Inventory & Quality Control Coordinator

Smith+Nephew•Fort Worth, TX

1d•Hybrid

About The Position

Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. Join our team as a Quality Control Coordinator at our Fort Worth, TX site and play a vital role in ensuring the highest standards of product safety and quality. This is an exciting opportunity to make an impact in a global organization committed to improving lives.

Requirements

Bachelor’s degree, or equivalent combination of education and experience in inventory management, quality control, or a regulated manufacturing environment.
At least 4 years of experience in a regulated aseptic processing environment.
Familiar with Good Documentation Practices (GDP).
Familiarity with GMP and regulatory requirements.
Strong attention to detail and ability to work independently.
Strong computer, organizational skills and excellent oral and written communication.
Self-motivated, adaptable to changing priorities, positive attitude, quick learner.

Responsibilities

Order, Monitor and Maintain accurate inventory levels and records.
Inspect incoming and existing inventory to ensure products meet quality standards and specifications.
Identify, document, and report defective or non-conforming materials.
Coordinate with Supply Chain and Supplier Quality to quarantine, return, or dispose of damaged or incorrect items.
Investigate inventory discrepancies and non-conformances as well as implement potential corrective actions.
Maintain quality control documentation, inspection logs, and inventory reports.
Assist with receiving processes to verify quantities, condition, and documentation of incoming goods.
Collaborate with Supply Chain, Procurement, and Supplier Quality teams to resolve quality or inventory issues.
Ensure compliance with Smith + Nephew procedures, safety standards, and regulatory requirements.
Support process improvement initiatives to increase inventory accuracy and operational efficiency.
Report and support investigations for OOS/OOT results and deviations.
Maintain laboratory cleanliness and laboratory storage space, and ensure compliance with GMP and safety.
Document and review test results in compliance with GDP and ALCOA+ principles standards.