Regulatory Officer to Sr Officer
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Educational Requirements
- Experience Requirements
- Required Skills
- Location & Salary
- Application Process
- Frequently Asked Questions
- Who can apply for this Regulatory Affairs position?
- Which markets will I work on?
- Is this role suitable for freshers?
- Where is the job located?
- How can I apply?
- Additional SEO Title Options
- Summary Table
Base Medico hiring Regulatory Affairs Officer to Sr Officer in Vadodara. B.Pharm/M.Pharm with 1–3 years experience eligible.
Base Medico Pvt. Ltd. is hiring Regulatory Affairs professionals for Officer to Senior Officer positions at its Vadodara manufacturing location. This opportunity is suited for pharmacy graduates with hands-on regulatory experience who are actively involved in dossier preparation and global regulatory submissions. The role offers direct exposure to emerging and regulated international markets and is ideal for candidates looking to build a long-term career in pharmaceutical regulatory affairs.
Company Overview
Base Medico Pvt. Ltd. is an Indian pharmaceutical company engaged in the development, manufacturing, and regulatory submission of quality pharmaceutical products for domestic and international markets. The company focuses on compliance-driven operations, robust documentation practices, and adherence to global regulatory standards.
With an expanding footprint across Africa, Latin America, and ASEAN regions, Base Medico continues to strengthen its regulatory affairs capabilities to support timely product registrations and lifecycle management. The organization emphasizes accuracy, regulatory intelligence, and continuous improvement, making it a strong workplace for regulatory professionals seeking practical exposure and career growth.
Job Role & Responsibilities
The Regulatory Affairs Officer to Senior Officer will be responsible for preparation, review, and submission of regulatory dossiers in compliance with country-specific requirements. This role requires strong technical knowledge of CTD and ACTD formats and the ability to manage submissions across multiple international markets.
Key Responsibilities
- Prepare and compile CTD and ACTD dossiers for pharmaceutical product registrations
- Handle regulatory submissions for Africa, LATAM, and ASEAN markets
- Coordinate with internal departments such as QA, QC, R&D, and production for dossier inputs
- Review regulatory documents to ensure accuracy, consistency, and compliance with guidelines
- Manage query responses and deficiency letters from regulatory authorities
- Support post-approval variations, renewals, and lifecycle management activities
- Maintain regulatory databases and submission trackers
- Ensure documentation is inspection-ready and audit-compliant
- Monitor changes in international regulatory guidelines and update internal teams accordingly
- Support senior regulatory staff in strategic submission planning
This role plays a direct role in expanding Base Medico’s international market presence while ensuring regulatory compliance and product quality.
Eligibility / Qualifications
Educational Requirements
Candidates must possess a pharmacy qualification from a recognized institution.
Relevant Courses (comma-separated):
B.Pharmacy, M.Pharmacy, Pharmaceutical Sciences, Regulatory Affairs
Experience Requirements
- 1 to 3 years of experience in pharmaceutical Regulatory Affairs
- Hands-on experience in CTD and ACTD dossier preparation
- Practical exposure to submissions for Africa, LATAM, and ASEAN regions
- Familiarity with country-specific regulatory requirements and guidelines
Required Skills
- Strong understanding of global regulatory submission processes
- High attention to detail and documentation accuracy
- Ability to manage multiple dossiers simultaneously
- Proactive approach and problem-solving mindset
- Good written and verbal communication skills
Location & Salary
- Job Location: Survey No. 570, Village Tundav, Savli – Vadodara Road, Vadodara, Gujarat – 391775
- Employment Type: Full-time
- Salary: Competitive and based on experience and current industry standards
Application Process
Interested candidates can apply through the following channels:
- Email your updated CV to: hr@basemedico.com
- Direct contact: 92743 95085
Frequently Asked Questions
Who can apply for this Regulatory Affairs position?
Candidates with B.Pharm or M.Pharm qualifications and 1–3 years of regulatory affairs experience can apply.
Which markets will I work on?
You will handle regulatory submissions for Africa, Latin America, and ASEAN regions.
Is this role suitable for freshers?
No. Prior hands-on regulatory experience is mandatory.
Where is the job located?
The position is based in Vadodara, Gujarat.
How can I apply?
Send your CV to hr@basemedico.com or contact the HR team at the provided phone number.
Additional SEO Title Options
- Base Medico Hiring Regulatory Affairs Officer – Vadodara Pharma Jobs
- Regulatory Affairs Vacancy at Base Medico – CTD / ACTD Experience Required
- Base Medico Vadodara Regulatory Affairs Careers – Officer to Sr Officer
Summary Table
| Company | Base Medico Pvt. Ltd. |
|---|---|
| Vacancies | Regulatory Affairs Officer, Senior Regulatory Affairs Officer |
| Required Education | B.Pharmacy, M.Pharmacy |
| Experience | 1–3 Years |
To apply for this job email your details to hr@basemedico.com
