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As a Field Service Engineer, you will delight our customers with timely onsite support of 10x Genomics instruments, ensuring compliance with company policy, cGMP, ISO, State Regulatory agencies, and the FDA.
$53 - $65 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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EXP is seeking an experienced and motivated Plumbing Designer/Engineer 2 to work in a flexible role that includes engineering, design and specification of building mechanical, electrical, plumbing, fire protection and process systems for Life Sciences, Research and Development, Pharmaceutical, and cGMP Projects.
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The Senior Quality Assurance Specialist provides Quality support for Petaluma site and ensures adherence to cGMP compliance in a regulated environment. Strong technical experience in a cGMP pharmaceutical setting.
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Bausch Health is a global company that develops, manufactures, and markets a differentiated product portfolio across multiple high-growth therapeutic areas including Gastroenterology, Generics, Neurology, Ortho Dermatologics, Medical Aesthetics and Dentistry.
$90,000 - $100,000 a yearFull-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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What You’ll BringA minimum of 10 years of process engineering design experience in cGMP, FDA, or other regulated manufacturing environments. Subject-matter expertise in cGMP regulations and standards (preferred.
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Lead packaging activities supporting multiple clinical programs in all phases of development, ensuring on-time delivery of project deliverables and compliance to current Good Manufacturing Practice (cGMP.
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Collaborates with internal functions and aligns goals and objectives for pre-clinical to commercial phase programs and products, ensuring cGMP, GCP, GVP and GLP compliance and realization of other value-added guidelines and best practices.
$315,000 - $320,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Expertise in Quality Systems and cGMP standards applicable to method validation for clinical and commercial products and AO/QC laboratory operations. May assist with cGMP compliance audits at contract partners and may interface with regulatory agencies during inspections.
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Support instruments in a cGMP/cGXP environment, while minimizing instrumentation and equipment downtime. Attend cGMP training as required by Department policy. Utilize computer skills to navigate and use corporate intranet, standard word processing, spreadsheet programs, maintenance management system, and calibration management system.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Plan and execute test method validation projects, including developing, performing, and documenting test method validation activities in accordance with cGMP. Draft, review, and approve design control documents (DHF documents) to support device developement deliverables, such as protocols, design verification, design validation, FMEA, risk management plans, change management plans, and design review.
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Neurodivergence, for example, attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder, dyslexia, dyspraxia, other learning disabilities. Excellent working knowledge, understanding and experience with the practical implementation of FDA and EMEA (or equivalent) regulations and guidelines in GLP, GCP and GXP environments.
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Ensure compliance with FDA and CGMP quality standards. Ensure compliance with FDA and CGMP quality standards. Knowledge of GMP and quality systems. High School Diploma; BS in Food Science preferred.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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We are a fully integrated contract development and manufacturing organization with sites in Belgium, United States, Japan, and India providing comprehensive development, cGMP manufacturing, and aseptic fill finish services.
$10Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Possess a strong knowledge of the FDA, cGMP, and GCP standards as well as regulatory guidance documents such as Annex 13. Possess clinical supplies experience/knowledge in forecasting, demand / supply planning , IRT systems, inventory management, clinical labeling and distribution including cold chain, import/export, and reverse logistics.
$70 - $80 an hourExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Technical knowledge of manufacturing systems, methods and procedures, biopharmaceutical manufacturing processes, knowledge of regulatory aspects (cGMP). Subject matter expert relative to manufacturing and MES Master Batch Records.
ExpandApply NowActive JobUpdated 9 days ago
cgmp job in South San Francisco, CA
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