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Chemical Engineer 38 Years of Consulting Experience in Global Process Industries Related to Polymers, Refinery Operations, Chemical and Biochemical Products. - Technical Consultant #1493

Chemical engineer for front end process design specializing in polymers, refinery operations, chemicals and biochemical products.Chemical engineering consulting for 38 years with extensive global experience in the process industries, primarily related to polymers, refinery operations, chemical and biochemical products.Supervising start up and commissioning of new chemical plants.Lead chemical engineer of many projects, with responsibility for all aspects of planning, process design and supervision of other engineers.Process engineer on a nuclear waste disposal project in the United Kingdom.Experienced in fast track front-end process engin...

Pharmaceutical Development and Regulatory Expert - Technical Consultant #2259

Pharmaceutical Regulatory Consultant with Broad SNDA, GMP, API Development Experience.Development of commercial manufacturing, FDA and international registration and approval for atracurium besylate, trifluoridine, bupropion hydrochloride, zidovudine, exosurf, mivacurium chloride, doxacurium chloride, pseudoephedrine hydrochloride, acrivastine, valciclovir, tramadol hydrochloride, topiramate, levofloxacin, surfaxin, vinorelbine tartrate and lamotrigine.Major process SNDAs for ofloxacin and leucovorin calcium.Regulatory documentation and approvals (FDA request for NDAs for grandfathered products) for digoxin, melphalan, azathioprine, thiogu...

Drug Product and Process Development, Process Manufacturing, and GMP Documentation Expert - Technical Consultant #2268

Consultant with Diverse Pharmaceutical Experience in Formulation Development, Manufacturing, Technology and Site Transfer, Process Design, Scale-Up, and ValidationPharmaceutical formulation development, manufacturing technology transfer, site transfer, process design optimization, and scale-up for domestic and international clients.Product development using QbD approach, process scale-up and optimization, process validation.Drive technology platforms such as solid and Liquid orals, aseptic filling, softgels, orally disintegrating granules, powders, MR products, X-ray contrast media, peptide injectable product, topicals, steroids and hormo...

Allergens and Analytical Method Development Consultant - Technical Consultant #2298

Chromatographic and Spectroscopic PhD. Analytical Chemist Chemistry in areas; LC-MS,GC-MS,ICP-MS, FT-IR,ICP-OES,CE for Drugs, Cosmetics, Pharmaceuticals, and Food.Analysis of drugs, pharmaceuticals, and cosmetics.Advanced Instrumental Analysis (LCMS,MS/MS,GCMS,ICPMS).Modern sample preparation techniques (SPE,QUECHERS).Laboratory quality management.Project management.Streamlining laboratory operations.Focused AreasGas chromatograph, (ECD/FID/FPD, GC and Mass spectrometry), head space sampler; High Performance Liquid Chromatograph ( PDA/UV/FLD/ELSD/RI); U(H)PLC; LC-MS(ESI,APCI);Ion chromatograph; on-line sample cleanup and enrichments for:...

Veterinary Drug Development And Registration Technical Consultant - Technical Consultant #2468

Veterinary Pharmacology and Pharmacokinetics, Bibliographic Assistance, Tissue Residues and Product RegistrationPharmacokinetics in domestic animals.Tissue residues of veterinary drugs.Milk residues of veterinary drugs.Pharmaco-toxicological monographs for veterinary drugs.Registration and development of veterinary pharmaceuticals.Expert-Pharmaceutical RegistrationTechnical support for the development and registration of more than 200 pharmaceutical products for veterinary use in Argentina and Latin America.Independent Consultant...

Pharmaceutical, Medical Device and Human Tissue Quality Auditor and Compliance Consultant - Technical Consultant #1824

Pharmaceutical Quality Auditor and Compliance Consultant for Human Tissue, Pharmaceuticals, and Medical DevicesQuality SystemSupplier quality system audits, supplier qualification, SCAR management and non-conforming material control and disposition.Quality system design: Medical device per QSR (21CFR PART 820) and ISO13485 requirements; and pharmaceutical per 21CFR 210.Designing Quality systems per 21CFR part 1271 (tissue and cellular therapy).Writing and reviewing Standard Operating procedures, SOPs and Work Instructions.Perform quality system audits per 21CFR 820 cGMPs (medical device), 221 cGMPs (pharmaceuticals), 600 cGMPs (biomedical)...

Sterile Process Validation, Steam Sterilization, and Aseptic Processing Microbiology Pharmaceutical Expert - Technical Consultant #2199

Pharmaceutical Microbiology Quality and Regulatory Consultant with Expertise in Process Validation, Steam Sterilization, PDA's, ASQ Certified.Regulatory affairs and quality assurance certified with ASQ.Over Twenty-five year's expertise in sterile process validation, steam sterilization and aseptic processing.Pharmaceutical microbiology, and chaired PDA's Microbiology and Environmental Monitoring Interest Group for over fifteen years.GMPs, data integrity, sterile process validation, steam sterilization, microbiology, environmental monitoring, regulatory updates, and conducting regulatory submissions.Expert Witness ExperienceInternational pa...

Biological-Clinical Manufacturing (Vaccines) Executive and Consultant - Technical Consultant #2534

Biological Manufacturing: Auditing, Root Cause Analysis, Corrective, Preventative Action and GxP compliance. Biological and clinical manufacturing operations executive, providing a wide range of experience in quality leadership across many facets. Create, develop and recommend program and system changes pertaining to vaccine product release and deviation management resulting in more efficient product release to market and improved "right-first-time" manufacturing metric. Articulate leader with unparalleled work ethic coupled with a strong sense of urgency, keen interest and passion in making quality a key ingredient to the success of...

Industrial Pharmacist-Distribution Operations, Manufacturing & Quality Management/ Expert - Technical Consultant #2536

Commissioning and Qualification of Solid Oral Dosage Facilities, Operation Excellence in Supply Chain, Drug Master Files Review, Validation of Analytic Control, Implement EHS Management Systems Quality management system: Design, Standard Operating Procedures (SOP) training, auditing, upgrading quality systems. Design of oral dosage manufacturing processes. Design of manufacturing process and equipment’s User Requirement Specification (URS). Commissioning and qualification of process equipment, clean rooms, HVAC, and purified water system. Market research, business plan, product targeting. Regulatory affairs: Review of parts 1...

Specialty Chemical and Bulk Pharmaceutical Supply Chain - Regulatory (GMP, MRP, ISO Certification) & Operations Expert - Technical Consultant #2542

Specialty Chemicals & Pharmaceutical Supply Chain-Change Agent, Regulatory, EPA, OSHA-PSM and Global Manufacturing ExpertPharmaceutical and specialty chemical operations with 20 years’ in supply chain Leadership for large facilities, providing technical solutions in challenging environments in union and non-union members. Manufacturing and operations professional, action-oriented, building effective teams and delivering positive results with unlimited drive for continuous improvement in fast paced, global businesses. Change agent and transformative leader in global manufacturing footprints leading to increased efficiency and throughp...