Top Medicine Jobs: Apply for Functional Quality Specialist I at Fortrea
If you’re searching for reliable medicine jobs that offer growth, global exposure, and long-term career development, Fortrea has an excellent opportunity for you. The Functional Quality Specialist I role is one of the most in-demand medical science jobs among professionals seeking impactful work in regulatory and safety operations. With fortrea jobs expanding in India—especially high-value jobs in Pune—this position offers an exciting pathway for candidates looking to advance their expertise in quality and clinical safety.
About the Company:
Fortrea is a global CRO offering advanced solutions in clinical research, drug safety, and regulatory operations. As one of the fastest-growing employers known for high-quality fortrea jobs, the company provides excellent opportunities for professionals looking to build strong careers in medicine jobs and medical science jobs.
- Job Title: Functional Quality Specialist I
- Location: Pune
- Time Type: Full time
- Application Deadline: End Date: December 5, 2025
- Job Requisition ID: 255882
Qualifications (Minimum Required):
- Bachelor’s/Master’s/PhD in Medicine, Alternative Medicine, Medical Science, Pharmaceutical Science, Nursing, Life Sciences, Biological Sciences, or related fields — ideal for applicants searching for medicine jobs or medical science jobs.
- Two+ years of experience in the pharmaceutical, biotech, or CRO industry, especially in Pharmacovigilance or Quality Review.
- Strong knowledge of medical and drug terminology, GCP, GVP, ICH guidelines, and global regulatory reporting.
- Excellent problem-solving and cross-functional communication skills.
- Technical proficiency with Microsoft Office.
Preferred Qualifications in Medicine Jobs at Fortrea:
- Experience generating quality metrics and trend analysis.
- Experience with CAPA documentation.
- Exposure to medical device reporting.
Job Description:
This medicine jobs opportunity ensures high-quality service to all internal and external clients with full compliance to the Health and Safety at Work Act 1974, COSHH regulations 1989, and EC Directives 1992/3 as detailed in Fortrea’s Health and Safety Manual. As part of the growing segment of medical science jobs, this role at Fortrea is ideal for professionals seeking challenging and rewarding career growth.
Key Responsibilities:
- Perform Quality review of assigned cases.
- Assist in addressing periodic client quality reviews.
- Assist in preparation of Corrective and Preventive Actions (CAPA) as requested.
- Ensure CAPA implementation and documentation in coordination with project managers.
- Perform ongoing review of various safety reports for global regulatory submissions for Fortrea clients.
- Assist in audit readiness, process review, and training coordination for new and existing team members.
- Support client audits, develop Quality Management Plans, and assist during regulatory inspections.
- Perform data analysis and recommend process improvement strategies.
- Execute drug safety data management processes, including call documentation and follow-up.
- Guide safety associates and support various QC, tracking, reconciliation, and process review tasks.
- Review global safety reports including Annual Reports, PSURs, PADERs, Investigator Brochures, and more.
Application Link: LINK TO ORIGINAL NOTIFICATION TO APPLY
