Life Science Jobs in Pune: Fortrea is Hiring Safety Writer | Apply Now
Looking to elevate your journey with life science jobs in Pune? The Fortrea career ecosystem in India continues to expand, and this new Safety Writer role in Pune offers life science graduates a chance to work on high-impact global safety documentation, regulatory submissions, and clinical research innovation. This is your opportunity to join a world-class team driving the future of drug safety.
Job Details:
- Job Title: Safety Writer
- Location: Pune, Maharashtra, India
About the Company:
Fortrea is a global Clinical Research Organization (CRO) committed to accelerating drug development and improving patient outcomes worldwide. As a fast-growing employer in India, Fortrea offers exceptional opportunities for professionals seeking life science jobs and long-term career growth in the clinical research ecosystem.
With operations spanning more than 90 countries, the company provides end-to-end support across clinical trials, pharmacovigilance, regulatory writing, data management, and medical affairs. For anyone exploring a Fortrea career, the organization is known for scientific excellence, a collaborative culture, and strong global quality standards.
Fortrea’s Pune office is one of its expanding hubs, making it a strong destination for candidates looking specifically for life science jobs in Pune. The company empowers employees through continuous learning, exposure to global projects, and clear development pathways making it a trusted name in the life sciences industry.
Key Responsibilities:
- Perform allied activities such as data collection for report planning, developing strategy, and leading kick-off meetings and discussion for comment resolution.
- Write various safety reports including Annual Reports, PSURs, PADERs, DSURs, RMPs, and others for global submissions.
- Perform quality review of safety reports prepared by junior writers.
- Author or contribute to ad hoc reports, benefit-risk evaluation reports, label update documents.
- Write CTD summaries including Non-Clinical and Clinical Overviews.
- Prepare medical information responses for HCPs.
- Author/contribute to signal reports and safety issue analysis reports.
- Write subject narratives for adverse drug reactions and serious adverse events.
- Communicate effectively with internal and client stakeholders.
- Conduct literature searches and propose updates.
- Implement consistent, efficient processes to meet timelines.
- Ensure compliance with regulatory standards.
- Maintain high customer service levels.
- Perform additional project-related activities as assigned.
Educational Requirements:
- Minimum of first degree in life sciences or equivalent
- Advanced degrees (PhD/Masters) preferred
- Relevant industry experience may substitute educational requirements
Experience:
At least 3 years’ experience in the pharmaceutical industry, or at least 2 years of it in medical writing.
Skills Required:
- Excellent written and spoken English
- Strong communication skills
- MS Office proficiency
- Good time management & organizational ability
- Excellent interpersonal skills
- Understanding of regulatory requirements, GVP & ICH-GCP guidelines
- Scientific or clinical research experience desirable
This is a strong opportunity for professionals seeking growth in life science jobs and those aiming to build a long-term Fortrea career in a global clinical research environment. If you want to work on impactful safety writing projects and grow in a structured, international setting, this Safety Writer role in Pune is an excellent next step.
