Lyrus Life Science Hiring Regulatory Affairs Officer/Executive
- Company Overview
- Job Role & Responsibilities
- Senior Officer / Executive – Regulatory Affairs
- Eligibility / Qualifications
- Location & Salary
- Application Process
- FAQs
- What experience is required for this RA role?
- Which regions should candidates be familiar with?
- Are freshers eligible?
- What dossiers are required?
- How do I apply?
- Summary Table
Regulatory Affairs Officer/Executive for B.Pharm/M.Pharm | Bengaluru
Apply for Senior Officer/Executive Regulatory Affairs at Lyrus Life Science, Bengaluru. Openings for B.Pharm/M.Pharm with 3–4 years RA experience.
Lyrus Life Science is hiring experienced Regulatory Affairs professionals for its Bengaluru operations. This opportunity is designed for candidates with hands-on dossier preparation skills and regional regulatory experience across EU, GCC, SA, and ROW markets. The role offers structured responsibilities, cross-functional interaction, and exposure to global regulatory standards.
Company Overview
Lyrus Life Science is a growing pharmaceutical organization focused on high-quality formulation development, regulatory excellence, and global market expansion. The company works across several regulated and semi-regulated markets, ensuring that products meet stringent international compliance and documentation requirements. With a strong commitment to innovation and operational discipline, Lyrus provides a stable environment for regulatory professionals to advance their expertise.
Job Role & Responsibilities
Senior Officer / Executive – Regulatory Affairs
This role requires solid understanding of regulatory frameworks, technical documentation, and market-specific submission requirements.
Key Responsibilities:
- Prepare and review dossiers (Modules 1–3) for EU, GCC, SA, and ROW submissions
- Coordinate with formulation, QC, QA, and documentation teams for data gathering
- Maintain regulatory databases and ensure timely updates related to submissions
- Support product lifecycle activities, variations, renewals, and amendments
- Ensure compliance with global guidelines and regulatory expectations
- Participate in audits, respond to regulatory queries, and manage submission timelines
Eligibility / Qualifications
Required Education:
- B.Pharm, M.Pharm
Experience:
- 3–4 years of Regulatory Affairs experience
Preferred Skills:
- Strong understanding of dossier structure (Modules 1–3)
- Exposure to EU, GCC, SA, and ROW regulatory systems
- Familiarity with CTD/eCTD requirements
- Strong documentation and communication abilities
Relevant courses include: Regulatory Affairs, Pharmaceutical Quality Assurance, Pharmaceutics, Industrial Pharmacy, Pharmaceutical Technology, Drug Regulatory Compliance.
Location & Salary
Location: Bengaluru, Karnataka
Salary details are not provided, but compensation will align with industry standards for RA professionals with 3–4 years of experience.
Application Process
Candidates can apply online and upload their CV using the link below:
Apply Here: https://rebrand.ly/LyrusRA
Additional company information:
Website: www.lyruslife.com
FAQs
What experience is required for this RA role?
Applicants need 3–4 years of experience in Regulatory Affairs with dossier preparation exposure.
Which regions should candidates be familiar with?
Experience with EU, GCC, SA, and ROW submissions is preferred.
Are freshers eligible?
No. This role is strictly for experienced candidates.
What dossiers are required?
Candidates must be able to prepare Modules 1–3 for regulated and semi-regulated markets.
How do I apply?
Use the official application link provided in the posting.
Summary Table
| Category | Details |
|---|---|
| Company | Lyrus Life Science |
| Vacancies | Senior Officer / Executive – Regulatory Affairs |
| Required Education | B.Pharm, M.Pharm |
| Experience | 3–4 years in Regulatory Affairs |

To apply for this job please visit rebrand.ly.