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QA Inspector II - DPI

Job in Hauppauge, Suffolk County, New York, 11788, USA
Listing for: Cipla USA
Full Time position
Listed on 2025-12-02
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 18.72 - 26 USD Hourly USD 18.72 26.00 HOUR
Job Description & How to Apply Below

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 Information
  • Job Title: DPI QA Inspector II
  • Organization Name: Inva Gen Pharmaceuticals, Inc.
  • Location: Unit 1 - 7 Oser Avenue, Hauppauge, NY 11788
  • Employment Type: Full Time
  • Shift: First Shift: 8:30 AM - 5:00 PM (may vary based on business needs)
  • Salary Range (Base/salary): $18.72/hr - $26/hr
  • Benefits: In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package including 401(k) savings plan and matching, health insurance (medical/dental/vision), health savings account (HSA), flexible spending account (FSA), paid time off (vacation/sick/flex time), paid holidays, short‑term and long‑term disability, parental leave, employee discounts, and other benefits.
Responsibilities / Accountabilities
  • 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, and sample collection as per protocols; specifically, to perform blend uniformity (BU) sampling.
  • Clean and maintain the sampling rods/dies/sample boxes used for BU sampling.
  • Perform IPQA testing on the manufacturing floor: LOD, bulk density, tapped density, leak test, weight variation test.
  • Ensure cleaning of manufacturing and packaging equipment, area and provide line clearance.
  • Post dispensed materials and samples into SAP (ERP system) and perform other necessary transactions.
  • Investigate deviations, OOS, OOT, or other non‑conformances.
  • Complete assigned training and follow company policies, safety requirements, cGMP and SOPs.
  • Review online batch records, area/equipment logbooks, calibration/PMP records, engineering records (temperature, humidity, calibration reports).
  • Ensure proper isolation of rejected material generated during batch process and accountability in the batch record.
  • Conduct daily quality rounds at the shop floor to ensure GMP compliance.
  • Report and, if necessary, escape to Manager QA about daily shop floor activities and any discrepancies during batch manufacturing and packing.
  • Perform additional duties as assigned by management.
Education & Experience
  • Minimum Science Graduate.
  • Minimum 1–2 years of pharmaceutical experience (DPI, MDI or Injectables) is preferred.
  • Preference for candidates with experience in generic pharmaceutical manufacturing.
Skills & Competencies
  • Knowledge of Good Manufacturing Practices and 21 CFR Part 820.
  • Ability to read, write and communicate effectively.
  • Basic computer skills (Microsoft Word, PowerPoint, Excel).
  • Self‑motivated, able to work in a fast‑paced manufacturing environment and handle multiple tasks simultaneously.
  • Excellent organization skills with strong attention to detail.
  • Strong fundamental mathematical skills and knowledge.
Physical Requirements
  • 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.
Other Information

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.

About the Company

Cipla is a leading global pharmaceutical company, dedicated to high‑quality, branded, and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and broadened our presence in key markets worldwide.

Inva Gen Pharmaceuticals, Inc. is a Cipla subsidiary engaged in the development, manufacture,…

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