At Baxter, we’re more than just a company—we’re a global community united by a shared mission: to save and sustain lives. Every role here, including yours, contributes to making a meaningful difference for millions of patients worldwide. For over 85 years, we’ve been at the forefront of medical innovation, delivering life-changing products and therapies to hospitals, clinics, and homes across the globe.
This is where you can do your best work. Where your purpose aligns with our mission. Where you’ll find a team that inspires, supports, and celebrates each other. Together, we create a place where happiness and success go hand in hand.
We’re Looking for a Regulatory Affairs (RA) Manager to Lead in KSA (Drugs and Devices)
As the RA Manager, you’ll play a pivotal role in shaping and executing regulatory strategies across KSA, ensuring compliance with local health authority regulations and Baxter’s global standards. You’ll be the bridge between Baxter and regulatory authorities, leveraging your expertise and network to keep our portfolio aligned with the latest updates and requirements.
This is your chance to lead, innovate, and make a lasting impact in a role that combines strategic thinking, collaboration, and a passion for improving lives.
What You’ll Do:
- Develop and implement global regulatory strategies to obtain and maintain product approvals.
- Stay ahead of health authority updates and communicate their impact to stakeholders.
- Ensure Baxter’s portfolio complies with local regulations and standards.
- Lead regulatory activities for a diverse product portfolio, managing submissions, approvals, and lifecycle processes.
- Provide expert regulatory guidance to cross-functional teams and mentor junior team members.
- Prepare, review, and approve labeling, SOPs, and promotional materials to ensure compliance.
- Represent Regulatory Affairs in project teams, driving alignment and progress.
What You’ll Bring:
- Experience: 5+ years in regulatory affairs or a related field within the pharmaceutical industry.
- Knowledge: Deep understanding of local and global regulatory requirements and scientific principles.
- Skills: Strong project management, negotiation, and communication skills.
- Mindset: A proactive, self-motivated approach with the ability to thrive in a fast-paced, multicultural environment.
- Education: Bachelor’s degree (or equivalent) in a scientific discipline.
- Languages: Fluency in English and Arabic.
Non-Negotiable Traits:
- Resilience under pressure and the ability to multitask effectively.
- Exceptional organizational and listening skills.
- A team player who can also work independently and deliver results.
- Strong communication skills, both written and verbal, with the ability to provide clear updates and explanations.
A Note on Our Transition:
As of February 1, Baxter has completed the sale of its Kidney Care business, which will now operate as Vantive. This role is part of a deferred market transition, meaning the employer of record will initially be Baxter and will later transition to Vantive. Vantive builds on Baxter’s 70-year legacy in kidney care, offering best-in-class therapies and meaningful work for those who join us.
Our Commitment to You:
Baxter is dedicated to creating an inclusive workplace. We provide reasonable accommodations for individuals with disabilities throughout the recruitment process. If you need assistance, please let us know.
Beware of Recruitment Fraud:
Unfortunately, recruitment scams are on the rise. Baxter will never ask for financial information or payment during the hiring process. If you encounter suspicious activity, please review our Recruitment Fraud Notice for guidance.
Ready to Accelerate Your Career While Making a Difference?
If you’re passionate about regulatory affairs and want to be part of a team that’s transforming healthcare, we’d love to hear from you. Apply today and join us at the intersection of saving and sustaining lives.
Together, we can create a healthier world.