Looking For Your Next Opportunity?
Search Our Open Jobs
QA Document Control Specialist
Clinical Pharmacology
Los Angeles, CA, US
Pay Rate Low: 28 | Pay Rate High: 30
Pay Rate Low: 28 | Pay Rate High: 30
- Added - 27/08/2025
Our client has over 50 years of experience and expertise, provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services.
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:
Qualifications:
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
INDBH
Close
Apply to Job
QA Document Control Specialist