Onsite Quality Assurance Associate – GMP Manufacturing

Kedrion Biopharma GmbH; Melville (NY); On-site; USD 32,000 - 34,000; Full time

Benefits offered by this job

Medical, Vision, Dental Insurance

Life Insurance & AD&D

Paid Holidays

PTO accrual

Job summary

Kedrion Biopharma Inc. in Melville, NY is seeking a Quality Assurance Associate to provide on-floor quality support in a GMP-regulated manufacturing environment.

You will monitor batch processing, inspect production areas, review logs, and identify compliance concerns in real time while collaborating with Quality, Operations, and Engineering teams. This daytime role (06:00 am – 06:00 pm, alternating weekends) offers permanent employment with a pay range of $23.00–$25.00 per hour and a full

Qualifications

• College degree preferred or equivalent combination of education and relevant experience.
• Experience in pharmaceutical manufacturing, quality, or operations is preferred.
• Understanding of GMP/GDP regulations is required.

Responsibilities

• Provide on-floor quality support in a GMP-regulated environment.
• Monitor batch processing and verify conformance with procedures and batch records.
• Review production logbooks, calibration, and preventive maintenance records.
• Support investigations, deviations, and quality system activities.

Skills

Attention to detail

Written communication

Verbal communication

Problem solving

Team collaboration

Education

College degree preferred or equivalent

Tools

Microsoft Office

Job description

Kedrion Biopharma Inc. in Melville, NY is seeking a Quality Assurance Associate to provide on-floor quality support in a GMP-regulated manufacturing environment.

You will monitor batch processing, inspect production areas, review logs, and identify compliance concerns in real time while collaborating with Quality, Operations, and Engineering teams. This daytime role (06:00 am – 06:00 pm, alternating weekends) offers permanent employment with a pay range of $23.00–$25.00 per hour and a full