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Online Resumes with "GMP documentation"
? Highly motivated and results orientated individual with over 9 years experience in the biotech and medical industries. ? Effectively manage different responsibilities simultaneously ? Highly Organized individual with a strong attention to detail ? Experience with documentation systems in a GMP Regulated environment. ? Ability to work independently or cooperatively as a team
Tags for this Online Resume: quality
Professional experience including: personnel supervision, manufacturing, hands on product marketing, Quality Control and Quality Assurance in the pharmaceutical industry. Success driven professional with exceptional follow through and proven track record of success in the areas of: Project Management, Market Development, Interview-Placement-Training of new employees, Excellent communication, Technical Writing Skills, Author...
I am seeking for a job in pharmaceutical company in an area like Quality Assurance, Quality Control,Validation and Regulatory Affairs, Manufacturing or Formulation & Development to explore my skills & experience which leads to systemic, structured and robust process for quality conformance and improvement in pharmaceutical industry.
Tags for this Online Resume: HPLC, GC, UV, Dissolution, Disintigration, GMP documentation, FDA regulation, KF titrator, PH meter, LOD, Melting point, TOC., Raw, intermediate, finished product testing, Impurity,Stability, calibration, Assay
I am an accomplished process design specialist with thirteen years experience in the pharmaceutical industry involving bacterial and viral vaccine production. Achievements have included authoring and co-authoring various cGMP documents. Broad based background encompassing a strong work ethic and commitment to organizational and team goals. Experienced in recognizing, recommending and introducing new processes and equipme...
To obtain a challenging position within the maintenance discipline in which my experience and edjucat
Tags for this Online Resume: 20+ years experience in Medical Device Manufacture, Experience with PLCs, Maintained GMP Documentation
Manage / implement a product stability program under current regulations; manage implementation of FDA requirements post 510(k) clearance
Ideal Companies: medical device companies; adjunct college professor; education manager within a company
SUMMARY * * Goal-oriented with strong analytical, problem solving, and writing abilities. Experienced in a number of chemical quantification and characterization techniques including FTIR, fluorescence spectroscopy, TGA, HPLC, UV-vis, and GC-MS systems as well as Quality Assurance skills such as data review, batch record review, and the drafting of cGMP documentation including SOPs and Master Batch Records.
Summary: Experienced commissioning engineer with over 12 years of practical experience in biotech. Proficient with most equipment related to cell culture fermentation, and oral solid dose pharmaceutical manufacturing facilities. Very strong in GMP documentation FDA, ISO 9000, cGMP, CFR title 21 and DEA regulatory compliance. Familiar with LIMS, BMS, Trackwise, Faciliworks, Word, and Excel.
Engineering Management Professional with over 15 years of experience with multinational Pharmaceutical companies. Recognized as a focused dedicated and highly motivated professional with a diverse project management background offering solid contributions. Budget and results-oriented with a strong business sense to design and implement engineering solutions to enhance user capabilities. Motivational leader team player and g...
Manage quality assurance operations for a dynamic company
Tags for this Online Resume: Quality Assurance, Quality Control, Validations, molecular diagnostics, Regulatory Affairs, GMP documentation, technical writing, microbiology, Audit, Compliance, Data Analysis, Data Queries, High Performance Liquid Chromatography (HPLC), Medical, Process Improvement, Quality, Management, Risk Analysis, Risk Management, Test, complaint trending and analysis, Failure Analysis
QUALIFICATIONS: Over 13 years of experience in the Pharmaceutical and Medical Device Industry. I have a proven desire to enhance team effort and first time quality concepts, Strong creative research skills, Strong detailed and task oriented skills. Work environment regulated by 21 CFR 820 and ISO 13485:2003 & 9001. Specialized in Quality Assurance, Regulatory Compliance, GMP, Document Control, QSR training, Excel, Power Poi...
Professional with a strong operational experience within the pharmaceutical industry. Vast knowledge of manufacturing operations including manufacturing packaging inventory systems engineering maintenance systems auditing process improvements (Lean) technology transfer for new products validations qualifications and facilities modifications/construction project management. Certified Project Management Professional. Trainer ...
Tags for this Online Resume: Manufacturing, Management, Project Management, Project Manager, Audit, Complaints, Customer Accounts, Pharmaceutical, Microsoft, Microsoft Project, "project management", manufacturing