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Eamonn Murphy personal email
Pharma lab leader with progressive and diversified experience in R&D and Quality at Allergan-Actavis. Highly motivated and diligent investigator with strong scientific reasoning and creativity. Practical experience in talent acquisition, mentoring and retention, leading by example. Passionate in enabling teams and stakeholders for innovative paths toward improved lab efficiency and product quality – compliance.Broad scientific background and extensive expertise in analytical method development, validation, technology transfer, method – drug product investigations, project management and method remediation project leadership in a GMP environment. • Subject matter expert for investigation and resolution of complex analytical - technical issues ensuring the uninterrupted supply of commercial drug products to the customer • Led global pharma organization through a strategic quality and compliance project by designing and implementing a cross-functional organization project plan that enabled compliance with new elemental impurity regulatory requirements • Built cross-functional teams involving AD, Quality (QA, QC), Regulatory, Manufacturing, Third Party CMO & CRO for complex project management and collaboration across departments • Established expert lab teams and GMP labs for LC-MS investigation support and ICP-MS labs for execution of non-routine lab analyses. Resulted in improved quality of investigations and significant cost savings for quality and manufacturing operations• Addressed FDA inspection queries, drafted deficiency responses, provided expert input for field alert investigations• Managed lab documentation (protocol, report, technical justification, SOP, specification) change control, CAPA creation to support GMP activities and maintain compliance
Matinas Biopharma
View- Website:
- matinasbiopharma.com
- Employees:
- 17
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Director Qc And AdMatinas BiopharmaBogota, Nj, Us
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Director Qc & AdMatinas Biopharma 2018 - PresentBedminster, New Jersey, Us
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Assoc. Director, Analytical Tech ServicesTeva Pharmaceuticals Aug 2016 - Dec 2017Tel-Aviv, Il• Managed and aligned the legacy Actavis Americas Elemental Impurities compliance project with the Teva standard. Managed the Elemental Impurities laboratory network (four labs) and program for Actavis commercial product. Project scope included fifteen sites globally with a central lab staff of fourteen scientists and technicians. Successfully completed method validation and screening for a total of four hundred products to demonstrate compliance with new regulatory requirement • Provided expert analytical method and product investigation support to Teva domestic sites. Several critical method issues and technical investigations were resolved resulting in uninterrupted supply of critical product to the market -
Sr. Manager, Analytical Global Pharm TechAllergan Mar 2015 - Aug 2016Dublin, Coolock, Ie• Managed the Actavis Americas Elemental Impurities compliance project. Coordinated project scope and managed the Elemental Impurities laboratory network (four labs) and program for Actavis commercial product. Project scope included fifteen sites globally with a central lab staff of fourteen scientists and technicians. Successfully completed method validation and screening for two hundred products to demonstrate compliance with new regulatory requirement • Managed analytical GMP lab group to support investigation and compliance based projects at the Elizabeth, NJ site. • Provided expert analytical method and product investigation support to domestic sites. Several critical method issues and technical investigations were resolved resulting in uninterrupted supply of critical product to the market• Managed commercial product method remediation at Actavis Elizabeth, NJ ensuring key commercial products supply to customer• Subject Matter Expert for Third Party Operations on method enhancement projects for compliance of drug products with current ICH guidelines• Reinforced organization compliance and quality culture with FDA inspectors by addressing FDA inspection queries, drafting 483 deficiency responses and providing expert input for field alert investigations. • Mentored and developed team of ten scientists to establish and maintain an efficient expert analytical lab group -
