Call Us:  +1.302.777.7774

CECON logo

Log in

Login to your account

Username *
Password *
Remember Me
Loading...
Show More

Search Module

(Either have testified or are willing)
Search for experts within miles of this zip code
Please enter your keywords above to get started on your search.

Hands on Experience in cGMP, GLP and FDA Regulatory Compliance, Blood and Plasma Processing and Laboratory Method Validation - Technical Consultant #886

Senior consultant in pharmaceutical and medical devices with emphasis in blood testingPharmaceutical and biotechnology quality assurance and control (QA, QC.)Regulatory compliance, consent decree and FDA batch record reviews-investigations; European audits.Plasma and blood collection centers and computerized donor record files.Blood and plasma quality assurance and control.Pharmaceutical QC methods development and review.Pharmaceutical validation of laboratory methods.Quality systems, quality control laboratory and development of standard operating procedures.Regulatory compliance audits; quality system audits.Vaccine stability, raw materi...

Expert in Pharmaceutical QC and Validation Protocols for Analytical, Laboratory and Production Equipment - Technical Consultant #935

Consulting Chemist and Chemical Engineer-Validation Protocols for Analytical EquipmentPharmaceutical and medical device process and equipment validation.Pharmaceutical quality control, quality review of pre-BLA (Biologic License Application) drug product, and stability analysis.Validation of HPLC, UV-Vis spectrophotometer, particle size analyzer, and atomic absorption instruments.Created and wrote IQ/OQ validation protocols for sterile washers, dry heat ovens, and robotic filling and capping equipment used in aseptic manufacturing of implantable controlled release systems.Executed validation protocols for fluid bed granulators, tablet pres...

Biostatistician for Pharmaceutical Data Analysis and Clinical Trial Support - Technical Consultant #1169

Experienced biostatistican to support pharmaceutical data analysis in drug development, efficacy screening and clinical trials.Statistical AnalysisProtocol Development - Pharmaceutical, Biotech, Medical Device, NIHPharmacokinetic (PK) AnalysisSAS ProgrammingStatistical Report WritingData and Safety Monitory BoardSensitivity Analysis2002 - Present Independent ConsultantStatistical services to the pharmaceutical, biotech, and medical device industries and the National Institute of Health (NIH).Statistical services...

Biomechanical engineering consultant for medical device evaluation and testing - Technical Consultant #1411

Experienced applying mechanical engineering tools to biomechanical applications, including computer aided design, (CAD) and finite element modeling, (FEM) techniques. Medical device evaluation and testing. Laboratory testing for hard and soft tissue, joints and other devices such as artificial limb prosthetics and external fixation devices. Medical device testing. Testing of spinal implants and orthopedic devices for FDA submission. Biomechanical evaluation and fatigue analysis of silicone breast implants.Medical device evaluation and testing.Skilled in mechanical laboratory testing and procedures for hard and soft tissue, joints and ot...

Chemical Consultant Skilled in China Chemical Trade, Polyurethane Chemistry and Regulatory and Environmental Compliance (OSHA, EPA , FDA, DOT, NHTSA, FTA, FAA) - Technical Consultant #1508

Urethane chemist with experience in specialty films, corrosion inhibitors and chemical trade with China.Chemical product commerce with China.Polyurethanes chemistry - polyurethane flexible foam production based on polyether and polyester polyols.Specialty films production by the solvent band casting process.Corrosion inhibitor production; specialty chemical production and sales; and production of artificial sweeteners.Operations, new product formulating, research and development.Plant and chemical process shut down.OSHA, EPA and regulatory compliance in chemical plant operations and chemical plant shut down.Increased profits after restruct...

Validation Consultant for Medical Devices - Technical Consultant #1588

Consultant for Medical device FDA/ ISO Regulatory Compliance.Medical device FDA/ ISO regulatory compliance.Design control systems, both hardware and software, for medical devicesRisk analysis, vendor qualifications and documentation related to medical devices.Software and process validations.Design and manufacturing engineering in flowmeters.Contract Manufacturer Organization (CMO) selection and qualification for medical devices.Drawing and document control systems, configuration and management.Human factors programs.Component acceptance procedures/ non conforming product disposition.Audits, gap analysis and response to FDA 483 forms and w...

Medical Device Regulatory Conultant - Technical Consultant #1648

Consultant for Medical Device Validation and Blood Bank Operations and Collection Devices per FDA RegulationMedical device submissions, regulatory affairs related to medical devices and pharmaceutical, good manufacturing practices (GMP) and Quality Systems Regulation (QSR).FDA compliance procedures including process validation, product validation, software validation, warning letters, consent decree resolution, compliance audits, supplier audits and ISO registrations.Extensive and broad knowledge of U.S. FDA quality and regulatory body regulations.Specializing in medical device submissions, regulatory affairs, and Good Manufacturing Prac...

Pharmaceutical and Medical Device Consultant for Portfolio Strategy, IT, Systems Design and Operational Excellence - Technical Consultant #1731

Broad Based Health Care Regulatory Consultant: Operational Excellence, IT, Product Portfolio Management, Health Care Product Portfolio Management and Quality System ConsultantOver 16 years in the pharmaceutical, medical device, biotechnology and healthcare industries.Subject matter expert in health care product portfolio management, project management, operational excellence, quality system improvements, system development life cycle (SDLC), computer system validation (CSV) and regulatory compliance in global operations.Assessments of business operations, quality assurance programs, regulatory, compliance, information technology and manufa...

Polypropylene Technical and Marketing Expert - Technical Consultant #1763

Polypropylene Technical and Marketing Expert in consumer, medical and industrial polyolefin marketsSenior Plastics Consultant with a marketing and finance MBA.Extensive new business and application development of polyolefins, bringing 28 years of experience.Created a technical team for a grassroots polypropylene plant.In depth understanding of polyolefin products, processes and applications.Detailed knowledge of the consumer, medical and industrial polyolefin markets.Technical and marketing support to Asia, South America and Africa for over seven years.Merger and acquisition evaluations.

Medical Device Expert in Product Development, R&D, and Regulatory Support (FDA, ISO, CE) - Technical Consultant #2032

Medical Device Consultant with Broad Experience in Business Management, R&D, and Regulatory Compliance: FDA, ISO, CEMedical device product development, market positioning, strategic planning, and branding strategy.Regulatory affairs and compliance, (FDA, ISO and CE approval processes).Technology leader providing equivalent support for the health care, security, intellectual property, and space industries while successfully developing new businesses in the U.S. and abroad.Budget and resource management, contract management and negotiation, change management and restructuring, profit and loss accountability, forecasting and trend analysis,...