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A career with a higher purpose

If you have a desire to learn, grow and innovate, you can find purpose and satisfaction at Baxter, and make a contribution to a greater good. Whether you’re interested in medical devices, pharmaceuticals or biotechnology – or all three – Baxter offers the opportunity to explore the path that’s right for you. Our combined expertise in these three areas is unique and it differentiates us from other companies in the healthcare industry.

Our employees around the world are connected by an enduring commitment to save and sustain lives. It’s this higher purpose that binds us as a company and as global citizens.

Discover how you can join Baxter and work in an innovative and exciting place while helping make a meaningful difference for millions of people around the world. Learn more.

Job Title Location Date
Regulatory Affairs Specialist CMCRL Wm Graham 2, IL, USA08/22/2014
Manager Regulatory Affairs Post Market CMC (Biosurgery)RL Wm Graham 2, IL, USA08/21/2014
Project Manager Regulatory Affairs ContractMississauga, ON, Canada08/12/2014
Director Regulatory Affairs Fluid SystemsRL Wm Graham 2, IL, USA08/11/2014
Regulatory Affairs Operations Sr. AssociateRL Wm Graham 2, IL, USA08/07/2014
Regulatory Affairs Operations Publisher ManagerRL Wm Graham 2, IL, USA08/07/2014
Regulatory Affairs Operations Associate Submissions ManagementRL Wm Graham 2, IL, USA08/05/2014
Manager Regulatory Affairs Device and Pharmaceutical Global LabelingRL Wm Graham 2, IL, USA07/30/2014
1 year contract Associate RA OperationsAllianceParkBraine R D Sales, Belgium, Belgium07/18/2014
Sr. Regulatory AssociateMississauga, ON, Canada07/08/2014
Regulatory Affairs AssociateRL Wm Graham 2, IL, USA06/23/2014
Manager Global Regulatory AffairsRL Technology, IL, USA06/23/2014
Regulatory Affairs ManagerRL Wm Graham 2, IL, USA06/10/2014
Mgr Reg Affairs CMC Small MoleculesWestlake Village, CA, USA05/30/2014
Director Regulatory Affairs CMCRL Wm Graham 2, IL, USA04/17/2014
Sr. Director of Regulatory AffairsDeerfield, IL, USA04/12/2014

Recent Jobs

Project Manager Regulatory Affairs Contract - Mississauga, ON
Description: Job Description Please note this is a 18-month contract: The Regulatory Project Manager is responsible for developing and maintaining a relationship with key stakeholders which will include Canadian and Global business and functional partners. The incumbent will manage regulatory projects from beginning to end, ensuring alignment between regulatory activities and corporate objectives and vision. In collaboration with busi...
Reference Code: 66101
Manager Regulatory Affairs Post Market CMC (Biosurgery) - RL Wm Graham 2, IL
Description: Job Description 1) Develop and execute CMC regulatory plans for complex projects including new products and maintenance of licenses/authorizations for existing marketing authorizations 2) Represent or lead the RA-CMC function on assigned cross-functional project teams 3) Monitor applicable regulatory requirements; assure compliance with Baxter and external standards 4) Establish appropriate communication within RA and oth...
Reference Code: 69084
Regulatory Affairs Specialist CMC - RL Wm Graham 2, IL
Description: Job Description Responsible for defining global chemistry, manufacturing and control (CMC) regulatory strategies and owning the CMC sections of regulatory submissions for new product development, global expansion, and the lifecycle maintenance of currently marketed products in the Medical Products Division. Develop and execute global regulatory CMC strategies for complex projects including new products and changes to exis...
Reference Code: 69643

About Regulatory Affairs Jobs

At Baxter, the Regulatory Affairs and Pharmacovigilance (GRAPV) function is responsible for ensuring that safe and effective biologics, medical devices and pharmaceuticals are available worldwide. GRAPV professionals at Baxter can help make a meaningful difference for patients around the world while also expanding their job related skills such as strategic planning, problem solving, scientific analysis, process/project quality standards, communication, submission and project management, risk assessment and contingency planning.

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