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Online Resumes with "cGMP"
I am looking for a pharmaceutical operations management position where I can utilize my advanced chemistry degree, expertise in quality assurance and background in safety compliance.
I'm seeking Full Time and $45,000.00 to $65,000.00.
Ideal Companies: Any.
Tags for this Online Resume: IT Support, Technical Support, Support Specialist, Help Desk, Associates Degree, Desktop, Network, PC, Infrastructure, Systems, LAN, Administrator, Technology, IS, IT, Technician, Information Systems, Telecommunications Management, Help Desk Level II, IT Analyst, Desktop Engineer, End User, Computer
Desires a position that combines skillsets such as pharmacuetical, clinical and training experiences. The ability to work in research, quality and clinical areas is parmount. However, not adverse to training others and travelling new new areas in the whole scientific arenas.
Quality Manager, FDA cGMP Compliance, Validation, Optimization of Analytical Metodologies, HAACP, Procurement, JIT
Seeking long term employment in a stable, growing company
Biotech or pharmaceutical manufacturing or research position in which I can apply my combined technical skills and ten years experience working in a cGMP and FDA regulated environment.
Consistently produced investigational medicinal products within aggressive timelines and according to cGMP guidelines as required by study protocols. Strong Program Management skills with an emphasis on the design and forecasting of accurate drug demands for multiple ongoing global Clinical Trials. Proficient in communicating with a diverse group of people including team members and vendors. Achieved objectives through my ...
Project Manager, Inside Sales Manager.
Ideal Companies: Medium to large progressive companies.
Personable, motivated and astute, business-minded life scientist with extensive experience in Quality Control labs using advanced molecular biology techniques in PCR, RT-PCR, qPCR; Excellent communicator with broad experience in CLIA-certified and FDA-regulated environments.
I am a strong contributor performing routine tasks and other duties assigned under cGMP and GLP methods. I am a versatile individual with keen attention to details and provide input to increase productivity and quality. I participate in IQ, OQ and PQ in
As a technician, I would bring focus on quality and ease of use to your system development. Furthermore, I am eager and determined to work as team in order to achieve success.
Methods Development • Procedure/SOP Writing • Method Validation Quality Control (NELAP, cGMP, GLP, ISO, FDA) • Organics Lab Start-up and Initialization • Process Improvement • Effective Communications Relationship Building • Strategic Planning • Resource Management • Problem Solving • Budgeting • Lab Safety • Laboratory Certification
Bio process Technician position using recent cGMP knowledge gained From taking the Bio Work Certificate course to ensure high quality Manufacturing of pharmaceutical products
my goal is to work as a quality control