Night QA Inspector II - Precision Pharma Quality

Cipla; Hauppauge, Northern (NY, KY); Hybrid; USD 33,000 - 43,000; Full time

Benefits offered by this job

401(k) matching

Health insurance

Health Savings Account

Flexible spending account

Paid time off

Paid holidays

Short-term disability

Long-term disability

Parental leave

Employee discounts

Job summary

InvaGen Pharmaceuticals, Inc. in Hauppauge, NY is hiring a DPI QA Inspector II for third shift to ensure quality throughout manufacturing and packaging processes. This role requires verifying materials, performing in-process checks, and posting data into SAP.

Minimum science graduate with 1–2 years pharma experience preferred; strong attention to detail and good communication are essential for success in a fast-paced GMP environment.

Qualifications

• Minimum science graduate with 1–2 years pharma experience preferred.
• Knowledge of cGMP and 21 CFR Part 820.
• Ability to read, write and communicate effectively.
• Basic computer skills (Word, Power and Excel).

Responsibilities

• Monitor and ensure product quality across manufacturing and packaging.
• Verify materials during dispensing and manage packaging materials.
• Perform in-process checks per batch instructions.
• Collect samples for BU, IPQA testing and analysis.
• Clean and maintain sampling tools and equipment.
• Record and post dispensed materials into SAP; support deviations investigations.
• Review batch records, logs and calibration PMP data.
• Observe safety, cGMP, SOPs and completed trainings.

Skills

Communication skills

Attention to detail

Organization

Math skills

Self-motivated

MS Office

Education

Science graduate

Tools

SAP

Excel

Word

Job description

InvaGen Pharmaceuticals, Inc. in Hauppauge, NY is hiring a DPI QA Inspector II for third shift to ensure quality throughout manufacturing and packaging processes. This role requires verifying materials, performing in-process checks, and posting data into SAP.

Minimum science graduate with 1–2 years pharma experience preferred; strong attention to detail and good communication are essential for success in a fast-paced GMP environment.