Quality Control Laboratory Specialist

Quality Control Laboratory Specialist

Location: Tarzana, CA

Onsite Flexibility: Onsite

Contract Details

• Position Type: Contract
• Contract Duration: 12 months
• Pay Rate: $31.00-$32.00 / Hour (USD)
• Shift / Schedule: Monday to Friday - 7:00 AM-3:30 PM (3 days/week); 5:00 AM-1:30 PM (2 days/week); weekend technical support required; schedule is subject to change
• Travel Requirements: Not specified
• Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Job Summary

This client is seeking an energetic and experienced individual with a cell therapy quality control background to join their Quality Control (QC) team. The successful candidate will contribute to the advancement of the product pipeline by playing a crucial role in Quality Control Operations - including sample management, equipment management, and reagent management - in the Quality Control Laboratory. This position is essential for ensuring that the laboratory meets the high standards required for CGMP Quality Control Operations . This position includes weekend technical support and operates on the described shift, which is subject to change.

Key Responsibilities

• Primarily responsible for the receipt, storage, inventory, distribution, and preparation of samples, controls, reagents, and standards used in analytical testing, utilizing paper and computer-based inventory systems.
• Responsible for the operation, organization, and maintenance of Temperature-Controlled Storage Units and ensure that samples, reagents, standards, and controls are stored in appropriate temperature conditions utilizing paper and computer-based asset systems.
• Support the calibration and maintenance activities required for QC equipment using computerised asset management software.
• Complete and document activities in accordance with CGMPs, SOPs, and protocols.
• Perform compendial assays and processing of samples as needed.
• Report deviation events to QC management.
• Contribute to ensuring that the laboratory meets the high standards required for CGMP lot release and stability testing.
• Contribute to the writing and revision of Standard Operating Procedures (SOPs) and other CGMP documentation.
• The position requires a strong background in laboratory practices, general testing methodology, assay troubleshooting, and familiarity with Quality Systems.
• Perform other duties as assigned.
• Ability to follow safety procedures outlined in the Safety, Health and Environmental requirements.

Required Skills

• Strong experience with receipt, storage, inventory control, and distribution of samples and reagents for analytical testing.
• Experience in customer service and strong communication skills.
• Familiar with basic computer applications such as Microsoft Outlook, Word, and Excel.
• Experience with labeling and preparation of reagents, controls, and reference standards.
• Experience operating and maintaining Temperature-Controlled Storage Units, including cryogenic (LN2) freezers.
• Excellent attention to detail, strong communication skills, and the ability to analyze raw data effectively.

Preferred Skills

• Experience in Cell &/or Gene Therapy.

Education Requirements

• Associate's degree, preferably in Biology or equivalent, required.
• Bachelor's degree, preferably in Biology or equivalent, preferred.

Required Experience

• 2-3 years of relevant CGMP laboratory experience (with Associate's degree or equivalent).
• 1-2 years executing routine and non-routine analysis for CGMP compendial assays (Appearance, pH, etc.).

Nice-to-Have Experience

• 1-2 years of relevant CGMP laboratory experience (with Bachelor's degree or equivalent).

Benefits

• Medical, Vision, and Dental Insurance Plans
• 401k Retirement Fund

Important Notes

• Interview Process: 1st round - 30-minute Teams call; 2nd round - onsite interview for one and a half hours, meeting the team and hiring manager.

About the Client

This client is a biopharmaceutical and life sciences organization with operations in strategic locations including the greater Los Angeles area of California. Specializing in cell therapy and advanced biologics, the company employs scientists, quality assurance specialists, research and development professionals, and regulatory affairs experts who collaborate to advance innovative product pipelines. With a strong emphasis on CGMP compliance and scientific rigor, the organization is a growing presence in the cell and gene therapy space.

About GTT

GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking, financial services, technology, life sciences, biotech, utilities, and retail sectors throughout the U.S. and Canada.

Job Number: 26-08149 Industry: Manufacturing & Operations

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