Quality Control Associate II

Pharmaron • Carlsbad, CA

2d • Onsite

About The Position

The Quality Control Associate II plays a critical role in ensuring the integrity, accuracy, and regulatory compliance of preclinical study data. This individual will serve as a key quality partner across scientific and operational teams, reviewing study documentation, identifying discrepancies, and ensuring adherence to GLP standards, protocols, and internal quality systems. This role offers strong exposure to preclinical research, regulatory frameworks, and cross-functional collaboration, with opportunities to grow into advanced QC, QA, or compliance-focused roles.

Requirements

• B.S. in Life Sciences or related field
• 3–6+ years of experience in Quality Control, Quality Assurance, or regulated laboratory environments
• Strong knowledge of GLP regulations, SOPs, and documentation practices
• Experience reviewing scientific data, study reports, or regulated documentation
• Proficiency in Microsoft Office (Word, Excel, Outlook)
• Experience in CRO, biotech, or pharmaceutical environments
• Familiarity with electronic quality systems (eQCM or similar)

Nice To Haves

• Exposure to preclinical or in vivo studies

Responsibilities

• Perform detailed reviews of study data, reports, and documentation to ensure accuracy, completeness, and GLP compliance
• Verify adherence to study protocols, SOPs, and regulatory requirements
• Identify, document, and follow up on deviations, ensuring timely resolution
• Support and maintain documentation within electronic quality management systems (eQCM)
• Ensure all records meet internal and regulatory standards for audit readiness
• Contribute to continuous improvement of document control and quality processes
• Partner with scientific and operational teams to resolve data discrepancies and improve data quality
• Coordinate training activities to ensure alignment with SOPs and quality expectations
• Work across departments to streamline workflows and enhance efficiency
• Support QC verification for study-related sample shipments
• Manage multiple priorities in a fast-paced, deadline-driven environment
• Contribute to departmental and quality improvement initiatives
• Other duties as determined by management.

Benefits

• Medical, Dental & Vision insurance with significant employer contributions
• Employer-funded Health Reimbursement Account
• Healthcare & Dependent Care Flexible Spending Accounts
• 100% Employer-paid Employee Life and AD&D Insurance, Short and Long Term Disability Insurance
• 401k plan with generous employer match
• Access to an Employee Assistance Program

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees