Baxter Associate Regulatory Affairs Jobs
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Required Education
- Skills & Competencies
- Location & Salary
- Application Process
- Why This Role Matters
- SEO-Focused Job Highlights
- Frequently Asked Questions (FAQs)
- Who can apply for this Regulatory Affairs position?
- Is this role suitable for freshers?
- What regulatory systems are required for this role?
- Where is the job located?
- Is this a global regulatory role?
- Is the application process safe?
- Equal Employment Opportunity
- Summary Table
Baxter Associate Regulatory Affairs Jobs in Bengaluru – B.Pharm / M.Pharm / MSc – Regulatory Affairs Vacancy
Baxter hiring Associate Regulatory Affairs in Bengaluru. B.Pharm, M.Pharm, MSc eligible. Regulatory Affairs vacancy with global exposure.
Baxter is hiring an Associate, Regulatory Affairs at its Bengaluru, Karnataka location. This opportunity is designed for life sciences and pharmacy professionals who want hands-on exposure to global regulatory operations, high-impact healthcare products, and structured compliance-driven environments. If you are building a long-term career in regulatory affairs, regulatory submissions, or global product registration, this role places you at the center of regulated healthcare innovation.
This position supports global and regional regulatory teams and plays a direct role in managing product registrations, regulatory change controls, and high-quality submissions to global regulatory authorities. It is a strong fit for candidates looking to work with regulated medical and healthcare products while developing expertise in regulatory systems like TrackWise8 and Veeva Vault RIMS.
Company Overview
Baxter is a globally recognized healthcare company with a legacy dating back to 1931. The organization is driven by a single mission: to save and sustain lives. Over the decades, Baxter has built a strong reputation for innovation, ethical operations, regulatory compliance, and patient-focused healthcare solutions.
With operations across multiple countries, Baxter plays a critical role in delivering essential medical products and therapies used in hospitals, clinics, and home-care settings worldwide. The company’s work directly supports patient safety, treatment continuity, and healthcare system reliability.
Baxter’s culture emphasizes accountability, collaboration, and continuous improvement. Employees are encouraged to take ownership of their work, engage with global teams, and contribute to solutions that impact patient outcomes at scale. Regulatory Affairs professionals at Baxter are trusted partners in ensuring that products meet global regulatory standards and reach patients safely and efficiently.
Job Role & Responsibilities
The Associate, Regulatory Affairs role focuses on execution and coordination of regulatory activities across global and regional teams. The position requires strong attention to detail, regulatory system expertise, and the ability to manage multiple regulatory workflows in a controlled and compliant manner.
Key Responsibilities
- Collaborate with Global and Regional Regulatory Affairs teams to align regulatory activities with business and compliance requirements.
- Support product registration activities across regulated markets by coordinating documentation, submissions, and lifecycle updates.
- Manage Change Control processes end to end, ensuring compliance with internal quality systems and regulatory expectations.
- Work extensively with TrackWise8 for Change Control Management activities.
- Handle regulatory submissions using RIMS – Veeva Vault, ensuring accuracy, completeness, and timely filings.
- Track the status and progress of regulatory filings and submissions across multiple regions.
- Maintain regulatory databases, trackers, and internal systems with high data integrity.
- Support internal stakeholders by providing regulatory updates, documentation status, and compliance-related information.
- Ensure all regulatory activities meet internal quality standards and external regulatory authority requirements.
This role directly contributes to regulatory compliance, product continuity, and patient safety. It offers practical exposure to regulated healthcare environments, making it highly valuable for professionals building expertise in global regulatory affairs.
Eligibility / Qualifications
Required Education
Candidates should have completed one of the following qualifications:
B.Pharm, M.Pharm, MSc (Pharmaceutical Sciences), MSc (Life Sciences), MSc (Biotechnology), MSc (Microbiology), MSc (Biochemistry), Pharm.D, or equivalent life sciences qualification.
Skills & Competencies
- Strong understanding of Regulatory Affairs fundamentals and product lifecycle management.
- Hands-on or working knowledge of TrackWise8 for Change Control Management.
- Experience or exposure to RIMS – Veeva Vault for regulatory submissions.
- Familiarity with regulatory documentation, submission tracking, and compliance workflows.
- Ability to manage multiple regulatory tasks with accuracy and consistency.
- Strong communication skills for interaction with global regulatory and cross-functional teams.
- High attention to detail and documentation quality.
Location & Salary
Job Location: Bengaluru, Karnataka, India
Application Process
Interested and eligible candidates should apply directly through the official Baxter careers portal.
Apply Online: https://jobs.baxter.com/en/job/-/-/152/89688779616
Applicants are advised to apply only through the official link to avoid recruitment fraud. Baxter does not request any payment during the hiring process.
Why This Role Matters
Regulatory Affairs is one of the highest-impact functions in the pharmaceutical and healthcare industry. This role ensures that life-saving products meet regulatory requirements and reach patients safely and legally across global markets.
At Baxter, Regulatory Affairs professionals act as gatekeepers of compliance and quality. Your work directly supports healthcare delivery, patient trust, and regulatory excellence. This position provides exposure to global regulatory systems, cross-border collaboration, and structured quality-driven processes.
SEO-Focused Job Highlights
- Regulatory Affairs jobs in Bengaluru
- Associate Regulatory Affairs vacancy in pharma
- Baxter Regulatory Affairs careers India
- High-paying regulatory affairs jobs
- Global regulatory submissions roles
- TrackWise8 regulatory jobs
- Veeva Vault RIMS regulatory positions
- Pharma regulatory compliance careers
Frequently Asked Questions (FAQs)
Who can apply for this Regulatory Affairs position?
Candidates with B.Pharm, M.Pharm, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, or equivalent qualifications can apply. Experience in regulatory systems is preferred.
Is this role suitable for freshers?
Candidates with relevant regulatory exposure, system knowledge, or internships may be considered. Prior hands-on experience in TrackWise8 or Veeva Vault is an advantage.
What regulatory systems are required for this role?
This role requires proficiency in TrackWise8 for Change Control Management and RIMS – Veeva Vault for regulatory submissions.
Where is the job located?
The position is based in Bengaluru, Karnataka, India.
Is this a global regulatory role?
Yes. The role involves collaboration with Global and Regional Regulatory Affairs teams across multiple geographies.
Is the application process safe?
Yes. Candidates should apply only through the official Baxter careers link. Baxter does not charge any fees for recruitment.
Equal Employment Opportunity
Baxter is an equal opportunity employer. All qualified applicants are considered without discrimination based on race, religion, gender, age, disability, or any legally protected status. Reasonable accommodations are available for candidates with disabilities during the hiring process.
Summary Table
| Company | Baxter Healthcare |
|---|---|
| Vacancies | Associate, Regulatory Affairs |
| Required Education | B.Pharm, M.Pharm, MSc Pharmaceutical Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharm.D |
| Experience | Regulatory Affairs / Regulatory Operations exposure preferred |
To apply for this job please visit jobs.baxter.com.
