To serve a company as a compliance agent, keeping all documentation, change controls, contracts, training up to date.
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Training Manager, Trainer, Engineering Support, Documentation Manager, Documentation Specialist, Documentation, Document Control
C and C++, application optimization, test and implementation concentrating on advanced techniques and architectures. Specializing in scripting languages, compilers and technology management. I have significant experience in systems/software engineering, and a proven record of leading and organizing diverse technical projects. I have also led in the development of internal development standards, change control processes, in...
I am a Information Technology Leader and Mentor. I am seeking a leadership position where I may use my skills, training and desire to grow an effective IT Team, to benifit the goals and mission of a progressive organization.
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ITILv3, Change Control, Help Desk, Infrastructure, Design, Leadership
24 years in Pharmaceuticals as a scientist/chemist.
Ideal Companies: Dupont, Invitrogen
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laboratory supervisor, Chemist, Cleaning Validation, Validation, Protocol, Risk management
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biotech, quality, pharmaceutical, assurance, regulatory, biotechnology, batch, validation, control, review, document, change, protocol, deviation, capa, management, manager, specialist, release, GMP
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Document Management, Change Control, CAPA, Customer Complaints, Auditing
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Strategic Manangement, Quality Audits, Compliance, Operations, Process Improvement, Revision Change Control, Project Management, Profit/Loss
Domestic and international regulatory strategy to market (medical device, pharmaceutical, combination and consumer products). Implement quality management systems; prefer start-up or small company environment where there is a lot of building (not maintaining) to do.
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CAPA, FDA, change control, PMA, complaint, CE Mark
My goal is to come into a company and improve efficiency and effectiveness of document controls systems to increase customer satisfaction, both internal and external.
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Document Control, Configuration Management, Change Control, Internal Auditing, Quality Systems
Quality Assurance professional with problem-solving abilities in Pharmaceutical and Biotechnology industries. Primary strengths include US (FDA) 21 CFR, and ICH Q7A Guidance for API Manufacture, Quality Systems development and implementation and strong auditing skills. Introduced and managed electronic document management software including validation, implementation, and maintenance, as well as project team leadership. R...
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Quality Assurance, FDA regulations, CAPA, Document Control, Change control
