Baxter International Jobs

- 2,941 Jobs

  • Supervisor I, Manufacturing 3rd Shift

    Baxter s products and therapies are found in almost every hospital worldwide, in clinics and in the home. No matter your role at Baxter, your work makes a positive impact on people around the world. Provide a positive and equitable working environment emphasizing the Baxter Shared Values: Respect / Responsiveness / Results. At Baxter, we are deeply connected by our mission.
    $37k-44k yearly est.17d ago

  • Production Fill Technician - 3rd Shift (BENEFITS DAY ONE)

    Baxter s products and therapies are found in almost every hospital worldwide, in clinics and in the home. No matter your role at Baxter, your work makes a positive impact on people around the world. At Baxter, we are deeply connected by our mission. At Baxter, we are committed to equitable pay for all our employees, and we strive to be mo
    $25.6 hourly17d ago

  • Raw Material Planner II

    Baxter s products and therapies are found in almost every hospital worldwide, in clinics and in the home. No matter your role at Baxter, your work makes a positive impact on people around the world. Develop knowledge of production planning in order to be the Finished Goods Planner Backup and be able to schedule finished goods (FG) production on manufacturing lines if needed. At Baxter, we are deeply connected by our mission.
    $56k-72k yearly est.11d ago

  • Senior Analyst, Sales Operations (Remote)

    Stryker is an EO employer -
    $57k-115.1k yearly1d ago

  • Staff Microbiologist (Remote, Hybrid, or Onsite)

    At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products. Stryker Spine is a global leader in complex spine and minimally invasive solutions. Stryker is hiring a Staff Microbiologist (Remote, Hybrid, or Onsite) to support our Spine Business! It is preferable that you reside within a commutable distance of either Leesburg, VA, or Allendale, NJ. As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better. As a Staff Microbiologist, you will be responsible for the Biosafety, i.e., Biocompatibility, Sterilization, Cleaning, and Disinfection of medical device activities within Stryker Spine.
    $83.1k-176.8k yearly11d ago

  • Associate Director, Knowledge Management (Remote)

    The Associate Director in Knowledge Management (part of Human Health Data Digital & Analytics organization), will oversee the end-to-end management of our global knowledge insight repository, system of record, OneSearch. We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States and Canada and MSD everywhere else.
    $117k-150k yearly est.11d ago

  • Cardiovascular & Metabolism Regional Medical Scientific Director (Remote - MI, OH & KY))

    The Cardiovascular & Metabolism Regional Medical Scientific Director (RMSD) is a credentialed (i.e., PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). We are seeking a Growth and Improvement minded Cardiovascular & Metabolism Regional Medical Scientific Director that can help drive our Strategic Operating Priorities.
    $175.4k-276.2k yearly6d ago

  • Product Design Lead

    As Johnson & Johnson expands its digital surgery eco-system and elevates the surgical care continuum, the MedTech organization is seeking to establish a data-driven, seamless, and accessible customer experience that enhances cross-franchise collaboration and improves customer engagement. Employees of Johnson & Johnson work with partners in healthcare to touch the lives of over a billion people every day, throughout the world. The people of Johnson & Johnson are inspired and united by the opportunity to care for the world one person at a time - and we have been for over 130 years. + Lead complex initiatives, producing scenarios, designing prototypes and writing specs that show how our digital products enhance the user experience and ecosystems
    $131k-225.4k yearly24d ago

  • Senior Clinical Research Associate- Northeast Region (REMOTE)

