Senior QA Associate - Onsite GMP Biotech Contract

AGW; Thousand Oaks (CA); On-site; USD 39,000 - 47,000; Full time

Benefits offered by this job

Medical

Vision

Sick Pay

Job summary

Aptask Global Workforce (AGW) seeks a Senior Quality Assurance Associate for an onsite 6+ month contract in Thousand Oaks, CA. This role provides daily QA oversight of Drug Substance manufacturing in a GMP environment and requires hands-on pharma/biotech experience.

The ideal candidate has familiarity with manufacturing and quality operations, cell culture knowledge, and a strong ability to follow SOPs and maintain documentation. 100% onsite with rotating shifts.

Qualifications

• 1–2+ years of hands-on experience in a regulated GMP environment (pharmaceutical, biotech, or food industries).
• Familiarity with manufacturing or quality operations.
• Knowledge of Cell Culture and Purification.
• Demonstrated ability to perform GMP operations, including following SOPs, maintaining training, and good documentation practices.
• Self-driven with strong teamwork ethic and communication skills.
• Bachelor's Degree in Biochemistry, Biology, Chemistry, or a related science field.

Responsibilities

• Provide daily oversight of Manufacturing and Facilities & Engineering areas.
• Perform electronic batch record review, SOP revision & approval, work order approval, and quality approval of minor deviations.
• Evaluate compliance issues, provide recommendations, and ensure progress of quality records to completion.
• Support GMP operations for manufacturing, providing quality oversight for GDP and GMP.
• Perform GMP record reviews and releases.

Skills

Teamwork

Communication skills

Self-driven

Education

Bachelor’s degree

Associate’s degree

High school/GED

Job description

Aptask Global Workforce (AGW) seeks a Senior Quality Assurance Associate for an onsite 6+ month contract in Thousand Oaks, CA. This role provides daily QA oversight of Drug Substance manufacturing in a GMP environment and requires hands-on pharma/biotech experience.

The ideal candidate has familiarity with manufacturing and quality operations, cell culture knowledge, and a strong ability to follow SOPs and maintain documentation. 100% onsite with rotating shifts.