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Darius Moily is listed as Sr Q.A Engineer/Technical writer at Pfizer, based in Walnut Creek, California, United States. AeroLeads shows a work email signal at westpharma.com, phone signal with area code 925, and a matched LinkedIn profile for Darius Moily.
Darius Moily previously worked as Sr Quality Engineer at Pfizer and Sr Technical writer at West Pharmaceutical Services. Darius Moily holds B.S, Electrical Engineering from San Francisco State.
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AeroLeads found 1 current-domain work email signal for Darius Moily. Compare company email patterns before reaching out.
I am a multilingual advanced manufacturing/Q.A engineer/ manager with 10 + years experience in introduction of new products to pilot and volume manufacturing and FDA remediation. I have worked in four different industries including, scientific instrumentation (Varian), semi conductors (Applied Materials), high precision optics (Tinsley Labs) and medical devices (Tyco/Covidien).My work included taking control of designs at 80% of prototype completion in R&D and revising all drawings and B.O.M for DFM and DFT through official ECO and following ISO and Six Sigma standards and guidelines. I am very familiar with working under FDA guidelines and have a lot of experience working with internal agencies such as regulatory, clinical and documentation. My work includes creation and implementation of the RoHS (Reduction of Hazardous Substances) program at Tyco.I was in charge of designing, building and training test beds for pilot and volume manufacturing. My work in Manufacturing included writing SOEs, DMRs, and Kan Ban design. I also have extensive experience working with OEM vendors on an international level.I have excellent writing and communication skills. In addition, I am fluent in French, English and Spanish. My extensive understanding of foreign cultures have helped me to be very efficient in cutting manufacturing costs, and achieving very high error free fabrication yields in overseas factories.Specialties: Certification in Labview, SolidWorks and AutoCad.How to Transfer Products from R&D to Manufacturing given by AMA, Certified Qualified Electrical Worker (To work on high voltage equipment) by Varian in Walnut Creek and Applied Materials in Santa Clara.Completed several courses in Semi conductor fabrication, Design, CVD and Lithography.View Logic, Math lab, Electronic workbench and Spice. CBEST (California Teaching Credentials) certificate. Fluent in English, French, Persian, Spanish
Listed skills include New Product Validation, Kaizen, Solidworks, View Logic, and 44 others.
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New York, New York, US
Design control and DHF remediation of complete design control suite of documents. From Risk Management, Input/ Output, all FMEAs, Design Verification/ Validation. This remediation effort was concentrated on Combination Medical Products.
Exton, PA, US
Please refer to previous experience at West for details of my duties.
This project involved the move of manufacturing facility. My work included creation of Quality Plans and Master Validation plans affecting all departments. Assuring all quality documents are updated for the move (Over 4000 docs). Assisting in all Process Verification at the new location. Assisting in the de-commissioning of the old facility.
Exton, PA, US
Remediation effort concentrating on "design controls" deficiencies. Specifically DHF/DMR documentation such as Project Plan, Design Input/ Output, Engineering protocols, Validation protocols, dFMEA, pFMEA with emphasis on both pre-mitigation and post mitigation and residual risk for risk reduction control. My work was concentrated on various drug delivery.
Raynham, MA, US
Remediation effort concentrating on "design controls" deficiencies found in FDA and internal audits.Concentrated effort on DHF remediation, Functional & Design Requirements, Verification & Validation, Risk Analysis, and post market surveillance. Remediation was concentrated on orthopedic bone fixation plate/screw constructs.
Chicago, IL, US
Remediation effort concentrating on "design controls" defficiencies found in FDA and internal audits.Heavy emphasis in V&V, including preparation of verification protocol, test scripts, sample size rationale, risk analysis. Test execution, test result protocol prep, Change orders and statistical analysis of data. DMR and DMR index preparation and.
Fridley, Minnesota, US
Engineer in charge of all issue on the assembly line for Trellis products (Advanced isolated Thrombolysis Catheter with 2 occluding balloons.).My work includes, line support, failure analysis, root cause and preventative investigation, statistical analysis based on risk factor, international supplier qualification, DCO, NMR, FMEA, and Engineering reports.
In charge of a team of a technician and two Sr programmers.Managed client’s technical IT needs and subsequent resolution.Developed road map for commercialization of revolutionary software in document management systems.Developed Beta test parameters for software product in house.
Fridley, Minnesota, US
· Formulated the full RoHS plan for all equipment produced in the Oximetry division, including: · Identified all non RoHS compliant parts in all products, from PCBs to mechanical shells. · Identified replacement RoHS compliant parts through vendors. · Changed all drawings; both Electrical and mechanical through official ECO release. · Sorted through all.
New York, NY, US
· Design of optical metrology tools and fixtures for the measurement of high precision lenses and mirrors including aspheres. · Discovered novel approach to polishing in the Angstrom regime which introduced in Situ sharpening of polishing tools and in the process cut down on final polish time by 30%. · Part of the main team for CCOS (Computer Controlled.
· Design and Trouble-shooting of components of high power microwave and RF enhanced CVD equipment. · Developed the control system for a novel tool used in measuring the thermal conductivity of thick and thin diamond films.
· Subjects included: Beg Math, Adv Math, Biology, English, French, Spanish, History and social sciences.
Santa Clara, CA, US
300 mm Chamber Work Center Manager/New Product Intro Electrical Engr· Responsible for Pilot manufacturing for all 200 and 300 mm Metal Deposition Chambers Including Process chambers such as TTN, IMP TaN, IMP Tin, SIP Cu, PVD Ti, PVD TaN, CVD, Preclean and Degas in the chamber work center and a staff of 32 assemblers, and 2 supervisors.· Implemented several.
· Responsible for the development of new products such as NGL (Next Generation Lithography) mask membrane material using PECVD processes for fabricating ultra thin, ultra smooth diamond films, low propagation loss films for SAW (Surface Acoustic Waves) devices application and inert coating for semiconductor equipment reactors.· Responsible for development.
· Responsible for implementation of cost reduction projects on all electronic components (Harnesses and PCBs) used on Mass Spectrometer products.· Worked with R&D engineers to reduce cost and ensure manufacturability of new designs prior to introduction.· Responsible for the design and implementation of functional test beds to support JIT manufacturing..
Quick answers generated from the profile data available on this page.
Darius Moily works for Pfizer.
Darius Moily is listed as Sr Q.A Engineer/Technical writer at Pfizer.
AeroLeads has found 1 work email signal at @westpharma.com for Darius Moily at Pfizer.
AeroLeads has found 1 phone signal(s) with area code 925 for Darius Moily at Pfizer.
Darius Moily is based in Walnut Creek, California, United States while working with Pfizer.
Darius Moily has worked for Pfizer, West Pharmaceutical Services, Codman/ Johnson & Johnson, Synthes, and Hill-Rom.
You can use AeroLeads to view verified contact signals for Darius Moily at Pfizer, including work email, phone, and LinkedIn data when available.
Darius Moily holds B.S, Electrical Engineering from San Francisco State.
Darius Moily is listed with skills including New Product Validation, Kaizen, Solidworks, View Logic, Labview, Statistical Analysis, Minitab, and Autocad.
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