Thermo Fisher Scientific is hiring for the Safety Reporting Specialist position in Hyderabad, India. The role focuses on receiving, preparing, submitting, and tracking expedited and periodic safety reports while ensuring compliance with regulatory timelines and country-specific requirements.
The position is listed as fully remote and full-time, with a standard Monday-to-Friday work schedule. Candidates with a bachelor’s degree and 0–2 years of comparable experience may be eligible to apply.
Job Details
| Particulars | Details |
|---|---|
| Company | Thermo Fisher Scientific |
| Job Role | Safety Reporting Specialist |
| Job Requisition ID | R-01372494 |
| Job Location | Hyderabad, India |
| Work Mode | Fully Remote |
| Employment Type | Full-Time |
| Work Schedule | Monday to Friday |
| Experience | 0–2 years (comparable experience) |
| Qualification | Bachelor’s degree or equivalent relevant qualification |
| Job Posting | Posted Today |
| Application Mode | Online |
Positions
Safety Reporting Specialist / Associate Safety Reporting Specialist
The job description describes the responsibilities of an Associate Safety Reporting Specialist, supporting safety report submissions, regulatory documentation, project tracking, and reporting metrics.
Responsibilities
Selected candidates will support the safety reporting team in the following activities:
- Receive, prepare, and submit safety reports to relevant parties within regulatory timelines.
- Track expedited and periodic safety report submissions and maintain evidence of submission.
- Identify and escalate quality issues or delays to the assigned lead or line manager.
- Coordinate with relevant teams on safety reporting activities.
- Support assigned leads with project management activities and potentially lead small projects.
- Generate reports and maintain up-to-date contact information in relevant systems and repositories.
- Prepare, maintain, and archive regulatory submission files according to work practice documents and applicable client standard operating procedures.
- Assist managers with compiling project metrics.
- Provide administrative support as required.
Eligibility and Qualifications
Candidates should meet the following requirements:
- Bachelor’s degree or equivalent relevant academic or vocational qualification.
- Approximately 0–2 years of comparable experience.
- Relevant education, training, or directly related experience may be considered as an alternative in some cases.
Required Skills
Applicants should have the following knowledge and skills:
- Basic knowledge of medical terminology.
- Good written and verbal communication skills.
- Proficiency in Microsoft Office applications.
- Basic understanding of safety database functionality.
- Basic knowledge of procedural documents.
- Working knowledge of global safety reporting requirements, including FDA regulations and guidelines.
- Strong organizational and time-management skills.
- Attention to detail and accuracy.
- Ability to handle sensitive information responsibly.
- Ability to collaborate effectively with different organizational levels and work within a team.
Work Environment
The job description identifies office, laboratory, and clinical environments as possible work settings. The listed requirements also include potential exposure to biological fluids and infectious organisms, electrical office equipment, and the use of personal protective equipment such as protective eyewear, garments, and gloves.
