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Were you looking for 21-CFR-Part-11 job results?
Click Here to search for 21-CFR-Part-11 in our 2.4M jobs.
Online Resumes with "21 CFR Part 11"
Sr. Quality Assurance Engineer with twenty years quality experience complying with FDA regulations. Energetic team player supporting quality within all manufacturing operations.
A dynamic, logical thinking, performance driven IT professional, with 15 years of experience out of which fourteen years of Lotus Notes Development including 5 years of Business Analysis experience and one year of Lotus Notes Administration experience using Notes version 7.01 & Notes version 8.4. Possess full knowledge of Software Development process including requirements definition, prototyping, Proof of concept, design,...
Tags for this Online Resume: SDLC, Agile, Scrum, Java, Project Management, Oracle, 21 CFR Part11, GCP, HIPAA, HL7, Software Architect , CTO, Healthcare, Clinical Research , Offshore Development, Open source technology, EDC, RDC
I have 14 years of experience in pharmaceutical industries. Results oriented individual with a track record of instituting and maintaining high levels of Quality Assurance and leadership. I’m seeking additional opportunities for professional development in consulting, validation, compliance or technical areas. Strong analytical and planning skills. Six Sigma Black Belt trained. Knowledge in FDA, cGMP, GLP, 21 CFR - Part 820...
Ideal Companies: Pharmaceuticals or food industries
Outgoing personality with strong ability to solve changing business/industry needs with application/database development. Versatile, independent thinker with team attitude.
Senior Scientist - six years; Associate Scientist II - three years; Bioprocess associate -threr years; Research associate for 5 years; Instructor (HS) - for five years
Experienced senior scientist with expertise in protein or antibody purification. Followed cGMP training with FDA 21CFR part 11 and demonstrated abilities in the scale-up and transfer of purification processes from the laboratory to production. The goal will be using my experience and knowledges for contributions to the biotech industry.
Tags for this Online Resume: Process Development for purification, Monoclonal Antibody purification, GMP Compliance, Large scale design for purification, techniques transfer and disposable technology , team management
Dear Hiring Manager, I am interested in exploring career opportunities with your company and have therefore enclosed my resume for your review. This position seems ideal for my experience, education, skills, and career interests. I am eager to contribute my enthusiasm and teamwork to your organization. My professional goal is to enhance my research development and senior leadership experience. I believe that I could...
Seeking position where I can maximize my quality management background in clinical trials, apply experience in SDLC and 21 CFR Part 11 and utilize my strong analytical and communication skills.
An IT professional with over 10 years experience as a validation specialist, senior/lead technical writer, documentation manager, analyst, tester, and end-user trainer. IT experience is complimented by solid management and leadership experience gained as a US Army officer.
A highly experienced and hands-on technical IT project manager and laboratory automation scientist with in-depth knowledge of the SDLC and pharmaceutical regulations (ie. 21 CFR part 11, and GLP regulations). 15 years of experience.