Regulatory Affairs Jobs at Cadila Pharmaceuticals | Pharma Graduates Apply!
A unique opportunity has arisen for individuals seeking regulatory affairs jobs at Cadila Pharmaceuticals Limited in Dholka, Ahmedabad. This position is ideal for those with a strong background in regulatory compliance and quality assurance in the pharmaceutical sector.
Job Details
- Designation: Sr. Executive – Regulatory Affairs, Formulations (US – Injectables Only)
- Location: Dholka, Ahmedabad
- CTC: Max 6.90 LPA
About the Company
Cadila Pharmaceuticals Limited is one of India’s leading pharmaceutical companies, dedicated to ensuring global compliance and delivering quality healthcare solutions. With a focus on innovation and quality, Cadila operates in various therapeutic areas and is committed to advancing healthcare through its comprehensive product portfolio. The company is headquartered in Ahmedabad, India, and has a significant presence in the global pharmaceutical market. Regulatory affairs jobs at Cadila offer a chance to contribute to its mission of improving health outcomes worldwide.
Job Description
The role of Sr. Executive in Regulatory Affairs at Cadila Pharmaceuticals involves working on US Injectable Regulatory Filings, including ANDA and CTD submissions. The successful candidate will engage in health authority interactions and ensure global regulatory compliance. This position requires adept documentation and dossier management skills, making it a vital role in maintaining the company’s commitment to quality and compliance in the pharmaceutical industry.
Key Responsibilities
- Manage US Injectable Regulatory Filings, including ANDA and CTD submissions.
- Facilitate health authority interactions and ensure compliance with global regulations.
- Oversee documentation and dossier management for regulatory submissions.
- Ensure adherence to quality standards and regulatory requirements.
- Collaborate with cross-functional teams to support product development.
- Stay updated on regulatory changes and industry trends.
- Prepare and review regulatory documents for accuracy and completeness.
- Assist in training and mentoring junior staff in regulatory affairs processes.
Eligibility Criteria
- Qualification: M. Pharma/B.Pharma (Mandatory – No other calls)
- Experience: 02 to 7 Years
- Strong understanding of US FDA regulations and guidelines.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Detail-oriented with strong analytical skills.
Required Skills
- Knowledge of regulatory submission processes for pharmaceuticals.
- Proficiency in documentation and dossier management.
- Strong organizational skills and attention to detail.
- Ability to interact effectively with health authorities.
- Familiarity with global regulatory compliance standards.
- Excellent verbal and written communication skills.
- Ability to work under pressure and meet deadlines.
- Proficient in using regulatory software and tools.
Why Join Cadila Pharmaceuticals?
Cadila Pharmaceuticals Limited is not just a workplace; it is a hub for innovation and quality in the pharmaceutical industry. By joining the team, candidates will have the opportunity to work on impactful projects that contribute to global health. The company values its employees and fosters a culture of continuous learning and professional development, making it an excellent choice for those pursuing regulatory affairs jobs.
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