Manager, QA (IC role)
Fortrea
5 - 10 years
Bengaluru
Posted: 26/07/2025
Job Description
Job Overview:
Manages and ensures proper execution of the audit and inspection programs.
Summary of Responsibilities:
- Oversees designated global audit programs for compliance with the master audit plan, (procedures, execution, QC, compliance to process, etc.)
- Identifies the scope and leads global audits and associated audit team.
- Facilitates prioritization of global projects for risk-based audits.
- Ensure the consistent implementation, use and review of SOPs.
- Escalate issues to management in a timely manner implementing appropriate solutions, including preventative actions.
- Negotiate with functional and operational internal stakeholders to improve quality and increase efficiencies.
- Analyze and interpret data to lead functional process improvement initiatives to drive efficiencies and effectiveness of Regulatory Compliance and Quality Assurance (RC and QA) processes.
- Lead and effectively manage constructive crucial interactions with clients or regulatory agencies.
- Lead functional process improvement initiatives to drive efficiencies and effectiveness of Regulatory Compliance and Quality Assurance (RC and QA) processes.
- Interpret applicable quality regulations/standards and create appropriate policies and procedures.
- Ensure Regulatory Compliance and Quality Assurance (RC and QA) management responsibilities, as indicated in applicable controlled documents, are followed.
- All other duties as needed or assigned.
Qualifications (Minimum Required):
- A minimum of a bachelor’s degree in Life Sciences preferred (or equivalent Life Science experience).
- Experience may be substituted for education.
Experience (Minimum Required):
- 10+ years of experience in regulatory environment (experience in GXP roles).
- Experience in conducting GCP and GVP audits.
- Experience and regulatory expertise of industry quality systems/standards.
- Ability to interpret applicable regulations/standards.
- Experience in leading process improvement initiatives.
- Ability to communicate and negotiate with internal stakeholders effectively.
Preferred Qualifications Include:
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Physical Demands/Work Environment:
- Some overtime required.
- Travel may be required.
- Office-Based (Hybrid), as requested by the line manager.
Learn more about our EEO & Accommodations request here.
About Company
Fortrea is a leading global Contract Research Organization (CRO) that provides comprehensive clinical development and consulting services to pharmaceutical, biotechnology, and medical device companies. Spun off from Labcorp in 2023, Fortrea specializes in managing clinical trials from early-phase research to late-stage development. With a global footprint, the company supports the development of new therapies by offering services in clinical trial management, regulatory consulting, data management, and more. Its mission is to help bring innovative, life-saving treatments to market faster and more efficiently.
Services you might be interested in
One-Shot Campaign
Reach out to ideal employees in one shot!
The intelligent campaign for reaching out to the ideal audience to whom you can ask for help (guidance or referral).