Joulé
Quality Control Associate I
Location: South San Francisco, CA
Type: Contract
Compensation: $25 - $29.26/hr
Job Description
Perform biochemical/immunological and cell‑based assays to support clinical and to‑be‑marketed products.
Support process development, product characterization, stability, and lot release testing in a cGMP environment.
Review and release assay data (electronic and paper‑based), prepare reagents, present results, and monitor assay quality.
Maintain compliance with Good Documentation Practices, ALCOA+ principles, data integrity, routine lab maintenance, 5S, and EHS safety practices.
Job Requirements
B.S. in Biological Sciences with 1‑2 years of relevant Quality Control experience.
Hands‑on experience performing immunological or cell‑based assays.
Experience with aseptic cell culturing and cGMP knowledge (required).
Ability to work independently, manage multiple projects, demonstrate initiative, and maintain exceptional attention to detail.
Effective verbal and written communication skills in a fast‑paced environment.
Proficiency in computer applications, data management, and electronic documentation systems.
Prior experience with GxP‑compliant systems such as Global SoftMax Pro, Single LIMS, and Veeva QMS is highly preferred.
Equal Opportunity Employer System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
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Type: Contract
Compensation: $25 - $29.26/hr
Job Description
Perform biochemical/immunological and cell‑based assays to support clinical and to‑be‑marketed products.
Support process development, product characterization, stability, and lot release testing in a cGMP environment.
Review and release assay data (electronic and paper‑based), prepare reagents, present results, and monitor assay quality.
Maintain compliance with Good Documentation Practices, ALCOA+ principles, data integrity, routine lab maintenance, 5S, and EHS safety practices.
Job Requirements
B.S. in Biological Sciences with 1‑2 years of relevant Quality Control experience.
Hands‑on experience performing immunological or cell‑based assays.
Experience with aseptic cell culturing and cGMP knowledge (required).
Ability to work independently, manage multiple projects, demonstrate initiative, and maintain exceptional attention to detail.
Effective verbal and written communication skills in a fast‑paced environment.
Proficiency in computer applications, data management, and electronic documentation systems.
Prior experience with GxP‑compliant systems such as Global SoftMax Pro, Single LIMS, and Veeva QMS is highly preferred.
Equal Opportunity Employer System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
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