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The company’s plant-based technology has revolutionized the current standard by stopping traumatic and surgical bleeds in seconds without the need for extended manual pressure. Collaborate with Quality teams to ensure compliance with regulatory standards, including but not limited to GMP, GLP, and GCP, as applicable.
$160,000 - $220,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Knowledge on Good Laboratory Practices (GLP) - Standard Operating Procedures (SOP) - Good Manufacturing Practice (GMP) This is a plastic manufacturing company; Candidates with plastic-manufacturing background are strongly encouraged to apply.
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The QC Reviewer is responsible for compliance with Standard Operating Procedures (SOP) and Good Laboratory Practice (GLP) requirements at Pharma Medica Research Inc (PMRI), as well as raw date verifications, preparation of analytical reports and maintenance of laboratory log sheets/books.
ExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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The candidate will be a member of the Developmental and Reproductive Toxicology group in an AAALAC-accredited, GLP-compliant facility and responsible for conducting studies from protocol review to in-life data collection, addressing QA audit findings, and running reports within the guidelines/protocols/Standard Operating Procedure (SOP)s.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The Associate Scientist - Microbiology performs and directs assays 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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Regulatory Submissions - Author relevant sections of regulatory submissions and response materials (e.g., IMPD, IND, MAA, BLA); interface with regulatory agencies on all components of stability and reference standard programs and analytical method qualification and validation.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Duties carried out in accordance with the HistoWiz QMS and Standard Operating Procedures (SOPs) to support GLP and non-GLP work. In-depth knowledge and experience with GLP and/or GCP regulations and industry standards (EPA, OECD, FDA, EU guidance.
$120,000 - $150,000 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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May serve as study director, principal investigator, or project leader for GLP and CGMP studies. The Principal Scientist is an advanced position, involved in planning own work and supervising day-to-day activities in the laboratory working under prescribed procedures (protocols, standard operating procedures, methods, etc.
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Ensures compliance with applicable Inova standard operating procedures (SOPs), ISO, FDA and other Quality System regulations, as well as applicable Environmental Health & Safety, Human Resources and all other regulatory and administrative policies.
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Conduct spot-check inspections/audits of production operations Participate in the internal audit program Write, review and approve Standard Operating Procedures (SOPs) as necessary May assist in supporting the Document Control program, record retention areas, and sample retention areas May support returned instrument processing Log returned instruments from the field.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Following Standard Operating Procedures (SOPs), Good Laboratory Practice(GLP) and Good Documentation Practice (GDP) This R&D/ Manufacturing Technician must also be comfortable safely operating some of the larger Manufacturing equipment.
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The LabsQA Team are responsible for the strategic development and delivery of a risk-based audit programme covering the following Quality Standards / areas: GLP, Lab GCP, Human Biological Samples, and our internal research quality standard “GLS” risk-based audit program.
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Knowledge on Good Laboratory Practices (GLP) – Standard Operating. Scan and enter material acceptances and rejections within MRP IQMS software. Quality Inspector oversee testing to ensure that products meet the established standards of appearance or performance.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Adhere to standard operating procedures, laboratory methods and protocols under GLP/GMP-like conditions for the production and analysis of a tissue engineered product. Familiarity with appropriate word processing, spreadsheet, presentation and related standard software.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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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.
ExpandApply NowActive JobUpdated 9 days ago
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