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SUBSIDIARY: Health Promotion Council (HPC)JOB OVERVIEW:The Assistant Director of Tobacco Prevention & Control is responsible for ensuring the quality and innovation of efforts within the Southeastern Pennsylvania Tobacco Control Project, identifying and pursuing fee-for-service projects and grant funding opportunities, identifying and building relationships with new partners, and integrating tobacco prevention and control efforts with other PHMC initiatives.
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Support technical problem solving for issues pertaining to GMP Quality Control. Perform daily GMP Quality Control laboratory testing activities at the iCTC facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations.
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Develop phase-appropriate analytical strategies, including characterization of CGT products, analytical method development or transfer, qualification/validation, specification development, quality control testing in a cGMP environment, stability studies, quality comparability, reference standard etc.
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Prepare erosion and sedimentation control/NPDES plans and post construction stormwater management designs in accordance with State best management practices/regulations. Individual should possess a strong knowledge of stormwater, erosion and sediment control, water and sewer design principles and should be able to interpret and apply municipal land use ordinances.
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Corporate Controller is experienced in leading global corporate accounting, control and enablement of efficient global accounting operations to support business and growth in an US headquartered multi-national enterprise across NAR, EMEA, LATAM and APAC regions.
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Serve as QA lead for quality system elements including Document Control, Training, Deviation Management, Internal and External Inspection, Supplier Management, Risk Management, Complaints, Recalls, etc.
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Required Education, Skills, and Knowledge Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Preferred (3) years of experience in the biopharmaceutical industry within a cGMP Quality Control roleExperience with different operational excellence concepts including (but not limited to) lean labs, lean practitioner, tier governance, coaching kata, gemba walks, job instruction, Kaizen, A3 problem solving, change management, leader standard work.
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One of Insight Global's large healthcare clients is looking for a Medical Technologist (MT) or Medical Laboratory Technologist (MLT) to join their team in Camden, NJ. The day-to-day responsibilities for this role include performing proper maintenance of chemical equipment, processing samples, the performance of routine and STAT laboratory testing/analysis, and quality control and reporting.
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Client Advocate is responsible for providing renewal quotation on all property, casualty and surety policies/contracts currently written through ECBM. Responsibilities Service clients on a book of assigned business in accordance with ECBM service and quality management standards and procedures.
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There are opportunities for personal and professional growth by serving on committees including GME, peer review, pharmacy and therapeutics, quality control, and credentialing, to name a few.
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Quality Assurance : Ensure data integrity and accuracy, conduct quality control checks, and adhere to Good Clinical Practice (GCP) guidelines and SOPs. Statistical Programming : Develop, validate, and maintain statistical programs using SAS or other software to support data analysis and reporting.
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We use an email quality control service to maintain security and a remove and dead address filter. Come join a company focused on growth by adding talented techs to their staff and providing highest quality certified services.
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Quality control of all Nuclear Medicine equipment. Follows all NRC and NJDEP regulations regarding radiation safety. Current ARRT - American Registry Radiology Tech License or. Acquisition and processing of all Nuclear Medicine exams.
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The Quality Control Specialist, Sterility Assurance will have substantial experience Analyzing QC sterility assurance program in a Pharmaceutical or Biotechnology environment. Minimum three (3) years of experience in the pharmaceutical industry within a Quality Control microbiology role.
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Daily activities include Inbound and outbound calling, setting appointments, performing presentations to members of unions that request our benefits, basic computer knowledge, completing the necessary paperwork, quality control, and leadership development.
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quality control jobs in Darby, PA
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