Astrix Technology
QA Document Control Specialist
Astrix Technology, Los Angeles, California, United States, 90079
QA Document Control Specialist
Clinical Pharmacology
Los Angeles, CA, US
Title:
Quality Assurance Document Control Specialist(Contract)
Location:
Fully Onsite – Torrance, CA
Schedule:
Mon – Fri 8-5pm
Pay rate:
$28–30/hr
Contract:
3 months with potential for extension
The QA Document Control Specialist will manage document control activities to ensure compliance with GMP and regulatory requirements. Responsibilities include reviewing, processing, and releasing controlled documents (SOPs, batch records, protocols, reports, specifications), maintaining records management systems, and supporting audits. This role requires collaboration across departments and contribution to process improvement initiatives.
Key Responsibilities:
Review and process controlled documents via Master Control
Manage records, logbooks, certificates, and archival processes
Create/revise product labels and specifications
Support regulatory/customer audits and quality system improvements
Participate in cross-site process harmonization and system implementation
Qualifications:
Bachelor’s degree in Chemistry, Biology, or related field
2+ years of QA document control experience in GMP biotech/pharma
Strong communication, organization, and multitasking skills
Proficiency with Microsoft Office; experience with Master Control preferred
Detail-oriented, proactive, and able to work independently or in teams
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
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Clinical Pharmacology
Los Angeles, CA, US
Title:
Quality Assurance Document Control Specialist(Contract)
Location:
Fully Onsite – Torrance, CA
Schedule:
Mon – Fri 8-5pm
Pay rate:
$28–30/hr
Contract:
3 months with potential for extension
The QA Document Control Specialist will manage document control activities to ensure compliance with GMP and regulatory requirements. Responsibilities include reviewing, processing, and releasing controlled documents (SOPs, batch records, protocols, reports, specifications), maintaining records management systems, and supporting audits. This role requires collaboration across departments and contribution to process improvement initiatives.
Key Responsibilities:
Review and process controlled documents via Master Control
Manage records, logbooks, certificates, and archival processes
Create/revise product labels and specifications
Support regulatory/customer audits and quality system improvements
Participate in cross-site process harmonization and system implementation
Qualifications:
Bachelor’s degree in Chemistry, Biology, or related field
2+ years of QA document control experience in GMP biotech/pharma
Strong communication, organization, and multitasking skills
Proficiency with Microsoft Office; experience with Master Control preferred
Detail-oriented, proactive, and able to work independently or in teams
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
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