QA Intern

Job Description

Position Summary:

The QA Intern performs quality assurance functions specific to material disposition to ensure continuous production in accordance with established procedures, guidelines and standards at the Stroudsburg, PA facility. This position will be responsible for the execution of Quality Assurance activity including but not limited to the review and disposition of raw materials, components, and finished goods while ensuring good manufacturing practices are followed throughout the facility.

Major Roles & Responsibilities:

Issues analytical summary sheets for all products manufactured or packaged at BioSpectra's Stroudsburg PA facility.

Issues Batch Records including all documentation for accountability of labels, seals, lot number assignment associated with the released of the manufactured product.

Reviews and approves Batch Records (for non-GMP and sample lots) including all documentation review associated with the release of the manufactured product.

Issues Certificate of Analysis for Finished Goods Shipments.

Notifies management of any non-conforming events and assists with writing or reviewing Investigation Reports.

Communicates any quality related requirements or findings to applicable department staff to ensure the correction or prevention of non-conforming events.

Performs Finished Good Inspection/QA Approval prior to Finished Good Shipments at BioSpectra's Stroudsburg, PA facility.

Performs review of Pest Control reports for Stroudsburg, PA facility.

Performs review of Temperature and Humidity Monitoring Assessments.

Performs quality review of Preventative Maintenance documentation.

Performs quality review of Maintenance Work Orders.

Inspects incoming Components and Raw Materials.

Approves and monitors the usage of regulated inventory in Sage ERP system.

Provides the placards detailing the disposition of material for placement in the facility Warehouses. Recommends modifications of existing quality or production standards to achieve optimum quality within limits of manufacturing capability.

Ensures Quality records are accurate, approved and in compliance with cGMP standards.

Ensures that the facility is functioning in accordance with established quality policies and procedures

through document review and approval, quality walk-throughs, communication with personnel and training support.

Other duties may be assigned as deemed appropriate by management.

Qualifications:

Student enrolled in a Bachelor's or Graduate Program in a science-related field

Has knowledge and understanding of cGMP & ICH Q7

Knowledge of relevant software applications including MS Office and Minitab

Knowledge of office systems and procedures

Knowledge of Supplier Approval Programs

Ability to communicate effectively with customers, regulatory agencies or member of the business community regarding inquiries or complaints.

Organized, Thorough, Neat

Confidentiality

Physical Requirements:

Lift up to 20 lbs. occasionally

Prolonged periods sitting at a desk and working on a computer Ability to see and distinguish color

Bend, stoop, and carry

Repeating motion that may include wrists, hands, and fingers