Senior Specialist Regulatory Affairs (m/w/d)

Vantive: A New Company Built On Our Legacy

Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.

At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us are driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support.

*Completion of the proposed separation of Kidney Care from Baxter into a standalone company (to be named Vantive) remains subject to the satisfaction of customary conditions.

Your role at Baxter

As Sr. Specialist Regulatory Affairs (m/f/d) within our Kidney Care Segment you will maintain regulatory files and provide regulatory advice to project teams.

This role is based in Hechingen/Baden-Württemberg

.

What you'll be doing

• With direction, develop and execute regulatory project plans 

• Identify and elevate key areas of regulatory risk 

• Maintain regulatory files in a format consistent with requirements 

• Maintain awareness of regulatory requirements; identify relevant requirements 

• Participate as an active team member and provide regulatory advice to project teams as required 

• Respond to questions from regulatory authorities within strict timelines 

• Compile and submit, in a timely manner, regulatory documents according to regulatory requirements 

• Maintain and update existing regulatory authorizations 

• Support regulatory activities relating to specific portfolio of products/projects 

• Prepare, review, and approve labeling and SOP’s 

• Represent or lead Regulatory Affairs in small project teams​ 

What you'll bring

• Bachelor’s degree or country equivalent in a scientific discipline

• Regulatory or equivalent experience within a pharmaceutical and/or medical device company, CRO, or similar organization

• Knowledge of regulations  

• Scientific knowledge 

• Project management skills 

• Manage multiple projects and deadlines 

• Ability to multitask and prioritize 

• Interpersonal and communication skills 

• Negotiation skills 

• Technical system skills (e.g., word processing, spreadsheets, databases, online research) 

• Ability to identify compliance risks and escalate when necessary​

•  Fluent German and English language skills

Have we sparked your interest?

If you like the sound of the above role, can thrive in a fast-paced working environment and are excited about working in a learning and growth culture, then we’d love to talk to you. Apply direct on our Online System. For further information please contact sigrid_bofinger@baxter.com

#IND-DACH

Reasonable Accommodations

Baxter 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.

Recruitment Fraud Notice

Baxter 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.