Life Science Jobs | BMS is Hiring a Specialist |
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Looking for advanced Life science Jobs in pharmaceutical quality and global compliance? Here’s an exciting opportunity under BMS Jobs in Hyderabad. The Specialist – Global Product Quality Complaint Triage and Network role is ideal for professionals in Life Sciences and bio engineering jobs who want to work in a global quality environment focused on patient safety and regulatory excellence.
- Job Title: Specialist, Global Product Quality Complaint Triage and Network
- Location: Hyderabad – TS – IN
About the Company
Bristol Myers Squibb is a leading global biopharmaceutical company dedicated to transforming patients’ lives through science. With strong expertise in oncology, hematology, immunology, and cardiovascular disease, BMS operates one of the industry’s most promising pipelines. The organization emphasizes innovation, global regulatory compliance, and quality excellence across its worldwide network.
Key Responsibilities
- Responsible for accurate & timely review, evaluation and assignment of incoming Product Quality Complaints (PQCs).
- Maintain expert knowledge and understanding of PQC intake routes.
- Manage PQC mailboxes as a source of intake for PQCs.
- Ensure critical thinking and risk-appropriate timelines for PQC processing.
- Deliver timely escalations to investigation sites, market quality, and senior management.
- Liaise with investigation sites to deliver high-quality, comprehensive investigation reports.
- Assess reported information for accuracy and completeness.
- Engage proactively with upstream and downstream partners to resolve triage assignment inaccuracies.
- Support continuous improvement of the triage & network processes for PQC.
- Be PQC inspection & audit-ready at all times.
- Provide Subject Matter Expert (SME) support during audits and inspections.
Qualifications & Experience
- Bachelor of Science in Life Sciences, or Bio-Engineering or related field.
- In-depth understanding of the global regulatory environment with respect to Product Quality Complaint processing.
- Minimum of 3 years of experience in a global Pharmaceutical/Bio-pharmaceutical/Device organization in a Quality role.
Skills Required
- Strong understanding of global regulatory environment for PQC processing
- Knowledge of pharmaceutical product formulations and defect categories
- Critical thinking and risk-informed decision-making skills
- Excellent organizational and multitasking abilities
- Strong communication skills (written and verbal English proficiency)
- Proficiency in electronic systems such as VEEVA, SAP, SharePoint, Excel, and related tools
- Ability to collaborate across global teams
If you are aiming for impactful Life science Jobs or exploring high-growth bio engineering jobs in pharmaceutical quality, this Specialist role under BMS Jobs offers global exposure, regulatory depth, and strong career advancement potential. Join a world-leading biopharmaceutical organization and contribute directly to patient safety and quality excellence.
