Overnight QC Production associate - ClinLab Staffing : Job Details

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

• 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.