QA Systems Lead – cGMP Quality, CAPA & Compliance

Grand River Aseptic Manufacturing; Grand Rapids (MI); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Medical benefits starting day 1

Paid volunteerism

Paid time off (PTO)

Wellness time off

Paid holidays

Job summary

Grand River Aseptic Manufacturing in Grand Rapids, MI is looking for a QA Systems Specialist to support quality systems in cGMP drug product manufacturing. This role includes management of processes like Non-Conformance, Corrective Action, and Quality Deliverables.

The ideal candidate holds a Bachelor's in Life Sciences or has equivalent work experience, with strong knowledge of QA principles, cGMP, and FDA standards. The position offers competitive pay based on experience and comprehensive benefits starting from day one.

Qualifications

• Bachelor's degree or 4-8 years relevant experience.
• Understanding of cGMP and FDA guidelines.
• Experience with quality systems regulations.

Responsibilities

• Manage oversight of quality systems.
• Lead continuous improvement initiatives.
• Train personnel on investigations tools.

Skills

Knowledge of QA principles

Experience in pharmaceutical manufacturing

Data analysis and reporting

Education

Bachelor's degree in Life Sciences or related field

Job description

Grand River Aseptic Manufacturing in Grand Rapids, MI is looking for a QA Systems Specialist to support quality systems in cGMP drug product manufacturing. This role includes management of processes like Non-Conformance, Corrective Action, and Quality Deliverables.

The ideal candidate holds a Bachelor's in Life Sciences or has equivalent work experience, with strong knowledge of QA principles, cGMP, and FDA standards. The position offers competitive pay based on experience and comprehensive benefits starting from day one.