Syneos Health hiring Regulatory Affairs Associate Mumbai 2026. Check eligibility, responsibilities, skills and apply for hybrid pharma job opportunity today now.
Introduction
If you are looking to build a strong career in regulatory affairs within the pharmaceutical industry, this opportunity is worth exploring. The Regulatory Affairs Associate at Syneos Health offers hands-on exposure to drug registration, compliance processes, and global regulatory systems. This role is ideal for candidates who want to work in a dynamic, fast-paced environment supporting drug development and commercialization.
Job Overview
| Particulars | Details |
|---|---|
| Job Title | Regulatory Affairs Associate |
| Company Name | Syneos Health |
| Location | Mumbai, India |
| Employment Type | Full-Time (Hybrid) |
| Department | Regulatory Affairs |
| Experience Required | Experience preferred |
| Education | Life Sciences / Pharmacy / Related Field |
| Salary | As per company standards |
Company Overview
Syneos Health is a globally recognized organization providing integrated clinical and commercial solutions to the pharmaceutical and biotechnology industries. The company partners with innovators to streamline drug development and commercialization processes. With a strong global presence and thousands of professionals worldwide, Syneos Health is known for delivering high-impact healthcare solutions and fostering a collaborative work environment.
Job Location & Employment Type
- Location: Mumbai, India
- Work Mode: Hybrid (combination of office and remote work)
- Employment Type: Full-Time
Open Positions / Department Details
- Department: Regulatory Affairs
- Role Level: Associate
- Focus Area: Drug registration, regulatory documentation, compliance management
Key Roles & Responsibilities
As a Regulatory Affairs Associate at Syneos Health, you will be responsible for:
- Supporting preparation and submission of regulatory documents for new drug registrations and renewals
- Managing documentation for site registrations, variations, and import licenses
- Assisting in preparation of tender-related documents
- Maintaining and updating internal databases related to dossiers and artwork
- Participating in regulatory strategy planning for bulk drug registrations
- Conducting literature and bibliographic searches when required
- Assisting in labeling updates and product lifecycle management activities
- Coordinating with internal teams and external stakeholders for regulatory submissions
- Ensuring documents are prepared according to submission timelines
- Handling administrative tasks such as filing, archiving, translation coordination, and documentation
- Organizing meetings and supporting departmental operations
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in:
- Pharmacy
- Life Sciences
- Biotechnology or related field
Experience
- Experience in regulatory affairs is preferred
- Freshers with strong knowledge and interest in regulatory processes may also be considered
Skills Required
- Knowledge of drug regulatory processes and documentation
- Understanding of dossier preparation and submission requirements
- Strong organizational and documentation skills
- Good communication and coordination abilities
- Ability to work with multiple stakeholders
- Basic research and data management skills
- Proficiency in MS Office tools
Salary & Benefits
- Salary: As per company standards
- Hybrid work flexibility
- Exposure to global regulatory processes
- Career development and training programs
- Opportunity to work with international clients
- Inclusive and supportive work environment
Selection Process
The recruitment process generally includes:
- Application screening
- Technical interview (Regulatory knowledge)
- HR interview
Candidates with strong documentation skills and regulatory understanding will be preferred.
How to Apply
Interested candidates can apply through the official Syneos Health careers portal.
- Apply as soon as possible (no fixed deadline mentioned)
Important Dates
- Last Date: Not specified (early application recommended)
Why Apply for This Job?
The Regulatory Affairs Associate at Syneos Health is a great opportunity for candidates who want to enter or grow in regulatory affairs. Here’s why:
- Gain real-world experience in drug registration and compliance
- Work with a global life sciences organization
- Build expertise in regulatory documentation and submissions
- Opportunity for long-term career growth in pharma regulatory roles
- Exposure to international regulatory standards and processes
FAQs
1. Who can apply for this job?
Candidates with a degree in pharmacy or life sciences can apply.
2. Is experience mandatory?
Experience is preferred, but freshers with relevant knowledge may also be considered.
3. What is the salary for this role?
Salary is offered as per company standards.
4. Is this a remote job?
It is a hybrid role, combining office and remote work.
5. What skills are required?
Key skills include regulatory documentation, communication, coordination, and knowledge of drug approval processes.
Conclusion
The Regulatory Affairs Associate at Syneos Health provides an excellent entry point into regulatory affairs with a global organization. With strong learning opportunities and exposure to international standards, this role can help you build a successful career in the pharmaceutical industry. Apply now to take advantage of this opportunity.
Disclaimer
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