QA Inspector II - DPI

Shift :
First Shift: 8:30 AM – 5:00 PM (May vary based on business needs)

The QA Inspector is responsible for monitoring and ensuring product quality is maintained through all phases of manufacturing or packaging in compliance with established specifications.

• Verification of raw materials during the dispensing process.
• Dispensing printed packaging materials to packaging.
• Perform in-process checks during batch manufacturing and packaging, as per manufacturing & batch packaging record instructions.
• Collection of in-process blend, finished product, validation samples for analysis, sample collection as per protocols. Specifically, to perform blend uniformity (BU) sampling.
• To clean and maintain the samplings rods/dies/sample boxes used for BU sampling.
• Perform IPQA testing on the manufacturing floor specifically LOD, Bulk Density, Tapped Density, Leak Test, Weight Variation test.
• Ensure cleaning of manufacturing and packaging equipment, area and provide line clearance.
• To perform posting of dispensed materials and samples into SAP system (ERP system) and to perform other transactions in SAP.
• Involve in investigation of Deviation, OOS, OOT, or any other non-conformances.
• Ensure completion of individual training assigned and follow company policies, safety requirements, cGMP and SOP's.
• Review of online batch records, area/equipment logbooks, calibration/PMP records etc.
• Ensure the proper isolation of rejected material generated during batch process and accountability in the batch record.
• Review of engineering records (temperature and humidity data, calibration reports and PMP records).
• To take daily Quality rounds at shop floor to ensure shop floor is maintained in state of compliance and per GMP requirement.
• Report, elevate to Manager quality assurance about daily shop floor activities and any discrepancy during batch manufacturing and packing.
• Other duties [additional support] that management may assign from time to time.

• Minimum Science Graduate
• A minimum of 1-2 years of pharmaceutical experience (DPI, MDI or Injectables) preferred.
• Preference will be given to candidates with experience in generic pharmaceutical manufacturing.
• Knowledge of Good Manufacturing Practices and 21 CFR Part 820.
• Ability to read, write and communicate effectively.
• Basic computer skills (Microsoft Word, Power and Excel).
• Self-motivated, with the ability to work in fast-paced manufacturing environment and handle multiple tasks simultaneously.
• Excellent organization skills with strong attention to details skills.
• Strong fundamental mathematical skills and knowledge.

• Work standing or walking unassisted for 75% or greater of an 8-hour period.
• Unassisted lifting up-to 35 lbs., may be required.
• Able to wear appropriate personal protective equipment at all times, when required.

This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required. Remote work and relocation are not supported in this position.