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Online Resumes with "CGMP"
At this time I would like to be a consultant or a temperary position to pharmaceutical companies for their quality or R&D problums. I have experience in dealing with FDA related issues in durg discovery and production. I can help the starter company to build up their quality system and train their employees to comply with the cGMP requirements by FDA. I do not mind to travel. I can speak, read and write Chinese in addition ...
Ideal Companies: Any company which can use my experience
Tags for this Online Resume: Qhality Assurance, QA, cGMP, FDA, ICH, Q7A, Inspection, Audit, Deviation Report, Change Control, OOS Report, Annual Report, DMF, validation, Purified Water, FDA Inspection
Successful pharmaceutical professional with over 36 years of cGMP supervisory and project management experience in a Lean parenteral manufacturing environment.
To obtain a challenging position that will fully utilize my talents and provide for growth and advancement.
I will become an accomplished scientist performing quality assurance and research and development investigations in the personal care and pharmaceutical industry. My work will directly improve the quality of life of those in our national and international communities. In the long term, I will mentor the up-and-coming generation of thinkers, especially those whose minds are undernourished and underappreciated.
Result-driven executive (18+ years, 35 Clinical Trail Designs and recruiting more than 3000 patients) with expertise commissioning and leading technology-based, Multi-million dollars revenue and growth initiatives ground solidly on business and economic value. As a Team Builder with extensive Clinical biostatistics (PK/PD, Clin. Operation & Clin. Trials), compliance with GCP, cGMP, and regulatory guidelines, Drug Developmen...
Tags for this Online Resume: RESEARCH AND DEVELOPMENT, PRECLINICAL PHARMACOLOGY, CLINICAL PHARMACOLOGY RESEARCH, CLINICAL PHARMACOLOGY RESEARCH, CLINICAL PHARMACOLOGY RESEARCH, CLINICAL PHARMACOLOGY RESEARCH, REGULAR AFFAIRS, REGULAR AFFAIRS, REGULAR AFFAIRS, REGULAR AFFAIRS
I’m looking for opportunities where I can mix the hands-on work with process troubleshooting/optimization in combination of managing of a product/project from the decision-making level regarding capital projects, project direction, etc. I have worked on all facets in the lifecycle of a process/product from the R&D side in its development and optimization coming into a fully validated manufacturing process and then supporti...
Looking for scientist position in Pharmaceutical/biotech companies
Senior scientist/clinical supply coordinator with broad experience managing and coordinating pharmaceutical clinical supply systems for API’s, Excipients, Packaging components, Finished drug products including Controlled substances, Reserve samples, and Chemical archives. Labeling and distribution of GMP Clinical supplies for worldwide GLP and GCP studies. Reconciliation and disposition of returned clinical supplies. Pro...
Over five years of diverse validation experience in the Pharmaceutical industry. Enthusiastic, ingenious, and results oriented professional. Highly effective in teamwork environment. Oriented towards resolution of problems. Knowledge of principal and supplemental FDA Regulatory Guidelines like: Solid Dosage Blend Uniformity, Dissolution Guideline, Stability Guidelines, cGMP, Conformance Standards, SUPAC and SOP’s. Expe...
over 3 years of experience as
Tags for this Online Resume: current Good Manufacturing Processes (cGMP) and Company Standard Operating Procedures (SOP)., of handle calibration, measuring & instruments , Proficient with MS Office Suite, Multilingual (Chinese, English, Japanese)
Draw upon strong mechanical aptitude to introduce process improvements that reduce production downtime, increase changeover efficiency, and decrease scrap materials as well as investigate and resolve equipment issues.
Go getter with a sense of humor. Loyal, trustworthy and full of life. Ready to take on any task given to me.
I am currently looking for an ethical company in the medical device or pharmaceutical industry that can utilize my experiences including but not limited to the scope of quality, of which I have been responsible for recruiting and adjusting personnel levels, QA Incoming Inspection (components and raw materials using sampling plans from ASQ Z1.4, MIL 105E and in-house specifications for inspections), QA Finished Product Relea...