Looking for Drug Safety Specialist ICSR jobs in Hyderabad? Mitocon Biopharma Pvt. Ltd. has announced an exciting opportunity for experienced Pharmacovigilance professionals with expertise in ICSR Case Processing. Candidates with 1โ3 years of experience in drug safety operations and strong knowledge of EMEA case processing, MedDRA coding, UKMHRA reporting, L2A & MLM case downloads, and case triage are encouraged to apply.
This is a 100% onsite, day-shift Pharmacovigilance role based in Begumpet, Hyderabad. Immediate joiners and candidates who can join within two weeks will receive preference.
Job Details
| Particular | Details |
|---|---|
| Position | Drug Safety Specialist |
| Department | Pharmacovigilance |
| Company | Mitocon Biopharma Pvt. Ltd. |
| Experience | 1โ3 Years |
| Location | Begumpet, Hyderabad |
| Work Mode | 100% Onsite |
| Shift | Day Shift (9:00 AM โ 6:00 PM) |
| Employment Type | Full-Time |
| Preferred Candidates | Hyderabad Local Candidates |
| Freshers | Not Eligible |
Key Responsibilities
As a Drug Safety Specialist, you will be responsible for:
- Perform Individual Case Safety Report (ICSR) case processing.
- Handle EMEA Pharmacovigilance case processing activities.
- Execute L2A and MLM case downloads.
- Perform UKMHRA reporting and case triage.
- Apply MedDRA coding accurately during case processing.
- Ensure compliance with global Pharmacovigilance regulations and SOPs.
- Maintain quality, accuracy, and timely submission of safety cases.
- Collaborate with internal Pharmacovigilance teams to meet regulatory timelines.
Eligibility Criteria
Candidates should possess:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, Medicine, or related healthcare discipline.
- 1โ3 years of Pharmacovigilance experience.
- Hands-on experience in ICSR Case Processing.
- Mandatory experience in EMEA Case Processing.
- Knowledge of:
- MedDRA Coding
- UKMHRA Reporting
- Case Triage
- L2A & MLM Case Downloads
- Strong communication and documentation skills.
- Immediate joiners or candidates available within two weeks are preferred.
- Only Hyderabad-based candidates will be considered.
Preferred Skills
- Pharmacovigilance Operations
- Drug Safety Case Processing
- EMEA Regulatory Requirements
- MedDRA Coding
- UKMHRA Guidelines
- Safety Database Knowledge
- Attention to Detail
- Regulatory Compliance
- Quality Documentation
Why Join Mitocon Biopharma?
- Opportunity to work on global Pharmacovigilance projects.
- Stable day-shift work schedule.
- Exposure to international regulatory reporting requirements.
- Collaborative and professional work environment.
- Career growth in Drug Safety and Pharmacovigilance.
How to Apply
Interested candidates meeting the eligibility criteria can send their updated resume to:
Email: sarvani.g@mitoconbiopharma.com
WhatsApp: 8019493434
Note:
- No phone calls.
- Immediate joiners are highly preferred.
- Freshers are not eligible.
- Only Hyderabad local candidates will be considered.
