Ahmedabad Gujarat Affairs lead Jobs – 13 Open Jobs Today

Senior Specialist
Baxter —Ahmedabad, Gujarat
- Word processing
- Project management
- Bachelor's degree
Clinical Evaluation Manager
Zydus Group —Ahmedabad, Gujarat
- Medicine
- Doctoral degree
- PMP
6d
Centre Manager
Medhavi —Naroda, Ahmedabad, Gujarat
- Microsoft Outlook
- Master's degree
- Business development
Quick apply
3d
Head - Accounts and Finance
Krish TechnoLabs Pvt Ltd —Ahmedabad, Gujarat
- Microsoft Excel
- Communication skills
- Tax experience
Business Development Manager (BDM)
Shanti Educational Initiatives Ltd —Navrangpura, Ahmedabad, Gujarat
- ₹45,000 - ₹50,000 a month
- Full-time
- Sales
- English
- Business development
- Health insurance
- Cell phone reimbursement
Quick apply
Manager – Medical Advisor
NewLife Medicals —Thaltej, Ahmedabad, Gujarat
- Medicine
- Doctoral degree
- Bachelor's degree
Deputy Manager/Assistant Manager-Process Development ( Downstream )
Zydus Group —Ahmedabad, Gujarat
5d
Medical Advisor
Cadila Pharmaceuticals —Ahmedabad, Gujarat
- Full-time
- Medicine
- Master's degree
- Analysis skills
- Health insurance
- Life insurance
Quick apply
Senior Quality Assurance Analyst (QMS)
DASH TECHNOLOGIES INC —Ahmedabad, Gujarat
- Computer Science
- Engineering
- Analysis skills
Quick apply
Assistant Manager, Regulatory Affairs
Amneal Pharmaceuticals —Ahmedabad, Gujarat
- Full-time
- Bachelor's degree
5d
Branding Manager
Cuatro Labs Pvt Ltd —Gandhinagar, Gujarat
- ₹20,000 - ₹40,000 a month
- Full-time
- CRM software
- Marketing
- English
Quick apply
Director, India Government & Public Affairs
Micron —Sanand, Gujarat
- AI
3d

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Senior Specialist

Baxter -
Ahmedabad, Gujarat

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Job details

Qualifications

Word processing
Project management
Bachelor's degree
Communication skills
Negotiation

Full job description

Req # 205795 Location Ahmedabad, Gujarat, India Job Category Regulatory Affairs Date posted 08/31/2026

This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

Summary:

Under limited supervision responsible for the implementation of global regulatory strategies, obtain and maintain marketing authorizations for product(s) and communication of general regulatory requirements in support of licensing of Baxter’s products. Support regulatory activities relating to specific portfolio of global products/projects.

Essential Duties and Responsibilities:

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

Qualifications:

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

Education and/or Experience:
Bachelor’s degree or country equivalent in a scientific discipline. Minimum of 2 years regulatory experience along with 8-10 years total experience within a pharmaceutical and/or medical device company, CRO, or similar organization.

Equal Employment Opportunity

Baxter 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

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.

Apply Now

Refine Your Search

affairs lead jobs in ahmedabad gujarat

Senior Specialist

Clinical Evaluation Manager

Centre Manager

Head - Accounts and Finance

Business Development Manager (BDM)

Manager – Medical Advisor

Deputy Manager/Assistant Manager-Process Development ( Downstream )

Medical Advisor

Senior Quality Assurance Analyst (QMS)

Assistant Manager, Regulatory Affairs

Branding Manager

Director, India Government & Public Affairs

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