    The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's/MSD policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and expands the territory for clinical research, finding and developing new sites. Participates in internal meetings and workstreams as SME for monitoring processes and systems. Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. **Responsibilities include, but are not limited to:** + Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. + Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. + Gains an in-depth understanding of the study protocol and related procedures. + Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready. + Participates & provides inputs on site selection and validation activities. + Performs remote and on-site monitoring & oversight activities using various tools to ensure: + Data generated at site are complete, accurate and unbiased + Subjects' right, safety and well-being are protected. + Conducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner. + Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out. + Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance. + Identifies, assesses and resolves site performance, quality or compliance problems and escalates per defined CRA Escalation Pathway as appropriate in collaboration with CRA Manager, CRM, TA Head and CRD as needed. + Works in partnership with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites. + Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines. + Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor and sharing best practices as appropriate/required. + Supports and/or leads audit/inspection activities as needed. + Performs co-monitoring visits where appropriate. + Following the country strategy defined by CRD and/or CRA manager, contributes to the identification of new potential sites and works closely with them to develop strong clinical research capabilities. + Mentors / buddies junior CRAs on process/study requirements and performs co-monitoring visits where appropriate. + Could perform Quality control visits if delegated by other roles and trained appropriately. **Extent of Travel:** + Ability to travel domestically and internationally approximately 65%-75% of working time. + Expected travelling ~2-3 days/week. + Current driver's license needed. **CORE Competency Expectations:** + Fluent in Local Languages and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively. + Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines. + Excellent understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines. + Hands on knowledge of Good Documentation Practices. + Proven Skills in Site Management including management of site performance and patient recruitment. + Demonstrated high level of monitoring skill with independent professional judgment. + Good IT skills (Use of MS office, use of various clinical IT applications on computer, tablet and mobile devices) and ability to adapt to new IT applications on various devices. + Ability to understand and analyze data/metrics and act appropriately. + Capable of managing complex issues, works in a solution-oriented manner. + Performs root cause analysis and implements preventative and corrective action. + Experience with conducting site motivational visit designed to boost site enrollment. + Capable of mentoring junior CRAs on process/study requirements and is able to perform co-monitoring visits where appropriate. **Behavioral Competency Expectations:** + Effective time management, organizational and interpersonal skills, conflict management, problem solving skills. + Demonstrated high level of monitoring skill with independent professional judgement. + Able to work highly independently across multiple protocols, sites and therapy areas. + High sense of accountability / urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment. + Works effectively in a matrix multicultural environment. + Ability to establish and maintain culturally sensitive working relationships. + Demonstrates commitment to Customer focus. + Works with high quality and compliance mind-set. + Positive mindset, growth mindset, capable of working independently and being self-driven. + Demonstrates and projects professional demeanor and communication consistent with organizational policies and practices. **Experience Requirements:** **Required:** + Min. 4 years of direct site management (monitoring) experience in a bio/pharma/CRO. **Educational Requirements:** **Preferred:** + B.A./B.S. with strong emphasis in science and/or biology **MRLGCTO** **\#EligibleforERP** We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we "follow the science" that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe. **Who we are ...** We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world. **What we look for ...** Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving, so if you are among the intellectually curious, join us-and start making your impact today. **NOTICE FOR INTERNAL APPLICANTS** In accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions. If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor. **Residents of Colorado** Click here (https://survey.sogosurvey.com/Survey1.aspx?k=SsQYWYYQsQRsPsPsP&lang=0) to request this role's pay range. **Employees working in roles that the Company determines require routine collaboration with external stakeholders, such as customer-facing commercial, or research-based roles, will be expected to comply not only with Company policy but also with policies established by such external stakeholders (for example, a requirement to be vaccinated against COVID-19 in order to access a facility or meet with stakeholders). Please understand that, as permitted by applicable law, if you have not been vaccinated against COVID-19 and an essential function of your job is to call on external stakeholders who require vaccination to enter their premises or engage in face-to-face meetings, then your employment may pose an undue burden to business operations, in which case you may not be offered employment, or your employment could be terminated. Please also note that, where permitted by applicable law, the Company reserves the right to require COVID-19 vaccinations for positions, such as in Global Employee Health, where the Company determines in its discretion that the nature of the role presents an increased risk of disease transmission.** Current Employees apply HERE (https://wd5.myworkday.com/msd/d/inst/1422$1533/rel-task/3001$14.htmld) Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld) **US and Puerto Rico Residents Only:** Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here (https://survey.sogosurvey.com/r/aCdfqL) if you need an accommodation during the application or hiring process. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Know Your Rights (https://www.eeoc.gov/sites/default/files/2022-10/22-088\_EEOC\_KnowYourRights\_10\_20.pdf) EEOC GINA Supplement Pay Transparency Nondiscrimination (https://www.dol.gov/sites/dolgov/files/OFCCP/pdf/pay-transp\_%20English\_formattedESQA508c.pdf) We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. Under New York City, Washington State and California State law, the Company is required to provide a reasonable estimate of the salary range for this job. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate's relevant skills, experience, and education. Expected salary range: $118,640.00 - $186,800.00 Available benefits include bonus eligibility, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and sick days. For Washington State Jobs, a summary of benefits is listed here (https://www.benefitsatmerck.com/) . Learn more about your rights, including under California, Colorado and other US State Acts (https://www.msdprivacy.com/us/en/CCPA-notice/) **Search Firm Representatives Please Read Carefully** Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. **Employee Status:** Regular **Relocation:** No relocation **VISA Sponsorship:** No **Travel Requirements:** 50% **Flexible Work Arrangements:** Remote Work **Shift:** **Valid Driving License:** Yes **Hazardous Material(s):** **Requisition ID:** R232520
    $118.6k-186.8k yearly4d ago

  • Digital Experience Platform Senior Manager

    Digital Experience Platform Senior Manager Kenvue, part of the Johnson & Johnson Family of Companies (Kenvue), is currently recruiting for:
    $129k-223.1k yearly39d ago

  • Drug Safety Scientist (f/m/d)

    at our central location in Vienna. No matter your role at Baxter, your work makes a positive impact on people around the world. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. At Baxter we are creating an organization and promoting a culture that respects each individual's unique character and life experiences, and reflects the diversity of our customers and markets. At Baxter, we are deeply connected by our mission.
    $85k-116k yearly est.Easy Apply40d ago

  • Drug Safety Scientist (m/w/d)

    Bei Baxter schaffen und f rdern wir eine Kultur, die den einzigartigen Charakter und die Lebenserfahrungen jedes Einzelnen respektiert und die Vielfalt unserer Kunden und M rkte widerspiegelt. No matter your role at Baxter, your work makes a positive impact on people around the world. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. At Baxter, we are deeply connected by our mission. Baxter beizutreten bedeutet, einem Team beizutreten, von dem Sie wirklich lernen k nnen!
    $85k-116k yearly est.Easy Apply42d ago

