Direct quality assurance for biopharma company, quality systems lot release investigations, audits, GLP GCP interface with GMP. Department of 20 -50, with increasing responsibility world-wide.
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quality assurance, biopharma, quality systems, lot release, investigations, GLP GCP interface with GMP
Greetings,
I hope this letter has found you in the middle of a very joyful work week. My name is Tyson. I have recently relocated to Little Rock AR and I am looking to find a suitable career vacancy. I have several years’ experience verifying and producing detailed reports for chemical analysis across a few different industries. My professional career has focused on chemical analysis and education. My laboratory backg...
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Teacher, Message Delivery, Communication, Analyst, Detailed, Coordinate, Validation, Analytical, Team Player
A laboratory animal technician position utilizing proven ability to work with research animals as well as my experience managing facilities and facility-related operations / services.
Diversified extensive hands-on experience in a pharmaceutical research setting. Strengths include:
• Provide 24/7 Monitoring of Animal barrier via lap top
• Primary animal care
• Facility maintenance / operation
• GLP Knowledge
• Rodent dosi...
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Animal Lab Supervisor
Over 18 years of top performance in optimizing operations for up to 60K+ SF R&D facilities.
A peak performer in establishing operational excellence in all facets of pre-clinical studies, encompassing best practices for quality, safety, compliance, and cost control. Adept at managing quality assurance for studies supporting pharmaceutical/biotech regulatory submissions by conducting independent audits, issuing audit reports...
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Operations Manager, Animal Research, GLP, Safety, Validation, FDA
Provide GLP and improvements on ISO related practices,while enjoying laboratory atmosphere.
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Chemist , Regulatory, ISO Auditor
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Certified Medical Technologist, Laboratory Expertise, GLP, GCP, FDA Compliance, Data Management, Quality Assurance, Biology
To obtain a position working as a Microbiology Business Analyst and Project Manager in a pharmaceutical/biotech validation environment, oriented toward management advancement. Over 20 years of experience in the Pharmaceutical Industry, 16+ years of those years are with GxP (GMP, GLP, GCP) systems compliance/QA and 21 CFR Part 11. Experience includes GxP system implementation projects, documentation/SOP writing/review.
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Molecular Biology, Cell Biology, Immunology, GMP and GLP, Cell Culture
Looking for an opportunity to contribute new peptide drug delivery technology for developing new peptide drug products.
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CSO (Chief scientific officer), peptide drug delivery, oral drug delivery sysytem, GLP-1 delivery, rHGH delivery, non-invasive peptid drug delivery
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ELISA, Flow cytometry, cell based assays, GLP, laboratory automation, ligand-binding assays
