Senior Specialist, Regulatory Affairs (Advertising and Promotion) (Remote)

This is where you save and sustain livesAt Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world.

You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives- where your purpose accelerates our mission.Your role at Baxter The Senior Specialist resides within the Global Regulatory Affairs, Advertising and Promotions Group.

This group owns the global Advertising and Promotions (Ad Prom) process, and the system that enables the process (Veeva PromoMats).

This role is responsible for creating the FDA submission package for promotional material in Veeva PromoMats, and also for general system administration and configuration for Veeva PromoMats.

An ideal candidate will have back-end experience with Ad Prom systems and software, or have general Information Technology or Systems Administration experience within a life science or other technical environment.What you'll be doing

Under general supervision, responsible for Veeva PromoMats, Tableau, and regulatory documents for FDA submission.Perform Veeva PromoMats system updates (i.

e., workflows, configurations, lifecycle management, XML management, spreadsheets, templates, etc.).Identify areas for improvement / modification.

Compile regulatory documents for FDA submission (eCTD experience preferred), including : tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as required, maintaining regulatory files in a format consistent with requirements, and staying aware of regulatory requirements.

Develop training material and liaise with cross-functional teams.Understand internal global processes (i.e., Advertising and Promotion process).What you'll bring

Bachelor's degree or country equivalent required.3+ years of pharmaceutical industry experience preferred; minimum 1 year of regulatory experience preferred or IT concentration in life sciences, technical / engineering or related field.

Understanding of Veeva software (i.e., PromoMats or RIM) design, Zinc software design, or similar system design.Understanding of Tableau software design.

Strong written and verbal communication skills, ability to organize, prioritize and meet deadlines.Strong analytical skills, including digital competency.

Strong technical systems skills (i.e., databases, XML and Microsoft Office 365 including SharePoint, Power Automate and Excel).

Proofreading and editing skills.Ability to contribute to multiple projects from a regulatory affairs perspective.Ability to multitask and problem solve.

Knowledge of regulations for FDA submission preferred.We 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 our employees, and we strive to be more transparent with our pay practices.

To that end, this position has a salary range of $80,000 to $110,000 and also includes an annual incentive bonus. The above range represents the expected salary range for this position.

The actual salary may vary based upon several factors including, but not limited to, relevant skills / experience, time in the role, business line, and geographic / office location.

Equal Employment OpportunityBaxter 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.Reasonable Accommodations

Take the next step in your career now, scroll down to read the full role description and make your application.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.

J-18808-LjbffrRemote working / work at home options are available for this role.