Associate Regulatory Affairs Job at Zoetis in Mumbai for B.Pharm M.Pharm professionals with experience in drug registration and regulatory submissions.
The pharmaceutical regulatory sector plays a crucial role in ensuring that medicines, vaccines, and medical devices meet safety and compliance standards before reaching the market. Regulatory Affairs professionals are responsible for managing product registrations, coordinating with regulatory authorities, and ensuring adherence to national and international guidelines.
Zoetis India has announced a career opportunity for the position of Associate – Regulatory Affairs in Mumbai. This role is suitable for B.Pharm or M.Pharm graduates with experience in pharmaceutical regulatory submissions and compliance processes.
The selected professional will support regulatory operations related to veterinary pharmaceuticals, vaccines, and medical devices across India and neighboring markets such as Sri Lanka, Nepal, and Bangladesh. This position provides valuable exposure to multi-country regulatory frameworks and product registration processes. Associate Regulatory Affairs Job at Zoetis
Company Overview
Zoetis Inc. is a global leader in animal health and veterinary pharmaceuticals, dedicated to developing medicines, vaccines, diagnostic products, and technologies that support the health of animals worldwide. The company works with veterinarians, livestock producers, and pet owners to deliver innovative healthcare solutions for animals.
With operations in multiple countries, Zoetis focuses on scientific innovation, regulatory compliance, and quality standards that ensure the safety and effectiveness of veterinary medicines. Its India operations support regional regulatory activities, product registrations, and compliance management across several markets.
Professionals joining Zoetis gain the opportunity to work in a dynamic regulatory environment that combines pharmaceutical expertise with animal healthcare innovation. Associate Regulatory Affairs Job at Zoetis
Job Overview (Job Details)
| Job Title | Associate – Regulatory Affairs |
|---|---|
| Company | Zoetis India Ltd |
| Department | Legal & Regulatory Affairs |
| Job Location | Mumbai, Maharashtra, India |
| Employment Type | Full-Time (Off Role) |
| Experience Required | 3 – 4 Years |
| Qualification | B.Pharm / M.Pharm |
| Industry | Pharmaceutical & Animal Health |
| Application Mode | Online Application |
| Job Status | Verified Job |
Job Location & Employment Type
- Location: Mumbai, Maharashtra, India
- Employment Type: Full-Time (Off Role)
- Department: Regulatory Affairs / Compliance
The role involves handling regulatory submissions and compliance management related to veterinary pharmaceutical products and medical devices. Associate Regulatory Affairs Job at Zoetis
Open Position
Associate – Regulatory Affairs
The selected candidate will assist regulatory operations related to product registrations, regulatory submissions, and documentation management for veterinary medicines, vaccines, and medical devices. Associate Regulatory Affairs Job at Zoetis
Key Roles & Responsibilities
Professionals hired for this role will work on various regulatory and compliance activities related to pharmaceutical product approvals and lifecycle management.
Regulatory Affairs Management
- Manage regulatory processes for veterinary drugs, vaccines, and medical devices in accordance with Drugs and Cosmetics regulatory requirements.
- Prepare and maintain documentation required for product registration and regulatory approvals.
- Ensure product dossiers comply with regulatory guidelines and company standards.
Regulatory Submissions & Documentation
- Perform regulatory submissions through the SUGAM and NSWS online portals.
- Maintain regulatory documentation required for product approvals, renewals, and variations.
- Coordinate with manufacturing facilities to prepare documents related to New Drug Applications and registration certificates.
Regulatory Coordination
- Work with regulatory liaison agents to facilitate smooth submission and approval of regulatory applications.
- Communicate with regulatory authorities including FDA and other government agencies.
- Provide responses to regulatory queries raised by authorities during the approval process.
Import License & Site Registration Management
- Maintain records related to import licenses and site registrations.
- Monitor regulatory compliance requirements for product import and distribution.
Packaging & Regulatory Updates
- Coordinate with internal teams to implement packaging changes or labeling updates required by regulatory authorities.
