What are the responsibilities and job description for the Inspector, Quality Assurance position at International Vitamin Corporation?
Overview:
- International Vitamin Corporation (IVC) is a leading global manufacturer of vitamins and nutritional supplements with more than half a century of private label and contract manufacturing experience, an impeccable quality and regulatory compliance record, and with new resources focused on enriching the health and lives of others.
- Provide direct support as QA Inspector in the QA Department, Granulation, Blending, Compression, Coating, Boxing (Bulk Packing) and Packaging.
QA Inspector must conduct audits in Granulation, Blending, Compression, Coating, Boxing and Packaging. QA Inspector is responsible in these departments for performing a daily walkthrough for product verification, SPC verification and product attributes.- Conduct Line clearance, in-process audits in packaging includes, verification of Packaging line clearance has been completed correctly, verifying that the proper cleaning has been performed by production. After Major “A”or Minor “B” verify that all previous components (with the exception of common components of back-to-back lots) have been removed from the room and approved components are on the line, corresponding to MPS, Master Packaging Specification.
- QA Inspector is responsible to perform all In-Process Inspections checks through Granulation, Compression, Blending (If applicable), Coating, Boxing, and Packaging.
- Perform AQL in Compression, Coating, Boxing and Packaging lines to confirm product is defect free and meets Quality requirements.
- Perform finished product testing in Compression/Coated for weight variation, Friability, Disintegration, pull samples and log into QA Retention logbook (If applicable).
- Report to QA Team Lead/QA Management Department any Non-Conformance issues which will be addressing by QA Team Lead through TrackWise system.
- Complete Quality Assurance documents as per QA SOP’s.
- Make sure product(s) manufactured at IVC-Philadelphia meets all regulatory and cGMP standards.
- Perform sampling throughout the job required in the workstation area according Batch records requirements.
- Check all logbooks through manufacturing and Packaging for correct and up to dated entries. QA Inspector must sign off on the bottom on each page once the full page is completed.
- Responsible to verify all entries through electronic logbooks in Granulation and Packaging areas.
- Make sure that every year the logbook is updated and replaced it accordingly.
- Responsible to perform and verify on daily basis the scale and weight logbook accuracy.
- Responsible to complete any IVC training or updated SOPs through “SmartSolve” and “ILearn-Share Point system”.
- Responsible for performing Inspections to the Incoming Components and Raw Materials.
- Responsible for issuing/returning bottle labels physically and systematically.
- Responsible as business needs, willing to support and work overtime as needed.
- Responsible for all other duites as assigned
- High School Diploma or GED.
- 2 to 4 years working experience as a QA in a manufacturing pharmaceutical environmental. Nutritional experience preferred.
- Working knowledge of cGMP, good documentation practice, Trackwise, Oracle will be plus.
- Demonstrate ability to work independently and communicate effectively with a wide variety of individual teams and cross-functional groups.
- Fluent with Microsoft Office (Word, Excel, Outlook).
- Good Documentation skill, both written and verbal.
- Good problem solving and reasoning skill, self-directed. Good Math skills.
- Good attendance, Good Organizational skills and a team player. Experience in Quality system, data entry skill will be a plus.
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