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Sofie Co.

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QC/Production Associate I

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Description:

QC/Production Associate I

Title | QC/Production Associate I

Location | Kansas City, MO

Department | Network Operations

Reports To | Facility Manager

Compensation Range | $28 - $30/hr

Work Schedule | Tuesday through Saturday

Overview

The QC/Production Associate I will operate the radiosynthesizers for the production of drug product, as well as operate analytical equipment for the quality control of drug product.

Essential Duties and Responsibilities

  • Perform FDG and NaF synthesis according to SOFIE Standard Operating Procedures (SOPs):

  • Ensure all materials/reagents are accepted according to SOPs and within expiry

  • Ensure all equipment is appropriately qualified prior to use

  • Operate the synthesis unit according to SOPs

  • Learn the basic operational principles of the synthesis unit and assist in routine maintenance of the synthesis unit

  • Perform FDG and NaF quality control (QC) processes according to SOPs:

  • Assist with basic maintenance of QC equipment

  • Ensure all equipment is appropriately calibrated and qualified prior to use

  • Operate the QC equipment according to SOPs

  • Ensure completion of applicable cGMP documentation.

  • Assist with inventory management:

  • Maintain production/QC/cleaning supply levels as appropriate

  • Assist with inventory reporting

  • Perform material acceptance according to SOPs

  • Communicate with local and Network support resources to troubleshoot equipment, production, or QC issues.

  • Perform basic computer-controlled cyclotron operations for FDG and NaF production under the advisement of site Cyclotron and Facility Engineer.

  • Maintain a clean and safe working environment.

  • Perform radiation safety duties according to SOFIE’s Corporate Radiation Compliance Program and site licensing requirements.

  • Maintain all qualification and validation requirements for entering ISO classified area.

  • Clean classified and non-classified areas according to SOPs.

  • Perform environmental monitoring of classified areas according to SOPs.

  • Report manufacturing metrics into data repository as required.

  • Complete cGMP documents as required and assist site and corporate Quality Assurance including, but not limited to:

  • Investigations

  • Corrective and Preventative Actions

  • Deviations

  • Out of Specifications

  • No or Atypical Yields

  • Manufacturing and QC Records

  • Logbooks

  • Attend internal meetings as required.

  • Other assigned duties as required.

Qualifications

  • High school diploma required; associates degree in chemistry, engineering, or natural sciences preferred.

  • Technical experience with computer-controlled automation preferred.

  • Efficient in the use of MS Office Suite required.

  • Ability to work various shifts and weekends required.

  • Ability to be detail-oriented, accountable, patient, organized, and work in a team environment required.

  • Ability to communicate professionally with colleagues and customers, have excellent attention to detail, and be dependable and responsible in a fast-paced, highly technical environment required.

  • Ability to lift ~50 lbs. required.

  • Up to 5% travel required.

Apply

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