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Carolina Components Group, Inc

Quality Inspector

Carolina Components Group, Inc, Durham, North Carolina, United States, 27703

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Title:

Quality Inspector

Job Type:

Full time

Location:

Durham, NC 27703

Summary:

The Quality Inspector is responsible for ensuring process, material, and assembly compliance to customer specifications, ISO 9001, cGMP, and Carolina Components Group standards. The individual is responsible for understanding and effectively/compliantly operating selected aspects of the quality management program.

Essential Duties and Responsibilities:

Responsible for accurately and completely processing assigned Orders through the Quality Department prior to shipment to customers per applicable procedures, work instructions, and customer specifications.

Responsible for performing and accurately documenting Inspection activities for incoming products, internally built assemblies, outgoing products, & other inspections as needed.

Responsible for performing incoming material inspection, labeling, and release for placement into inventory.

Responsible for maintaining daily work schedule in coordination with Operations and Manufacturing personnel.

Responsible for working with Inventory Management to stage incoming material for inspection in a manner designed to prevent mixing of unreleased and released product.

Responsible for reviewing and approving various logbooks/forms for accuracy and compliant entries.

Responsible for identifying, containing, and issuing appropriate documentation for non-conforming materials inclusive of internal non-conforming events, supplier corrective actions, corrective action preventive actions, investigations, etc.

Responsible for maintaining proper segregation, documentation, and inventory of Quarantined materials.

Identifying and implementing Quality improvement initiatives.

Responsible for conforming to other job duties as assigned.

Desired Education:

High School Diploma or equivalent (minimum requirement)

Associate degree (preferred)

Desired Experience:

0-2 Years Quality Assurance Experience

1-2 Years Pharmaceutical/Biotech Manufacturing experience

Acumatica (ERP) experience

Strong computer skills

Strong Organizational skills

Effective communication skills a must

Must be able to work collaboratively in a fast-paced environment.

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