{"schemaVersion":"jobsearcher.job.v1","id":"0da26a2e149e47cb3f7a0439","url":"https://jobsearcher.com/jobs/0da26a2e149e47cb3f7a0439","canonicalUrl":"https://jobsearcher.com/jobs/0da26a2e149e47cb3f7a0439","title":"QC Production Associate","description":"Description:\n\nJoin our team as a QC/Production Associate I, where you’ll play a key role in producing life-changing drug products and ensuring their quality through hands-on work with advanced radiosynthesizers and analytical equipment.\n\n*QC/Production Associate I*\n\n*Title *| QC/Production Associate I\n\n*Department *| Network Operations\n\n*Reports To* | Facility Manager\n\n*Compensation | *$27-$30/hr\n\n*Overview*\n\nThe 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.\n\n*Essential Duties and Responsibilities*\n\n* Perform FDG and NaF synthesis according to SOFIE Standard Operating Procedures (SOPs):\n* Ensure all materials/reagents are accepted according to SOPs and within expiry\n* Ensure all equipment is appropriately qualified prior to use\n* Operate the synthesis unit according to SOPs\n* Learn the basic operational principles of the synthesis unit and assist in routine maintenance of the synthesis unit\n* Perform FDG and NaF quality control (QC) processes according to SOPs:\n* Assist with basic maintenance of QC equipment\n* Ensure all equipment is appropriately calibrated and qualified prior to use\n* Operate the QC equipment according to SOPs\n* Ensure completion of applicable cGMP documentation.\n* Assist with inventory management:\n* Maintain production/QC/cleaning supply levels as appropriate\n* Assist with inventory reporting\n* Perform material acceptance according to SOPs\n* Communicate with local and Network support resources to troubleshoot equipment, production, or QC issues.\n* Perform basic computer-controlled cyclotron operations for FDG and NaF production under the advisement of site Cyclotron and Facility Engineer.\n* Maintain a clean and safe working environment.\n* Perform radiation safety duties according to SOFIE’s Corporate Radiation Compliance Program and site licensing requirements.\n* Maintain all qualification and validation requirements for entering ISO classified area.\n* Clean classified and non-classified areas according to SOPs.\n* Perform environmental monitoring of classified areas according to SOPs.\n* Report manufacturing metrics into data repository as required.\n* Complete cGMP documents as required and assist site and corporate Quality Assurance including, but not limited to:\n* Investigations\n* Corrective and Preventative Actions\n* Deviations\n* Out of Specifications\n* No or Atypical Yields\n* Manufacturing and QC Records\n* Logbooks\n* Attend internal meetings as required.\n* Other assigned duties as required.\n\n*Qualifications*\n\n* High school diploma required; associates degree in chemistry, engineering, or natural sciences preferred.\n* Technical experience with computer-controlled automation preferred.\n* Efficient in the use of MS Office Suite required.\n* Ability to work various shifts and weekends required.\n* Ability to be detail-oriented, accountable, patient, organized, and work in a team environment required.\n* 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.\n* Ability to lift ~50 lbs. required.\n* Up to 5% travel required.\n\nJob Type: Full-time\n\nPay: $27.00 - $30.00 per hour\n\nBenefits:\n* 401(k)\n* 401(k) matching\n* Dental insurance\n* Health insurance\n* Health savings account\n* Life insurance\n* Paid time off\n* Relocation assistance\n* Retirement plan\n* Vision insurance\n\nExperience:\n* TLC: 1 year (Preferred)\n* GC: 1 year (Preferred)\n* HPLC: 1 year (Required)\n\nLicense/Certification:\n* RPH License (Preferred)\n\nShift availability:\n* Overnight Shift (Required)\n\nAbility to Commute:\n* Miami, FL 33134 (Required)\n\nWork Location: In person","company":"Sofie","rawCompany":"sofie","city":"Miami","state":"FL","isRemote":false,"isActive":false,"createdAt":"2026-08-27T12:47:34.141Z","occupations":[{"code":"19-4031.00","title":"Chemical Technicians","slug":"chemical-technicians"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"19-2031.00","title":"Chemists","slug":"chemists"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325998","title":"All Other Miscellaneous Chemical Product and Preparation Manufacturing","slug":"all-other-miscellaneous-chemical-product-and-preparation-manufacturing"},{"code":"325413","title":"In-Vitro Diagnostic Substance Manufacturing","slug":"in-vitro-diagnostic-substance-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"QC Production Associate","description":"Description:\n\nJoin our team as a QC/Production Associate I, where you’ll play a key role in producing life-changing drug products and ensuring their quality through hands-on work with advanced radiosynthesizers and analytical equipment.