  • Bilingual Customer Service Representative

    * Accountable for providing outstanding service to all external customers, patients, and Baxter team members. No matter your role at Baxter, your work makes a positive impact on people around the world. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. At Baxter, we are deeply connected by our mission. You will speak with the patients whose lives are saved and sustained by Baxter products. Collaboration with cross functional departments: Product Information, Distribution Centers, Planning and Deployment, Credit and Collections, Customer Master, various sales representatives, Center for One Baxter, and others.
    $36k-90k yearly3d ago

  • Customer Service Representative

    * Accountable for providing outstanding service to all external customers, patients, and Baxter team members. No matter your role at Baxter, your work makes a positive impact on people around the world. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. At Baxter, we are deeply connected by our mission. * 2+ years customer service or supply chain experience You will speak with the patients whose lives are saved and sustained by Baxter products. Collaboration with cross functional departments: Product Information, Distribution Centers, Planning and Deployment, Credit and Collections, Customer Master, various sales representatives, Center for One Baxter, and others. At Baxter, we are committed to equitable pay
    $36k-90k yearly3d ago

  • Customer Service Representative

    * Accountable for providing outstanding service to all external customers, patients, and Baxter team members. No matter your role at Baxter, your work makes a positive impact on people around the world. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. At Baxter, we are deeply connected by our mission. * 2+ years customer service or supply chain experience You will speak with the patients whose lives are saved and sustained by Baxter products. Collaboration with cross functional departments: Product Information, Distribution Centers, Planning and Deployment, Credit and Collections, Customer Master, various sales representatives, Center for One Baxter, and others. At Baxter, we are committed to equitable pay
    $36k-90k yearly3d ago

  • Bilingual Customer Service Representative

    * Accountable for providing outstanding service to all external customers, patients, and Baxter team members. No matter your role at Baxter, your work makes a positive impact on people around the world. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. At Baxter, we are deeply connected by our mission. You will speak with the patients whose lives are saved and sustained by Baxter products. Collaboration with cross functional departments: Product Information, Distribution Centers, Planning and Deployment, Credit and Collections, Customer Master, various sales representatives, Center for One Baxter, and others.
    $36k-90k yearly3d ago

  • Sr. Manager, Regulatory Affairs - Advertising & Promotion (Open to Remote)

    No matter your role at Baxter, your work makes a positive impact on people around the world. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. At Baxter, we are deeply connected by our mission. Manager of Regulatory Affairs-Advertising/Promotion reports to the Director Global Regulatory Affairs-Advertising & Promotion and is responsible for the review of Advertising and Promotional (Ad Prom) materials and accountable for all operational aspects of regulatory submissions providing planning and technical support for Baxter's products for one or more business units/countries. 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 salary range of $112,000 to $216,000 and also includes an annual incentive bonus and equity target.
    $112k-216k yearly4d ago

  • Data Engineer - Procurement Systems and Analytics (Remote/Hybrid)

    No matter your role at Baxter, your work makes a positive impact on people around the world. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. This Data Engineer is responsible for building the future data infrastructure required for transforming Procurement at Baxter into a data driven function. At Baxter, we are deeply connected by our mission. 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.
    $68k-156k yearly7d ago

  • Senior Software Engineer, Azure Cloud (US Remote)

    No matter your role at Baxter, your work makes a positive impact on people around the world. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. At Baxter, we are deeply connected by our mission. As a Senior Software Engineer, you will be responsible for the research and development of advanced vision care cloud solutions, saving vision for diabetic patients in primary healthcare settings. As a Senior Software Engineer, Azure Cloud at Baxter, your work directly contributes to making a significant impact on others.
    $60k-132k yearly7d ago

  • Data Engineer - Procurement Systems and Analytics (Remote/Hybrid)

    No matter your role at Baxter, your work makes a positive impact on people around the world. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. This Data Engineer is responsible for building the future data infrastructure required for transforming Procurement at Baxter into a data driven function. At Baxter, we are deeply connected by our mission. 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.
    $68k-156k yearly7d ago

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Updated March 26, 2023

Zippia gives an in-depth look into the details of Baxter International, including salaries, political affiliations, employee data, and more, in order to inform job seekers about Baxter International. The employee data is based on information from people who have self-reported their past or current employments at Baxter International. The data on this page is also based on data sources collected from public and open data sources on the Internet and other locations, as well as proprietary data we licensed from other companies. Sources of data may include, but are not limited to, the BLS, company filings, estimates based on those filings, H1B filings, and other public and private datasets. While we have made attempts to ensure that the information displayed are correct, Zippia is not responsible for any errors or omissions or for the results obtained from the use of this information. None of the information on this page has been provided or approved by Baxter International. The data presented on this page does not represent the view of Baxter International and its employees or that of Zippia.

Baxter International may also be known as or be related to Baxter International, Baxter International Inc, Baxter International Inc., Baxter International, Inc. and baxter.