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Online Resumes with "CGMP"
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.
Highly accomplished PRODUCTION and PROJECT MANAGER with multi-Project Management experience in the Pharmaceutical/Biotech Industry (Generic Drug Production, Drug Discovery, Assay Development and High-Throughput Laboratory Automation and equipment). Proven track record in the arena of Robotic Engineering including on-time delivery of custom Automated Robotic Screening Platforms for High-Throughput Screening (HTS), as well as...
Tags for this Online Resume: project management, HTS, screening, robotic , laboratory equipment, biology, chemistry , pharma, Environmental Health and Safety, pharmaceutical , academic, Drug Discovery, automation
Hands on work in laboratory (R&D) setting; Interested in working in the nano-technology environment.
To be able to extant my professional & interested field - Quality control system compliment and formulation developments for specialty chemicals & nutraceuticals supplements.
EXECUTIVE LEVEL QUALITY PROFESSIONAL with extensive expertise working in a cGMP, FDA, DEA regulated pharmaceutical environment. Validations, (developing and executing validation protocols) calibrations, SOP’s and training are my areas of expertise. Self motivated, team player, a great leader with over 25 years of experience in all aspects of quality
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.
Ten years experience as a Manufacturing Production Technician. Knowledgeable of cGMP and safety regulations in a production environment. Experienced in analyzing batch records. Able to process the set up, calibration, production and shut down of pharmaceutical batches. Able to work independently as well as part of a team.
I'm looking to go further in the Pharma industry, or make the switch to oil & gas, or aerospace. Colorado is preferred. Willing to relocate.
n innovative graduate student in Biomanufacturing at NC State University seeking employment in downstream processing, purification or characterization of biopharmaceuticals. Experience includes summer internship in analytical technology at Biogen Idec, hands on in recombinant proteins purification, and cGMP compliance
To work for a company utilizing my knowledge of cGMP compliance, FDA and international regulatory requirements, extensive experience in QC/QA operations and analytical methods development and validation. I am experienced Project Manager and was leading cross-functional teams in multiple projects ranging from 3 months duration to 1.5 years.
implimentaion of FDA & OTHER CGMP CFR , SOP ETC
Acquire a position in the field of chemistry that emphasizes my strengths in team building, management and regulatory control