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7 Hours Ago
Tijuana, Baja California, MEX
Junior
Junior
Healthtech • Other
The EHS Associate at Baxter is responsible for developing and implementing environmental, safety, and health programs at a medical device manufacturing facility. This role includes problem-solving, administrative coordination, and ensuring compliance with regulations while promoting a culture of safety within the organization.
7 Hours Ago
Skaneateles, NY, USA
88K-121K Annually
Mid level
88K-121K Annually
Mid level
Healthtech • Other
As a Senior Quality Engineer at Baxter, you will lead compliance investigations, corrective action projects, and quality risk assessments. Your role involves analyzing operational data, conducting root cause investigations, and driving quality improvements. You'll also manage multi-departmental teams to ensure product compliance and implement effective inspection criteria. Strong communication and organizational skills are essential to succeed in this position.
7 Hours Ago
Skaneateles, NY, USA
88K-121K Annually
Senior level
88K-121K Annually
Senior level
Healthtech • Other
The Senior Quality Engineer will lead quality processes for new product launches, ensuring compliance with regulatory standards. Responsibilities include validating new processes, conducting root cause analyses, improving product quality, and managing corrective actions. This role involves collaborating across teams to enhance operational efficiencies and uphold quality in manufacturing processes.
7 Hours Ago
Tijuana, Baja California, MEX
Senior level
Senior level
Healthtech • Other
The Specialist Supplier Quality at Baxter monitors supplier performance and coordinates quality problem resolution for supplied parts. The role involves conducting audits, developing inspection techniques, managing corrective actions, and providing engineering support for non-conforming materials.
Top Skills: Engineering
11 Hours Ago
Skaneateles, NY, USA
76K-105K Annually
Mid level
76K-105K Annually
Mid level
Healthtech • Other
The Quality Associate II is responsible for managing document control and training requirements at Baxter. This includes overseeing the document change control process, ensuring compliance with quality management systems, maintaining training records for employees, and working closely with managers to develop and monitor training plans. The role also involves supporting audits and collaborating with various functions within the organization.
Junior
Healthtech • Other
As a Subassembly Operator at Baxter, you will operate and monitor assembly machinery, perform quality checks, load production supplies, and document manufacturing processes to ensure the production of life-saving products. You will work collaboratively in a fast-paced environment while adhering to quality standards and safety procedures.
11 Hours Ago
Haina, Bajos De Haina, DOM
Mid level
Mid level
Healthtech • Other
The Strategic Project Engineer II at Baxter will enhance capital projects management systems focusing on optimizing facility layouts, analyzing cost of goods sold, leading project feasibility analysis and supporting new product launches while ensuring alignment with financial goals and regulatory commitments.
11 Hours Ago
Remote
United States of America
80K-110K Annually
Senior level
80K-110K Annually
Senior level
Healthtech • Other
The Senior CCMS Administrator at Baxter manages and supports the MadCap IXIA CCMS system, prepares translation packages, troubleshoots issues, develops specifications for projects, and trains team members on CCMS usage. The role also involves data analysis and implementation project management.
Top Skills: XML
15 Hours Ago
Round Lake, IL, USA
96K-132K Annually
Senior level
96K-132K Annually
Senior level
Healthtech • Other
As a Research Associate III at Baxter, you'll perform critical chemical and physical analyses, lead study evaluations, mentor junior team members, ensure compliance with regulations, and collaborate cross-functionally to support product development and stability testing.
Top Skills: HplcUplc
15 Hours Ago
Batesville, IN, USA
104K-143K Annually
Senior level
104K-143K Annually
Senior level
Healthtech • Other
The Principal Engineer will oversee quality and regulatory matters for medical bed devices, ensuring compliance with QSR regulations. Responsibilities include collaboration with engineering and quality organizations, supporting validation processes, and analyzing quality data to drive improvements while maintaining strong professional relationships across departments.
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