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Online Resumes with "Good Manufacturing Practices GMP "
Quality Control Chemist-10 years experience-Sample Analysis / Processing • Good Laboratory Practice (GLP) • Product Analysis
Quality Control • Analytical Workflow • Compendia Testing • Stability Analysis • Process Improvement • Recall Process• Equipment Validation/Calibration • Good Manufacturing Practice (GMP) • Data Collection/Analysis• FDA Compliance • Sterile Production / Manufacturing • Manufacturing Specification Development
Analytical Chemist / Trainer
I am looking for a position that utilizes my experience. I have over 30 years of experience with analytical instrumentation (GC/MS, LC/MS) and customer and employee training. I am skilled at laboratory method development. I could be extremely productive in a laboratory, instrument sales or a training position.
Ideal Companies: Covance, Case Laboratories, Eli Lilly and Company, American Testing Laboratories
Tags for this Online Resume: LCMS, GCMS, Powerpoint, Closing, cGMP, Training, Methods, Development, Interpretation, MSMS
Warehouse Technician with background in aerospace/pharmameuticals/logistic, OSHA/IATA,HAZMAT and DEA,FORKLIFT certified
Stabiliy,room for growth with the company.
Ideal Companies: Aerospace, Pharmacueticals, Warehouse/Supply Chain/Logistic, Nike, Cytech
Tags for this Online Resume: OSHS/IATA Certified, DOT/HAZMAT Certified, DEA Clearance, Forklift Certified, Inventory Control/Supply Chain/Logistics, Order Pulling/Stocking/FIFO, Warehouse
Training and Documentation Specialist
Energetic professional looking for training, project management, or documentation opportunities.
Ideal Companies: SAP, Oracle, Microsoft,
Production Supervisor -- 14 years experience
These sentences are to express my interest in the Production Supervisor position based on my skills in administration, leadership, communication, technical, development, performance management, statistical and computer knowledge, and problem solving.
I am confident that I would be a great addition to your team.
My resume that highlights my knowledge in manufacturing environment is enclosed on medical industry mainly....
Tags for this Online Resume:
Production Supervisor
Featured Profile
PhD Research Scientist With 12+years of Experience in Biomedical Sciences
I am seeking opportunities to contribute as a scientist within preclinical drug development or drug discovery research for the bio-pharmaceutical industry to support the primary or secondary screening and characterization of the molecular mechanism of action of lead drug candidates enabling target validation. I specialize in the development of cell-based assays using genomic, proteomic and biochemical approaches implementin...
Ideal Companies: Biogen Idec, Joule Scientific, Novartis NIBR, Aveo Oncology, Agios, Pfizer, Millipore, Merck, EMD serono, Third rock ventures, Cambridge Scientific, Alkermes, Enlight Biosciences
Tags for this Online Resume:
Lentiviral Retroviral shRNA RNA knockdown screens, Flow Cytometry, RTPCR, Immunopreciptations, Reporter assays, Cell based Assays, ELISA, Migration, Stable and Transient Transfections, Genomic and Proteomic Studies, Cloning, Transient siRNA knockdowns, Phenotyping Mammalian cell lines, Gene Overexpression, Subcloning to expression Vectors, Construct Stable Inducible Cell lines, Protein Kinase Assay, Pulse Chase Experiments, Transfection, Transduction, Transformation, Polyoma virus DNA tumor virus replication, Research Scientist, Cell Biology Protein Biochemistry Genetics Molecular Bioliogy Oncology Virology, FACS
Featured Profile
Validation Documentation Writer, Validation Coordinator, Quality Assurance - 10 years Experience - Indianapolis
To work in a quality-driven environment, such as the biotechnical field, as a Validation Coordinator, Validation Writer, or Quality Assurance Manager.
