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Online Resumes with "small molecule drug"
Biologist - 10 Years of Experience
PROFESSIONAL SUMMARY * Highly motivated and versatile scientist with experience in in vitro/cell-based assay development, validation and execution, in vivo pharmacology, including 5+ years of industry experience * Extensive experience in discovery and development of small molecule inhibitors against protein homeostasis * Expertise in defining strategy and providing leadership in various aspects of in vivo POC, target identi...
Tags for this Online Resume: drug discovery, in vitro/cell-based assay development, in vivo pharmacology, RT-PCR/q-PCR, Protein Biochemistry, PD biomarker, CRO expereince, program management, PK/PD relationship, disease animal models, mammalian/primary/cancer/iPS cell culture, co-cultures
Analytical chemist - 15+ years eperience HPLC, LCMS; pharma-biotech
HPLC and LCMS method development and validation in support of small molecule drug discovery programs, reglatory submissions, or related area
Tags for this Online Resume: HPLC and UHPLC, LCMS and LCMS/MS, analytical chemistry, method development and validation, cGMP and GLP, regulatory submissions
Life Scientist - 20 Years of Experience - Near 19335
Summary An experienced toxicologist with a successful track record supporting drug discovery research and development to progress biologic-based and/or small molecule drug candidate (s) through all phases of nonclinical development (Phase 1-4). Multiple successful NDA approvals, along with BLA approval for a respiratory biologic and successful IND submissions. Extensive and broad based expertise in conceptualizing and desig...
Tags for this Online Resume: Audit, Research, Test, Toxicology, Protocol, Compliance, Training, Evaluate, Medical, Medical Devices, oncology, protocol, pharmaceutical, ich, nonclinical, Regulatory Affairs, Quality Assurance, GXP
Life Scientist - 20 Years of Experience - Near 19335
Summary An experienced toxicologist with a successful track record supporting drug discovery research and development to progress biologic-based and/or small molecule drug candidate (s) through all phases of nonclinical development (Phase 1-4). Multiple successful NDA approvals, along with BLA approval and successful IND submissions. Extensive and broad based expertise in conceptualizing and designing nonclinical developmen...
Tags for this Online Resume: Audit, Research, Test, Toxicology, Protocol, Compliance, Training, Evaluate, Medical, Medical Devices
Pharmaceutical CMC Development | cGMP Manufacturing | Product Quality
Senior manager and director of pharmaceutical process chemistry, manufacturing and controls (CMC) specializing in cGMP, quality and regulatory compliance of novel small and large molecule therapeutic drugs including peptides, nucleotides, protein biologics and antibody drug conjugates (ADCs). Skilled in technology transfer, analytical method development and validation, quality risk assessment, deviation management, investi...
Ideal Companies: Shire, Biogen, Lonza, Genzyme, Sarepta.
Tags for this Online Resume: Chemical Process Development, API, cGMP Manufacture, Technology Transfer, Management, Quality, Risk Assessment, Pharmaceutical Operations, FDA and ICH Drug Regulations, CRO, CDMO and CMO Oversight, CMC Process Chemistry, TrackWise QMS, Change Controls, Deviation Management, Investigations, Root Cause Analysis, CAPA, Antibody Drug Conjugates, IND, IMPD, NDA, MAA and BLA
