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Nesco Resource · 2 days ago

Analytical Development/Quality Control Associate

South San Francisco, CA

Full-time

Onsite

Entry Level

$30/hr - $35/hr

1+ years exp

Nesco Resource is a company that specializes in providing staffing solutions, and they are seeking an Analytical Development/Quality Control Associate to conduct quality control testing on products and materials. The role involves analyzing test results, ensuring compliance with GMP and regulatory standards, and documenting quality control procedures and findings.

ConsultingHuman ResourcesStaffing Agency

Responsibilities

Conduct quality control testing on products and materials

Analyze test results and report deviations

Ensure compliance with GMP and regulatory standards

Document quality control procedures and findings

Assist in troubleshooting and root cause analysis

Perform biochemical/immunological and cell-based assays in support of clinical and to-be-marketed products

Support process development, product characterization, stability, and lot release testing with established procedures in a cGMP environment

Routine execution of sample preparation and testing

Compliance review and release of assay data (electronic and paper-based)

Preparing reagents

Presenting results

Monitoring assay quality

Demonstrating Good Documentation Practices

Demonstrating ALCOA+ principles

Data integrity

Routine lab maintenance

Following EHS safety practices

Qualification

Immunological assaysCell-based assaysAseptic cell culturingData managementElectronic documentationLaboratory testingGMP complianceEHS safety practicesBiological Sciences degreeBenchlingFACSDiva/FACSLyricFlowJoSoftMax ProSingle LIMSVeeva QMSProblem-solvingCommunication skillsAttention to detailTeamworkInitiativeFast-paced environmentDocumentation Practices

Required

B.S. in Biological Sciences with 1-5 years of relevant laboratory experience

Hands-on experience with performing immunological or cell-based assays including ELISA, PCR, cell killing, and flow cytometry assays

Experience with aseptic cell culturing is required

Ability to work independently as well as with a team, handle multiple projects, demonstrate initiative while maintaining exceptional attention-to-detail

Demonstrate effective verbal and written communication skills

Ability to work in a fast paced environment

Required proficiency in computer applications, data management, and electronic documentation systems

Preferred

Prior experience with Benchling, Client FACSDiva/FACSLyric, and FlowJo along with GxP-compliant systems such as global SoftMax Pro, Single LIMS, and Veeva QMS is highly preferred

Experience with laboratory testing preferred