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Temporary Lab Administrator

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  • Job
    Full-time
    Junior Level
  • Science
  • San Diego

Requirements

  • BS degree in general sciences or an associate degree with equivalent experience.
  • Excellent organizational and communication skills.
  • Proven time management abilities and experience managing a high-volume workflow.
  • Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) background is highly preferred.

Responsibilities

  • Generation of Certificate of Analysis (COA) for GMP and client specific jobs.
  • Receive, verify, track, and stage all test samples that require QC analysis.
  • Receive and assemble data packets from contract labs for review.
  • Perform instrument qualifications and maintenance checks by performing tests including - - Balances, pH, conductivity, and pipettes.
  • Maintain sample management and reagents inventory in a Quality Control environment and order buffers as needed.
  • Daily and weekly maintenance of instruments per SOP and appropriate instrument logs.
  • Perform other functions and duties as required.

FAQs

What is the job title for this position?

The job title is Temporary Lab Administrator.

What company is offering this job?

TriLink BioTechnologies is offering this job.

What team will the Temporary Lab Administrator be a part of?

The Temporary Lab Administrator will be part of the Quality Control team.

What are the primary responsibilities of this role?

The primary responsibilities include generating Certificates of Analysis (COA), managing test samples, assembling data packets from contract labs, performing instrument qualifications and maintenance checks, maintaining sample and reagent inventory, and conducting daily and weekly maintenance of instruments.

What qualifications are required for this position?

A BS degree in general sciences or an associate degree with equivalent experience is required.

What skills are essential for success in this role?

Essential skills include excellent organizational and communication abilities, proven time management skills, and experience managing a high-volume workflow.

Is prior experience in GMP and GLP necessary for this position?

A background in Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) is highly preferred.

What kind of environment should an applicant be familiar with?

Applicants should be familiar with a high-throughput, fast-paced environment.

What specific tasks will involve instrument maintenance?

Tasks involving instrument maintenance include performing instrument qualifications and maintenance checks on equipment such as balances, pH meters, conductivity meters, and pipettes.

Are there any additional duties apart from those listed?

Yes, the role may require performing other functions and duties as required.

Is this position permanent or temporary?

This position is temporary.

Extraordinary science. Everyday miracles.

Science & Healthcare
Industry
501-1000
Employees
2014
Founded Year

Mission & Purpose

Maravai brands set the standard in nucleic acid products and services, enzyme development, and biologics safety testing. From producing revolutionary mRNA technologies that drive infectious disease vaccines, cancer vaccines, and other cell and gene therapies to delivering gold-standard bioprocess impurity detection solutions, Maravai is helping life sciences companies overcome their biggest development and manufacturing challenges to streamline and scale from research through clinical trials to commercialization. For over 35 years, Maravai’s brands have served as proven catalysts for innovative, lifesaving technology for humanity. Across our portfolio of brands, we hold numerous patents and offer more than 1,500 innovative products and services, including CleanCap® technology, CleanAmp® hot start PCR, Antibody Affinity Extraction™, EndonucleaseGTP®, PROTEIN A MIX-N-GO™, MockV®, Sterling™, Glen Pak™, Glen Gel-Pak™. Each of our brands are ISO-9001:2015 certified and have earned hundreds of thousands of citations in peer-reviewed scientific publications.