Overview
Supplier Quality Engineer Jobs in California, Missouri, USA at Kindeva Drug Delivery Company
Location: California
Posted Thursday, May 15, 2025 at 4:00 AM
Our Work Matters
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
The Supplier Quality Engineer’s primary responsibility is to manage assigned supplier relationships and quality program deliverables. Provides oversight, evaluation, and corrective action of all production and supplier quality related issues for external supplier processes and suppliers based on commodity class assigned. Generates reports, memos, files, and presentations necessary to manage the issues according to site procedures.
Role Responsibilities
Primary Quality contact for assigned suppliers within an assigned commodity class.
Responsible person for Quality Tracking System (Trackwise) records within Change Management, Investigations, SCAR, and Commitment Tracking modules ensuring timely completion and appropriate documentation of work completed in support of the record closure.
Reviews and approves supplier change notifications, investigations, and corrective actions.
Ensures component and tooling qualification activities are completed and meet SOP requirements.
Issues Supplier Corrective Action Request (SCAR) and reviews/approves SCAR responses.
Coordinates activities cross-functionally (QA, Operations, Purchasing, Product Design & Development) to ensure appropriate prioritization of deliverables, by the QE as well as the supplier.
Ensure compliance with company procedures, quality standards, and government regulatory requirements.
Responsible for review, redline and changes for assigned supplier quality plan (SQP), QC Test Report (QCTR) and controlled drawings.
Owner for assigned projects, responsible for project management and task execution.
Assists in identifying root causes and coordinates corrective action to quality issues.
Ensures product or component traceability and quarantine as necessary.
Basic Qualifications
BS in an a scientific/engineering discipline.
2+ years of cGMP industry experience.
Knowledge of computerized systems (MS Office suite).
Fundamental understanding of statistical analysis utilizing software
Demonstrated ability to manage multiple priorities.
Preferred Qualifications
Experience with in medical device or quality engineering.
Professional certification (i.e. Certified Quality Engineer, Six Sigma Green Belt, Certified Quality Auditor).
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
Do you see yourself as part of the Kindeva mission? Click Apply Now Today!
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Title: Supplier Quality Engineer
Company: Kindeva Drug Delivery Company
Location: California, Missouri, USA
Category: Engineering (Quality Engineering), Quality Assurance – QA/QC (Quality Engineering)
