Onsite Senior Manufacturing Associate - CAPA/EV Lead

AGW; Thousand Oaks (CA); On-site; USD 57,198,000 - 95,330,000; Full time

Benefits offered by this job

Medical

Vision

Sick Pay

Job summary

Aptask Global Workforce (AGW) is seeking a Senior Associate Manufacturing - Onsite for a 6+ month contract in Thousand Oaks, CA. The role leads CAPAs and EVs for Manufacturing Clinical Supply, driving quality and compliance in a cross-functional team.

The candidate will implement continuous improvement, manage projects with PM tools, and ensure timely CAPA ownership while collaborating with quality, engineering, validation, and regulatory partners, adhering to cGMP and SOP standards.

Qualifications

• Master’s degree in engineering, science, or related field.
• 3+ years of Manufacturing or Operations experience with degree.
• Experience with CAPA and EV, preferably using Veeva Systems.

Responsibilities

• Lead and execute CAPAs and EVs related to biopharmaceutical manufacturing.
• Identify and implement continuous improvement opportunities to improve process efficiency and safety.
• Gather CAPA Applicability responses and ensure timely completion.
• Use project management tools to plan, monitor, and report CAPAs and project progress.
• Communicate with quality, engineering, validation, regulatory, and suppliers.
• Adhere to cGMP, SOPs, and EHS policies.

Skills

Analytical thinking

Problem solving

Communication skills

Independence and collaboration

Education

Master’s degree in engineering or life sciences

Bachelor’s degree + 3 years manufacturing/ops

Associate’s degree + 5 years manufacturing/ops

High school diploma + 10 years manufacturing/ops

Engineering/Science degree or related field

Tools

Veeva Systems

Job description

Aptask Global Workforce (AGW) is seeking a Senior Associate Manufacturing - Onsite for a 6+ month contract in Thousand Oaks, CA. The role leads CAPAs and EVs for Manufacturing Clinical Supply, driving quality and compliance in a cross-functional team.

The candidate will implement continuous improvement, manage projects with PM tools, and ensure timely CAPA ownership while collaborating with quality, engineering, validation, and regulatory partners, adhering to cGMP and SOP standards.