Tony Sacre, Pmp work email
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Tony Sacre, Pmp personal email
Project Manager with unique background combining leadership and product development skills. Customer facing liaison for internal/external customers. Managing ophthalmology products in Development through Life Cycle stage. PMO R&D representative for EU MDR project. Managed dermatology, pharmaceutical (Rx), medical device, and cosmetic projects from concept to launch. Dependable team leader with demonstrated ability to communicate with internal and external customers. Strong analytical problem-solving skills used effectively to launch new products and reduce cost of goods for existing products. Project Management expertise integrating cross-functional teams including Quality Assurance, Quality Control, Marketing, Supply Chain management, Regulatory Affairs, and Manufacturing.Specialties: Project/Portfolio Management, Waterfall, Agile, analytical chemistry, CMC, CTD, Device, Rx, Cosmetic
Dayne'S Craft Barbecue
View- Website:
- daynescraftbarbecue.com
- Employees:
- 4
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PitmasterDayne'S Craft BarbecueFort Worth, Tx, Us
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Project ManagerAbbott Apr 2022 - PresentAbbott Park, Illinois, Us -
Project ManagerAlcon Laboratories, Inc. Jul 2011 - Jan 2022Geneva, Switzerland, ChSr. Manager PMO Surgical Systems and Processes. Global deployment of SalesForce/ServiceMax solutions, Portfolio , Communications, and Change Management.Project Manager for Alcon. Vision Care Ocular Health R&D projects. Project Manager for life cycle management (LCM) projects for Vision Care and Surgical business franchises 2011 - 2020.PMO R&D representative for EU Medical Device Regulation (MDR) project. Company wide effort to convert Tech Files from MDD to MDR format. Point of contact for R&D, interface with Quality, Supply Chain, Commercial, Clinical, and Medical Safety. Represented R&D in company wide web cast for project. Point of contact for internal and external customers, providing guidance and support to adhere to local governance processes. -
Sr. Quality EngineerReckitt Benckiser Feb 2011 - Jun 2011Slough, Berkshire, GbInterpret regulatory requirements and provide guidance for effective compliance, as well as providing coordination / support for programs and projects.Provide oversight and management of various Quality Processes such as; Internal Audit Program, Corrective and Preventive Actions System, Change Control, Supplier / Contract Manufacturer Quality Management, Non-Conforming Material, etc.Improve existing and develop new Quality Processes, writing and implementing associated procedures and other documentation.Conduct investigations of undesirable trends in production processes performance and unplanned events, perform root cause analysis, and develop and implement corrective and preventive actions.Conduct audits of suppliers and contract manufacturing firms in order to determine the effectiveness of their quality systems, as well as their capability to provide compliant goods and services.Provide technical guidance and facilitate problem-solving methodologies regarding quality-related issues. -
Project Manager, PmpCoria Labs Aug 2007 - Dec 2010• Project Manager for Coria Labs, distributor of dermatological products. Served as point of contact for internal and external customers.• Launched new cosmetic pressed powder in nine months by independently sourcing contract manufacturer and custom packaging. Led cross functional teams in multiple regions to accomplish goals.• Launched new line extension cosmetic brand extension in six months from concept to commercial, including sourcing a new contract manufacturer. Led teams in multiple regions.• Researched alternate packaging solution enabling major cosmetic brand entrance into world wide retailer, significantly increasing revenues.• Led project teams in commercial launch activities of NDA, ANDA, and 510(k) products.• Served as project leader to improve pharmaceutical process and scale up activities which increased efficiency and reduced manufacturing losses.• Served as liaison to Regulatory, Quality, Supply Chain, Marketing, and Sales providing a vast array of product history and information.• Submitted dossier to National Eczema Association for review and approval for branded cosmetic.
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Sr. ScientistHealthpoint Sep 2005 - Aug 2007• Authored, reviewed, and edited technical documents such as SOPs, CTDs, technical reports, batch records, analytical methods, protocols, etc.• Performed Stability trending analysis and shelf life assignments performed using linear regression and confidence intervals.• Reviewed manufacturing and testing procedures for compliance with cGMP, ICH, and relevant FDA guidelines. -
Group Leader, Analytical ChemistryDpt Laboratories Aug 2001 - Aug 2005San Antonio, Tx, Us• Group Leader responsible for supervision of laboratory employees, equipment maintenance and operation, lab operations, and point of contact for analytical services.• Developed and validated analytical methods to support product development, product release, and stability throughout entire life cycle of product.• Authored, reviewed, and edited technical reports, protocols, and documentation in support of submissions, investigations, and product development. -
Director, Quality ControlTextract Laboratories Jun 1999 - Jul 2001• Approved or rejected all components, containers, closures, in-process materials, packaging materials, labeling, and drug supplies as stipulated in 21CFR210 and 211.• Authored and edited SOPs for Quality Unit in support of drug product manufacturing.• Reviewed all production records for compliance with cGMP and corporate SOPs.• Developed and validated assay for botanical drug product per ICH guidelines.• Operated and maintained aseptic production area for aqueous extract of botanical product as in-process intermediate and lyophpilization for drug product.
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Group Leader, Analytical ChemistryIlex Oncology Nov 1997 - Jun 1999• Group Leader responsible for supervision of laboratory employees, equipment maintenance and operation, lab operations, and point of contact for analytical services.• Developed and validated analytical methods to support product development, product release, and stability throughout entire life cycle of product.
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Analytical ChemistDpt Laboratories Sep 1995 - Oct 1997San Antonio, Tx, Us• Developed and validated analytical methods to support product development, product release, and stability throughout entire life cycle of product.
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Analytical ChemistCedra Corporation Sep 1992 - Aug 1995• Developed and validated analytical methods for drug candidates in biological matrices to support preclinical and clinical studies.
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Staff ChemistCubix Aug 1990 - Aug 1992• Provided full contract service for mobile emission source testing per EPA and state environmental agencies. Prepared cost quotations, planning, executing onsite testing including results summary, formal report, and closing service to customer.
Tony Sacre, Pmp Skills
Tony Sacre, Pmp Education Details
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Texas State UniversityChemistry
Frequently Asked Questions about Tony Sacre, Pmp
What company does Tony Sacre, Pmp work for?
Tony Sacre, Pmp works for Dayne's Craft Barbecue
What is Tony Sacre, Pmp's role at the current company?
Tony Sacre, Pmp's current role is Pitmaster.
What is Tony Sacre, Pmp's email address?
Tony Sacre, Pmp's email address is to****@****bal.net
What schools did Tony Sacre, Pmp attend?
Tony Sacre, Pmp attended Texas State University.
What skills is Tony Sacre, Pmp known for?
Tony Sacre, Pmp has skills like Analytical Chemistry, Capa, Cmc, Ctd, Change Control, Cosmetics, Cross Functional Team Leadership, Fda, Formulation, Glp, Gmp, Gas Chromatography.
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