Legacy Pharmaceutical Packaging
Quality Control Inspector - 10HR Night (8pm - 6am Mon - Thurs)
Legacy Pharmaceutical Packaging, Earth City, Missouri, United States, 63045
Job Details
Job LocationMO - Earth City, MO
Position TypeFull Time
Education LevelHigh School Diploma or GED
Travel PercentageNone
Job ShiftDay
Job CategoryManufacturing
Description
Job Title:
Quality Control Inspector
Department:
Quality
Reports To:
Quality Control Manager
PRIMARY PURPOSE or JOB SUMMARY
The Quality Control Inspector is responsible for the in-process and finished goods inspection activities at Legacy. The Quality Control Inspector shall fully comply with all regulatory / cGMP guidelines and Legacy Pharmaceutical Packaging standards and policies.
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.Promote and enforce cGMP and SOP compliance in an FDA regulated pharmaceutical manufacturing environment, ensuring product integrity, safety and compliance with standards.Possess a working knowledge of cGMPs, FDA and DEA regulations and Legacy Pharmaceutical Packaging policies and procedures.Perform and document in-process and finished good quality inspections of product and material.Perform and document containment of quality events.Perform and document line clearance of production room cleansVerification of materials issued for packaging.Monitor, review, and document Temperature Chart Recorder data.Perform daily review of in-process packaging batch records.Provide support to and coordinate with other departments to ensure product integrity.Perform and Check/Verify return quantities of Labeling Components in the batch record.Print and apply green release tags for production component returns as needed.Initiate and document Event Reports for in-process nonconformities (failure to adhere to a product requirement, process, or procedure).Comply with all Legacy Pharmaceutical Packaging standards and policies.Perform other duties as required.
ACCOUNTABILITY
The Quality Control Inspector shall be held accountable for the compliance, accuracy and timeliness of responsibilities and work assigned.
SUPERVISORY RESPONSIBILITIES
None
Qualifications
High School diploma or GED certificate requiredMust be able to understand and apply cGMP and Quality System ProceduresFamiliarity with Microsoft Office (Outlook Email, Word, Excel)Familiarity with data entry into electronic quality softwareMust be highly focused and detail orientedStrong interpersonal communication and accurate documentation skillsDEA clearance required including drug testing
WORKING CONDITIONS
Production areas and/or warehouse environment
ADDITIONAL COMMENTS
Experience in a cGMP environment preferred
Job LocationMO - Earth City, MO
Position TypeFull Time
Education LevelHigh School Diploma or GED
Travel PercentageNone
Job ShiftDay
Job CategoryManufacturing
Description
Job Title:
Quality Control Inspector
Department:
Quality
Reports To:
Quality Control Manager
PRIMARY PURPOSE or JOB SUMMARY
The Quality Control Inspector is responsible for the in-process and finished goods inspection activities at Legacy. The Quality Control Inspector shall fully comply with all regulatory / cGMP guidelines and Legacy Pharmaceutical Packaging standards and policies.
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.Promote and enforce cGMP and SOP compliance in an FDA regulated pharmaceutical manufacturing environment, ensuring product integrity, safety and compliance with standards.Possess a working knowledge of cGMPs, FDA and DEA regulations and Legacy Pharmaceutical Packaging policies and procedures.Perform and document in-process and finished good quality inspections of product and material.Perform and document containment of quality events.Perform and document line clearance of production room cleansVerification of materials issued for packaging.Monitor, review, and document Temperature Chart Recorder data.Perform daily review of in-process packaging batch records.Provide support to and coordinate with other departments to ensure product integrity.Perform and Check/Verify return quantities of Labeling Components in the batch record.Print and apply green release tags for production component returns as needed.Initiate and document Event Reports for in-process nonconformities (failure to adhere to a product requirement, process, or procedure).Comply with all Legacy Pharmaceutical Packaging standards and policies.Perform other duties as required.
ACCOUNTABILITY
The Quality Control Inspector shall be held accountable for the compliance, accuracy and timeliness of responsibilities and work assigned.
SUPERVISORY RESPONSIBILITIES
None
Qualifications
High School diploma or GED certificate requiredMust be able to understand and apply cGMP and Quality System ProceduresFamiliarity with Microsoft Office (Outlook Email, Word, Excel)Familiarity with data entry into electronic quality softwareMust be highly focused and detail orientedStrong interpersonal communication and accurate documentation skillsDEA clearance required including drug testing
WORKING CONDITIONS
Production areas and/or warehouse environment
ADDITIONAL COMMENTS
Experience in a cGMP environment preferred