Pharma QA Lead — GMP, Audits & Compliance

Tower-Laboratorie; Montague Township (MI); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Medical insurance

HSA option

Vision insurance

401(k) with employer contribution up

Paid time off

9 paid holidays

Long-term disability coverage

Company-paid life insurance

Job summary

Tower Laboratories is seeking a Quality Assurance leader to supervise QA auditors at the Montague facility, ensuring product release and compliance with cGMP and FDA requirements. The role involves cross-functional collaboration, training, and audits to support manufacturing operations.

Ideal candidates will have 5+ years in QA leadership within the pharmaceutical industry, strong problem-solving abilities, and proficiency with MS Word and Excel in a quality control context.

Qualifications

• Five years experience in Quality Assurance leadership in the pharmaceutical industry.
• Demonstrated current knowledge of cGMP regulations and industry standards.
• Ability to train others and provide guidance.
• Strong organizational skills; ability to delegate and manage multiple tasks.

Responsibilities

• Oversee daily QA Auditor activities; provide direction and training.
• Familiar with FDA rules and processes; ensure compliance.
• Conduct packaging audits; verify packaging specs and AQL.
• Lead investigations to identify root causes of deviations.
• Perform internal GMP audits to ensure cGMP compliance.
• Audit finished batch production documents and release products.
• Communicate deficiencies to key personnel and cross‑functional teams.
• Review BOM and packaging specifications; ensure proper documentation.

Skills

Quality Assurance leadership

Team player

Problem solving

Analytical skills

Attention to detail

Communication

Education

Bachelor’s degree in Science

Tools

MS Word

MS Excel

Job description

Tower Laboratories is seeking a Quality Assurance leader to supervise QA auditors at the Montague facility, ensuring product release and compliance with cGMP and FDA requirements. The role involves cross-functional collaboration, training, and audits to support manufacturing operations.

Ideal candidates will have 5+ years in QA leadership within the pharmaceutical industry, strong problem-solving abilities, and proficiency with MS Word and Excel in a quality control context.