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Online Resumes with "GCP GMP"
Experienced Certified Clinical Research Professional and Certified Critical Care Nurse with excellent communication skills and proven track record of accomplishment in assisting potential and established investigative sites to meet and or exceed established goals. Recognition Awards for communication and cooperation with Co-workers and Sr. Project Management. Excellent knowledge of FDA CFR, GCP/GMP, ICH guidelines. Highly ...
I'd like to use my people and organization skills to communicate compliance requirements to cross-functional departments emphasizing the legal obligation biotech/pharma has to regulatory agencies and patients in an organization who supports the Quality Systems.
Cover Letter Ignace Vallejo, MS. GCP and GMP QA Manager Certified Quality Auditor GMP; by CFPA. Certified Six Sigma “Black belt”. 525 Neptune Ave, Brooklyn, NY 11224. Apt 22 F Home # 718 946 0556. Mobile # 917 359 3028. firstname.lastname@example.org Good Clinical Practice (GCP). Audits were followed according to our SOPs and ICH GCP regulations and Guidelines. The vendor audits were preformed, as follows: • On Octo...
Solutions-focused Project Manager - 20+ years experience - combining scientific, business, account management, and client relations - Princeton, NJ
Tags for this Online Resume: Bilingual English and Japanese, Project Management, Clinical Drug Development, Pre-Clinical Research, Client Relations and Support, GLP / GCP / GMP, Strategic Planning / Execution, Business Development
Customer Support, Regulatory Compliance, and Account Management professional, experienced in the pharmaceutical, biotech, and software fields; knowledgeable in industry compliance standards of GCP, GMP, GDP, and CAPA management; commended by clients for 24/7 support readiness, responsiveness, audit preparedness, and reference ability; recognized for superior organizational, communication, documentation, mentoring, and team ...
My goal is to leverage my strong scientific, medical, and clinical trial experience as the foundation for building a career in Pharmaceuticals and Biotech companies. The positions I am interested are Clinical Scientist, Drug Safety Scientist, PV scientist, Non-MD Study Clinician, Clinical Trial Manager and other opportunities in San Francisco bay area. I am open to both permanent and contract positions.
SUMMARY Extensive management and technical experience with pharmaceutical companies in the areas of Quality Assurance, Quality Control, Manufacturing Support and Product Development. Back ground includes: * Risk Management * Process Improvement Projects * Clinical Investigator Site Audits GCP/GMP/PV Internal/ External Audits * Documentation audits * GMP, GCP Deviations/Investigations Change Control Management * Complaints H...
Summary Highly skilled medical doctor with more than 15 years medical knowledge in various therapeutic area. 5 years' experience as Clinical Data Manager ensuring that data for clinical trials is properly collected, validated and clean. Diligently evaluate data, verify results and present conclusions. Excellent track record when it comes to consistent quality and reliability in carrying out research duties according to regu...