Technician, Quality Control - Day Shift

Orca Bio•Sacramento, CA

3h•Onsite

About The Position

The Technician, Quality Control - Day Shift conducts routine and non-routine testing to ensure the highest quality standards in our cell therapy manufacturing facility. Your work will play a crucial role in maintaining the integrity and safety of our cell therapy products.

Requirements

A.S. or B.S. in a relevant scientific discipline (biology, microbiology, etc.) required
High attention to detail and a commitment to data integrity
Strong organizational, communication, and problem-solving skills
Ability to work both independently and collaboratively in a fast-paced, regulated setting
Flexible and responsive to changing priorities and team needs
Must have visual acuity of 20/20 (corrected or uncorrected) and normal color vision to safely perform critical tasks such as visual inspection of materials, equipment, and labeling, including distinguishing color-coded components in a GMP environment.
Must be able to meet cleanroom gowning requirements, including wearing full gowning (face coverings, gloves, hoods, goggles) for extended periods, as needed.
Use of cosmetics (makeup, painted nails), jewelry, or facial piercings is not permitted in the cleanroom, and any skin conditions that cause shedding must be disclosed.

Nice To Haves

Experience with analytical assays (e.g., flow cytometry, ELISA, PCR)
Familiarity with aseptic technique in a GMP or biotech setting

Responsibilities

Perform a range of basic to moderately complex analytical tests following cGMP guidelines
Test routine and non-routine samples; document results with accuracy and compliance
Maintain, calibrate, and troubleshoot lab equipment to ensure functionality
Prepare reagents and aliquot samples, including aseptic techniques when needed
Monitor and maintain inventory of lab supplies
Support assay transfers, validations, and equipment qualifications
Aliquot samples as required, including aseptic aliquoting
Actively participate in group and project teamwork; project and process improvements
Work cross-functionally with Manufacturing, QC, and QA to resolve issues and implement corrective actions
Follow all cGMP documentation and procedural standards
Perform additional duties as assigned to support the Quality team