QA Associate: Digital Quality & GMP Transformation

Mennonite Economic Development Associates (MEDA); Pomona (CA); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Health Insurance

401(k) plan

Paid time off

Life insurance

Employee assistance program

Job summary

Bimeda in Pomona, CA is seeking a QA Associate to join the quality assurance team. The role focuses on core GMP responsibilities, including product release, change control, APRs, deviations and CAPA resolution, while supporting digital quality systems adoption and data-driven decision making.

Reporting to the QA Manager, you will drive quality improvements, oversee auditing activities, and champion Lean QA practices.

Qualifications

• Knowledge of pharmaceutical QA methodologies and cGMP.
• Strong attention to detail and organizational skills.
• Proficiency with Microsoft Office and document management systems.
• Minimum 2–3 years of experience in pharmaceutical QA and GMP compliance.

Responsibilities

• Review batch records and determine disposition (release, reject, or hold).
• Perform internal QA audits on manufacturing lines and finished products.
• Investigate product complaints, deviations, and OOS results; implement CAPAs.
• Support e-QMS, LIMS, and electronic batch records adoption and data-driven decisions.
• Provide training on documentation practices and evolving digital quality tools.

Skills

QA methodologies

cGMP knowledge

Data analytics

Education

Bachelor's degree in a related science field

Tools

ZenQMS

TrackWise

MasterControl

Job description

Bimeda in Pomona, CA is seeking a QA Associate to join the quality assurance team. The role focuses on core GMP responsibilities, including product release, change control, APRs, deviations and CAPA resolution, while supporting digital quality systems adoption and data-driven decision making.

Reporting to the QA Manager, you will drive quality improvements, oversee auditing activities, and champion Lean QA practices.