Production Technician III

TekWissen•Norcross, GA
•Onsite

About The Position

The Production Technician III provides day-to-day operations support for all manufacturing areas. The role supports production schedules and customer deliveries by preparing bottles, assembling manifolds and other components, performing washroom activities, staging production supplies, and maintaining inventory. It also involves weighing, diluting, and verifying chemicals for in-process solutions. The technician helps ensure materials, equipment, and tooling are available, assists with documentation review, and may be cross-trained to support other production areas. The position requires following GMP documentation, safety and compliance procedures, and applicable FDA and ISO standards, including OSHA regulations for bloodborne pathogens. This is a three-month temporary, onsite assignment in Norcross, Georgia.

Requirements

  • 5–7 years of work experience.
  • Ability to lift and carry up to 50 pounds or more without assistance.
  • Ability to stand and 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 documentation, safety procedures, and applicable compliance standards.

Responsibilities

  • Fulfill the daily and weekly production support schedule, adapting to schedule and personnel changes to meet internal and external customer needs and delivery requirements.
  • Assemble bottle preparation items 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 materials, equipment, and tooling are available as required and maintain inventory.
  • Complete training on assigned procedures and cross-train 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.
  • Support ongoing FDA compliance and follow OSHA safety regulations for bloodborne pathogens.
  • Understand and follow applicable FDA and ISO standards and the consequences of non-conformance.
  • Create legible and accurate written records.
  • Work cooperatively with coworkers and supervisors or managers in other departments, receive direction from superiors, and follow RITA values.
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