GMP QA Associate | Biotech Batch Release Oversight

Astrix; California (MO); On-site; USD 48,216 - 68,880; Full time

Benefits offered by this job

Medical insurance

401(k)

Vision insurance

Job summary

A biotech staffing agency is seeking a QA Associate II/III to support quality operations within a manufacturing facility. The role ensures compliance with cGMP requirements and involves reviewing GMP documents, supporting product release, and providing QA oversight. Ideal candidates have a Bachelor’s degree and 1-3 years of experience in a GMP-regulated environment. This contract position offers benefits such as medical insurance and a 401(k).

Qualifications

• 1–3+ years of experience in a GMP-regulated environment, preferably in Pharma or Biotech.
• Working knowledge of cGMP and regulatory guidelines.

Responsibilities

• Review and approve GMP documents, including SOPs, specifications, and batch records.
• Perform batch record reviews and support product release activities.
• Support deviation, CAPA, investigation, and change control processes.

Skills

Attention to detail

Communication skills

Education

Bachelor’s degree in a scientific or related field

Job description

A biotech staffing agency is seeking a QA Associate II/III to support quality operations within a manufacturing facility. The role ensures compliance with cGMP requirements and involves reviewing GMP documents, supporting product release, and providing QA oversight. Ideal candidates have a Bachelor’s degree and 1-3 years of experience in a GMP-regulated environment. This contract position offers benefits such as medical insurance and a 401(k).