Laboratory Technician

Aequor

Houston (TX)

On-site

USD 45,000 - 55,000

Full time

14 days+

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

A leading company in pharmaceutical manufacturing is seeking an Environmental Monitoring Microbiology Technician I for a night shift in Houston. This role involves conducting environmental monitoring tasks to support the production of clinical-grade products. Candidates with a Bachelor's degree in Life Sciences or relevant lab experience are encouraged to apply for this contract position with potential for extension.

Qualifications

Bachelor's degree preferred or high school diploma with relevant lab experience.
Basic lab experience in a cGMP environment preferred.

Responsibilities

Conducts Environmental Monitoring tasks for GMP production.
Prepares buffers and components; operates environmental monitoring equipment.
Coordinates equipment needs with the QC EM team.

Skills

Lab experience

Aseptic technique

Education

Bachelor's Degree in Life Sciences

High school diploma

Job description

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

Base pay range

$20.00/hr - $27.00/hr

Direct message the job poster from Aequor

Title: Environmental Monitoring Microbiology Technician I

Location: Houston, TX

Duration: 01+ year with possibility of extension

Shift: Night Shift - 12-hour rotating shifts - 2 days on, 2 days off, 3 days on, 3 days off

Must be available to train on first shift - 5 days/week for the first 4-6 weeks

Day shift: 7:00 PM - 7:30 AM

Job Summary: The Environmental Monitoring (EM) Core Technician will be responsible for conducting EM tasks in support of production and aseptic processing of clinical-grade products. The core tech will also be responsible for maintaining, stocking, and setting up the clean room environment.

Job Duties:

Participates in the Environmental Monitoring process as part of GMP production of viral therapies
Cell culture and product purification using aseptic technique when required
Coordinates EM equipment needs with QC EM team for manufacturing processes
Drafting, completing, and revising manufacturing documents including Batch Records and EM forms
Buffer and component preparation including operation of steam autoclave
Operation of manual, semi-automated, and automated equipment in support of routine clinical production
Operating environmental monitoring equipment such as Solairs, ApexZ50, active counters

Qualifications:

Bachelor's Degree in Life Sciences preferred. Basic lab experience with a Bachelor's degree or intermediate lab experience within a cGMP clinical production environment, or a high school diploma.
Lab experience preferred.

Seniority level