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
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 21CFR job results?
Click Here to search for 21CFR in our 2.4M jobs.
Online Resumes with "21CFR"
Design/Develop/Sell/Manage/Travel
Outgoing personality with strong ability to solve changing business/industry needs with application/database development. Versatile, independent thinker with team attitude.
Ideal Companies: HP, IBM, IT SERVICES COMPANY, LOOKING TO MOVE INTO IT SALES
Tags for this Online Resume: JAVA, JSP, MySQL, SQL, SAS, Database, Programming, SQL Server, ACCESS, Microsoft Office, Web Development, Design, Development, Web, TERADATA, UNIX, PROGRAMMER, ORACLE
Production Supervisor with over nineteen years experience in the Biotechnical Industry. Solid background in Bioreactors, Column Chromatography, and Validation. Comprehension of 21CFR, cGMPs, and ISO to ensure FDA compliance. Experienced in training and
I am looking for a position that can use my vast knowledge in Biotech, equipment or Supervisory skills. I also will consider other positions outside the Biotech/Pharmaceutical field. I can work in a team atmosphere or as an individual working on my own projects. I have worked very closely with QA so I believe I could fit in very well with a similiar position. With my supervisor skills I can fit into many leadership role...
Tags for this Online Resume: cGMP, Asceptic Technique, Validation, Manufacturing
Compliant, but flexible...the best of both worlds
I am primarily interested in obtaining a VP position and using my knowledge to truly direct and enhance a companies experience with quality systems and to provide their customers with products that meet or exceed customer expectations.
Ideal Companies: Medical Device Manufacturers
Tags for this Online Resume: Quality Assurance, Project Management, Auditor, ISO 13485:2003, 21 CFR 820, QSR, Regulatory, Management, Medical Devices
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
Clinical Trials Manager
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...
Quality Control manager
Quality Manager with 17 years of experience within the Pharmaceutical Industry. Extensive experience in laboratory operation, laboratory start-up, laboratory automation, manufacturing compliance, new site start-up, deviation assessment, analytical method development and analytical method validation. Strong knowledge and skilled in securing compliance with regulations such as GMP’s, GLP’s and Quality System (21 CFR 820.180)....
Quality Assurance Manager - Clinical
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.
Tags for this Online Resume: Clinical Quality, SDLC, Part 11, Quality Audit
Computer System validation Specialist
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.
Tags for this Online Resume: validation, documentation
Mechanical Inspector- L-3 Communications 5 yrs- Ca
CMM Inspector, Opg , ISO-9000 and ISO-13485,21 CFR820, Mil-std
