Production Technician III

TekWissen•Norcross, GA

21h•Onsite

About The Position

The Production Technician III provides day-to-day operational support across manufacturing areas. The role supports production schedules by preparing bottles, assembling manifolds and other components, performing washroom activities, staging production materials, and maintaining inventory. It also involves weighing, diluting, and verifying chemicals for in-process solutions; ensuring materials, equipment, and tooling are available; and maintaining an organized, clean workspace. The technician follows standard operating procedures and manufacturing records, assists with reviewing documentation such as equipment logs and manufacturing records, and maintains accurate written records. The role requires adherence to safety and compliance requirements, including applicable FDA and ISO standards and OSHA rules for bloodborne pathogens. The technician may be cross-trained to support other production areas and is responsible for training on assigned procedures.

Requirements

5–7 years of work experience.
Ability to lift and carry up to 50 pounds or more without assistance.
Ability to work on feet for long durations.
Ability to operate heavy equipment and use an autoclave.
Ability to work with weights and measurements when preparing in-process solutions.
Ability to follow GMP documents, safety requirements, and applicable FDA and ISO standards.

Responsibilities

Fulfill daily and weekly production support schedules, adapting to schedule and personnel changes to meet customer needs and delivery requirements.
Assemble bottle preparation for manufacturing use, manifolds, and other components.
Perform washroom activities, stage and set up bottles for production, and maintain inventory.
Weigh, dilute, and verify chemicals for in-process solutions using weights and measurements.
Ensure required materials, equipment, and tooling are available and maintain inventory.
Train on all assigned procedures and be cross-trained to assist other production areas or departments as needed.
Maintain an organized and clean workspace.
Assist with reviewing documentation for assigned functions, including equipment logs and manufacturing records.
Follow GMP documents, including SOPs and manufacturing records, with strict adherence to safety and compliance requirements.
Maintain ongoing FDA compliance and follow OSHA safety regulations for bloodborne pathogens.
Create legible and accurate written records.
Cooperate with coworkers and supervisors or managers in other departments, receive direction from superiors, and follow the Client RITA values.