2nd Shift Quality & Compliance Auditor (GMP)

Tower-Laboratorie; Montague Township (MI); On-site; USD 55,000 - 85,000; Full time

Job summary

Tower-Laboratorie is a 2nd shift Quality/Compliance Auditor role focused on enforcing our quality systems and conducting audits across drug, medical device, and non-drug products to ensure cGMP compliance.

The position emphasizes strong writing, communication, and teamwork, with at least two years of pharmaceutical QA experience and a high school diploma. Hours are Mon-Thu, 3:00 PM–1:00 AM.

Qualifications

• Minimum of 2 years of pharmaceutical QA or regulatory experience.
• Solid knowledge of cGMP regulations and industry standards.
• Ability to read and follow directions and to communicate in English.
• Strong writing and organizational skills.

Responsibilities

• Perform audits of manufacturing and packaging processes to verify compliance.
• Inspect documentation and in-process tests for accuracy and adequacy.
• Investigate deviations and collect data to determine root causes.
• Contribute to internal cGMP audits and policies.
• Review batch production records prior to release.

Skills

Quality auditing

cGMP knowledge

MS Word

MS Excel

English communication

Attention to detail

Team player

Education

High school diploma

Tools

MS Word

MS Excel

Job description

Tower-Laboratorie is a 2nd shift Quality/Compliance Auditor role focused on enforcing our quality systems and conducting audits across drug, medical device, and non-drug products to ensure cGMP compliance.

The position emphasizes strong writing, communication, and teamwork, with at least two years of pharmaceutical QA experience and a high school diploma. Hours are Mon-Thu, 3:00 PM–1:00 AM.