Mandhela Kalan Delhi Regulatory affairs specialist Jobs – 16 Open Jobs Today

RA Senior Specialist (Regulatory Affairs)
Baxter —Gurugram, Haryana
- Project management
- Bachelor's degree
- Communication skills
14h
Regulatory and Quality Specialist
Grifols India Healthcare —Gurugram, Haryana
- Full-time
- English
- Organisational skills
- Communication skills
8d
Safety & PV Specialist I
サイネオス・ヘルス —Gurugram, Haryana
- Medicine
- B.Sc
- Master's degree
Product Stewardship & Regulatory Specialist - CB3 - NM
ACS India Private Limited —Gurugram, Haryana
- Full-time
- Salesforce
- English
- Microsoft Office
- Health insurance
- Paid time off
Quick apply
8d
Staff Clinical Affairs Specialist
Stryker —Gurugram, Haryana
- Full-time
- Azure
- Project management
- SharePoint
- Health insurance
Specialist Deputy Legal Manager - Office of General Counsel
Deloitte —Gurugram, Haryana
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
2d
Specialist - Insurance - P&C Claims 4A
Genpact India Pvt. Ltd. —Gurugram, Haryana
- Full-time
- Hybrid work
- English
- Finance
- Master's degree
Quick apply
Senior Product Specialist - Telepresence & Microscopy (Maharashtra) (m/f/d)
KARL STORZ —Delhi, Delhi
- Call employer
- Health insurance
International Registration
ABCD ASIA —Gurugram, Haryana
- ₹13,00,000 - ₹14,00,000 a year
- Full-time
Quick apply
Global Senior Environmental Data Manager
Reckitt —Gurugram, Haryana
- Microsoft Powerpoint
- English
- Databases
- Health insurance
11d
SBU HEAD – CRITICAL CARE
Fresenius Medical Care —Gurugram, Haryana
- Full-time
- Master's degree
- Business Administration
- MBA
Business Marketing Manager
Siemens Healthineers —Delhi, Delhi
- Weekend availability
- Hybrid work
- English
- Analysis skills
- Bachelor's degree
- Flexible schedule
Quick apply
Specialist - Regulatory Affairs - Operations 4A
Genpact India Pvt. Ltd. —Gurugram, Haryana
- Full-time
- English
- Master's degree
- Bachelor's degree
Quick apply
Specialist - Regulatory Affairs - Operations 4B
Genpact India Pvt. Ltd. —Gurugram, Haryana
- Full-time
- English
- Master's degree
- Bachelor's degree
Quick apply
4d
Sr. Specialist - Regulatory Affairs - Operations 4C
Genpact India Pvt. Ltd. —Gurugram, Haryana
- Full-time
- Azure
- English
- Master's degree
Quick apply

Related jobs to explore

Based on your search for regulatory affairs specialist

Social Impact Associate
Kyndryl —Gurugram, Haryana
As a Social Impact Specialist, you will support the design, coordination, and execution of social responsibility initiatives that create measurable community…
1d
RA Senior Specialist (Regulatory Affairs)
Baxter —Gurugram, Haryana
Monitor changes in regulatory requirements, regulatory intelligence, and industry trends, and communicate relevant risks, requirements, and potential business…
14h

I want to receive the latest job alerts for regulatory affairs specialist in mandhela kalan delhi

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

regulatory affairs specialist jobs near mandhela kalan delhi

Regulatory Specialist jobs in Gurugram, Haryana

Insurance Specialist jobs in Gurugram, Haryana

Marketing Manager jobs in Delhi, Delhi

Regulatory Affairs Medical Devices jobs in Chennai, Tamil Nadu

Regulatory Affairs Specialist jobs in Pune District, Maharashtra

Regulatory jobs in Coimbatore, Tamil Nadu

Regulatory Affairs Specialist jobs in Chandigarh, Chandigarh

Regulatory Affairs Specialist jobs in Electronics City, Bengaluru, Karnataka

Regulatory Affairs Specialist jobs in Bopal, Ahmedabad, Gujarat

Ministry Of External Affairs, India Photographer jobs in Delhi, Delhi

Regulatory Affair jobs in Bengaluru, Karnataka

Regulatory Affairs Pharma, Internship jobs in Bengaluru, Karnataka

Talent Acquisition Specialist jobs in Bengaluru, Karnataka

Food Regulatory jobs in Gurugram, Haryana

Regulatory Affairs Specialist jobs in Savli, Vadodara, Gujarat

Regulatory Affairs, Trainee jobs in Mumbai, Maharashtra

Regulatory Affairs Specialist jobs in Navi Mumbai, Maharashtra

Medical Documentation Specialist jobs in Mumbai, Maharashtra

Medical Affairs jobs in Mumbai, Maharashtra

Google Ads Specialist jobs in Bengaluru, Karnataka

RA Senior Specialist (Regulatory Affairs)

Baxter -
Gurugram, Haryana

Apply Now

Job details

14 hours ago

Qualifications

Biotechnology
Project management
Bachelor's degree
Pharmacy
Communication skills
Information management
Negotiation

Full job description

Req # 207680 Location Gurgaon, Haryana, India Job Category Regulatory Affairs Date posted 09/04/2026

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.

