Quality Control Specialist (Contract)
Pay Rate: Up to $49.84/hour
Duration: Temporary Assignment — August 24, 2026 through December 18, 2026
Hours: Full-Time
Location: San Diego, CA (Onsite)
Summary
We are seeking a detail-oriented Quality Control Specialist to support quality activities, documentation, review processes, issue tracking, and continuous improvement initiatives. In this role, you will work closely with cross-functional teams to help ensure processes and documentation meet established quality standards, procedures, and compliance expectations.
The ideal candidate has experience supporting quality operations, documentation, process execution, or functional projects within a regulated or highly structured environment. Strong attention to detail, organization, analytical thinking, and the ability to manage multiple priorities are essential for success in this role.
What You'll Do
• Support day-to-day quality activities, documentation, reviews, and process execution within the Quality Control function
• Review records, procedures, reports, and supporting documentation for accuracy, completeness, and alignment with established standards
• Coordinate issue tracking, investigations, corrective actions, change records, and other quality events as applicable
• Maintain quality systems, trackers, metrics, and documentation to support operational visibility and inspection or audit readiness
• Partner with cross-functional teams to support compliant execution of processes and timely resolution of quality-related issues
• Assist with process improvement initiatives designed to strengthen quality, efficiency, and consistency
• Support training coordination and updates to quality-related procedures and documentation
• Analyze quality trends and identify potential risks, discrepancies, or areas for improvement
• Provide recommendations and support corrective actions to improve quality outcomes
• Maintain accurate and organized records while ensuring documentation meets established quality standards
What You Bring
• Bachelor's degree in a related scientific, healthcare, business, or technical field, or equivalent combination of education and experience
• 2+ years of relevant experience supporting quality, operations, functional projects, documentation, analysis, or process execution
• Working knowledge of quality systems, documentation practices, issue tracking, and procedural or compliance requirements
• Ability to review records and documentation, identify discrepancies, and support investigations or corrective actions
• Strong organizational skills and exceptional attention to detail
• Ability to follow established procedures while exercising sound judgment when identifying issues or potential risks
• Strong analytical and problem-solving skills with the ability to identify trends and recommend improvements
• Excellent written and verbal communication skills
• Ability to collaborate effectively with cross-functional teams and stakeholders
• Ability to manage multiple priorities and deadlines in a fast-paced environment
Bonus Points If You Have
• Experience working within a regulated industry such as pharmaceutical, biotechnology, healthcare, medical devices, or life sciences
• Experience with quality management systems (QMS) or electronic quality management systems
• Experience supporting audits, inspections, CAPA, deviations, change controls, or other quality processes
• Experience analyzing quality metrics, trends, or operational KPIs
• Experience supporting continuous improvement or process optimization initiatives
TCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation.
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