Specialist Quality Control
Advanced Bio-Logic Solutions Corp, Thousand Oaks, CA, United States
Location:
Onsite
- Thousand Oaks, CA
Employment Type:
Contingent Worker (Contract, W2)
Contract Length:
12 months (possible extension)
Compensation:
$39/$55 per hour (based on experience)
Summary of the Role
Serve as a System Administrator supporting business processing environments for a big biopharma leader. Oversee installation, configuration, and maintenance of operating systems, servers, and layered products while ensuring compliance. Troubleshoot technical issues, schedule system upgrades, and play a key role in the validation and deployment of GxP laboratory systems in regulated environments.
Key Responsibilities
Install, configure, and maintain operating systems, servers, and ancillary products with compliance to licensing and maintenance agreements
Troubleshoot, respond to escalations, and perform hardware or software repairs as needed
Schedule and oversee hardware and software installations and upgrades
Participate in process engineering activities and facilitate new business SOPs, forms, and manuals for evolving electronic workflows
Participate in system requirement gathering, configuration, and design activities for the new ELN system
Verify and manage site master data
Coordinate ELN Template development and review with site subject matter experts
Support development and review of Operational Qualifications (OQ), User Acceptance Testing (UAT), and Data Migration Verification
Contribute to the review and input of training materials, and support instrument qualification activities at the site
Required Experience & Skills
Extensive experience with GxP laboratory systems and computer systems validation, including hands‑on IQ, OQ, PQ, UAT, and data migration verification for ELN, LIMS, and LMES platforms aligned with GAMP and 21 CFR Part 11 requirements
Proven background in electronic laboratory workflow design, configuration, validation, and deployment for global QC operations in regulated biopharmaceutical environments
Strong expertise in quality systems within biopharmaceutical QC environments, including SOP development, deviation and change control management, CAPA support, audit readiness, and inspection defense
Top 3 Must Have Skills
1. GxP laboratory systems and computer systems validation (IQ, OQ, PQ, UAT, data migration for ELN/LIMS/LMES; GAMP; 21 CFR Part 11)
2. Electronic laboratory workflow configuration, validation, and deployment; electronic procedures/templates; global QC support in biopharma
3. Quality systems expertise: SOP development, deviation/change control, CAPA, audit readiness, inspection defense
Day-to-Day Responsibilities
Install and upgrade software and hardware components per schedule
Troubleshoot escalated technical issues and execute repairs
Lead ELN system process engineering and facilitate new business documentation
Participate in requirements gathering, system design, and configuration
Coordinate with site SMEs for ELN Template development and review
Execute and verify UAT and data migration efforts
Review, develop, and support training materials
Assist in planning and executing site instrument qualifications
Basic Qualifications
Doctorate degree
Masters degree and 2 years of experience
Bachelors degree and 4 years of experience
Associates degree and 8 years of experience
High school diploma / GED and 10 years of experience
This posting is for Contingent Worker, not an FTE
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Onsite
- Thousand Oaks, CA
Employment Type:
Contingent Worker (Contract, W2)
Contract Length:
12 months (possible extension)
Compensation:
$39/$55 per hour (based on experience)
Summary of the Role
Serve as a System Administrator supporting business processing environments for a big biopharma leader. Oversee installation, configuration, and maintenance of operating systems, servers, and layered products while ensuring compliance. Troubleshoot technical issues, schedule system upgrades, and play a key role in the validation and deployment of GxP laboratory systems in regulated environments.
Key Responsibilities
Install, configure, and maintain operating systems, servers, and ancillary products with compliance to licensing and maintenance agreements
Troubleshoot, respond to escalations, and perform hardware or software repairs as needed
Schedule and oversee hardware and software installations and upgrades
Participate in process engineering activities and facilitate new business SOPs, forms, and manuals for evolving electronic workflows
Participate in system requirement gathering, configuration, and design activities for the new ELN system
Verify and manage site master data
Coordinate ELN Template development and review with site subject matter experts
Support development and review of Operational Qualifications (OQ), User Acceptance Testing (UAT), and Data Migration Verification
Contribute to the review and input of training materials, and support instrument qualification activities at the site
Required Experience & Skills
Extensive experience with GxP laboratory systems and computer systems validation, including hands‑on IQ, OQ, PQ, UAT, and data migration verification for ELN, LIMS, and LMES platforms aligned with GAMP and 21 CFR Part 11 requirements
Proven background in electronic laboratory workflow design, configuration, validation, and deployment for global QC operations in regulated biopharmaceutical environments
Strong expertise in quality systems within biopharmaceutical QC environments, including SOP development, deviation and change control management, CAPA support, audit readiness, and inspection defense
Top 3 Must Have Skills
1. GxP laboratory systems and computer systems validation (IQ, OQ, PQ, UAT, data migration for ELN/LIMS/LMES; GAMP; 21 CFR Part 11)
2. Electronic laboratory workflow configuration, validation, and deployment; electronic procedures/templates; global QC support in biopharma
3. Quality systems expertise: SOP development, deviation/change control, CAPA, audit readiness, inspection defense
Day-to-Day Responsibilities
Install and upgrade software and hardware components per schedule
Troubleshoot escalated technical issues and execute repairs
Lead ELN system process engineering and facilitate new business documentation
Participate in requirements gathering, system design, and configuration
Coordinate with site SMEs for ELN Template development and review
Execute and verify UAT and data migration efforts
Review, develop, and support training materials
Assist in planning and executing site instrument qualifications
Basic Qualifications
Doctorate degree
Masters degree and 2 years of experience
Bachelors degree and 4 years of experience
Associates degree and 8 years of experience
High school diploma / GED and 10 years of experience
This posting is for Contingent Worker, not an FTE
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