Cipla USA→
QA Inspector I
Entry LevelOn-site
Location
Central Islip, NY
Salary
$48k–$62k/yr
Experience
Not specified
Posted
1 week ago
Skills
manufacturing practicessapbasic computer skillscommunication skillsself-motivatedorganization skills
Job Description
Summary: Cipla USA is a leading global pharmaceutical company dedicated to high-quality medicines. The QA Inspector I is responsible for monitoring and ensuring product quality throughout the manufacturing process 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, escalate 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
Required Qualifications:
- Minimum High school diploma
- Minimum 1-2 years' experience in manufacturing or packaging pharmaceuticals
- 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, Power and Excel)
Required Skills: Manufacturing Practices, SAP
Important Skills: Basic computer skills
Nice-to-Have Skills: Communication skills, Self-motivated, Organization skills