Senior QA Specialist – GMP, Documentation & Improvement

Greenfield Global; Brookfield (CT); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Health and dental benefits

Disability and life insurance

Paid time off

Retirement savings program

Job summary

Greenfield Global in Brookfield, CT is seeking a Senior Quality Assurance Specialist to join our QA team. The role provides experienced QA and document management support in a GMP-regulated manufacturing environment, independently executing core QA activities and leading investigations and continuous improvement to sustain product quality.

The successful candidate will review batch records, manage labeling control, and support quality systems across the site, collaborating with cross-functional

Qualifications

• Minimum 3 years of QA experience in a regulated environment.
• Experience with batch records, labeling, and document control.
• Knowledge of GMP and ISO quality systems.
• Strong analytical and problem-solving abilities.
• Excellent communication and ability to work independently.

Responsibilities

• Issue and control labels, batch records, and other controlled documents.
• Review Batch Production Records for completeness, accuracy, and compliance.
• Disposition of raw materials, intermediates, and finished products; review Certificates of Analysis.
• Lead investigations of deviations, OOS results, complaints, and CAPAs; support audits.
• Analyze quality trends and metrics; support site quality improvement initiatives.

Skills

Quality Assurance experience

Document management

Batch record review

Investigations

Audits

GMP/ISO knowledge

Analytical skills

Communication skills

Cross-functional collaboration

Regulated manufacturing

Education

High School Diploma or GED

Quality certifications preferred

Job description

Greenfield Global in Brookfield, CT is seeking a Senior Quality Assurance Specialist to join our QA team. The role provides experienced QA and document management support in a GMP-regulated manufacturing environment, independently executing core QA activities and leading investigations and continuous improvement to sustain product quality.

The successful candidate will review batch records, manage labeling control, and support quality systems across the site, collaborating with cross-functional