Technician I, Microbiology, Quality Control

ADMA Biologics Inc•South Burlington, VT

33d•Onsite

About The Position

The Technician I, Microbiology, Quality Control performs environmental monitoring and water sampling within controlled manufacturing areas and QC laboratory.

Requirements

Ability to follow the cGMP's and procedures with great attention to detail
Demonstrated ability to achieve goals, overcome obstacles, and meet deadlines
Possess time management skills and be able to balance multiple job assignments at once
Familiarity with microbiological testing is desired.
Self-motivated and able to work autonomously while responsible for multiple priorities.
Strong attention to detail and commitment to data integrity.
Ability to follow SOPs and work in a regulated environment.
Effective communication and teamwork skills.
Ability to gown into controlled manufacturing areas multiple times per day.
Function in areas subject to exposure to infectious material (human-source products), toxic chemicals, chemical fumes/odors, electrical hazards, and temperature extremes within coolers/freezers.
Ability to work flexible shifts, weekends, or holidays as required.
Associate's or Bachelor's degree in a science discipline.
0-3 years of experience in a laboratory setting.

Responsibilities

Perform environmental sampling within the controlled manufacturing areas in accordance with approved Standard Operating Procedures (SOPs) (e.g. viable air, total airborne, and surface test methods).
Perform water, compressed gas, and utility system sampling according to established SOPs.
Ensure calibration and maintenance of monitoring/test equipment are current.
Record, label and transport samples accurately to the laboratory for analysis.
Document results in logbooks, worksheets and electronic systems in compliance with Good Documentation Practices (GDP).
Identify, report and participate in the generation of alert and action-level excursion documentation, as needed.
Maintain awareness of safety, contamination control, and environmental conditions within the manufacturing facility.
Participate in data trending, reporting and continuous improvement initiatives.
Support audit and inspection readiness initiatives.
Perform other duties, as directed by the supervisor/management, to support company directives and initiatives.