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Experience in basic molecular biology (RNA,/DNA/plasmid extraction, qPCR and Droplet Digital PCR). Experience in basic molecular biology (RNA,/DNA/plasmid extraction, qPCR and Droplet Digital PCR.
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We're seeking a Document Control Specialist to work at a premier client in Alachua, FL. Sound good? What's a typical day as a Document Control Specialist? Apply to be a Document Control Specialist today.
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The Sr. Manager of Health, Safety, and Environment (HSE) is responsible for providing HSE technical and regulatory support to the Alachua, Florida operational campus which includes the Advanced Development and Manufacturing (ADM) facility, the ADM Expansion Building and the Process Development Laboratory Building.
$171,250 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Knowledge of regulatory requirements governing biopharmaceutical manufacturing, including cGMP, EMA, and ICH guidelines. In-depth knowledge of Drug Substance and Drug Product manufacturing processes, including formulation, process development, scales-up, and technology transfer.
$217,500 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Ensure inter-agency collaboration with principle stakeholders in child and adult protection and domestic violence systems, i.e., DOH, DOE, DJJ, university schools of social work, Ounce of Prevention, child advocates, child advocacy centers, Department of Elder Affairs, etc.
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Systems Technology and Reclamation (STaR) technical roles such as Network and Imaging Lab Technician. These positions will require specific skills in roles such as Graphic Artist, Color Press Operator, Web Press Operator, Binding and Finishing, Ink mixer and Ink Jet Operators etc.
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6 months experience operating industrial, production, or manufacturing equipment/machinery (e.g. Folder, Collator, Inserter, Printing Press) Paid time off benefits include parental leave, family care leave, bereavement, jury duty, and voting.
$35.3 an hourPart-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Experience with IT compliance and regulatory requirements (FDA, GxP, CFR part 11, GDPR). The IT Integration Lead will direct the integration of IT networks, infrastructure, systems and processes for a newly acquired company in compliance with FDA, GxP, and GDPR regulatory requirements.
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A strong understanding of molecular biology techniques for analysis of gene therapy products: to include (but not limited to) PCR, Infectivity, Potency, and various ELISA methods. In addition, review and approve CTL assay development and validation reports, relevant sections of clinical documents pertaining to AAV analytical testing and documentation for submission to regulatory agencies.
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As the only regenerative medicine company that offers a differentiated portfolio of allograft and xenograft biomaterials at scale, RTI provides customers across a diverse set of market segments with leading-edge expertise, scale, and flexibility across end-to-end services including design, development, regulatory support, verification and validation, manufacturing, and supply chain management.
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Milton Hershey School (MHS) is one of the world's best private schools, where students in pre-K through 12th grade from disadvantaged backgrounds receive an exceptional career-focused education with housing, meals, and more—and all costs are covered.
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We are seeking a Regulatory Affairs Specialist to join our team. Assist in hosting audits from various regulators and customers pertaining to Regulatory Affairs issues.
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The Technical Support Specialist will also work closely with our frontline team to introduce new products, assist with commissioning, and deliver all the necessary training. Additionally, the Technical Support Specialist will: Review Continuous Product Improvement cases with machine technical issues, concerns, or suggestions from sales areas, collaborating with Technical Support team members, Engineering, Sales, Product Management and Manufacturing to give accurate technical advice on solutions.
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Cross-Functional Collaboration:Work closely with R&D, regulatory affairs, quality, and commercial teams to ensure clinical program alignment with business objectives. In-depth knowledge of clinical trial design, regulatory requirements, and GCP.Experience with FDA submissions, including INDs, BLAs, PMAs, and/or 510(k)s.
$148,526 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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By utilizing the food service team, this manager is responsible for the efficient execution of all fresh food/ food service programs in compliance with corporate and regulatory guidelines and supporting the General Manager in all facets of running the store.
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regulatory affairs specialist molecular imaging jobs Title: sr specialist in Alachua, FL
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