Quality Assurance Inspector II - 12 Hour Schedule - Day Shift

Description:

The QA Inspector II plays an important role in supporting our commitment to quality by overseeing the sampling, inspection and testing of incoming raw materials, packaging components and returned goods to ensure they meet established specifications. This role also supports quality oversight throughout all phases of drug manufacturing and helps maintain compliance at every step. In addition, the QA Inspector II is responsible for receiving, inspecting, releasing and controlling labels and outserts, as well as ensuring quality standards are upheld before, during and after each packaging run. This role follows a 12-hour rotating schedule, working from 6:00 AM to 6:30 PM

Essential Functions:

• All Functions of QA Inspector I, Perform Inspection, sampling and testing where applicable on all incoming raw materials, packaging components and returned goods following detailed written procedures. 
• Preparation of samples for chemical and microbiological (where required) analysis and delivering them to the QC lab. 
• Inspection and test of packaging components utilizing various measuring devices such as scales, micrometers and height gauges to determine conformance to specifications. Maintaining detailed records of sampling, inspections and testing activities. 
• Assigning and verification of expiry date and retest date for all the GMP raw materials through vendor COA and in-house COA. Collection of packaged product samples for annual stability.
• Perform room, equipment, and packaging line checks (where applicable) prior to each stage of manufacturing following detailed written procedures. Conduct in process testing per manufacturing and packaging batch record instructions. 
• Prepare controlled / uncontrolled / packaged finished product samples for QC lab and QA retains, following detailed documentation procedures. Maintenance of standard weights required to perform daily verification of balances.
• Labeling component receipt, visual examination, counting, preliminary inspection and sampling.
•  Preparation of labeling components/outserts inspection reports; quarantine and release labels and maintaining incoming components log and corresponding inventory cards. 
• Issuance of labeling components/outserts according to packaging order and regular monitoring and auditing of label room. 
• Fill out the QA final labeled product inspection report, final line clearance which includes labeling and packaging reconciliation paperwork.
• Compliance of Warehouse area in terms of Isolation of Quarantine, Released, In-Process, Finished Product, Packaged Product, Returned Goods, and Rejected areas.
• Ensure the proper isolation of rejected material generated during batch process and accountability in the batch record. Monitor facility and product environmental operating conditions. Plus the following:
• Review of engineering records (temperature and humidity data calibration and PM records, Pest control records and contractor related functions)
• Review of online batch records in terms of completeness of signatures, entries, and actual reconciliation / yields prior to initiation of next processing step
• Verification of functionality of all the equipment and associated controls during the batch run
• Maintenance of retention sample room and monitoring of temperature and humidity, replacement of chart records as per schedule, review of log and disposition of samples.

Additional Responsibilities:

• Disposition of rejected material and returned drug products as per SOP
• Performs environmental monitoring in accordance with established schedule (where applicable)
• Perform applicable testing and prepare report for customer complaints
• Other duties that management may from time to time assign.

Additional Requirement: 

This position requires successful completion of an OSHA-compliant Respirator Fit Test

 

Education:

• High School or GED - Required

Experience:

• 2 years or more in 2 or more years experience in QA or related field

Specialized Knowledge:

• Good basic math knowledge 
• Excellent attention to details.
• Records observations for improving processes.

 

The hourly rate for this position ranges from $21.00-$27.00 per hour. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, as well as a long-term incentive award, such as restricted stock units, with this position within the first 12 months. 

Amneal ranges reflect the Company’s good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the po