CV, Curriculum Vitae and Online Resumes Search

Recruiters - Try Postings!

Postings.com™ is a must-have for recruiters who want to:

  • Find Qualified Candidates
  • Find Job orders and Post Splits
  • Be Found in Search Engines
  • Implement a Social Sourcing Strategy
30-Day Free Trial!



Job Seekers - Look Here!

Hitting a wall with your job search? Try Climber Premium.

  • Top the Search Engines
  • Unsurpassed Candidate Marketing
  • Power Career Networking
  • Fresh Jobs from the Net

Were you looking for fda-regulations job results?
Click Here to search for fda-regulations in our 2.4M jobs.



Online Resumes with "fda regulations"



Clinical Research Associate, seeking entry-level, in-house opportunity

I am an excellent candidate for a Clinical Research Associate position due to my unique combination of experience in Preclinical Research and Development, Pharmaceutical Sales, and CRA Training. In addition to the skills and accomplishments detailed in my c.v., please consider the following highlights: Certification from Barnett International (July 2012): 10-Week CRA & CRC Beginner Program. Coursework emphasized FDA reg...

Certified Production Technician/ Supplier Operator - Avon Products Inc.

Machine operator @ Avon with extensive experience in operating various machines, Anderson-Filler/Nabach-Crimper and Case packers,to name a few, also have been trained as a material supplier in an FDA regulated environment. Aware of SOP's and complience with cGMP's.

Tags for this Online Resume: machine operator, production worker, material handler, line supplier, material supplier

Lead Research Analyst

Recent medical school graduate with seven years of previous experience in the biotechnology industry. Experience includes leadership roles in research and quality control supporting the manufacture of several different drugs and vaccines under strict FDA regulations. Dedicated to combining the skills and knowledge acquired in biotechnology with my medical degree in support of the eradication of some of the diseases that hav...

Head, Quality & Regulatory Affairs, CA, MD in US; Singapore, Australia, Taiwan, China Japan in Asia

In charge of corporate quality and regulatory affairs function in Asia Pacific Region of international giant pharmaceutical or biotech companies. English and Chinese-speaking countries. GXPs experts. Registrations, audits, trainings.

Tags for this Online Resume: Regulatory Head, Quality Compliance, Asia, China, Pharmaceutical, Bioteh, Quality and Regulatory Compliance, Inspection, , Pharmaceutical/Bioteh/Medical Device Industry, FDA Quality and Regulatory Compliance, , FDA Inspection, US/EU Market, US/Asia Mobile, Lifecycle Total Management, US/Asia Mobile for Job Locations, 30+ years Experience in FDA Regulated Industry

Operations Manager - Medical Device Manufacturing - FDA Regulated Inductry

To successfully lead an organization into higher quality, higher efficiency manufacturing.

Software Testing/QA Engineer, 6 years experience

SOFTWARE TESTING professional recognized as someone counted on to “take most challenging tasks with a 'cool and helpful presence'“ and for going out of the way to learn new technical subject areas. Known for a combination of focused analytical skills and interpersonal strengths. With six years of experience having deep background in the design, development and testing of software with expertise in manual testing while worki...

Medical Technologist/Regulatory Affairs Professional with 7 clinical research and laboratory science years experience and extensive knowledge of cGMP, FDA regulations, CAP/CLIA, SOP preparations and editing, clinical research project management.

Seeking a position within an esteemed organization where my expertise would add great value.

Tags for this Online Resume: Clinical Research Specialist, Clinical Laboratory Specialist, Biologist, QA/QC International Coordinator, Regulatory Affairs Professional, Drug Safety Associate

Regulatory and clinical affairs -- 20 years experience

A position in regulatory affais/medical writing for human clinical trials

Tags for this Online Resume: medical writing, regulatory affairs, FDA regulations, clinical. research, clinical trials, medical research

Featured Profile

Sr. Quality Engineer, 20 years FDA regulations, CQA, Midwest

Sr. Quality Assurance Engineer with twenty years quality experience complying with FDA regulations. Energetic team player supporting quality within all manufacturing operations.

Tags for this Online Resume: Quality Engineer, CQA, Risk Management, Quality Systems , FDA, 21CFR Part 11

Featured Profile

Featured Profile