Environmental Monitoring (EM) Core Technician

VIVOS Professional Services, LLC; Houston (TX); On-site; Full time

Job summary

A leading company in pharmaceutical manufacturing is seeking an Environmental Monitoring (EM) Core Technician in Houston. This role involves supporting GMP-compliant manufacturing of clinical-grade viral therapies, maintaining cleanroom conditions, and performing vital environmental monitoring tasks. The ideal candidate should have basic lab experience and a degree in life sciences.

Qualifications

• 1-3 years of relevant experience required.
• Intermediate lab experience in cGMP clinical production environment acceptable.
• Cleanroom experience is a plus.

Responsibilities

• Perform Environmental Monitoring (EM) during GMP viral therapy production.
• Prepare buffers and components; operate steam autoclave.
• Draft and revise documentation including Batch Records and EM forms.

Skills

Basic to intermediate lab experience

Environmental monitoring

Aseptic techniques

Education

Bachelor’s Degree in Life Sciences

High School Diploma

Job description

2 days ago Be among the first 25 applicants

VIVOS Professional Services, LLC provided pay range

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

Base pay range

$23.00/hr - $26.00/hr

Direct message the job poster from VIVOS Professional Services, LLC

Job Title: Environmental Monitoring (EM) Core Technician

Location: Houston, TX (Onsite)

Pay Range: $23-26/hr. on W2

Shifts Available: Day & Night Shifts

• Night Shift: 7:00 PM – 7:30 AM (12-hour rotating schedule: 2 days on, 2 days off, 3 days on, 3 days off)
• Day Shift: 7 AM - 7 : 30 PM (12-hour rotating schedule: 2 days on, 2 days off, 3 days on, 3 days off)
• Training Requirement: Must be available to train on first shift (Monday–Friday, 5 days/week) for the first 4–6 weeks

Qualifications:

• Bachelor’s Degree in Life Sciences preferred
• High School Diploma with intermediate lab experience in a cGMP clinical production environment acceptable
• 1–3 years of relevant experience
• Basic to intermediate lab experience required
• Cleanroom experience and aseptic techniques are a plus

Job Summary:

The EM Core Technician is responsible for supporting GMP-compliant manufacturing of clinical-grade viral therapies by performing environmental monitoring (EM), maintaining cleanroom conditions, and assisting in related laboratory and documentation tasks.

Key Responsibilities:

• Perform Environmental Monitoring (EM) during GMP viral therapy production
• Utilize aseptic technique during cell culture and product purification tasks (as needed)
• Coordinate EM equipment and supply needs with the QC EM team
• Prepare buffers and components; operate steam autoclave
• Operate EM equipment including Solairs, ApexZ50, and active air counters
• Draft, complete, and revise documentation including Batch Records and EM forms
• Operate manual, semi-automated, and automated production equipment
• Support cleanroom maintenance, setup, and stocking

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Contract

Job function

• Job function

  Manufacturing

• Industries

  Pharmaceutical Manufacturing

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