Lab Technician

Collabera; Irvine (CA); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading company in the pharmaceutical and biotechnology sectors is hiring a Laboratory Technician in Irvine, CA. The role involves managing laboratory equipment, ensuring compliance with GMP regulations, and coordinating vendor services. Ideal candidates will have a BS in molecular biology or biochemistry and relevant experience in a regulated environment.

Qualifications

• At least three years of relevant experience in a GMP regulated environment.

Responsibilities

• Manages laboratory equipment and ensures GMP compliance.
• Coordinates vendor maintenance and calibration services.
• Reviews vendor documentation for accuracy.

Skills

cGMP

FDA regulations

EMA GMP regulation

molecular biology

biochemistry

Education

BS in molecular biology

BS in biochemistry

Job description

1 day ago Be among the first 25 applicants

This range is provided by Collabera. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$30.00/hr - $32.00/hr

Direct message the job poster from Collabera

Creating the Next Together | #Hiring for #Pharmaceuticals, #Biotechnology, and #MedicalDevice roles with Fortune 500 clients

To discuss more about this job opportunity, please reach out to Himanshu Kumar Singh(LinkedIn URL - https://www.linkedin.com/in/himanshu-kumar-singh-57b782258/), email your updated resume at Email - [e-mail] or give me a call at [phone]. Thank you!

Pay Rate: $30 - $32/hour

Location: Irvine, CA 92612

Job Description:

• Manages and ensures proper functioning and GMP compliance of laboratory equipment.
• Coordinates vendor maintenance, calibration and validation services.
• Reviews vendor documentation for accuracy and completeness and completes associated work orders in the asset management system.
• Performs and documents equipment out of tolerance investigations.
• Ensures equipment information and vendor contracts are updated in the asset management system.
• Serves as point of contact for lab personnel and external vendors regarding equipment-related issues.

Required Skills:

• Strong working knowledge of cGMP, FDA and EMA GMP regulation and ICH guidance documents.
• Experienced in GMP regulated drug development environment.
• Must possess a BS in molecular biology, biochemistry, or related field with at least three years of relevant experience.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Contract

Job function

• Job function

  Research and Analyst

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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