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Over 20 years experience in pharmaceuticals. Expertise and knowledge in Granulation, Drying, Milling, Blending and Compounding. Knowledge of Compression (Kikusui, Sejong) and Coating (Vector and Glatt). Excellent troubleshooting skills due to technical knowledge and work experience. Strong work ethic with commitment to quality and meeting schedule requirements to support company goals
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Sr. Manufacturing ManagerTris Pharma Feb 2021 - PresentMonmouth Junction, New Jersey, United States -
Manufacturing ManagerTris Pharma Sep 2016 - Jun 2022Monmouth Junction, New Jersey -
Senior Manufacturing SupervisorTris Pharma Sep 2012 - Sep 2016Monmouth JunctionManufacturing Supervisor• Supervise 30+ Technicians on 1st shift in meeting weekly production goals on a 24 hour/7-day schedule manufacturing both intermediate and final powder/liquid suspensions• Support off shifts by setting up the daily schedule and ensuring all raw material are available• Perform on the floor batch record reviews• Assign technicians to work areas on daily basis• Perform safety reviews/training as needed• Perform SOP training of technicians• Communicate with, support and motivate assigned technicians and participate in performance assessment, training and development.• Work with Class 2 and 3 Controlled drugs.• Monitor and approve timecards utilizing ADP system• Monitor Access to Controlled Substance Vaults• Troubleshoot equipment issues and recommend improvements to management• Work closely with QA/Packaging/Maintenance departments in order to keep department running efficiently• Perform managerial responsibilities during absences• Write investigations as needed and follow through to closure -
Shift LeaderAustarpharma, Llc Oct 2009 - Sep 2012Edison, New Jersey• Assist in the support and manufacturing of products for contract manufacturing. • Assist formulation department in scale up and manufacturing of batches• Maintain GMP facility• Schedule and coordinate calibration of equipment• Implement and maintain production department SOP’s• Train other departments on proper procedures in the cGMP facility.• Breakdown, clean and setup equipment. -
Shift LeaderAbbott Laboratories Apr 2003 - Aug 2009I was responsible for overseeing the 2nd Shift manufacturing team. My areas of responsibilty were granualtion, drying, blending, compression and coating. I performed Batch Record reviews and I performed performance evaluations for 2nd shift team. Communicate directly with maintenance, managers and QA in order to continue processing at all times. -
Production Technician IiHoffmann-La Roche Jan 1990 - Oct 1999• Experienced in wet granulation, spheronizing, fluid bed, milling and using PK blender and other production equipment• Developed batch record for new product launch• Assisted in validation for new product launch• Assisted in cleaning validation qualifications• Conformance to GMP and SOP requirements by following batch records accurately in granulation processing and encapsulation.• Performed setup, cleaning and troubleshooting of encapsulation machines.• Participated in stock build to prepare for product launch
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Frequently Asked Questions about William Layden
What company does William Layden work for?
William Layden works for Tris Pharma
What is William Layden's role at the current company?
William Layden's current role is Sr. Manufacturing Manager at Tris Pharma.
What is William Layden's email address?
William Layden's email address is de****@****hoo.com
What is William Layden's direct phone number?
William Layden's direct phone number is +173294*****
What schools did William Layden attend?
William Layden attended Ucnj Union College Of Union County, Nj.
What skills is William Layden known for?
William Layden has skills like Validation, Gmp, Quality Assurance, Capa, Pharmaceutical Industry, Formulation, Cleaning Validation, 21 Cfr Part 11, Change Control, Quality System, Customer Service, Structural Drying.
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William Layden
Division Chief Of The Organization And Personnel Division At Department Of DefenseSan Antonio, Tx3amedd.army.mil, mail.mil, defense.gov -
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