- Ensure packaging compliance with applicable regulatory requirements.
Cross-Functional Collaboration
- Work closely with regulatory, quality, and operational teams to ensure regulatory compliance.
- Support internal stakeholders in regulatory documentation and product registration processes.
Affiliate Quality Support
- Assist affiliate quality teams in addressing logistics service provider compliance requirements.
- Support resolution of quality queries and product complaints.
- Maintain regulatory and quality compliance data related to affiliate operations.
Associate Regulatory Affairs Job at Zoetis
Eligibility Criteria
Candidates applying for this role should meet the following educational and professional requirements.
Education
Applicants must hold one of the following qualifications:
- B.Pharm (Bachelor of Pharmacy)
or - M.Pharm (Master of Pharmacy)
Degree must be in pharmacy or a related pharmaceutical discipline.
Experience
- Minimum 3–4 years of professional experience in Regulatory Affairs or Drug Registration.
- Experience working with regulatory documentation and submission processes.
Experience in the following areas will be considered an advantage:
- Medical device registration
- Pharmacovigilance
- Quality assurance processes
- Veterinary pharmaceutical regulatory compliance
Skills Required
Applicants should possess the following professional skills:
- Strong knowledge of Indian pharmaceutical regulatory requirements
- Hands-on experience with SUGAM portal regulatory submissions
- Familiarity with regulatory filing procedures related to the Department of Animal Husbandry and Dairying
- Good understanding of product registration documentation
- Strong communication and coordination skills
- Ability to analyze regulatory requirements and propose solutions
- Proficiency in Microsoft Office tools such as Excel, Word, and PowerPoint
Associate Regulatory Affairs Job at Zoetis
Salary & Benefits
Salary for this position will be as per company norms and industry standards.
Working with Zoetis may also provide additional benefits such as: Associate Regulatory Affairs Job at Zoetis
- Professional development opportunities
- Exposure to global regulatory practices
- Experience in veterinary pharmaceutical regulatory systems
- Collaborative work environment with industry experts
Selection Process
The recruitment process may include the following stages:
- Application review and resume screening
- Technical interview focusing on regulatory knowledge
- HR interview and final evaluation
- Selection and offer issuance
Shortlisted candidates will be contacted by the company for further recruitment steps. Associate Regulatory Affairs Job at Zoetis
How to Apply
Interested candidates should submit their applications through the official Zoetis careers portal or recruitment platform.
Applicants are advised to upload an updated resume highlighting experience in: Associate Regulatory Affairs Job at Zoetis
- Regulatory affairs
- Drug registration
- Regulatory submissions
- Compliance management
Important Dates
- Application Deadline: Not specified by the company
Candidates are advised to apply early to avoid missing this opportunity.
Why Apply for This Pharma Job?
This role offers valuable exposure to pharmaceutical regulatory operations across multiple countries.
Key advantages include:
- Opportunity to work with a global animal health company
- Exposure to multi-country regulatory environments
- Experience with regulatory filings for veterinary pharmaceuticals and vaccines
- Career development in regulatory affairs and pharmaceutical compliance
- Opportunity to collaborate with regulatory authorities and industry experts
Professionals looking to build a long-term career in pharmaceutical regulatory affairs will benefit greatly from this opportunity. Associate Regulatory Affairs Job at Zoetis
Important Note
IndiaPharmaJobs.in is an independent job information platform that publishes pharmaceutical job updates for informational purposes only.
We are not affiliated with any company mentioned in this article and do not charge any fees for job applications. Candidates should apply only through official company recruitment channels. Associate Regulatory Affairs Job at Zoetis
Final Call-to-Action
If you are a B.Pharm or M.Pharm professional with experience in regulatory affairs and pharmaceutical product registration, this opportunity with Zoetis India can help you advance your career. Eligible candidates should apply online and take the next step toward a rewarding regulatory affairs career in the pharmaceutical industry. Associate Regulatory Affairs Job at Zoetis