Manager, Analytical Tech ServicesActavis Plc (Now Allergan) Jan 2010 - Mar 2015Dublin, Ie• Established and managed a GMP lab and expert analytical lab group to support investigation and compliance based projects at the Elizabeth site • In 2013-2014, designed and implemented the Actavis Americas Elemental Impurities compliance project. Established and managed the Elemental Impurities laboratory network (four labs) and program for Actavis Americas commercial product. Project scope included fifteen sites globally with a central lab staff of fourteen scientists and technicians. • Provided expert analytical method and product investigation support to three domestic sites. Several critical method issues and technical investigations were resolved resulting in uninterrupted supply of critical product to the market• Managed commercial product method remediation at Actavis Elizabeth, NJ and Lincolnton, NC sites from 2010 onwards ensuring key commercial products supply to customer• Subject Matter Expert for Third Party Operations on method enhancement projects for compliance of drug products with current ICH guidelines• Reinforced organization compliance and quality culture with FDA inspectors by addressing FDA inspection queries, drafting 483 deficiency responses and providing expert input for field alert investigations. • Mentored and developed team of six scientists to establish an efficient expert analytical lab group. Group increased to ten scientists by 2015. • From 2012 onward, responsible for the assessment of API Supplier Change Notifications / DMF Updates (10-12 per year) for the Actavis Elizabeth NJ site -
Manager Analytical ServicesActavis Totowa Jan 2008 - Jan 2010• Lead on method remediation project for two product re-introductions under consent. Product re-introductions were key commercial successes for site• Provided expert analytical method and product investigation support. Several critical method issues and technical investigations were resolved resulting in uninterrupted supply of critical product to the market• Managed internal Actavis lab with two resources for investigation support through identification of impurities by HPLC mass spectrometry. Prompt identification ensured uninterrupted market supply of product
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Principal ScientistActavis Totowa Llc Jul 2004 - Jan 2008Dublin, Ie• Provided expert analytical method and product investigation support to site. Several critical method issues and technical investigations were resolved resulting in uninterrupted supply of critical product to the market• Managed commercial product method remediation ensuring key commercial products supply to customer• Established and managed an internal Actavis lab with two resources for investigation support through identification of impurities by HPLC mass spectrometry. Prompt identification ensured uninterrupted market supply of product -
Chemist / Glp Study DirectorCarbogen Ag Jun 2001 - Mar 2004• Supervised GLP projects with three direct report chemists in the characterization of primary reference standards for drug substance and impurities for Novartis Animal Healthcare in Basel• Liaised with Novartis Animal Healthcare, Carbogen AG Management, Quality, and R&D chemist group to ensure timely completion of projects within budget• Authored characterization protocols, reports, documentation for reference standard characterization• Responsible for administration of characterization/recertification, documentation and storage of standards at Carbogen AG, and international distribution of standards for Novartis Animal Healthcare, Basel• Interpreted and reported on non-routine external CRO and internal analytical data including pyrolysis-GC-MS and multinuclear NMR experiments, as examples, for investigation support• Operated in a GMP compliant paperless lab environment with SQL LIMS
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ChemistCardinal Health 2004 - 2004Dublin, Oh, Us -
ResearchEth Zurich 1998 - 2001Zürich, Ch -
Research At Inorganic Chemistry InstituteUniversity Of Goettingen 1994 - 1997Göttingen, Niedersachsen, De
Eamonn Murphy Skills
Eamonn Murphy Education Details
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Ph.D.Chemistry
Frequently Asked Questions about Eamonn Murphy
What company does Eamonn Murphy work for?
Eamonn Murphy works for Matinas Biopharma
What is Eamonn Murphy's role at the current company?
Eamonn Murphy's current role is Director QC and AD.
What is Eamonn Murphy's email address?
Eamonn Murphy's email address is ef****@****ine.net
What schools did Eamonn Murphy attend?
Eamonn Murphy attended Ph.d..
What skills is Eamonn Murphy known for?
Eamonn Murphy has skills like Pharmaceutical Industry, Gmp, Standard Operating Procedure, Good Laboratory Practice, U.s. Food And Drug Administration, Technology Transfer, Validation, Corrective And Preventive Action, Change Control.
Who are Eamonn Murphy's colleagues?
Eamonn Murphy's colleagues are Gabriel Ramírez, Geetanjali Vaidya, Chris Marcinek, Cpa, Carlos Duran, Gerardo Zelaya, David Boalleti.
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