COD Research Hiring Executive Regulatory Affairs

B.Pharm/M.Pharm/M.Sc – Executive Regulatory Affairs | Ahmedabad

Apply for Executive – Regulatory Affairs at COD Research, Ahmedabad. B.Pharm, M.Pharm, M.Sc candidates with 2–4 years experience eligible.

---

COD Research, a trusted name in pharmaceutical research and regulatory excellence, is inviting applications for the role of Executive – Regulatory Affairs at its Ahmedabad facility. This is an exceptional opportunity for candidates passionate about contributing to global healthcare compliance and regulatory standards.

---

Company Overview

COD Research is a leading organization known for delivering high-quality regulatory, clinical, and analytical research solutions for the global pharmaceutical industry. The company upholds stringent international standards and maintains compliance with major regulatory agencies worldwide, including the USFDA, EMA, and WHO. With a culture that values innovation, accuracy, and integrity, COD Research offers an environment where skilled professionals thrive and contribute meaningfully to advancing pharmaceutical development.

---

Job Role & Responsibilities

As an Executive in Regulatory Affairs, you will play a crucial role in ensuring that all regulatory documentation and submissions meet international standards and comply with the evolving requirements of health authorities. Your core responsibilities include:

• Submission Preparation: Compile and format key regulatory documents (IND, NDA, BLA, MAA, etc.) in eCTD format to meet global health authority specifications.
• Quality Control: Conduct document formatting, apply hyperlinks and bookmarks, and validate submissions using publishing tools to ensure compliance and accuracy.
• Technical Coordination: Manage the technical aspects of electronic submissions, troubleshoot issues, and ensure timely delivery.
• Regulatory Compliance: Stay updated on evolving guidelines from global authorities to ensure company-wide adherence to the latest regulatory practices.
• Submission Management: Track submission lifecycles and oversee timely electronic delivery through regulatory gateways.
• Collaboration: Work closely with regulatory leads, medical writers, and cross-functional teams to align workflows and timelines.
• Documentation & Archival: Maintain version control and secure archiving of all regulatory submission packages.
• Process Improvement: Contribute to process enhancement initiatives and the development of new regulatory workflows.

---

Eligibility / Qualifications

• Qualification: B.Pharm, M.Pharm, or M.Sc (Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, or related fields)
• Experience: 2–4 years of relevant experience in Regulatory Affairs (Regulatory Publishing experience preferred)
• Skills Required:
  • Strong knowledge of global regulatory submission formats (IND, NDA, MAA, eCTD)
  • Proficiency in regulatory publishing tools
  • Familiarity with ICH, USFDA, and EMA guidelines
  • Excellent communication and documentation skills

---

Location & Salary

• Location: Ahmedabad, Gujarat
• Salary: Competitive and commensurate with experience

---

Application Process

Interested candidates may send their updated resume to: career@cod-research.com
Apply before 10th November 2025 to secure your opportunity to join COD Research’s regulatory excellence team.

---

Why Join COD Research?

• Opportunity to work on global regulatory submissions.
• Exposure to international regulatory frameworks (USFDA, EMA, MHRA, WHO).
• Collaborative work environment encouraging continuous learning.
• Competitive compensation and structured career progression.

---

Frequently Asked Questions (FAQs)

1. Who can apply for this position?
Candidates with a B.Pharm, M.Pharm, or M.Sc degree and 2–4 years of experience in regulatory affairs or publishing are eligible.

2. Is regulatory publishing experience mandatory?
Not mandatory but preferred. Candidates with relevant experience in eCTD or submission formatting are prioritized.

3. What are the working hours and environment like?
COD Research maintains a professional, collaborative, and technology-driven work environment with standard industry working hours.

4. How do I apply?
Submit your updated CV to career@cod-research.com with your current and expected CTC details.

5. Is this role open for freshers?
No, this opportunity is for candidates with a minimum of 2 years of experience.

---

Summary Table

Company	COD Research
Vacancies	01 – Executive (Regulatory Affairs)
Required Education	B.Pharm, M.Pharm, M.Sc (Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology)
Experience	2–4 years in Regulatory Affairs (Publishing preferred)
Location	Ahmedabad, Gujarat
Application Email	career@cod-research.com