Ideal Companies: Convance, Clarian, Roche Diagnostics
Tags for this Online Resume:
GxP guidelines, Planning Documentation, Regulus, CFR21 Part 11, Testing Documentation, TrackWise, Good Documentation Practices, Microsoft Office
Risk Management/IT Auditor
Regulatory, risk management and food safety/compliance professional with operational and IT Audit experience in Governance, Risks and Compliance (GRC), Hazards Analysis Critical Control Point (HACCP), International Foods Standards (IFS),Good Manufacturing Practices (GMP) and Food and Drug Administration (FDA) guidelines or frameworks, is seeking a senior leadership or consultant role. Has extensive compliance experience ut...
Tags for this Online Resume:
IT Auditor, SAP- Governance, Risks and Compliance (GRC), Hazards Analysis Critical Control Point (HACCP), International Foods Standards (IFS), Good Manufacturing Practices (GMP), Microsoft Great Plains (GP)
Supply chain analyst- Focused on developing and implementing process controls and quality improvement initiatives that reduce costs and increase company revenue
I am a supply chain professional who is keen on advancing my career in logistics and manufacturing with particular interest in the food and beverage industry. I am conversant with HACCP techniques and 5S trained according to Good Manufacturing Practices (GMP) and Standard Operating Procedures put out by the International Standard organization (ISO).I am also familiar with a host of Warehouse Manufacturing Systems (WMS) used...
Department Manager - 6 Years of Experience - Near 01440
Dear Hiring Manager;
I am writing to express my interest in the position of QA Manager, advertised as being open with your company. I am a highly talented and motivated manufacturing manager with an extensive background of Good Manufacturing Practices (GMP), and I am familiar with all facets of quality management. I would like to bring my expertise to your company.
My experience as a manager in manufacturing includes the...
Tags for this Online Resume:
QA manager, GMP, Auditor, Massachusetts, Central, non-conforming, Manufacturing, policies
Chemical Engineer - 5 Years of Experience
Energetic and trilingual quality engineer (member of OIQ) with experience in medical devices, pharmaceuticals and the bottling industry. Offers work experience in a highly regulated (FDA) pharmaceutical environment using Good manufacturing practices (GMP), Good laboratory practices (GLP), Good documentation practices (GDP) as well as Health and Safety issues (CSST). Solid record in designing and validating changes which imp...
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Los Angeles, Irvine, Quality
PhD Research Scientist With 12+years of Experience in Biomedical Sciences
I am seeking opportunities to contribute as a scientist within preclinical drug development or drug discovery research for the bio-pharmaceutical industry to support the primary or secondary screening and characterization of the molecular mechanism of action of lead drug candidates enabling target validation. I specialize in the development of cell-based assays using genomic, proteomic and biochemical approaches implementin...
Ideal Companies: Biogen Idec, Joule Scientific, Novartis NIBR, Aveo Oncology, Agios, Pfizer, Millipore, Merck, EMD serono, Third rock ventures, Cambridge Scientific, Alkermes, Enlight Biosciences
Tags for this Online Resume: Lentiviral Retroviral shRNA RNA knockdown screens, Flow Cytometry, RTPCR, Immunopreciptations, Reporter assays, Cell based Assays, ELISA, Migration, Stable and Transient Transfections, Genomic and Proteomic Studies, Cloning, Transient siRNA knockdowns, Phenotyping Mammalian cell lines, Gene Overexpression, Subcloning to expression Vectors, Construct Stable Inducible Cell lines, Protein Kinase Assay, Pulse Chase Experiments, Transfection, Transduction, Transformation, Polyoma virus DNA tumor virus replication, Research Scientist, Cell Biology Protein Biochemistry Genetics Molecular Bioliogy Oncology Virology, FACS
Validation Documentation Writer, Validation Coordinator, Quality Assurance - 10 years Experience - Indianapolis
To work in a quality-driven environment, such as the biotechnical field, as a Validation Coordinator, Validation Writer, or Quality Assurance Manager.
Ideal Companies: Convance, Clarian, Roche Diagnostics
Tags for this Online Resume: GxP guidelines, Planning Documentation, Regulus, CFR21 Part 11, Testing Documentation, TrackWise, Good Documentation Practices, Microsoft Office
