QA Specialist II: OOS & Deviation Excellence

Dawar Consulting; El Segundo (CA); On-site; USD 50,000 - 71,000; Full time

Benefits offered by this job

Medical Benefits

Paid Sick Leave

401K

Job summary

Dawar Consulting seeks a Quality Specialist II for OOS deviation & compliance in El Segundo, CA. This long-term contract role balances QA oversight with regulatory alignment to GMP standards.

The ideal candidate will manage deviations, CAPAs, change controls, and quality events while ensuring timely, accurate documentation and cross-functional collaboration with Manufacturing, QA, and Engineering teams.

Qualifications

• Master's degree in Biological Sciences or related field or equivalent experience.
• Bachelor's degree with 2+ years of relevant experience, or
• Associate degree with 4+ years of relevant experience, or
• High School diploma with 5+ years of relevant experience.

Responsibilities

• Provide QA oversight and approval for deviations, OOS investigations, CAPAs, change controls, and quality events.
• Ensure quality records are initiated, investigated, documented and closed within timelines.
• Escalate deviations and quality issues per procedures.
• Support resolution of manufacturing, environmental, facility, equipment, and material quality issues.
• Collaborate with Manufacturing, QA, Engineering and cross-functional teams.
• Support QA activities during campaigns, including occasional weekends or nights.
• Maintain compliance with GMP and regulatory requirements.

Skills

QA oversight

Deviations

OOS investigations

CAPAs

Change Controls

Quality events

Cross-functional collaboration

Documentation

Education

Master's degree in Biological Sciences

Bachelor's degree + 2+ years experience

Associate degree + 4+ years experience

High School diploma + 5+ years experience

Job description

Dawar Consulting seeks a Quality Specialist II for OOS deviation & compliance in El Segundo, CA. This long-term contract role balances QA oversight with regulatory alignment to GMP standards.

The ideal candidate will manage deviations, CAPAs, change controls, and quality events while ensuring timely, accurate documentation and cross-functional collaboration with Manufacturing, QA, and Engineering teams.