About The Position

This Compounding role performs functions associated with cGMP manufacturing operations within a biologics production facility. The technician works with engineers on setup and calibration tasks and performs rework and quality testing related to the production of parts, components, and final materials. The role uses programs such as LIMS, SAP, and automated control systems to collect and evaluate operating data, supporting on-line adjustments to products, instruments, or equipment. The technician determines and may assist in developing methods and procedures to control or modify the manufacturing process. The position works under close supervision, completing routine assignments with limited judgment and receiving detailed instructions. The schedule is B2 Shift: 5:45 p.m.–6:30 a.m., Wednesday through Friday and every other Saturday.

Requirements

  • High school diploma or GED.
  • At least 2 years of experience, or equivalent experience; alternatively, an associate degree in science with at least 1 year of relevant experience, or a bachelor's degree with 0 years of relevant experience.
  • Ability to acquire job skills and learn company policies and procedures to complete routine tasks.
  • Ability to recognize deviations from accepted practices.

Responsibilities

  • Ship finished materials.
  • Maintain inventory levels.
  • Sample in-process and raw materials.
  • Run the glass washer and autoclave.
  • Prepare buffers and media.
  • Prepare equipment using CIP/SIP.
  • Perform cell culture activities from vial thaw through production scale.
  • Perform column chromatography.
  • Perform tangential flow filtration.

Benefits

  • Paid time off, including vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) for eligible employees.
  • Eligibility to participate in short-term incentive programs.
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