Baxter Hiring Senior Specialist – Regulatory Affairs 2026
Looking for an experienced Regulatory Affairs job in Ahmedabad?
Baxter is hiring a Senior Specialist – Regulatory Affairs to support regulatory strategies, product registrations, marketing authorizations, and submission activities.
This full-time opportunity is suitable for experienced professionals with 8–10 years of total relevant experience, including at least 2 years of regulatory experience, in pharmaceutical, medical device, CRO, or related organizations.
About Baxter
Baxter is a global healthcare company focused on developing products and solutions designed to save and sustain lives.
The organization operates across the healthcare industry with a strong emphasis on scientific innovation, quality, regulatory compliance, and operational excellence.
For regulatory professionals, Baxter provides opportunities to work with global regulatory requirements, product portfolios, submissions, and cross-functional project teams.Job Overview
| Job Details | Information |
|---|---|
| Company | Baxter |
| Position | Senior Specialist – Regulatory Affairs |
| Department | Regulatory Affairs |
| Location | Ahmedabad, Gujarat |
| Experience | 8–10 Years Total |
| Regulatory Experience | Minimum 2 Years |
| Qualification | Bachelor’s Degree in a Scientific Discipline |
| Employment Type | Full-Time |
| Work Type | On-site |
| Job Requisition ID | JR-205795 |
| Application Deadline | September 18, 2026 |
Senior Specialist – Regulatory Affairs Job Description
The Senior Specialist will support regulatory activities across product portfolios and help implement regulatory strategies.
The role involves preparing and maintaining regulatory documentation, monitoring regulatory requirements, supporting submissions, and providing regulatory guidance to project teams.
Key Focus Areas
- Global regulatory strategy
- Regulatory submissions
- Marketing authorization maintenance
- Regulatory documentation
- Product labeling
- SOP review
- Compliance risk management
- Regulatory authority communication
Eligibility Criteria
Candidates should have:
- A Bachelor’s degree or equivalent qualification in a scientific discipline
- At least 2 years of regulatory affairs experience
- 8–10 years of total relevant professional experience
- Experience in pharmaceutical, medical device, CRO, or related industries
- Strong understanding of regulatory requirements
- Ability to manage multiple projects and deadlines
Experience with global regulatory environments will be valuable for this position.
Skills Required
Regulatory Skills
- Regulatory strategy
- Submission preparation
- Marketing authorization management
- Regulatory documentation
- Product labeling
- SOP review
- Compliance assessment
- Regulatory risk identification
Professional Skills
- Project management
- Stakeholder management
- Negotiation
- Written and verbal communication
- Analytical thinking
- Problem-solving
- Time management
- Ability to prioritize multiple activities
Technical Skills
- Word processing applications
- Spreadsheets
- Databases
- Online research tools
- Regulatory documentation systems
Key Responsibilities
As a Senior Specialist – Regulatory Affairs, responsibilities include:
- Develop and execute regulatory project plans under appropriate direction
- Identify and escalate important regulatory risks
- Maintain regulatory files according to required standards
- Monitor changes in applicable regulatory requirements
- Provide regulatory guidance to project teams
- Respond to questions from regulatory authorities within required timelines
- Compile and submit regulatory documents
- Maintain and update existing marketing authorizations
- Support regulatory activities for assigned product portfolios
- Prepare, review, and approve labeling materials
- Review and support SOP activities
- Represent Regulatory Affairs on small project teams
- Coordinate with cross-functional stakeholders to meet submission timelines
Regulatory Affairs Career Opportunities
Regulatory Affairs professionals play an important role in ensuring that healthcare products meet applicable regulatory requirements before and after commercialization.
Experience gained in this role can support career progression toward positions such as:
- Regulatory Affairs Manager
- Senior Regulatory Affairs Manager
- Regulatory Project Manager
- Global Regulatory Lead
- Regulatory Strategy Lead
- Regulatory Operations Manager
The role can be particularly valuable for professionals seeking broader exposure to pharmaceutical and medical device regulations.
Benefits & Career Opportunities
Working at Baxter can provide:
- 🌍 Exposure to a global healthcare organization
- 📋 Experience with regulatory submissions and authorizations
- 🧪 Exposure to pharmaceutical and medical device regulatory processes
- 📚 Learning and professional development opportunities
- 🤝 Cross-functional collaboration
- 🚀 Long-term career growth
- ❤️ Opportunity to contribute to healthcare products designed to improve patient care
How to Apply
Verified Job Posting
Interested candidates should apply through the official Baxter careers portal.
Job Requisition ID
JR-205795
Search for:
“Senior Specialist”
📅 Application Deadline: September 18, 2026
Candidates should submit their updated resume and complete the online application before the closing date.
⚠️ Important: Baxter does not charge candidates recruitment fees. Be cautious of anyone requesting payment in exchange for a job opportunity.
Why Should You Apply?
This position is a strong fit for professionals who already have substantial experience in Regulatory Affairs and want to move into a senior specialist role.
The Ahmedabad position combines regulatory strategy, submissions, compliance, authorization maintenance, and cross-functional project work—providing broad exposure to the regulatory lifecycle.
Frequently Asked Questions
1. Who can apply for the Baxter Senior Specialist role?
Candidates with a Bachelor’s degree in a scientific discipline, at least 2 years of regulatory experience, and approximately 8–10 years of total relevant experience can apply.
2. Is this a fresher job?
No. This is a senior-level position requiring significant professional experience.
3. Where is the Baxter job located?
The position is based in Ahmedabad, Gujarat, India.
4. What is the required regulatory experience?
A minimum of 2 years of regulatory experience is specified, along with 8–10 years of total relevant experience.
5. What industries are relevant?
Experience in pharmaceuticals, medical devices, CROs, or similar organizations is relevant to the position.
6. What is the job requisition ID?
The Baxter job requisition ID is JR-205795.
