Latest pharma jobs 2026 at Syneos Health for Regulatory Affairs Associate in Mumbai hybrid role apply online today now
Introduction
The demand for skilled professionals in regulatory affairs continues to grow in the pharmaceutical industry, especially in India’s expanding drug market. A new opportunity is now open at Syneos Health for the position of Regulatory Affairs Associate in a hybrid work model based in Mumbai. This role is ideal for candidates with 1–3 years of experience who are looking to build a strong career in pharma jobs. Freshers with relevant exposure and experienced professionals alike can explore this opportunity to work with a globally recognized life sciences organization known for innovation and excellence.
Job Overview
| Job Title | Regulatory Affairs Associate |
|---|---|
| Company Name | Syneos Health |
| Qualification | B.Pharm, M.Pharm, Life Sciences |
| Experience | 1–3 Years |
| Job Location | Mumbai (Hybrid) |
| Salary | As per company standards |
Company Overview
Syneos Health is a leading global organization specializing in integrated biopharmaceutical solutions. The company supports clients throughout the drug development and commercialization lifecycle, helping bring innovative therapies to patients faster.
With a strong presence worldwide, Syneos Health has contributed to the development of a majority of newly approved drugs by regulatory authorities such as the FDA and EMA. The organization focuses on combining clinical expertise with commercial insight, making it a trusted partner in the healthcare and pharmaceutical sectors.
The company is also known for its inclusive work culture, employee development programs, and commitment to innovation. Professionals working here gain exposure to global regulatory frameworks and cutting-edge healthcare solutions.
Job Description
The Regulatory Affairs Associate will play a crucial role in supporting regulatory operations for the India market. This position involves working closely with internal teams and external stakeholders to ensure smooth execution of drug registration and compliance activities.
The selected candidate will be responsible for preparing and managing documentation related to new drug registrations, renewals, and import licenses. The role also requires hands-on experience with the SUGAM portal, which is essential for regulatory submissions in India.
In addition to documentation, the associate will contribute to strategic planning for product registrations and ensure that all regulatory processes align with current guidelines. This role offers an excellent opportunity to gain exposure to regulatory frameworks and build expertise in pharma regulatory affairs.
Eligibility Criteria
Qualification
Candidates must have a degree in Pharmacy or Life Sciences such as B.Pharm, M.Pharm, or equivalent. Additional certifications in regulatory affairs will be considered an advantage.
Experience
Applicants should have 1–3 years of relevant experience in regulatory affairs, preferably in the India market. Knowledge of drug registration processes and regulatory compliance is essential.
Key Responsibilities
- Prepare and manage regulatory documents for new drug registrations and renewals
- Handle site registrations, variations, and import licenses for bulk drugs
- Work on SUGAM portal submissions and documentation
- Support tender documentation and submission processes
- Maintain and update internal databases related to dossiers and artworks
- Assist in regulatory strategy planning for product approvals
- Conduct bibliographic research when required
- Coordinate with internal teams and external stakeholders
- Ensure timely preparation and submission of regulatory documents
- Support administrative tasks such as documentation, filing, and meeting coordination
Required Skills
- Strong understanding of regulatory affairs in the pharmaceutical industry
- Hands-on experience with SUGAM portal
- Excellent documentation and data management skills
- Knowledge of drug registration and compliance processes
- Good communication and coordination abilities
- Ability to work in a team-oriented environment
- Strong attention to detail and organizational skills
- Basic knowledge of global regulatory frameworks is a plus
Selection Process
The selection process typically includes multiple stages to evaluate both technical knowledge and communication skills. Candidates may go through:
- Initial screening of application
- Technical interview focusing on regulatory knowledge
- HR interview to assess communication and cultural fit
Final selection is based on overall performance and suitability for the role.
How to Apply
Follow these steps to apply online for this pharma job:
- Visit the official careers page of Syneos Health
- Search for “Regulatory Affairs Associate India Market”
- Review the job details carefully
- Click on the apply online button
- Register or log in with your account
- Upload your updated resume and required documents
- Submit the application and wait for confirmation
Make sure your resume highlights relevant regulatory experience and technical skills.
Important Dates
- Application Deadline: Not specified (early application recommended)
Conclusion
This is an excellent opportunity for candidates seeking pharma jobs in regulatory affairs with a reputed global company. If you have relevant experience and want to grow in a dynamic environment, apply online today and take the next step in your career.