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QA Document Control Specialist (Contract) – BioPhase
Location : San Diego, CA (Hybrid : 1-3 days onsite per week)
Pay Rate : $41 - $45 per hour
BioPhase is seeking a QA Document Control Specialist (Contract) to support our client in the biotechnology sector. This role will focus on managing and improving document control systems, training administration, and quality processes within a GXP-regulated environment. The ideal candidate will have experience with MasterControl, strong organizational skills, and a keen eye for compliance in a biotech or pharmaceutical setting.
Key Responsibilities
Manage controlled documents throughout their lifecycle (creation, formatting, review, approvals, implementation, retention, archival).
Administer the Learning Management System (LMS), including onboarding / offboarding training.
Oversee Electronic Document Management Systems (EDMS), ensuring compliance with GLP, GCP, GMP, and GDPR.
Provide training and technical support for users on system processes.
Track and report document control and training metrics.
Support software upgrades, system troubleshooting, and process improvements.
Ensure compliance with periodic document review SOPs.
Assist with SOP development and quality assurance tasks as needed.
Qualifications
2-4 years of document control experience in biotech or pharma.
Experience working in a GXP, GMP, or GCP environment.
MasterControl experience is required (certification is a plus).
Bachelor’s degree in a scientific discipline (preferred, but not required).
Strong organizational, communication, and time management skills.
Ability to work cross-functionally and support regulatory compliance efforts.
Why Join Us?
Competitive hourly pay : $41 - $45 / hr.
Hybrid work flexibility (1-3 days onsite per week in San Diego).
Opportunity to work in a fast-paced biotech environment with leading industry professionals.
Interested? Apply today to join our team and contribute to meaningful projects in biotech and pharma!