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Every service event gives us the opportunity to be great and prosperous,Good customer relationships come from honesty and integrity in the way we do business .

After 26 years of field Service I would like to transition into project management or technical sales. I have extensive medical devices back ground and laboratory sciences.

Ideal Companies: Perkin Elmer, Siemens, Agilent, Phillips medical, Trump, Berchtold, Skytron, Mercedes Benz, Google

Tags for this Online Resume: Management, Test, Project Management, Quality Assurance, TQM (Total Quality Management), Infection control, Siemens, Support, Surgical, Technical Support

EPMO / PMO Leader

Information Technology Resumes - Manager Resumes - Montvale, NJ

Pharmaceutical Information Technology Professional with over 20 years of application design, development, testing, and implementation experience. Areas of expertise include implementing systems and processes to help organizations achieve sustained business performance applied locally and on global program basis. Background includes a unique blend of business acumen, technical expertise, and financial discipline which enable...

Ideal Companies: Medco, Barr, Eisai, Becton Dickinson, Roche

Tags for this Online Resume: IT, Information technology, IS, Information Systems, Technology, Healthcare, PMO, EPMO, Portfolio Management, Project Management

Clinical Research Associate

Research Resumes - Analyst Resumes - Osseo, MN

To obtain a Clinical Research Position in the Minnesota Area.

Tags for this Online Resume: Knowledge of 21 CFR, Quality System Regulation (QSR), Medical Device Reporting, Regulatory Compliance , Regulatory Submissions , ICH GCP Guidelines

Production Supervisor

Manufacturing & Production Resumes - Aircraft Rigging Assembler Resumes - West Covina, CA

Jaime Giron 1250 S. Rimsdale Drive West Covina, Ca. 91791 626-456-2587 Greetings, I have been in the pharmaceutical industry for twenty + years and have worked for several well known companies. I seek the opportunity to be part of the manufacturing / management team if given the opportunity to do so. I have worked in all aspects in the pharmaceutical industry from Technician, Lead, Validations, Q.A., Q.C., Documentation C...

Tags for this Online Resume: Pharmaceutical, GMP's, FDA, 21 CFR, Nutraceutical, SOP's

10years bio analytical experience CV

Research Resumes - Analyst Resumes - ,

Dear Sir, I believe that my initiative drive and capability for hard work will make me suitable to your organization. I am a person who believes in career satisfaction along with care growth, and it is an organization like yours, which gives utmost priority to employee satisfaction that, will suit my career needs. Here with Iam enclosing my Curriculum vitae for your kind perusal. Hoping to hear positively from your e...

Tags for this Online Resume: Bioanalytical method development, Bioanalytical method Validation, Bioanalytical Subject Analysis in GLP conditions, Experience in LC-MSMS handling, Experience Protocal Review and Reports Review, Experience in 21CFR Part 11

Quality Manager

Manufacturing & Production Resumes - Quality Manager Resumes - Sussex, WI

I am a quality/lean professional who has worked in highly regulated environment and know what it takes to have manufacturing and office process compliant to regulations with minimum impact to productivity.

Tags for this Online Resume: ISO 9001:2008, Electro-Mechanical Integration, MINITAB, ISO 13485:2003 , FDA 21CFR820 , Lean Manufacturing

Medical Device / Pharmaceutical Quality and Validation Engineer

Engineering & Architecture Resumes - Process Engineer Resumes - Brighton, MA

I am seeking permanent opportunities as a Medical Device or Pharmaceutical Quality / Process / Validation Engineer. I have enjoyed my experiences in Software and Equipment Validations as well as Engineering Studies and Process Monitoring and Improvement.

Tags for this Online Resume: Validation, Bioprocessing, Specifications, 21 CFR part 11, IQ, OQ, PQ, process monitoring, manufacturing database, Medical Device, Process Improvement

Quality Engineer - 20 Years of Experience - Near 30022

Manufacturing & Production Resumes - Quality Engineer Resumes - Alpharetta, GA

I have been involved with numerious FDA regulated manufacturers in both the pharmaceutical as well as the medical device industry sectors in supporting them in meeting their FDA warning letter violations. These directives encompass 21 CFR Part 210 / 211 and 21 CFR Part 803, 806, 809 & 820 compliance statues. I pride myself in assisting team members in not only understand what the FDA is asking of them, but to enhance the ...

Tags for this Online Resume: quality assurance, regulatory compliance, engineering

Quality Engineer - 9 Years of Experience - Near 07305

Manufacturing & Production Resumes - Quality Engineer Resumes - Jersey City, NJ

apply my skill set in new product development technical reporting laboratory testing of new products guided by 21CFR.820 QSR QSM cGMP and standards ASTM ISO CE

Tags for this Online Resume: Jersey City, cGMP QSR QSM, 21CFR.820, DMR CAPA, QA Engineering, technical specifications, food production, consulting services

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