Quality Control Analyst I/II

United States·AlamedaContract to Hiremid

OtherQuality Control AnalystLaboratory & Life Sciences

2 views0 saves0 applied

Apply Now

Quick Summary

Overview

Technical Tools

excel

GeneFab is seeking a Quality Control Analyst I/II to help ensure consistent quality of our cell manufacturing process. You will perform laboratory tests on incoming raw materials, in-process samples, and final product samples before distribution. You will carefully and consistently analyze this data to ensure product specifications are met, or perform peer reviews of other analyses. As part of this role, you will also review current GMP documentation related to SOPs, testing methods, and protocols.

Successfully execute and document laboratory procedures and experiments with great attention to detail

Perform QC testing on raw materials, in-process and final product samples

Assess data to ensure product specifications are met

Assist in reviewing data

Perform technical root-cause investigations for aberrant results and deviations relating to analytical methods

Responsible for raw materials inspection, sampling and testing in support of clinical and commercial products in compliance with GMP requirements.

Collaborate closely with Interdepartmental MSAT and Manufacturing groups to support, execute, and/or provide oversight in the execution of method optimization, characterization, troubleshooting, transfer, and qualification

Perform additional duties as assigned

B.S. degree in biology or related field with experience in cell therapy, immunology, cancer biology, or a closely related field, and 0-3 years (QC Analyst I) or +3 years of industry experience (QC Analyst II)

Experience with relevant technologies with an emphasis on multicolor flow cytometry, MSD, Immunospot, cell culture (e.g., aseptic techniques, cell line expansion), multiplexed immunoassay, NGS, qPCR, and dPCR methods

Experience with relevant QC Microbiological assays is a plus

Experience with assay development, method qualification, and routine testing in GLP and/or GMP environment

Experience with contract laboratories and or CDMO is a plus

Knowledge related to laboratory information management systems (LIMS) and electronic lab notebook record keeping (ELN) is a plus

Proficient in MS Word, Excel, Project, and PowerPoint

Experience with gene and cell therapies or the pharmaceutical industry is a plus

Availability to work extended hours to meet deadlines when necessary

Comfortable in a fast-paced environment with minimal direction and able to adjust workload based on changing priorities

Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of the initial job description

The base salary range for this role is $35-45; starting pay is determined by multiple job-related factors including a candidate’s skills, education and experience level, benchmark, and internal parity

We offer an excellent benefits program including a selection of Medical, Dental and Vision plans, FSA, HSA, Company paid holidays, employee assistance program, commuter benefits, wellbeing resources, perks and more!

Significant growth opportunity as the company expands