Lab Quality Analyst: Regenerative Medicine & Compliance

Actalent; Dayton (OH); On-site; USD 34,000 - 37,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

401(k) plan

PTO

Job summary

Actalent seeks a Quality Specialist for a Dayton, OH laboratory and manufacturing setting. This role focuses on documentation review, investigations, CAPA management, deviation tracking, and ensuring regulatory compliance within a fast-paced environment.

Duties include batch review, QMS support across cGMP departments, and collaboration with lab, manufacturing, and quality teams to uphold safety and quality standards.

Qualifications

• Bachelor's degree in a scientific discipline (Biology, Chemistry, Microbiology, Biochemistry) or related field.
• Minimum of 6 months' experience in a regulated laboratory, manufacturing, quality, or other highly regulated environment.

Responsibilities

• Review batch production records and manufacturing documentation for lot release.
• Coordinate CAPAs, NCRs, and deviation records with timely closure.
• Support investigations, root cause analysis, and process improvement efforts.

Skills

Quality systems

Investigations

CAPA management

Deviation tracking

Documentation review

Batch record review

Cross-functional collaboration

Education

Bachelor's degree in Biological/Chemical/ Life sciences

Job description

Actalent seeks a Quality Specialist for a Dayton, OH laboratory and manufacturing setting. This role focuses on documentation review, investigations, CAPA management, deviation tracking, and ensuring regulatory compliance within a fast-paced environment.

Duties include batch review, QMS support across cGMP departments, and collaboration with lab, manufacturing, and quality teams to uphold safety and quality standards.