatory, Quality, Patient Safety, R&D, Marketing, Commercial, and other functions when appropriate, including support related to product complaints, safety questions, launches, and customer needs within established Medical Affairs boundaries.
Lead and support medical information activities associated with product launches, congresses, scientific booths, and other Medical Affairs initiatives, ensuring readiness of scientific content and response materials.
Perform other duties and responsibilities consistent with the scope, purpose, and level of the role, as assigned, to support evolving Medical Affairs and organizational priorities.

What you'll bring

Excellent medical and scientific writing, oral communication, and literature-search skills, with demonstrated ability to synthesize complex evidence into accurate, balanced, and audience-appropriate scientific responses.
Strong critical thinking skills with attention to detail. The ability to evaluate study design, data quality, clinical relevance, limitations, and the strength of supporting evidence.
Working knowledge of regulatory and compliance requirements applicable to medical communications, unsolicited requests, scientific exchange, promotional review, and approved product information.
Excellent presentation, teaching, and interpersonal skills, including the ability to communicate effectively with healthcare professionals and cross-functional stakeholders.
Ability to work collaboratively across Medical Affairs pillars and in cross-functional teams, manage conflict, competing priorities, and contribute effectively in a changing environment.
Advanced functional expertise, strategic judgment, and organizational acumen, with demonstrated ability to independently lead complex cross-functional initiatives, influence senior stakeholders, navigate ambiguity, and deliver results without formal authority.

Education and/or Experience

Bachelor's degree in a clinical, scientific, or healthcare discipline required; advanced clinical or scientific degree and/or relevant professional licensure or certification preferred.
Substantial progressively responsible relevant experience demonstrating advanced proficiency in Medical Information and broader Medical Affairs organization, including independent ownership and successful delivery of complex initiatives or special projects; level placement should reflect significant depth and years of applicable experience.
Experience responding to medical or scientific inquiries, conducting literature evaluation, developing scientific content, or performing medical/scientific review is preferred.
Experience in infusion therapy, pharmacy, nursing, nutrition, medical devices, pharmaceuticals, or other relevant therapeutic/technology areas is preferred, depending on assigned portfolio.
Experience working within regulated healthcare or life sciences environments and with cross-functional review processes is preferred.
Ability and willingness to travel up to 20% to support business meetings, scientific activities, team collaboration, and other Medical Affairs priorities.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

#LI-MS1

US Benefits at Baxter (except for Puerto Rico)

Equal Employment Opportunity

Know Your Rights: Workplace Discrimination is Illegal

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