Core Technician - Viral Therapeutics

Lonza•Houston, TX

1d•Onsite

About The Position

The purpose of this role is to participate in aseptic processing of clinical grade product. Responsible for maintaining and stocking clean room environment, cleaning and up-keep of GMP suites and surrounding supportive areas. Responsible for monitoring temperatures, expiration of materials and calibrated equipment during processing.

Requirements

Basic Lab experience with a bachelor’s degree, or Intermediate Lab experience within a cGMP clinical production environment and a High School Diploma.
Ability to perform aseptic manipulations without causing product contamination.
Ability to read, understand and follow SOP’s.
Ability to stand for up to 6 hours.
Ability to routinely lift up to 50 lbs.

Nice To Haves

Ability to read, understand and follow production schedule.

Responsibilities

Stocks cleanroom suites and supports areas with released inventory.
Supports cleanroom environment maintenance at below alert limits by following established cleaning practice.
Monitors expiry of critical raw materials as needed.
Participate in aseptic processing of clinical grade product.
Maintain and stock clean room environment.
Clean and up-keep of GMP suites and surrounding supportive areas.
Monitor temperatures, expiration of materials and calibrated equipment during processing.
Carry out production processes in a GMP facility, with tasks including cell culture.
Read, understand and follow production schedule.
Perform aseptic manipulations without causing product contamination.
Read, understand and follow SOP’s.
Perform aseptic gowning on a daily basis.