The pharmaceutical and vaccine regulatory landscape is rapidly evolving, creating strong demand for experienced regulatory professionals. Techinvention has announced an exciting opportunity for the position of Assistant Manager โ Regulatory Affairs at its office in Navi Mumbai.
This role is ideal for professionals who have experience handling regulatory submissions, compliance, and communication with health authorities. Candidates with a strong background in pharmaceutical or life sciences regulatory work can play a critical role in ensuring vaccines and pharmaceutical products meet national and international compliance standards.
If you have experience in regulatory documentation, approvals, and lifecycle management within the pharmaceutical industry, this position offers an excellent opportunity to advance your career in regulatory affairs.
Author: Pharmabharat Editorial Team
Job Overview
Position: Assistant Manager โ Regulatory Affairs
Company: Techinvention
Location: Navi Mumbai
Industry: Pharmaceutical / Vaccines / Regulatory Affairs
Experience Required: 5โ6 Years
Qualification: MSc in Regulatory Affairs, Pharmaceutical Sciences, Life Sciences, or related fields
Key Roles and Responsibilities
The selected candidate will be responsible for handling regulatory submissions and ensuring compliance with regulatory standards across different regions.
Main responsibilities include:
- Managing regulatory submissions, approvals, and communications with health authorities
- Ensuring compliance with local, regional, and international vaccine regulations
- Preparing and submitting regulatory documentation such as:
- New Drug Applications (NDAs)
- Variations
- Renewals
- Collaborating with cross-functional teams including:
- Research & Development
- Production
- Quality Assurance
- Legal teams
- Monitoring regulatory updates and implementing necessary compliance measures for vaccines and pharmaceutical products
Required Qualifications
Candidates applying for this regulatory affairs job should meet the following criteria:
- MSc in Regulatory Affairs, Pharmaceutical Sciences, Life Sciences, or a related discipline
- 5โ6 years of professional experience in regulatory affairs within the pharmaceutical industry
- Hands-on experience in:
- Regulatory submissions
- Product approvals
- Product lifecycle management
- Strong understanding of regulatory frameworks and vaccine compliance standards
- Excellent documentation and coordination skills
Salary and Benefits
Although the company has not officially disclosed the salary, candidates with 5โ6 years of regulatory affairs experience in the pharmaceutical industry can expect a competitive compensation package.
Estimated Salary Range: โน8,00,000 โ โน12,00,000 per year (depending on experience and expertise)
Additional benefits may include:
- Professional growth in vaccine regulatory projects
- Exposure to international regulatory standards
- Collaborative work with R&D and quality teams
- Career advancement opportunities in regulatory leadership roles
Job Location
The position is based in:
Navi Mumbai
Navi Mumbai is one of Indiaโs major pharmaceutical and biotech hubs, offering strong career opportunities in regulatory affairs, research, and pharmaceutical manufacturing.
How to Apply
Interested and eligible candidates can apply by sending their updated CV to the official email addresses:
Email:
hr@techinvention.biz
connect@techinvention.biz
Applicants are advised to mention โApplication for Assistant Manager โ Regulatory Affairsโ in the email subject line to ensure faster processing.
Conclusion
This Regulatory Affairs job in Navi Mumbai is a great opportunity for experienced pharmaceutical professionals who want to grow in regulatory strategy and vaccine compliance. With strong industry exposure and collaboration with multiple departments, the role offers valuable experience in regulatory lifecycle management.
