Jesus Juárez-Brambila, Bs, Ms, Phd. Email & Phone Number
@axsome.com
1 phone found area 201
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Who is Jesus Juárez-Brambila, Bs, Ms, Phd.? Overview
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Jesus Juárez-Brambila, Bs, Ms, Phd. is listed as Director, Analytical Development, CMC at Axsome Therapeutics, Inc., a with 48 employees, based in Jemison, Alabama, United States. AeroLeads shows a work email signal at axsome.com, phone signal with area code 201, and a matched LinkedIn profile for Jesus Juárez-Brambila, Bs, Ms, Phd..
Jesus Juárez-Brambila, Bs, Ms, Phd. previously worked as Associate Director, Analytical Development at Axsome Therapeutics, Inc. and Principal at Juarez Consulting Group. Llc. Jesus Juárez-Brambila, Bs, Ms, Phd. holds Ph.D., Synthetic Organic Chemistry from University Of California, Santa Cruz.
Email format at Axsome Therapeutics, Inc.
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About Jesus Juárez-Brambila, Bs, Ms, Phd.
Experienced Pharmaceutical Professional Chemist with over 24 + years of experience in:• Research and Process Development of new drugs from Discovery to launch.• Analytical Development of new drugs from Discovery to commercial products• Analytic Method development, method validation and method transfer for small molecules DS API’s: raw materials, isolated intermediates and finished goods. DS and DP stability studies, dissolution, forced degradation. Isolation, identification and synthesis of impurities • Instrumentation: LC-UV, LC-MS, GC-HS : Waters, Agilent, Shimadzu; NMR, IR, MS, KF, TLC, PSD, DSC, XRPD, Dissolutors, Ion Chromatography among others.• Software for data acquisition and interpretation: Empower, EZstart, Chemstation, Chem Bio Office, MestreNova, Chromeleon, Microsoft Office among others.• Work under strictly regulated environment by international agencies (FDA, ICH, COFEPRIS, JP BP, EMA, etc.)• Co-writing IND and NDA FDA submissions. • Member of the CMC group• Enjoy managing projects, and working with teams to complete business objectives, leading to a successful completion of projects• Focused on exceeding expectations, while innovating and delivering new ways to look at a product or chemical intermediate.• Effective leader to ensure that projects are completed with a high level of excellence, on time, and within budget. • Working with others allows me to share my analytical and synthetic expertise and experience, while gaining new skills and perspectives.• Assertiveness to maximize my contribution to projects through development of interpersonal relationships and clear communication.
Listed skills include Hplc, Analytical Chemistry, Chromatography, Pharmaceutical Industry, and 46 others.
Jesus Juárez-Brambila, Bs, Ms, Phd.'s current company
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Jesus Juárez-Brambila, Bs, Ms, Phd. work experience
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Associate Director, Analytical Development
CurrentPrincipal
CurrentProfessional and Superior Service for the Chemical, Biotechnology & Pharmaceutical Industry.
Senior Analytical Chemist
Analytical Method Validation Chemist - Contract
Essential Duties and Job Functions:Develop analytical method validation remediation plan for the site in conjunction with Sr. ManagementManage, guide and coordinate all activities associated with Validant Analytical method validation teamsEngage with site Management & Laboratory Teams as requiredEnsure validation protocols and reports are produced in a timely fashionMonitor team progress and report to Site & Validant Management
Ra Iii, Analytical Development Chemist - Contract
As Analytical Development Chemist, I applied NEKTAR analytical methods for• Routine and non routine analysis of: Raw Materials, In Process Checks, Active Pharmaceutical Ingredients, Product Development and Stability samples.• Use of Agilent and Waters instrumentation.• Use of Empower, Chemstation, and Chromeleon software for HPLC, GC, UV, IC, etc. for lab management, data acquisitions and data analysis.• Product Development Support.• Data Analyis, Troubleshooting and Complex Problem Solving• Assist with the training of analysts.• Applies cGMP, ICH and GxP on daily basis.
Qc Analytical Chemist - Contract
As method validation chemist, I revised 183 test methods used by the QC unit for analytical testing, cleaning and microbiological applications for raw materials, intermediate products, stability, bulk and final products, over the counter and prescription products. The main focuses was a detailed revision of the validation reports for current validated methods and suggest any changes needed to revalidated any method up to modern qualifications and international governing agencies regulations.• Investigation of stability failures and evaluation of analytical methods validation reports.• Worked with R&D and interfaced with the Chemists in the QC Lab.• Analyzed methods to check for accurateness and robustness. • Interacted with all levels of the organization.• Investigated stability testing methodologies in gel caps.• Wrote validation protocols for method validation.
Senior Research Chemist
• Successful process development of a purine nucleoside phosphorylase (PNP) inhibitor currently in the pivotal stage of clinical trials• Tech transfer of key process steps from lab scale to pilot scale to manufacture multi-kilos of drug substance to support clinical program• Conducted spiking studies to support justification of starting materials for successful filing with the Agency. Based on this data, the Agency has accepted the two building blocks as registered GMP starting materials• Successfully synthesized multi-kilos of a broad based antiviral compound to support ongoing toxicology studies• Identification, isolation, synthesis and full analytical characterization of process impurities for ongoing drug development programs as part of the regulatory requirement • Purification of process sludge using preparatory high pressure liquid chromatography to isolate process degradents prior to manufacturing of registration lots• Responsible for analytical method development for ongoing drug development programs• Synthesized labeled drug substance to be used as internal standards (stable isotopes) for BioAnalytical department• Coordinated activities with product development group on polymorph and salt selection of potential new drug candidates• Responsible for efficient functioning and upkeep of the cGMP facility to be in compliance• Proficient in handling small to large scale reactors, Biotage columns, prep HPLC, NMR, prep LC, IR, MS and Karl-Fisher equipment• Participated as a project sub-team member on various drug development programs• Responsible for drafting technical documents and writing various sections of the IND and NDA• Trained in GMP and GLP environment and familiar with current regulatory guidance• Responsible for procurement of chemicals, reagents and maintenance of the scale-up lab
Research Scientist
• Created and developed new chemical compounds for this bulk pharmaceutical company, which supplies lipid products to researchers and pharmaceutical companies worldwide• Successfully completed the synthesis and scale-up of multiple sophisticated compounds including JBT-2000, Safingol, Lipid A, synthetic ether lipids, synthetic platelet activating factor and analogs• Synthesized, purified, and performed full spectroscopic analysis on new chemical compounds • Customized new chemicals to specifications by adapting pre-existing synthesized chemicals• Developed expertise in synthesis within argon and nitrogen atmospheres, as well as extra-dry glassware• Utilized laboratory equipment and analytical instrumentation including NMR spectrometers, gas chromatography, mass spectrometers, and infrared spectrometers• Complied with cGMP and GLP regulations, SOPs, and Analytical Test Methods
Research Scientist
• Taught 200-level organic chemistry courses at 17,000-student university• Supervised laboratory and teaching assistants. Performed research and applied for grants• Worked with local companies and post-graduate students on special projects and research-related activities• Participated in research involving the synthesis of new Magnetic Resonance Imaging (MRI) compounds• Synthesized innovative chemical ligands that show promising application with MRI for diagnosis of myocardial ischemic disease• Researched methods to create new compounds with greater contrast efficiency and improved bio-distribution• Performed complete synthesis, purification, and full spectroscopic analysis of new chemical compounds • Purified compounds using partition chromatography, distillation, recrystallization, thin layer chromatography, and flash chromatography • Taught courses, conducted lectures, and participated in laboratory demonstrations.
Posdoctoral Fellow
Explore new methodologies for pulp bleaching.
Colleagues at Axsome Therapeutics, Inc.
Other employees you can reach at axsome.com. View company contacts for 48 employees →
Mike Cabrera
Colleague at Axsome Therapeutics, Inc.Miami, Florida, United States
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Kelly Santiago, Mba
Colleague at Axsome Therapeutics, Inc.Kenosha, Wisconsin, United States
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Doug Moore
Colleague at Axsome Therapeutics, Inc.Spring Hill, Tennessee, United States
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Ashley Varghese
Colleague at Axsome Therapeutics, Inc.New York City Metropolitan Area, United States
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Matthew Distasi
Colleague at Axsome Therapeutics, Inc.New York, United States
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Bianca Cruz
Colleague at Axsome Therapeutics, Inc.New York City Metropolitan Area, United States
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Corey Pauline
Colleague at Axsome Therapeutics, Inc.Bridgeville, Pennsylvania, United States
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Christie Maranto
Colleague at Axsome Therapeutics, Inc.Lafayette, Louisiana Metropolitan Area, United States
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Darren S.
Colleague at Axsome Therapeutics, Inc.Austin, Texas, United States
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Pam Anderson
Colleague at Axsome Therapeutics, Inc.United States
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Jesus Juárez-Brambila, Bs, Ms, Phd. education
Ph.D., Synthetic Organic Chemistry
Ms, Synthetic Organic Chemistry
Bachellor In Science, Chemistry, Biology And Pharmaceutical Sciences
Frequently asked questions about Jesus Juárez-Brambila, Bs, Ms, Phd.
Quick answers generated from the profile data available on this page.
What company does Jesus Juárez-Brambila, Bs, Ms, Phd. work for?
Jesus Juárez-Brambila, Bs, Ms, Phd. works for Axsome Therapeutics, Inc..
What is Jesus Juárez-Brambila, Bs, Ms, Phd.'s role at Axsome Therapeutics, Inc.?
Jesus Juárez-Brambila, Bs, Ms, Phd. is listed as Director, Analytical Development, CMC at Axsome Therapeutics, Inc..
What is Jesus Juárez-Brambila, Bs, Ms, Phd.'s email address?
AeroLeads has found 1 work email signal at @axsome.com for Jesus Juárez-Brambila, Bs, Ms, Phd. at Axsome Therapeutics, Inc..
What is Jesus Juárez-Brambila, Bs, Ms, Phd.'s phone number?
AeroLeads has found 1 phone signal(s) with area code 201 for Jesus Juárez-Brambila, Bs, Ms, Phd. at Axsome Therapeutics, Inc..
Where is Jesus Juárez-Brambila, Bs, Ms, Phd. based?
Jesus Juárez-Brambila, Bs, Ms, Phd. is based in Jemison, Alabama, United States while working with Axsome Therapeutics, Inc..
What companies has Jesus Juárez-Brambila, Bs, Ms, Phd. worked for?
Jesus Juárez-Brambila, Bs, Ms, Phd. has worked for Axsome Therapeutics, Inc., Juarez Consulting Group. Llc, Cambrex, Roche, and Nektar Therapeutics.
Who are Jesus Juárez-Brambila, Bs, Ms, Phd.'s colleagues at Axsome Therapeutics, Inc.?
Jesus Juárez-Brambila, Bs, Ms, Phd.'s colleagues at Axsome Therapeutics, Inc. include Mike Cabrera, Kelly Santiago, Mba, Doug Moore, Ashley Varghese, and Matthew Distasi.
How can I contact Jesus Juárez-Brambila, Bs, Ms, Phd.?
You can use AeroLeads to view verified contact signals for Jesus Juárez-Brambila, Bs, Ms, Phd. at Axsome Therapeutics, Inc., including work email, phone, and LinkedIn data when available.
What schools did Jesus Juárez-Brambila, Bs, Ms, Phd. attend?
Jesus Juárez-Brambila, Bs, Ms, Phd. holds Ph.D., Synthetic Organic Chemistry from University Of California, Santa Cruz.
What skills is Jesus Juárez-Brambila, Bs, Ms, Phd. known for?
Jesus Juárez-Brambila, Bs, Ms, Phd. is listed with skills including Hplc, Analytical Chemistry, Chromatography, Pharmaceutical Industry, Gmp, Organic Chemistry, Organic Synthesis, and Chemistry.
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