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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.
Job Responsibility:
Lead and develop the Quality Training team to ensure strong performance and engagement
Oversee the design, deployment, and continuous improvement of all sitewide training programs
Partner with functional leaders to build and maintain role‑based training plans
Implement and maintain global and site-level training SOPs to ensure compliance
Ensure training programs meet cGMP, GDP, and regulatory requirements (21 CFR Parts 7, 11, 803, 806, 810, 820)
Support Quality System training needs, including CAPA, NCR, Change Control, Audits, and controlled documentation
Manage creation, revision, and governance of OJT materials, curricula, and qualification processes
Deliver or oversee New Hire, Annual, and Quality Systems training across the site
Serve as Master Trainer and conduct qualifications as needed
Lead training readiness efforts for regulatory and internal inspections
act as site SME with auditors
Manage and report training metrics, dashboards, KPIs, and training effectiveness insights
Administer the Learning Management System (LMS) and drive process standardization, innovation, and change management initiatives
Requirements:
Bachelor’s degree in science, engineering, business, or a related field
5+ years of experience in training, quality, manufacturing, or a cGMP‑regulated environment
supervisory experience required
Strong knowledge of cGMP, GDP, and relevant FDA regulations
Solid understanding of Quality System processes and audit/inspection expectations
Ability to lead and develop high‑performing teams
Experience with Learning Management Systems (LMS)
Strong analytical, problem‑solving, and influencing skills
Excellent facilitation, presentation, and interpersonal abilities
Ability to manage multiple priorities in a matrixed environment
Strong project management and thoughtful planning capabilities
What we offer:
Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts
educational assistance programs
paid holidays
paid time off ranging from 20 to 35 days based on length of service