{"schemaVersion":"jobsearcher.job.v1","id":"fbfb350c62864088f8d2e721","url":"https://jobsearcher.com/jobs/fbfb350c62864088f8d2e721","canonicalUrl":"https://jobsearcher.com/jobs/fbfb350c62864088f8d2e721","title":"Associate Director, Quality","description":"Req # 206344 Location Hayward, California, United States Job Category Quality Date posted 08/06/2026\n\nOverview\nThis is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives.\nSupport for Parents\nContinuing Education/ Professional Development\nEmployee Heath & Well-Being Benefits\nPaid Time Off\n2 Days a Year to Volunteer\nSuccess Profile\nWhat makes a successful Quality team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.\nDetail Oriented\nContinuous Learner\nCourageous\nCollaborative\nCritical Thinker\nInfluential\n\nThis is where your work makes a difference.\nAt 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.\nOur 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.\nHere, you will find more than just a job—you will find purpose and pride.\nYour Role\nThis position is responsible for being Most Senior plant level Quality Management Representative, developing and deploying the quality system for the plant, assuring systems and procedures for regulatory compliance are established and deployed\nWhat You'll Be Doing\nServe as the Management Representative for Quality and lead the Quality organization within a mid-to-large manufacturing facility.\nBuild and develop a high-performing Quality organization with a clear vision and mission that supports business growth and global expansion.\nOversee batch review and product release activities.\nFulfill the responsibilities of the Person Responsible for Regulatory Compliance (PRRC), including ensuring device conformity is appropriately verified in accordance with the Quality Management System before release.\nEnsure Post-Market Surveillance (PMS) obligations are fulfilled.\nEnsure vigilance reporting requirements are met in accordance with Articles 87-91 of the Medical Device Regulation (MDR).\nDirect large-scale programs and departmental initiatives in support of division-wide and company-wide objectives.\nMaintain accountability for product quality, regulatory compliance, and adherence to Baxter quality policies.\nDevelop, implement, and maintain quality systems, including Management Review, CAPA, Design Controls, and Process Controls, to ensure products meet defined requirements.\nEnsure compliance with applicable regulatory requirements and manage regulatory inspections and audits.\nConduct periodic reviews of the Quality Management System with executive leadership to ensure effectiveness and continued suitability.\nDrive continuous improvement initiatives across processes and systems while supporting deployment of divisional and corporate quality programs.\nAssess and advise senior leadership on quality-related aspects of acquisition targets.\nCollaborate effectively with stakeholders across functions, business units, and global locations.\nServe as the primary quality representative in interactions with customers and regulatory agencies regarding products, systems, and processes.\nEnsure adherence to established specifications, procedures, and standards supporting product quality and regulatory compliance.\nDevelop and manage the Quality organization budget and ensure effective utilization of departmental resources.\nLead coaching, training, performance management, employee development, and succession planning initiatives for the Quality team.\nWhat You'll Bring\nIn-depth knowledge of the regulatory environment governing the manufacture of medical devices and therapeutics.\nProven leadership experience managing large teams in a complex, regulated environment.\nDemonstrated ability to lead within a matrix organization and collaborate effectively across global, cross-functional teams.\nStrong analytical, problem-solving, and decision-making skills.\nExcellent verbal and written communication skills.\nProven success working with multifunctional and global teams.\nStrong interpersonal, influencing, and negotiation skills.\nExtensive knowledge of applicable quality systems, regulatory standards, and industry regulations.\nExperience in risk management, validation, analytics, and microbiology within a GMP-regulated environment.\nQuality expertise supporting technology transfer initiatives.\nAbility and willingness to work within ISO 7 and ISO 8 cleanroom manufacturing environments, including required gowning procedures.\nEducation & Experience\nBachelor's degree in Science, Engineering, or a related technical discipline required; advanced degree preferred.\nMinimum of 10 years of experience in Quality, Manufacturing, or a related field within the medical products industry.\nMinimum of 7 years of management experience.\nWe 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 $160,000 - $220,000 annually. The estimated salary is meant to reflect an anticipated salary range for the position. We may pay more or less than the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on 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.\nApplicants 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.\nUS Benefits at Baxter (except for Puerto Rico)\nThis 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\nEqual Employment Opportunity\nBaxter 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.\nKnow Your Rights: Workplace Discrimination is Illegal\nReasonable Accommodations\n\nBaxter 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.\nRecruitment Fraud Notice\n\nBaxter 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.","company":"Baxter","rawCompany":"baxter","city":"Hayward","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-08-08T14:21:50.528Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"11-9199.01","title":"Regulatory Affairs Managers","slug":"regulatory-affairs-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"}],"industries":[{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Associate Director, Quality","description":"Req # 206344 Location Hayward, California, United States Job Category Quality Date posted 08/06/2026\n\nOverview\nThis is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives.