Mitocon Biopharma is hiring experienced professionals for the position of Scientific Writer at its Hyderabad location. Candidates with expertise in pharmacovigilance, clinical overview reports, non-clinical summaries, and regulatory scientific documentation are encouraged to apply for this exciting pharmaceutical scientific writing opportunity.
This latest pharma job opening in Hyderabad is ideal for candidates searching for scientific writer jobs in pharma, pharmacovigilance documentation jobs, clinical overview writing careers, regulatory medical writing jobs, and drug safety scientific writing opportunities in India.
Professionals with 2–5 years of experience in preparing regulatory dossiers, Health Hazard Assessment (HHA) reports, and CTD summaries can build a rewarding career with Mitocon Biopharma’s growing regulatory and scientific documentation team.
Job Details
| Category | Details |
|---|---|
| Job Role | Scientific Writer |
| Company | Mitocon Biopharma |
| Experience | 2–5 Years |
| Job Type | Full-Time |
| Work Mode | Onsite |
| Location | Begumpet, Hyderabad |
| Industry | Pharmaceutical / Biopharma |
| Department | Scientific Writing / Pharmacovigilance |
Key Responsibilities
Candidates selected for the Scientific Writer role at Mitocon Biopharma will be responsible for:
- Preparing and reviewing scientific and regulatory documentation for pharmaceutical submissions
- Drafting Health Hazard Assessment (HHA) / Evaluation reports
- Preparing CTD modules including:
- 2.4 Clinical Overview Reports
- 2.5 Clinical Summary Reports
- 2.6 Non-Clinical Overview Reports
- 2.7 Non-Clinical Summary Reports
- Supporting pharmacovigilance and drug safety documentation activities
- Coordinating with cross-functional regulatory and clinical teams
- Ensuring accuracy, compliance, and scientific integrity in documentation
- Managing timelines in a fast-paced pharmaceutical environment
Required Qualifications & Skills
Candidates applying for this pharmaceutical scientific writing job should possess:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or related field
- Mandatory experience in Pharmacovigilance
- Strong experience in scientific writing and regulatory documentation
- Hands-on expertise in HHA report drafting
- Knowledge of CTD documentation and regulatory submission standards
- Excellent analytical, communication, and documentation skills
- Ability to work collaboratively within regulatory and medical teams
Preferred Keywords for Search Visibility
This opportunity is highly relevant for professionals searching:
- Scientific Writer jobs in Hyderabad
- Pharmacovigilance jobs in India
- Regulatory medical writer jobs
- Pharma documentation jobs
- Clinical summary writer jobs
- Non-clinical overview report drafting careers
- CTD scientific writing jobs
- Biopharma regulatory writing openings
- Drug safety documentation jobs
- Pharmaceutical scientific writer vacancy 2026
Why Join Mitocon Biopharma?
Working with Mitocon Biopharma offers professionals an opportunity to:
- Work on impactful global healthcare projects
- Gain exposure to regulatory scientific documentation
- Collaborate with experienced pharmacovigilance professionals
- Build expertise in clinical and non-clinical regulatory writing
- Grow within a quality-driven and innovation-focused organization
Application Process
Interested candidates can apply by sharing their updated resume through:
