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Online Resumes with "Quality System Documentation"
Organized highly motivated quality focused manger/ team leader with 16 years experience, in organizing, directing, training and leading organization to meeting and exceed ISO requirements. Strong communication skills written and verbal, at all levels of the quality system documentation. A trainer, mentor able to maintain a sense of humor under pressure. Diplomatic and tactful with professionals and non-professionals, intern...
My goal is to provide a leadership role in a Quality System with emphasis on ISO9000 and associated documentation control.
James C. Robinson 217 E. Cranberry Lane, Greenville, South Carolina 29615 Telephone: (864) 675-9668 / Alt. Phone: (864) 270-5344 / E-Mail: email@example.com Experienced Gas Turbine Technical Professional seeking a challenging position utilizing skills and experience in any combination of the following areas: ◙ Project Management ◙ Technical Advisor ◙ Installation and Maintenance Technician ◙Purchasing and Inventor...
Seeking an opportunity in Quality Assurance or Regulatory Compliance. Small and mid-sized companies offering variety and challenge are preferred, but will consider all full-time or consulting positions in the northern NJ/southern NY area that fit my experience.
Objective is to work for a pharmaceutical, biopharma or chemical company where my quality system and documentation experience can be utilized.
My range of experience began with hands-on work testing and measuring products, and I then went on to supervision and documentation. When I moved into a corporate role I became an expert on administration of Quality Systems and Documentation Systems, adapting this infrastructure to address new product classifications, new manufacturing sites, and new regulatory requirements. I was responsible for monitoring regulatory chan...
To be a part of a pharmaceutical professional organization that would enhance and elevate my credentials towards the growth of the organization and myself.
Tags for this Online Resume: Maintaining Quality Management Systems like: Change control, Deviations, CAPA, OOS and OOT., Performing Annual Product Quality Reviews, Vendor Qualification, Qualification of Equipments (FAT, SAT, DQ, IQ, OQ PQ)., Prepare, maintain, control and issued quality system documents while adequately maintaining the Documents Management System, Performing Batch Release, In-process Control Management,
I am a Regulatory Analyst with 5 years of professional experience in developing and implementing Quality System documentation and regulatory submissions for medical devices, pharmaceuticals and biotech products. Thorough understanding of business processes such as R&D, nonclinical, clinical, pre-approval and post-approval submissions.
A highly motivated professional with a verifiable record of accomplishment spanning several years. Highly creative, recognized as a results-oriented and solution-focused individual. Responsible for timely and accurate completion of projects that are of average complexity or completion of portions of projects that are above average complexity. Professional that utilizes verbal and written communication skills to maintain a c...
Accomplishments * Implemented, Trainer and Lead Author of AS9100 Quality System Documents * Reviewed, Wrote, Trained and implemented new Laboratory Safety procedures * JEDEC task group member (Radiography) and performed Chair duties
Summary of Qualifications Dedicated and solutions oriented professional with 14 years of medical device background mainly in Quality & Compliance * Highly motivated with demonstrated ability to set appropriate and effective priorities and implement decisions to achieve both immediate and long-term goals while managing multiple tasks and completing priorities. * Effective communication and inter-personal skills with all leve...