\nSupport for Parents\nContinuing Education/ Professional Development\nEmployee Heath & Well-Being Benefits\nPaid Time Off\n2 Days a Year to Volunteer\nSuccess Profile\nWhat makes a successful Quality team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.\nDetail Oriented\nContinuous Learner\nCourageous\nCollaborative\nCritical Thinker\nInfluential\n\nThis is where your work makes a difference.\nAt 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.\nOur 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.\nHere, you will find more than just a job—you will find purpose and pride.\nYour Role\nThis position is responsible for being Most Senior plant level Quality Management Representative, developing and deploying the quality system for the plant, assuring systems and procedures for regulatory compliance are established and deployed\nWhat You'll Be Doing\nServe as the Management Representative for Quality and lead the Quality organization within a mid-to-large manufacturing facility.\nBuild and develop a high-performing Quality organization with a clear vision and mission that supports business growth and global expansion.\nOversee batch review and product release activities.\nFulfill the responsibilities of the Person Responsible for Regulatory Compliance (PRRC), including ensuring device conformity is appropriately verified in accordance with the Quality Management System before release.\nEnsure Post-Market Surveillance (PMS) obligations are fulfilled.\nEnsure vigilance reporting requirements are met in accordance with Articles 87-91 of the Medical Device Regulation (MDR).\nDirect large-scale programs and departmental initiatives in support of division-wide and company-wide objectives.\nMaintain accountability for product quality, regulatory compliance, and adherence to Baxter quality policies.\nDevelop, implement, and maintain quality systems, including Management Review, CAPA, Design Controls, and Process Controls, to ensure products meet defined requirements.\nEnsure compliance with applicable regulatory requirements and manage regulatory inspections and audits.\nConduct periodic reviews of the Quality Management System with executive leadership to ensure effectiveness and continued suitability.\nDrive continuous improvement initiatives across processes and systems while supporting deployment of divisional and corporate quality programs.\nAssess and advise senior leadership on quality-related aspects of acquisition targets.\nCollaborate effectively with stakeholders across functions, business units, and global locations.\nServe as the primary quality representative in interactions with customers and regulatory agencies regarding products, systems, and processes.\nEnsure adherence to established specifications, procedures, and standards supporting product quality and regulatory compliance.\nDevelop and manage the Quality organization budget and ensure effective utilization of departmental resources.\nLead coaching, training, performance management, employee development, and succession planning initiatives for the Quality team.\nWhat You'll Bring\nIn-depth knowledge of the regulatory environment governing the manufacture of medical devices and therapeutics.\nProven leadership experience managing large teams in a complex, regulated environment.\nDemonstrated ability to lead within a matrix organization and collaborate effectively across global, cross-functional teams.\nStrong analytical, problem-solving, and decision-making skills.\nExcellent verbal and written communication skills.\nProven success working with multifunctional and global teams.\nStrong interpersonal, influencing, and negotiation skills.\nExtensive knowledge of applicable quality systems, regulatory standards, and industry regulations.\nExperience in risk management, validation, analytics, and microbiology within a GMP-regulated environment.\nQuality expertise supporting technology transfer initiatives.\nAbility and willingness to work within ISO 7 and ISO 8 cleanroom manufacturing environments, including required gowning procedures.\nEducation & Experience\nBachelor's degree in Science, Engineering, or a related technical discipline required; advanced degree preferred.\nMinimum of 10 years of experience in Quality, Manufacturing, or a related field within the medical products industry.\nMinimum of 7 years of management experience.\nWe 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 $160,000 - $220,000 annually. The estimated salary is meant to reflect an anticipated salary range for the position. We may pay more or less than the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on 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.\nApplicants 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.\nUS Benefits at Baxter (except for Puerto Rico)\nThis 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\nEqual Employment Opportunity\nBaxter 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.\nKnow Your Rights: Workplace Discrimination is Illegal\nReasonable Accommodations\n\nBaxter 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.\nRecruitment Fraud Notice\n\nBaxter 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.","datePosted":"2026-08-08T14:21:50.528Z","dateModified":"2026-08-08T14:21:50.528Z","hiringOrganization":{"@type":"Organization","name":"Baxter","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Hayward","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"fbfb350c62864088f8d2e721"},"url":"https://jobsearcher.com/jobs/fbfb350c62864088f8d2e721"}}