GMP Quality Assurance Analyst

Otsuka Pharmaceutical Co., Ltd; New Albany (OH); On-site; USD 46,000 - 76,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

401(k) match

Wellness benefits

Annual bonus

Job summary

Pharmavite in Ohio is seeking a Manufacturing Documentation Specialist to ensure quality across GMP manufacturing and packaging operations. You will issue, track, and review documents and records, and collaborate with cross-functional teams to uphold quality standards.

The role emphasizes accurate data handling, attention to detail, and adherence to retention policies while supporting continuous improvement in manufacturing processes.

Qualifications

• High School Diploma or GED or equivalent work experience.

Responsibilities

• Review bulk, components, labels, lab test records, and finished goods for specifications.

Skills

Quality testing

English proficiency

Communication

Data entry

Excel

Math calculations

Prioritization

Organizational skills

Attention to detail

Education

High School Diploma/GED

Tools

Microsoft Word

Excel

Job description

Pharmavite in Ohio is seeking a Manufacturing Documentation Specialist to ensure quality across GMP manufacturing and packaging operations. You will issue, track, and review documents and records, and collaborate with cross-functional teams to uphold quality standards.

The role emphasizes accurate data handling, attention to detail, and adherence to retention policies while supporting continuous improvement in manufacturing processes.