On-Site QA Specialist: cGMP, Batch Records & CAPA

Germer International - Pharmaceutical Recruiting; Madison (WI); On-site; USD 85,000 - 95,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Paid maternity leave

Job summary

A recruitment firm in the pharmaceutical sector is seeking a QA Specialist in Madison, WI. This full-time, mid-senior level role requires a Bachelor's degree and at least 2 years of experience in a cGMP setting. The position involves providing quality assurance support, reviewing batch records, and ensuring proper documentation of facility events. Benefits include medical and vision insurance, a 401(k), and paid maternity leave.

Qualifications

• Bachelor's degree or above required.
• 2+ years of experience required in a cGMP setting.
• Experience in quality assurance documentation preferred.

Responsibilities

• Provide QA support independently.
• Assure proper documentation for facility events.
• Review executed batch records.
• Perform inspection and disposition of raw materials.
• Write deviations, investigations, change controls.
• Perform shipping release procedures.
• Assist in preparation of Annual Product Review documentation.

Skills

cGMP experience

Quality Assurance support

Inspection procedures

Document generation for QA

Education

Bachelor's degree or above in Scientific discipline

Job description

A recruitment firm in the pharmaceutical sector is seeking a QA Specialist in Madison, WI. This full-time, mid-senior level role requires a Bachelor's degree and at least 2 years of experience in a cGMP setting. The position involves providing quality assurance support, reviewing batch records, and ensuring proper documentation of facility events. Benefits include medical and vision insurance, a 401(k), and paid maternity leave.