\n\n*QC/Production Associate I*\n\n*Title *| QC/Production Associate I\n\n*Department *| Network Operations\n\n*Reports To* | Facility Manager\n\n*Compensation | *$27-$30/hr\n\n*Overview*\n\nThe 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.\n\n*Essential Duties and Responsibilities*\n\n* Perform FDG and NaF synthesis according to SOFIE Standard Operating Procedures (SOPs):\n* Ensure all materials/reagents are accepted according to SOPs and within expiry\n* Ensure all equipment is appropriately qualified prior to use\n* Operate the synthesis unit according to SOPs\n* Learn the basic operational principles of the synthesis unit and assist in routine maintenance of the synthesis unit\n* Perform FDG and NaF quality control (QC) processes according to SOPs:\n* Assist with basic maintenance of QC equipment\n* Ensure all equipment is appropriately calibrated and qualified prior to use\n* Operate the QC equipment according to SOPs\n* Ensure completion of applicable cGMP documentation.\n* Assist with inventory management:\n* Maintain production/QC/cleaning supply levels as appropriate\n* Assist with inventory reporting\n* Perform material acceptance according to SOPs\n* Communicate with local and Network support resources to troubleshoot equipment, production, or QC issues.\n* Perform basic computer-controlled cyclotron operations for FDG and NaF production under the advisement of site Cyclotron and Facility Engineer.\n* Maintain a clean and safe working environment.\n* Perform radiation safety duties according to SOFIE’s Corporate Radiation Compliance Program and site licensing requirements.\n* Maintain all qualification and validation requirements for entering ISO classified area.\n* Clean classified and non-classified areas according to SOPs.\n* Perform environmental monitoring of classified areas according to SOPs.\n* Report manufacturing metrics into data repository as required.\n* Complete cGMP documents as required and assist site and corporate Quality Assurance including, but not limited to:\n* Investigations\n* Corrective and Preventative Actions\n* Deviations\n* Out of Specifications\n* No or Atypical Yields\n* Manufacturing and QC Records\n* Logbooks\n* Attend internal meetings as required.\n* Other assigned duties as required.\n\n*Qualifications*\n\n* High school diploma required; associates degree in chemistry, engineering, or natural sciences preferred.\n* Technical experience with computer-controlled automation preferred.\n* Efficient in the use of MS Office Suite required.\n* Ability to work various shifts and weekends required.\n* Ability to be detail-oriented, accountable, patient, organized, and work in a team environment required.\n* 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.\n* Ability to lift ~50 lbs. required.\n* Up to 5% travel required.\n\nJob Type: Full-time\n\nPay: $27.00 - $30.00 per hour\n\nBenefits:\n* 401(k)\n* 401(k) matching\n* Dental insurance\n* Health insurance\n* Health savings account\n* Life insurance\n* Paid time off\n* Relocation assistance\n* Retirement plan\n* Vision insurance\n\nExperience:\n* TLC: 1 year (Preferred)\n* GC: 1 year (Preferred)\n* HPLC: 1 year (Required)\n\nLicense/Certification:\n* RPH License (Preferred)\n\nShift availability:\n* Overnight Shift (Required)\n\nAbility to Commute:\n* Miami, FL 33134 (Required)\n\nWork Location: In person","datePosted":"2026-08-27T12:47:34.141Z","dateModified":"2026-08-27T12:47:34.141Z","hiringOrganization":{"@type":"Organization","name":"Sofie","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Miami","addressRegion":"FL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"0da26a2e149e47cb3f7a0439"},"url":"https://jobsearcher.com/jobs/0da26a2e149e47cb3f7a0439"}}