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Online Resumes with "SOPs Validation"
Chemist - Organic, Polymer, Analytical, QC - 10 years experience - research and development
Looking for a stable company that requires the skills and experience of a Chemist (Organic Synthesis, Polymer, Analytical, QC). Looking for an opportunity to participate in the research and development of new organic molecules, polymers, advanced materials, identification using analytical instrumentation (NMR, MS, GPC, FTIR, UV-VIS). Advancement within a company toward a management position and supervisory role.
Ideal Companies: Exxon-Mobil, Merck, Dow Chemical, Bristol Myers Squibb, Glaxo Smith Kline, Johnson and Johnson, BASF, DuPont, Genentech, Sigma-Aldrich, Eastman Chemical Company, Scering-Plough, Biogen Idec
Tags for this Online Resume: Organic Chemistry, Polymer Chemistry, Analytical Chemistry, NMR, HPLC, Synthesis, Process Development, SOP, GPC, Quality Assurance/ Quality Control, Medicinal Chemistry, Laboratory, Chemistry
QUALITY TECHNICIAN Specialist
Tags for this Online Resume: SOP, CAPA, EXCEL, PP, WINDOW,OUTLOOK, SAP, EBR, EDM, ETQ, SOP ,Validation Protocol, CAPA, NC, SAP R3 y Mercury R6, EDM, ETQ,Track wise, SOP, Validation Protocol, SAP, R3 and Mercury R6, EDM, ETQ, Track Wise
SR. PHARMACEUTICAL QUALITY SYSTEMS & VALIDATION PROFESSIONAL
Seeking Pharmaceutical QA Position - - Full Time or Consulting Position SR. PHARMACEUTICAL QUALITY SYSTEMS AND VALIDATION PROFESSIONAL with a broad knowledge of regulatory compliance and quality control and assurance expertise in cGMP manufacturing, operations, regulatory, supply chain management, and validation as applied to aseptic parental pharmaceutical products, tablets, APIs, and medical devices. My experience in...
Ideal Companies: Pharmaceutical or Medical Device Companies, (Abbott; Abbvie; Hospira, Johnson & Johnson)
Tags for this Online Resume: North Carolina, South Carolina, Florida, Texas, Missouri, Chicago, Atlanta, Associate Director of Quality Assurance, Quality Assurance Manager, Sr. Compliance QA Manager, Associate Director of Validation, Validation Director, CAPA Management, Supplier QA Manager, Director of Supplier Assurance, CMO QA Manager, Pharmaceutical QA Manager, Medical Device QA Manager, Corporate QA Auditor, CAPA Manager, API Manufacturer, Sterile Fill Pharmaceutical Manufacturer, Medical Device Manufacturer, Sr. Quality Engineer, Oklahoma, Illinois, Milwaukee WI, Validation Manager, Internal QA Auditor
Chemist - 15 Years of Experience - Near 10965
I am a QC analytical scientist with chemistry/biochemistry, immunochemistry background, and certified in Quality Auditing (CQA) I have in-depth knowledge and experience of Quality Affairs and Regulatory Affairs (QA/RA). I am looking for an opportunity in Pharmaceutical/Biotech company as QA as Associate QA scientist, Quality Auditor, Compliance Specialist, or Regulatory Affairs Specialist(entry level).
Tags for this Online Resume: Regulatory/Quality Audits, cGMP/GLP, Compliance, HPLC/EMPOWER, Document Control, SOPs/Validation, LIRs/CAPA, NY/NJ
Medical Scientist - 13 Years of Experience - Near 21136
HIGHLIGHTS OF QUALIFICATIONS: * 2+ years of clinical research monitoring experience and 25+ years pre-clinical experience * Knowledge of clinical trial procedures and approval processes. * In-depth knowledge of ICH GCP guidelines * Knowledge of FDA regulations * Knowledge of clinical trials for investigative biomedical and pharmaceutical studies. * Good working knowledge of Pharmacology, Epidemiology, Biology, Chemistry, Ph...
Tags for this Online Resume: Cancer, Leadership, Medical, Patient Care, Quality, Quality Assurance, Quality Control, Trauma, Troubleshooting, Phlebotomy
Quality Assurance Director - 13 Years of Experience - Near 60453
SUMMARY * 17 years of experience in pharmaceutical, Medical Devices, and FDA regulated environment including Quality Assurance and Process Computer System Validation. * Experience in generating all validation documents, including Validation Plan (MVP), Gap Analysis, Design Specifications, IQ, OQ, and PQ Test Protocols, Standard Operating Procedures (SOPs), and Validation Summary Reports. * Experience in Manufacturing Proces...
Tags for this Online Resume: Compliance, Manufacturing, ISO, Filing, Management, MDR, Process Improvement, Quality, Quality Assurance, Quality Management
Clinical Research
Summary . Research Scientist with experience on and off the bench in a GxP environment. Extensive experience with R&D, assay development, clinical testing documentation, compliance, managing regulated equipment, overseeing lab moves and modifications, change controls, SOPs, Validation and Qualification protocols internal audits, project management *
Ideal Companies: regeneron, pfizer, siemens
Tags for this Online Resume: Ariba, Asset Management, Compliance, ELISA, Genotyping, High Performance Liquid Chromatography (HPLC), Immunization, Inventory, Inventory Control, Management
Quality Assurance Specialist - 14 Years of Experience - Near 07871
SUMMARY Manager and Project Coordinator of Scientific Systems with over 25 years of experience in the Pharmaceutical and Scientific field. Well versed in FDA Regulations for scientific data collection validation. Proven ability to work in coordination with Clients and Project Teams to conform to FDA Regulations. Ability to meet deadlines, working independently or as a team member. Expertise includes: * Instem Centrus Suite ...
Tags for this Online Resume: Pathology, Toxicology, CVS, Pre-clinical, Validation, GLP, Legacy, Project Leader
Biochemist - 20 Years of Experience - Near 95051
Professional Summary: * Superior problem solving skills, QC/QA validation, GLP protocol expert, FDA * qPCR designs, Elisa, SOP validation, Automated System Specialist, Statistical analysis * HPLC, Flow Cytometry, Chromotography, Analytical Chemistry, Sample preparation and Analysis
Tags for this Online Resume: Research, Filing, Packaging, Product Launch, Protocol, Allergy, Analytical Chemistry, Applications, Biomedical Industry, Chemistry
Biochemist
Professional Summary: * Superior problem solving skills, QC/QA validation, GLP protocol expert, FDA facility and 510k * qPCR designs, Elisa, SOP validation, Automated System (Tecan), Statistical analysis * HPLC, Flow Cytometry, Chromotography, Analytical Chemistry, Real Time PCR
Tags for this Online Resume: Research, Product Launch, Protocol, Quality, Quality Assurance, Quality Control, Filing, Packaging, Problem Solving, Problem Solving Skills
