2nd-Shift GMP Quality & Compliance Auditor

DaMar Staffing; Michigan; On-site; USD 55,000 - 85,000; Full time

Job summary

Tower Laboratories, Ltd. seeks an experienced QA Auditor to enforce the company’s quality system on the 2nd shift (Mon–Thu, 3:00 PM–1:00 AM).

You will perform production and packaging audits, drive root-cause investigations, and ensure adherence to cGMP and internal procedures while maintaining calibration of equipment. Ideal candidates have at least 2 years in pharma QA or regulatory roles, strong writing and communication skills, and a keen eye for detail to uphold product safety and

Qualifications

• Minimum of 2 years of pharmaceutical experience, in the Quality Assurance or Regulatory field.
• Demonstrated current knowledge of cGMP regulations and industry standards.
• Working knowledge of MS Word and MS Excel.
• Ability to read and follow directions, complete paperwork and communicate effectively in English.
• Strong writing skills.
• Excellent organizational skills; strong attention to detail.
• Good interpersonal skills; ability to communicate effectively with all levels of plant personnel.
• Strong team player, demonstrated team attitude and behaviors.

Responsibilities

• Enforce Tower Laboratories, Ltd. quality system and ensure cGMP compliance.
• Perform audits of production processes to verify specifications and quality.
• Audit packaging and components to meet acceptance criteria.
• Investigate deviations and collect information for root-cause analysis.
• Coordinate with QA Manager and other departments to address deficiencies.
• Ensure calibration of instrumentation and proper documentation.
• Contribute to internal cGMP audits and procedural compliance.
• Support safety and company procedures in daily tasks.

Skills

GMP compliance

Auditing

Attention to detail

English communication

Education

High school diploma

Tools

MS Word

MS Excel

Job description

Tower Laboratories, Ltd. seeks an experienced QA Auditor to enforce the company’s quality system on the 2nd shift (Mon–Thu, 3:00 PM–1:00 AM).

You will perform production and packaging audits, drive root-cause investigations, and ensure adherence to cGMP and internal procedures while maintaining calibration of equipment. Ideal candidates have at least 2 years in pharma QA or regulatory roles, strong writing and communication skills, and a keen eye for detail to uphold product safety and