Overnight Quality Operations Associate – GMP (Manufacturing)

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

Benefits offered by this job

Medical, vision and dental insurance

Life and AD&D insurance

Paid holidays

PTO accrual

Job summary

Kedrion Biopharma Inc. is seeking a Manufacturing Quality Associate for an overnight shift (6:00 pm–6:00 am) in Melville, onsite.

You will help ensure quality and compliance on the production floor, working with QA and Operations to monitor activities and resolve issues in real time. The role emphasizes review of documentation, adherence to GMP/GDP, and involvement in continuous improvement and quality systems.

Qualifications

• Strong written and verbal communication skills.
• Demonstrated problem-solving skills and attention to detail.

Responsibilities

• Monitor batch processing activities for cGMP compliance.
• Conduct routine inspections of manufacturing operations and equipment.
• Review production logbooks and batch records for critical parameters.
• Support plasma and component inspection activities for quality.
• Document and trend operational observations for quality metrics.

Skills

Communication skills

Problem solving

Attention to detail

Education

College degree

Tools

Microsoft Office

Email systems

Job description

Kedrion Biopharma Inc. is seeking a Manufacturing Quality Associate for an overnight shift (6:00 pm–6:00 am) in Melville, onsite.

You will help ensure quality and compliance on the production floor, working with QA and Operations to monitor activities and resolve issues in real time. The role emphasizes review of documentation, adherence to GMP/GDP, and involvement in continuous improvement and quality systems.