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Online Resumes with "GDP"
Chemical Engineer - 5 Years of Experience
Energetic and trilingual quality engineer (member of OIQ) with experience in medical devices, pharmaceuticals and the bottling industry. Offers work experience in a highly regulated (FDA) pharmaceutical environment using Good manufacturing practices (GMP), Good laboratory practices (GLP), Good documentation practices (GDP) as well as Health and Safety issues (CSST). Solid record in designing and validating changes which imp...
Tags for this Online Resume: Los Angeles, Irvine, Quality
IT Field service Engineer Consultant / Intelligent Technology
A challenging position as a Communications Consultant in a the bio-medical intelligent Technology. 7+ years of experiences
Ideal Companies: Looking for Company with improvement of growth and ownership of a franchise etc.
Tags for this Online Resume: Peripheral, palm Pilot etc.
Operations Manager - 18 Years of Experience - Santo Domingo,Dominican Republic,Near 10216
The opportunity to grow in my professional experience and serve as a facilitator in promoting the objectives of the company, contributing to the achievements of the goals.
Tags for this Online Resume: Logistic, Warehouse , SAP, JDEdwards, GMP, GDP- LEAN, Process, Manufacturing
Quality Coordinator - 15 Years of Experience - Near 08807
Customer Support, Regulatory Compliance, and Account Management professional, experienced in the pharmaceutical, biotech, and software fields; knowledgeable in industry compliance standards of GCP, GMP, GDP, and CAPA management; commended by clients for 24/7 support readiness, responsiveness, audit preparedness, and reference ability; recognized for superior organizational, communication, documentation, mentoring, and team ...
Tags for this Online Resume: Princeton, Compliance, Quality, Support, Regulatory, Customer Service, Testing, Software
Quality Coordinator - 7 Years of Experience - Near 91352
Tags for this Online Resume: CAPA, Green Belt, GMP, GDP, Lean
Medical Scientist - 14 Years of Experience - Near 30269
I'm a Bilingual, Army –Trained Medical Professional with pharmaceutical experience to include GxP, quality control immunoassay testing, environmental monitoring, laboratory investigations, and exception reporting. My Army Service includes 10 years experience in Clinical and Research applications of microbiology, phlebotomy, hematology, resource management, safety, risk assessment and mitigation, process improvement and emp...
Tags for this Online Resume: GMP, GDP, GLP, MP, Quality Conol , Pharmaceutical, 21 CFR 211, Non Conformance reporting, CAPA, Quality Control Associate, Root Cause Investigations, Scientist, Microbiology, Environmental Monitoring, Assessments, Audit, ELISA, Quality, Quality Assurance, Quality Control, Research, Test
QA ASSOCIATE - 3 Years of Experience - 08873
• Ensure implementation of cGMP, GLP and GDP • Monitoring processing and laboratory activities in the facility on a daily basis • Hosting regulatory audits • Member of internal audit team • Preparation and implementation of Standard Operating Procedures, Stability Protocols, Master Batch Production Records, etc. • Evaluation and Qualification of vendors for raw materials, packaging materials and contract services • Samplin...
Tags for this Online Resume: QUALITY ASSURANCE, QA TECNICIAN, VALIDATION, DOCUMENTATION, QA AUDITOR, BMR, Test, Audit, Documentation, Internal audit, Manufacturing, Microsoft, Microsoft Office, Packaging
Sr. Project and Quality management Specialist
Quality Engineering and /or Compliance position that will utilize my knowledge of design control, regulations, auditing and project management skills to ensure regulatory and quality compliance in the design of products for a world-class company with significant impact on Public Health and enhance company’s profitability.
Tags for this Online Resume: CROSS FUNCTIONAL PROJECT TEAM LEADERSHIP , PROJECT MANAGEMENT SKILLS , CORPORATE AND DEPARTMENTAL SOP DEVELOPMENT , COMPLIANCE, QSR, ISO, GLP/GDP AND GMP , LEAD AUDITOR, INTERNAL/SUPPLIER AUDITOR
Electromechanical Equipment Assembler - 1 Years of Experience
SUMMARY: * More than 5 years of Experience in cGMP regulated environment. * Manage control of changes, Deviations, OOSIR and CAPA * Review batch records and releases lots * Prepare and revise Standard Operating Procedure for cGMP Equipment * Work both independently and in team to finish project on-time. * Knowledge of FDA regulations and 21 CFR 210 & 211, cGMP/GLP/GDP guidelines for solid and liquid drug products.
Tags for this Online Resume: Manufacturing, Packaging, Documentation, Management, Quality, Quality Assurance, Quality Management, Test, Audit, Quality Control
Biologist - 3 Years of Experience
Project summary: Apomimetic peptides are novel drug candidates to treat atherosclerosis because of their ability to mimic the native apolipoprotein functions. Human PON1 (Paraoxonase1) activity was known to increase in presence of apomimetic peptide-lipid complexes. This increase in PON1 activity may be attributed to 'alterations' in secondary structural components (possibly tertiary structure) of PON1. The project includes...
Tags for this Online Resume: cGMP, Electrophoresis, ELISA, Protein purification, Chromatography, Filtration and diafiltration, Procurement, Chromatography systems, Formulation, English Language, Validations, CIP and SIP, Nanofiltration, UV spectroscopy, GDP, CAPA, Incidents and Deviations
Director of Quality - 15 Years of Experience
SUMMARY Certified Quality Auditor for Life Science Practice Lead as senior Quality System Auditor with compliance acumen delivering outstanding returns through comprehensive knowledge and hands on experience. Vendor qualification and management plus remediation efforts ensuring delivered products meet requirements for direct to stock fulfillment. Certified Quality Auditor/Project Manager for Quality Management Systems for m...
Tags for this Online Resume: Audit, Quality, Quality Assurance, Services, Test, Compliance, Infrastructure, Management, Risk Management, Training
Quality Engineer - 10 Years of Experience - Near 00782
PROFESSIONAL SUMMARY QUALIFICATIONS ASQ member, CAPA Expert Certified, CQA, Quality Risk Management - FMEA, Introduction and Internal Auditor for ISO 9001. Knowledge in cGMP Regulations and International Standard (ISO) as 21CFR820, ISO 13485, 21CFR210 & 211, ISO 9001 & ISO 14001. OSHA Rules, Quality Assurance & Control, Manufacturing, Production, Warehouse, Pest Control. Computer skills: Trackwise, SAP, Maximo, LIMS, Visio,...
Tags for this Online Resume: Manufacturing, Documentation, Quality Assurance, CAPA, Audit, Complaints, Investigations, Good Manufacturing Practices, Internal audit, Management, Systems
