IpharMed Services is hiring for the position of Regulatory Affairs Associate – Trainee in Bangalore. The opportunity is suitable for freshers, recent graduates, final-year students, and candidates with up to 1 year of relevant experience.
Candidates with a Bachelor’s or Master’s degree in Pharmacy, Biotechnology, Biochemistry, Life Sciences, or a related STEM field can apply for this position.
The selected candidates will receive training and mentorship in regulatory documentation, dossier preparation, document review, regulatory submissions, and health authority requirements.
IpharMed Services Recruitment 2026 – Job Details
| Particular | Details |
|---|---|
| Company | IpharMed Services |
| Position | Regulatory Affairs Associate – Trainee |
| Department | Regulatory Affairs |
| Job Type | Full-Time |
| Job Location | Bangalore |
| Experience | 0–1 Year |
| Eligible Candidates | Freshers, Recent Graduates, Final-Year Students |
| Qualification | Bachelor’s/Master’s Degree |
| Application Mode |
Role Overview
As a Regulatory Affairs Associate – Trainee, candidates will support regulatory activities related to pharmaceutical products and regulatory submissions.
The role provides exposure to CTD, eCTD and ACTD dossier preparation, technical document review, regulatory guideline monitoring, regulatory document archiving and responses to health authority queries.
Candidates will work with experienced regulatory professionals and coordinate with different departments to collect information required for regulatory submissions.
Key Responsibilities
- Assist in preparing, compiling and formatting CTD, eCTD and ACTD regulatory dossiers.
- Support market authorization and renewal submission activities.
- Review technical documents and raw data for accuracy and completeness.
- Assist with the review of Batch Manufacturing Records (BMR) and analytical method validation documents.
- Track regulatory guideline updates issued by authorities and organizations such as FDA, EMA, CDSCO and ICH.
- Communicate relevant regulatory updates to internal teams.
- Coordinate with R&D, QC, QA and Supply Chain teams to collect information required for regulatory filings.
- Maintain regulatory databases and electronic records.
- Archive submitted dossiers, approval letters, regulatory commitments and post-approval variations.
- Assist in preparing responses to health authority queries and deficiency letters.
Eligibility Criteria
Candidates should meet the following requirements:
- Bachelor’s or Master’s degree in Pharmacy, Biotechnology, Biochemistry, Life Sciences or a related STEM discipline.
- Experience of 0–1 year.
- Freshers and recent graduates can apply.
- Final-year students may also be considered as mentioned in the job information.
- Relevant internship experience can be beneficial.
- Coursework or certification in Regulatory Affairs or Drug Regulatory Affairs (DRA) is an advantage.
Required Skills
Candidates should have:
- Good attention to detail.
- Interest in Regulatory Affairs.
- Ability to understand and manage technical documents.
- Basic understanding of regulatory compliance.
- Good communication and coordination skills.
- Ability to work with cross-functional teams.
- Willingness to learn pharmaceutical regulatory processes.
Training and Benefits
According to the job information, the role includes:
- One-on-one training and mentorship from experienced regulatory professionals.
- Career development opportunities in Regulatory Affairs.
- Exposure to regulatory workshops, certifications and industry seminars.
- Collaborative work environment.
- Entry-level compensation.
- Health insurance.
- Paid leave.
- Performance-based bonuses.
How to Apply
Interested and eligible candidates can apply by sending their updated CV and a short cover letter explaining their interest in Regulatory Affairs.
Application Email: bd@ipharmed.com
Job Location: Bangalore
Experience: 0–1 Year
Employment Type: Full-Time
Candidates should mention the position “Regulatory Affairs Associate – Trainee” in the email subject line while applying.