To monitor and ensure all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. To monitor and ensure all phases of drug manufacturing are in compliance with established specifications. To receive, inspect, release and control of labels and outserts. To ensure quality compliance before, during and after each packaging run.
Essential Functions:
All requirements from Inspector II,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 reconcilaiton / yields prior to initiation of next processing stepVerification of functionality of all the equipment and associated controls during the batch runMaintenance of retention sample room and monitoring of temperature and humidity, replacement fo chart records as per schedule, review of log and disposition of samples. plus the following:
Monitor and release of Purified Water System
Generates, proof read and issues "in-house" labels as in accordance with Process Study protocols and master batch records.
performs rinse and swab sampling for microbial cleaning verification
Handling complaint samples, visual inspection or retention / complaints samples, Batch record review for the receipt of complaint batches, collection of complaints / retention samples for analytical testing in case of complaint investigation
Identification of gaps in the manufacturing and packaging equipment and assess the impact on the quality of product
Coordination with manufacturing and engineering teams to resolve compliance issues in a timely manner
Additional Responsibilities:
Performs rinse and swab sampling for microbial cleaning verification
Handling complaint samples, visual inspection or retention / complaints samples, Batch record review for the receipt of complaint batches, collection of complaints / retention samples for analytical testing in case of complaint investigation
Identification of gaps in the manufacturing and packaging equipment and assess the impact on the quality of product
Coordination with manufacturing and engineering teams to resolve compliance issues in a timely manner
Other duties that management may from time to time assign.
Education:
High School or GED - Required
Experience:
3 years or more in 3 or more years experience in QA or related field
Skills:
Good basic math knowledge and excellent attention to details - Intermediate
Thorough understanding and familiarity with GMP regulations including 21 CFR 210 and 211, ICH guidelines - Intermediate
High energy level and organizational skills - Intermediate
A certain degree of creativity and latitude is required - Intermediate
Computer Skills ( Word and Excel) - Intermediate
The hourly base salary for this position ranges from $25.00 to $30.00 per hour. Amneal ranges reflect the Company’s good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life’s many other commitments and opportunities.
