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TITLEQC Microbiology AnalystSUMMARYThe QC Analyst is responsible for performing environmental monitoring and microbiological test methods on in-process intermediates and varying stages of drug products under minimal supervision and within cGMP guidelines, to support further manufacturing of commercial and clinical therapeutics.
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Production Lead Skills and Requirements: Extensive experience operating a sit down/stand up forklift Accuracy and attention to detail pulling orders and tracking inventory properly Ability to lift up to 50lbs throughout the day Experience in manufacturing or production environment Computer skills, basic data entry Valid CA Driver’s License.
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Other continuing education initiatives highly desirable (e.g., Six Sigma, Lean Manufacturing, industry specific coursework). These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.
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Gibson operates via a central headquarters based in Nashville, TN, supporting five manufacturing facilities as well as four regionally-based support centres that enable the sales, marketing, and distribution activities in each of four different worldwide regions.
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Demonstrated knowledge of cGMPs, Health Authority Regulations, Quality Systems and technical expertise in manufacturing processes. Ability to comprehend technical information related to analytical methods, manufacturing processes and regulatory expectations.
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Attention to detail, clear and proactive communication– Aptitude to learn manufacturing processes which include materials, technical understanding of manufacturing and packaging. Qualifications– Minimum Associate Degree required– Advanced computer skills with focus on expertise in Excel.
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Start or continue a career in real estate development and management with EAH Housing.
$270,000 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Join our team as a full-time Assembler/Shipping Assistant, where you will be responsible for various manufacturing, shipping, and warehouse support duties. Your role will involve assembling irrigation controllers that help customers conserve water.
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The Quality Control Analytical Supervisor is responsible for supervising the biological, biochemical and chemical evaluation of in-process, drug substance, studies and investigational samples in support of the manufacturing process of commercial and clinical drug products.
$132,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Biotech manufacturing, Cell Culture, depth and tangential flow filtration, column chromatography, protein purification and formulation, buffer and media operations, SOP. Knowledge of biotech manufacturing processes and equipment, including cell culture, depth and tangential flow filtration, column chromatography, protein purification and formulation, and buffer and media operations.
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Knowledge of biotech manufacturing process and equipment including cell culture, depth and tangential flow filtration, column chromatography, protein purification and formulation and/or buffer and media operations.
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Leads the strategic sourcing of new and existing direct materials (ingredients or packaging material) to support the manufacturing of finished goods according to established procedures, practices, and policies.
$166,800 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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We are looking for a highly motivated chemist, biochemist and/or chemical engineer to join in our newly commissioned state-of-art therapeutic oligonucleotide GMP manufacturing facility in Petaluma, CA. This individual will work in a Process Development lab to help develop, transfer and trouble-shoot processes for smooth transfer to GMP and non-GMP manufacturing.
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GMP grade oligonucleotide manufacturing. In-Process oligonucleotide manufacturing. Additionally, our primary manufacturing capabilities enable customization and bulk (OEM) manufacture of reagents such as key NGS enzymes for high volume applications.
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Direct and broad experience in GMP manufacturing across multiple platforms (biologics, synthetics, oral dose, parenteral manufacturing, packaging). Support the CMO selection process by evaluating CMO capabilities against applicable manufacturing, quality, and compliance requirements and needs - both operational capabilities & strategic objectives.
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manufacturing job Title: vp Company: Ashley Furniture in Novato, CA
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