Quality Assurance Specialist

Kelly Services; South San Francisco (CA); On-site; USD 55,000 - 58,000; Full time

Job summary

Kelly Science & Clinical in South San Francisco is seeking a Quality Assurance Specialist for a 6-month contract onsite. You will support ongoing manufacturing operations on the production floor, ensuring adherence to SOPs and cGXP requirements.

The role involves reviewing batch records, supporting deviations and quality events, and assisting with raw material release to keep production compliant and efficient in a fast-paced environment.

Qualifications

• Quality Assurance professional with manufacturing experience.
• Knowledge of cGMP standards and compliant documentation.
• Experience reviewing batch records and handling deviations.

Responsibilities

• Provide real-time QA support to day-to-day manufacturing activities, ensuring operations are executed in alignment with SOPs and cGMP.
• Review batch records, production logs, and related documents for accuracy and compliance with cGMP.
• Support deviations and quality events investigations, including root cause analysis and timely resolution.
• Assist with review and release of raw materials for manufacturing.

Skills

QA

cGMP

Deviation handling

Documentation

Root cause analysis

Batch records review

Job description

.Kelly® Science & Clinical is seeking a Quality Assurance Specialist for a 6-month contract opportunity with one of our clients, a biotechnology company in South San Francisco that has pioneered cell therapy manufacturing solutions. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Position type: 6-month contract

Workplace: Onsite in South San Francisco, CA

Pay Range: $40-42 per hour

Are you passionate about bringing the next generation of cell therapies to patients and ensuring the highest standards of product quality? We are seeking a dedicated and detail-driven Quality Assurance Specialist to join a leading, mission-focused biotechnology company dedicated to advancing cell therapy manufacturing. This is a contract position employed via a staffing partner, and you will play a critical role onsite in South San Francisco as part of our dynamic team.

About the Opportunity

As a Quality Assurance Specialist, you will directly support ongoing manufacturing operations, serve as a key resource for quality on the production floor, and help drive compliance and continuous improvement across cGMP operations. This hands‑on role offers the unique opportunity to gain comprehensive experience in quality operations, documentation management, deviation handling, and cross‑functional collaboration, all within an innovative and fast‑paced environment at the forefront of cellular therapeutics.

Responsibilities

• Provide real-time QA support to day‑to‑day manufacturing activities, ensuring operations are executed in alignment with approved Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGxP).
• Review batch records, production logs, and associated documents for accuracy, completeness, and compliance with cGMP requirements.
• Support the identification, documentation, and investigation of deviations and quality events, including root cause analysis and timely resolution.
• Assist with the review and release of raw materials for manufacturing.
• Conduct routine QA walkthroughs of the manufacturing floor, escalating and addressing quality events as appropriate....