QA Inspector II - 2nd Shift

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title: QA Inspector II - 2nd Shift  FLSA Classification: Full-Time, Non - Exempt Professional   Work Location: Fall River, MA  Work Hours: second Sh ift: 3:00 PM – 11:30PM (may vary based on business needs) Reports To: Quality Control Manager Salary Range:$26 - $33 Job Purpose: The purpose of the QA Inspector position is to monitor and ensure shop floor activities and ensure product quality is maintained throughout all phases of the manufacturing and packaging process in compliance with established specifications and standard operating procedures (SOPs). Duties and Responsibilities: The QA Inspector (MDI) position is an individual contributor role and a member of the InvaGen Pharmaceuticals Plant Quality Team. The essential and typically expected job duties for this position include but are not limited to the following: Working knowledge of shop floor QA activities (Line clearance, in-process checks, sampling, calibration and verification of equipment’s). Perform line clearance, in-process testing as per batch record instructions. Review of batch records. Preparation, issuance and review of logbooks. Conduct room and equipment checks (where applicable) prior to each stage of manufacturing by following detailed written procedures. Execute sampling and inspections as required. Inspect in-process and finished product samples (where applicable) for the Quality Control (QC) Lab. Maintain records of standard weights and perform daily verification of balances. Ensure the proper isolation of rejected material generated during batch process and accountability in the batch record. Monitor facility and product environmental operating conditions. Review of engineering records such as temperature and humidity data, calibration and PM records, Pest control records and contractor related functions. Assess online batch records in terms of completeness of signatures, entries, and actual reconciliation / yields prior to initiation of next processing step. Verify the functionality of all the equipment and associated controls during the batch run. Identify and report any non-conformances and/or discrepancies to management if applicable. Education and Experience: Minimum high school diploma Advanced vocational training or education in pharmaceutical manufacturing, industrial management, or related field of study from an accredited college/university is preferred. Experience in quality assurance in a cGMP pharmaceutical manufacturing operation and work environment is preferred. Minimum of 3 years’ experience in quality assurance in a cGMP pharmaceutical manufacturing operation and work environment. Experience in MDI or combination products is preferred. Proficient user of personal computer hardware and…