BioMatrix walk-in Regulatory Affairs
- Company Overview
- Job Role & Responsibilities
- International Regulatory Affairs (IRA)
- Eligibility / Qualifications
- Required Education:
- Relevant Courses:
- Experience Required:
- Skills Required:
- Location & Salary
- Salary:
- Application Process
- Walk-in Interview Details:
- Venue:
- Email Application:
- Contact Numbers:
- Why Join BioMatrix Healthcare?
- FAQs
- Who can apply for BioMatrix IRA roles?
- What experience is required?
- What skills are important?
- Is global regulatory experience required?
- What markets will I work on?
- Final Thoughts
Meta Title: BPharm 15+ IRA Jobs BioMatrix Ahmedabad Walk-in
Meta Description: B.Pharm, M.Pharm, M.Sc candidates apply for 15+ IRA vacancies at BioMatrix Ahmedabad. Regulatory affairs jobs with global exposure.
BioMatrix Healthcare Pvt. Ltd. is conducting a walk-in interview for International Regulatory Affairs (IRA) professionals at its Ahmedabad corporate office. This is a high-value opportunity for candidates targeting regulatory affairs jobs in pharma, dossier preparation roles, CTD/eCTD submission careers, and global pharmaceutical compliance jobs.
If you are looking to build a strong career in regulatory affairs, international submissions, or pharmaceutical documentation with exposure to EU-GMP, USFDA, and global markets, this role offers long-term growth and high earning potential.
Company Overview
BioMatrix Healthcare Pvt. Ltd. is a research-driven multinational pharmaceutical company headquartered in Ahmedabad, India. Established in 2007, the company has built a strong reputation in the development and manufacturing of oral solids, liquids, and dry syrup formulations.
The company operates under multiple global regulatory approvals including WHO-GMP, EU-GMP, Health Canada, UK-MHRA, ANVISA, and USFDA compliance standards. With exports to 40+ countries and 1000+ product registrations, BioMatrix plays a key role in supplying affordable, high-quality medicines worldwide.
Working at BioMatrix provides exposure to global regulatory frameworks, international markets, and advanced pharmaceutical documentation practices.
Job Role & Responsibilities
International Regulatory Affairs (IRA)
- Prepare and compile regulatory dossiers for ROW and semi-regulated markets
- Handle submissions for Asia, LATAM, CIS, Africa, GCC, and European regions
- Work on CTD, ACTD, and eCTD dossier formats
- Manage product lifecycle activities including renewals, variations, and query responses
- Review regulatory documents for accuracy and compliance
- Coordinate with cross-functional teams for submission readiness
These responsibilities are critical for ensuring global drug approvals and maintaining compliance with international regulatory authorities.
Eligibility / Qualifications
Required Education:
- B.Pharm
- M.Pharm
- M.Sc
Relevant Courses:
Regulatory Affairs, Pharmaceutics, Pharmaceutical Analysis, Drug Regulatory Affairs, Clinical Research, Quality Assurance
Experience Required:
- 1 to 10 Years in regulatory affairs or related domain
Skills Required:
- Dossier preparation and submission
- CTD / eCTD documentation expertise
- Regulatory compliance knowledge (EU, USFDA, MHRA, etc.)
- Strong documentation and communication skills
- Experience in global pharmaceutical markets preferred
Location & Salary
- Job Location: Ahmedabad (Corporate Office)
Salary:
- Competitive salary based on experience
- High growth potential in regulatory affairs domain
Application Process
Walk-in Interview Details:
- Date: 10th May 2026 (Sunday)
- Registration Time: 09:30 AM – 01:00 PM
Venue:
BioMatrix Healthcare Pvt. Ltd.
Corporate Office, 502-B, Times Square Grand
Sindhu Bhavan Road, Thaltej, Ahmedabad – 380059
Email Application:
Contact Numbers:
- 6357410551, 6358970525
- 9725901031, 9228893058
Why Join BioMatrix Healthcare?
- Work with EU-GMP, USFDA, and Health Canada approved systems
- Exposure to international regulatory markets (LATAM, EU, CIS, Africa)
- Strong career growth in regulatory affairs and global pharma compliance
- Opportunity to work on high-value dossier submissions and approvals
- Experience in multinational pharmaceutical operations
These roles directly contribute to global medicine approvals and access to healthcare worldwide.
FAQs
Who can apply for BioMatrix IRA roles?
Candidates with B.Pharm, M.Pharm, or M.Sc qualifications.
What experience is required?
1–10 years in regulatory affairs or related pharmaceutical roles.
What skills are important?
Dossier preparation, CTD/eCTD submissions, regulatory compliance, and documentation.
Is global regulatory experience required?
Preferred but not mandatory for junior roles.
What markets will I work on?
Asia, LATAM, CIS, Africa, GCC, and Europe.
Final Thoughts
This BioMatrix Healthcare hiring drive is ideal for professionals aiming to grow in regulatory affairs, pharmaceutical documentation, and global compliance roles.
With increasing demand for regulatory professionals in international markets, careers in CTD submissions, dossier management, and pharma regulatory jobs offer strong salary potential and long-term stability.
If you are targeting high-CPC pharma keywords such as regulatory affairs jobs, dossier preparation roles, CTD submission jobs, or pharma compliance careers, this opportunity is highly valuable.
| Company | BioMatrix Healthcare Pvt. Ltd. |
|---|---|
| Vacancies | Regulatory Affairs Officer, Executive, Assistant Manager |
| Required Education | B.Pharm, M.Pharm, M.Sc |
| Experience | 1–10 Years |
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