Quality Assurance Lead: Production & Compliance

Cencora, Inc.; Columbus (OH); On-site; USD 24,000 - 34,000; Full time

Job summary

Cencora, Inc. in Columbus, OH is seeking a QA/Production team member to oversee daily QA and production activities.

The role requires attention to batch records, compliance, and close collaboration with cross-functional teams to ensure product quality. The successful candidate will audit records, perform serialization tasks, and assist in investigations and deviations as part of our continuous improvement initiatives, while adhering to cGMP and safety standards.

Qualifications

• Requires high school diploma, GED or equivalent.
• Ability to read and understand English documents and labels.
• Good written skills for accurate compliance documentation.
• Basic mathematical skills for production checks.
• Strong interpersonal and organizational abilities.
• Good verbal and written communication across teams.
• Proficient with ERP systems and Microsoft Office.

Responsibilities

• Provide direction and guidance to daily QA and production activities.
• Audit production batch records for accuracy and compliance.
• Conduct final audit prior to Product Release.
• Perform serialization tasks to support production needs.
• Verify and correct discrepancies in products and packaging components.
• Escalate non-conformance issues and assist root-cause analysis.
• Participate in site internal audits and continuous improvement efforts.

Skills

English reading

Written communication

Mathematical skills

Interpersonal skills

Organizational skills

Verbal communication

Computer literacy

Education

High school diploma or GED

Tools

ERP Systems

Microsoft Office (Outlook, Word, Excel)

Job description

Cencora, Inc. in Columbus, OH is seeking a QA/Production team member to oversee daily QA and production activities.

The role requires attention to batch records, compliance, and close collaboration with cross-functional teams to ensure product quality. The successful candidate will audit records, perform serialization tasks, and assist in investigations and deviations as part of our continuous improvement initiatives, while adhering to cGMP and safety standards.