Quality Specialist II (Supplier Quality Review Analyst)
Thermo Fisher Scientific · Bengaluru · onsite · Posted 29d ago
Undisclosed3–4 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Work Schedule
Standard (Mon-Fri) Environmental Conditions
Office Job Description
As part of the Thermo Fisher Scientific team, you ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Role Title
Quality Specialist II (Supplier Quality Review Analyst)
Role Purpose
Support the periodic review of existing suppliers by collecting quality data, issuing supplier questionnaires, compiling required evidence, and providing completed review packs to the relevant divisions for decision-making. Maintaining score cards.
Key Responsibilities
- Maintain the supplier review schedule for existing suppliers.
- Issue supplier questionnaires and follow up on responses.
- Collect and collate supplier quality data from agreed sources.
- Compile supplier review reports using the approved template.
- Highlight missing information, overdue responses, trends, or potential concerns.
- Submit completed review packs to site Quality / Supplier Quality teams.
- Maintain a tracker for open, completed, and overdue reviews.
- Ensure review records are complete, accurate, and audit-ready.
Required Skills
- Strong attention to detail.
- Good data handling and reporting skills.
- Ability to follow a defined process consistently.
- Clear written communication.
- Strong organisation and follow-up skills.
- Comfortable working with suppliers and internal stakeholders of all organisational levels.
- Basic understanding of quality records, supplier questionnaires, NCRs, CAPAs, audits, and quality data.
- Knowledge of ISO standards (13485), and international regulatory requirements
- Experience with quality management systems and documentation (TrackWise, Master Control, or equivalent)
- Experience in deviation investigations, CAPA, change control, and root cause analysis
- Technical writing and documentation skills
- Analytical and problem-solving abilities
Experience Level
Suitable for someone with 3 -4 years experience in Quality, Supplier Quality support, Quality Systems, Document Control, Procurement Support, or a regulated operational environment.
Experience in IVD, medical device, diagnostics, pharmaceutical industry would be essential.
Disclaimer: This job posting and location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
Skills
trackwisetechnical writingDiagnosticsdata handlingauditsiso standardsCAPAChange ControlCancerRoot Cause Analysispharmaceutical industryQuality SystemsProcurementSupplier QualityPharmaceuticalquality management
About Thermo Fisher Scientific
Thermo Fisher Scientific
Biotechnology
4.8k+
employees
1956
70 years old
Waltham,Massachusetts
United States
About
Thermo Fisher Scientific enables their customers to make the world healthier, cleaner and safer.
Industries
BiotechnologyBiotech & Life sciencesInternetAnalytics & KPOPharma
Employee ratings
1,052 reviews
3.8/ 5
Culture
3.7
Career growth
3.0
Work-life
3.8
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