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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.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Proven track record of success in a fast-paced production environment at a biotech/pharmaceutical company preferably in GMP or GLP. At least 5 years of QA or Manufacturing experience in a GMP manufacturing environment with a Bachelor’s Degree in Biology, Chemistry, Chemical engineering, Biomechanical engineering, Bioengineering, Biomedical Engineering, Biochemistry or related field.
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Experience in Quality Management, Good Laboratory Practices (GLP), and Good Manufacturing Practice (GMP) Analytical Skills: must have the ability to interpret analytical assay data. The QA/QC Manager, a pivotal role in our organization, will be responsible for quality control, quality assurance, quality management, and Good Manufacturing Practice (GMP.
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Work with the BST network of specialty labs to support delivery of high quality bioanalytical and biomarker data to clinical programs, ensuring adherence to the requirements of quality, and ethical and regulatory standards, including ICH/GDPR/GCP/IVDR/GLP.
$209,000 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Minimum of 5+ years of progressive Quality experience working in regulated environment preferably in the field of biotechnology, biopharma, and/or cell/gene therapy (deep experience with GLP or GCP preferred.
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About Research Models & ServicesFundamental to basic research and discovery is the use of in vivo models to help identify disease targets and determine potential biological pathways that regulate the condition.
$18ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Knowledge of GLP/GCLP and GCP global regulatory requirements for clinical trial submissions (USA, UK & EU), understanding of 21CFR Pt. 11 with respect to clinical systems (QMS). Extensive experience managing deviations, RCA and CAPAs in a GLP/GCP environment.
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In-depth working knowledge of the applicable cGMP/GCP/GLP/GVP regulations and guidelines in a pharmaceutical environment. This role will develop strong relationships, collaborate, and interact with various departments (i.e., Quality Operations, Quality Systems, Chemistry Manufacturing, and Controls (CMC), Analytical, Regulatory Affairs, Pharmacovigilance, Procurement), and all levels of management at Akebia to accomplish company objectives.
$189,501 a yearFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Strong familiarity with regulatory / compliance environment (cGMP, GLP) associated with parenteral drug manufacture. The Sr. Associate Compliance provides scientific support in the root cause analysis and closure of OOS investigations, OOT investigations and product quality complaints; ensures compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP) and Quality Management System standards, compiles monthly Quality metrics for internal and corporate review, and analyzes trends to implement corrective and preventive actions to mitigate adverse trends.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Strong background in GLP and cGMP standards, with hands-on experience in assay development and validation. Strong background in GLP and cGMP standards, with hands-on experience in assay development and validation.
$32 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Familiarity with GLP, cGMP, and QA/QC personal care industry best practices. WHAT WE SEEK:Bachelor’s or master’s degree in Chemistry, Chemical Engineering, Cosmetic Science, or a related field.
$140,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Review and resolve denials Process referrals and submit clinical support documentation to insurance carriers File documentation into a patient's chart Pharmacy Technician Qualifications:Minimum of three years Pharmacy Technician experience with prior authorizationsCoverMyMeds experienceExperience with prior auths for anti-obesity medications, such as GLP-1 such as Saxenda, Ozempic, Wegovy, and Mounjaro.
$20 - $25 an hourRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Lead investigations into significant quality issues, scientific misconduct and suspected serious breach of GCP or GLP; facilitate identification of root cause and development of appropriate corrective and preventive actions; track actions and confirm effectiveness; ensure reporting of potential or confirmed violations to regulatory authorities, as appropriate.
$200,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Knowledge of relevant regulations, including Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and Occupational Safety and Health Administration (OSHA) requirements. Knowledge of relevant regulations, including Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and Occupational Safety and Health Administration (OSHA) requirements.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Partners with all line functions to ensure GMP, GLP and GCP compliance for all clinical development programs by providing guidance and serving as an expert in the interpretation regulatory requirements and expectations.
Full-timeExpandApply NowActive JobUpdated 2 months ago
glp job Company: Pci Services in Woburn, MA
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