Core Technician I

Planet Pharma; Houston (TX); On-site; USD 50,000 - 65,000; Full time

Job summary

A leading biotechnology company in Houston is seeking an Environmental Monitoring Core Technician to support the production of clinical-grade products. The role involves conducting environmental monitoring tasks, maintaining the cleanroom environment, and performing cell culture as needed. Candidates should have a Bachelor's degree in Life Sciences and lab experience, alongside strong organizational and communication skills. The company offers a supportive work environment and expects dedication to team-oriented projects.

Qualifications

• A Bachelor's degree in Life Sciences is preferred.
• 1-3 years of lab experience in a clinical environment.
• Ability to pass Class 10,000 gowning qualification.

Responsibilities

• Support aseptic processing of clinical-grade products.
• Perform environmental monitoring tasks.
• Draft and revise manufacturing documentation.

Skills

Aseptic technique

Cell culture and serological methods

Microsoft Office proficiency

Organizational skills

Effective communication skills

Education

Bachelor’s Degree in Life Sciences

High School Diploma

Tools

Environmental monitoring equipment

Steam autoclave

Job description

Overview

Must be available to train on first shift, 5 days per week, for the first 4–6 weeks.

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 and a High School Diploma
• Lab experience preferred
• 1–3 years of experience

Job Summary

The Environmental Monitoring (EM) Core Technician supports production and aseptic processing of clinical-grade products by performing environmental monitoring tasks. This role is also responsible for maintaining, stocking, and setting up the cleanroom environment.

Key Responsibilities

• Participate in the Environmental Monitoring (EM) process as part of GMP production of viral therapies
• Perform cell culture and product purification using aseptic techniques when required
• Coordinate EM equipment needs with the QC EM team for manufacturing processes
• Draft, complete, and revise manufacturing documentation, including batch records and EM forms
• Prepare buffers and components, including operation of steam autoclave
• Operate manual, semi-automated, and automated equipment in support of routine clinical production
• Operate environmental monitoring equipment such as Solairs, Apex Z50, and active counters

Required Skills

• Aseptic technique; experience in cell culture and serological methods preferred
• Ability to pass Class 10,000 gowning qualification
• Computer software proficiency, including Microsoft Office
• Strong organizational, recordkeeping, time management, and multitasking skills
• Effective written and verbal communication skills
• Team-oriented with the ability to work independently and demonstrate a strong work ethic