QA Systems Lead — cGMP Quality & CAPA Expert

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

Benefits offered by this job

Medical benefits starting day 1

Paid volunteerism

Generous PTO

Wellness time off

Paid holidays

Job summary

Grand River Aseptic Manufacturing Inc. in Grand Rapids, MI is looking for a QA Systems Specialist. You will support quality systems related to the manufacturing and testing of cGMP drug products, focusing on Non-Conformance, CAPA, and Change Control.

The ideal candidate will have a Bachelor’s degree in Life Sciences or equivalent experience, knowledge of QA principles, and a passion for continuous improvement. Benefits include medical insurance from day 1, paid volunteerism, and generous PTO.

Qualifications

• Bachelor’s degree or 4-8 years relevant experience.
• Knowledge of cGMP and FDA guidelines required.
• Experience in regulated products is essential.

Responsibilities

• Daily management of quality systems.
• Lead continuous improvement initiatives.
• Train personnel on Root Cause Analysis tools.

Skills

Knowledge of QA principles and procedures in pharma

Data analysis and reporting

Experience in aseptic manufacturing

Root Cause Analysis

Education

Bachelor’s degree in Life Sciences or related field

4-8 years of related work experience

Job description

Grand River Aseptic Manufacturing Inc. in Grand Rapids, MI is looking for a QA Systems Specialist. You will support quality systems related to the manufacturing and testing of cGMP drug products, focusing on Non-Conformance, CAPA, and Change Control.

The ideal candidate will have a Bachelor’s degree in Life Sciences or equivalent experience, knowledge of QA principles, and a passion for continuous improvement. Benefits include medical insurance from day 1, paid volunteerism, and generous PTO.