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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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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.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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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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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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Familiarity with GLP (good lab practices) and food safety certification - HACCP is a plus. The Lab Manager – R&D will report to the Associate Director of Innovation, with day-to-day responsibilities that include managing a robust product development pipeline that includes rapid concept development, existing formula optimization, and validation of new ingredients and suppliers.
$140,000 a yearFull-timeExpandApply NowActive JobUpdated Today - 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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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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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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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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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.
$175,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months 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.
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Familiar with GLP, cGMP, and QA/QC personal care industry best practices. High level of downstream experience formulating a wide range of products such as creams, lotions, solutions, serums, mousses, surfactant systems, and aerosols.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Certification in pharmacovigilance (e.g., RQAP-GLP, PVQA) or quality management (e.g., ASQ Certified Quality Auditor) is a plus. Minimum of 6 years of experience in drug safety/pharmacovigilance quality assurance or compliance within the pharmaceutical or biotech industry.
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glp job Company: Pci Services in Boston, MA
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