QA Inspector

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 I

FLSA Classification
:
Hourly $16.64 - $22.88

Work Location
:
Central Islip, NY

Work Hours: Second Shift 3:00PM - 11:30PM (may vary based on business needs)

Reports To
: QA Supervisor

Job Overview: The QA Inspector is responsible for monitoring and ensuring product quality is maintained through all phases of manufacturing in compliance with established procedures.

Responsibilities:

• Verification of raw materials during the dispensing process.
• To perform posting of dispensed materials and samples into SAP system and to perform other transactions in SAP.
• Maintenance of standard weights and perform daily verification of balances
• Perform in-process checks during batch manufacturing, as per manufacturing record instructions.
• Collection of in-process blend, finished product, validation samples for analysis, sample collection as per protocols. Specifically, to perform blend uniformity sampling.
• Perform in-process testing (e.g., weight, thickness, hardness, disintegration, friability, etc.) as per manufacturing batch record instructions.
• Ensure cleaning of manufacturing and equipment, area and provide line clearance.
• 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.
• Perform AQL, Blend sampling, In-process Sampling, and inspections as required.

Skills:

• Knowledge of Good Manufacturing Practices and Good Documentation Practices.
• Ability to read, write, and communicate effectively.
• Self-motivated, with the ability to work in a fast-paced manufacturing environment and handle multiple tasks simultaneously.
• Excellent organization skills with the ability to focus on details.
• Basic computer skills (Microsoft Word, PowerPoint and Excel).

Educational

Qualification:

Minimum High school diploma.

Work Experience: Minimum 1-2 years’ experience in manufacturing or packaging pharmaceuticals.