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Relevant experience in good laboratory/manufacturing practices (GLP/cGMP), laboratory quality control or stability, and interaction with quality assurance is required. Must be able to communicate effectively with manufacturing and quality personnel.
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Performs Cell Culture and Cell-Based assays (BSL2 and BSL2+) according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs.
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The Associate GLP QA Auditor coordinates auditing activities to ensure compliance with SOPs and GLP requirements. Pharmaron is a premier contract research organization that offers a broad spectrum of R&D and manufacturing service capabilities throughout the entire drug discovery, preclinical, clinical development and commercialization process.
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The QC Analyst Lead Microbiology provides essential support to manufacturing by leading in conjunction with the Laboratory Supervisor, with a deep understanding of environmental monitoring principles and laboratory testing, including Endotoxin, Mycoplasma, Sterility, and growth promotion, the Lead Analyst serves as a backup to the supervisor, performs qualification testing, trains staff, manages supplies, reviews data accurately, and contributes to data analysis and reporting.
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Overview of PositionThe Electro-Mechanical Technician I is responsible for maintaining and repairing manufacturing equipment in standard conditions to minimize equipment downtime, increase product yield, and optimize machine reliability while meeting Environmental Health & Safety (EHS) and Quality requirements.
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Formal education (including short courses) on GLP, GMP, SQF, Food Defense, PCQI, or HACCP. Kelly Engineering is seeking a Quality Technician with a food manufacturing background to join our client's quality team.
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We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
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Creates and implements SOPs for Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP) studies, conducts internal audits, and provides training to laboratory staff and trainees to qualify the facility.
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The company also provide therapeutic protein drug cGMP manufacturing, from GLP IND to clinical phase manufacturing. JOINN Biologics is a contract manufacturing service company, located in San Francisco Bay Area with professional team and cGMP facility in JOINN Innovation Park. JOINN Biologics offers process development, including cell line development and cell culture, upstream process development, downstream process development, analytical services.
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Immunological Assay Development, ELISA, Immunohistochemistry (IHC), Ligand Receptor Binding, Good Laboratory Practices (GLP), & Good Manufacturing Practice (GMP) Work under Good Laboratory Practices (GLP) at all times, and work under Good Manufacturing Practices (GMP) where required.
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Skills: HPLC, Chemistry, Chromatography, GLP (Good Laboratory Practice), GCP (Good Clinical Practice), GMP (Good Manufacturing Practice) Solid use of instruments including HPLC, GC, MS, UV/VIS, APC. Solid documentation skills, familiarity of GMP, GLP. Able to present findings to larger groups.
$30 - $38.18 an hourFull-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Frontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China, and growing over 30% YOY. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
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At least 5 years of QA or Manufacturing experience in a GMP manufacturing environment with a Bachelors Degree in Biology, Chemistry, Chemical engineering, Biomechanical engineering, Bioengineering, Biomedical Engineering, Biochemistry or related field.
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The Director, Quality Assurance, will manage a GLP QAU, including Good Laboratory Practice / Good Manufacturing Practice (GLP/GMP) within the Gene Therapy Program (GTP) at the University of Pennsylvania, supporting the development, manufacture, and testing of viral vectors for clinical trials.
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Knowledge of Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP) and/or Good Pharmacovigilance Practice (GPvP) Experience with Data Science and Digital Health (including Real World Evidence/Real World Disease.
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