As a Senior RA Specialist, Regulatory Affairs, you will be responsible for the

execution and maintenance of Regulatory Affairs activities for Baxter's

pharmaceutical and medical device product portfolios across India, while

supporting regulatory activities for Bangladesh and Sri Lanka under limited supervision.

In this role, you will

Supports product registrations, lifecycle management, renewals, variations, regulatory submissions, health authority interactions, and compliance activities to ensure timely product approvals and continued market access.
Works closely with Regulatory Affairs, Quality, Commercial, Supply Chain, Marketing, Global Regulatory Affairs, and distributor partners to support business objectives and regulatory compliance.
Prepare and execute regulatory submissions, renewals, variations, and lifecycle management activities for assigned pharmaceutical and medical device product portfolios in India, while supporting regulatory activities for Bangladesh and Sri Lanka.
Compile, review, and submit regulatory dossiers, authority responses, and supporting documentation in accordance with local regulatory requirements and established timelines.
Support regulatory submissions, authority queries, approvals, and post-approval activities with Indian health authorities, including medical device, pharmaceutical, import, and registration applications through applicable regulatory systems and portals such as SUGAM.
Perform regulatory assessments of product, manufacturing, labeling, artwork, supplier, and site changes to determine regulatory impact, reporting requirements, and submission strategies.
Maintain product registrations and regulatory approvals by ensuring timely completion of renewals, post-approval changes, commitments, regulatory notifications, and lifecycle management activities.
Monitor changes in regulatory requirements, regulatory intelligence, and industry trends, and communicate relevant risks, requirements, and potential business impacts to internal stakeholders.
Liaise with health authorities, distributors, license holders, and external regulatory partners to support product registrations, regulatory approvals, regulatory queries, and compliance activities.
Review and support approval of product labeling, artwork, promotional materials, and regulatory documentation to ensure compliance with applicable local regulations and Baxter requirements.
Support health authority inspections, regulatory audits, recalls, and responses to regulatory queries, observations, and commitments in collaboration with cross-functional stakeholders.
Collaborate closely with Global Regulatory Affairs, Quality, Supply Chain, Commercial, Marketing, Medical Affairs, and external partners to support regulatory submissions, product launches, lifecycle management activities, compliance initiatives, supply continuity, and business objectives.

Qualifications :

Bachelor's Degree in Pharmacy, Life Sciences, Biomedical Sciences, Biotechnology, Chemistry, Regulatory Affairs, or a related scientific discipline.
Minimum 5 years of Regulatory Affairs experience within the pharmaceutical, medical device, biologics, nutrition, or healthcare industry, including product registrations, lifecycle management, regulatory assessments, and health authority interactions.
Strong knowledge of India and South Asia regulatory requirements, including CDSCO regulations, SUGAM submissions, product registrations, lifecycle management, regulatory intelligence, compliance activities, and health authority interactions.
Strong project management, communication, stakeholder management, coordination, and negotiation skills, with the ability to manage multiple regulatory activities, identify compliance risks, escalate issues when necessary, and collaborate effectively within a matrix and multicultural environment.
Experience supporting regulatory activities in India and working with distributors, license holders, or regulatory partners across South Asia is preferred.
Experience using Regulatory Information Management Systems (RIMS), TrackWise, SUGAM, and other regulatory management tools is preferred

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

regulatory affairs specialist jobs in mandhela kalan delhi

RA Senior Specialist (Regulatory Affairs)

Regulatory and Quality Specialist

Safety & PV Specialist I

Product Stewardship & Regulatory Specialist - CB3 - NM

Staff Clinical Affairs Specialist

Specialist Deputy Legal Manager - Office of General Counsel

Specialist - Insurance - P&C Claims 4A

Senior Product Specialist - Telepresence & Microscopy (Maharashtra) (m/f/d)

International Registration

Global Senior Environmental Data Manager

SBU HEAD – CRITICAL CARE

Business Marketing Manager

Specialist - Regulatory Affairs - Operations 4A

Specialist - Regulatory Affairs - Operations 4B

Sr. Specialist - Regulatory Affairs - Operations 4C

Related jobs to explore

I want to receive the latest job alerts for regulatory affairs specialist in mandhela kalan delhi

Explore jobs in more locations

In this role, you will

Qualifications :

Jobseeker tools

Employer Tools

Browse

Stay Connected