QC​/Production Associate III

Description:

QC/Production Associate III Title | QC/Production Associate III Location | Totowa,NJ Department | Network Operations Reports To | Facility Manager Overview The QC/Production Associate III will operate and maintain the radio synthesizers for the production of drug product, as well as operate and maintain analytical equipment for the quality control of drug product. They will also aid the Facility Manager in training of QC/Production personnel as applicable.

Essential Duties and Responsibilities Perform FDG, NaF, and 1-2 other products’ 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 Operate a semi-preparative HPLC system Learn the basic operational principles of the synthesis unit and semi-preparative HPLC and perform routine maintenance of the synthesis unit and semi-preparative HPLC Perform FDG, NaF, and 1-2 other products’ quality control (QC) processes according to SOPs:
Perform basic maintenance and qualification of QC equipment Ensure all equipment is appropriately calibrated and qualified prior to use Operate the QC equipment according to SOPs Prepare reagents for QC Perform troubleshooting of QC equipment under advisement of Corporate QC Department or others Ensure completion of applicable cGMP documentation. Perform inventory management:
Maintain production/QC/cleaning supply levels as appropriate Perform 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, NaF, and 1-2 other products’ 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 Assist with training of QC/Production Associate I personnel. Attend internal meetings as required. Other assigned duties as required. Qualifications High school diploma required; associates degree in chemistry, engineering, or natural sciences preferred. 6-years’ experience in radiopharmaceutical manufacturing and quality control required. Technical experience with computer-controlled automation required.

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 10% travel required.