| Resume alert | Resumes 21 - 30 of 78 |
Manager Customer Service
Easton, PA, 18042
... Member of the site Quality Leadership Team (QLT) Additional Responsibilities and Laboratory Experience Trained on all applicable ISO 9001, FDA, and current Good Manufacturing Practices (cGMPs) as they pertain to the industrial gases industry Proven ... - 2017 Oct 07
... Member of the site Quality Leadership Team (QLT) Additional Responsibilities and Laboratory Experience Trained on all applicable ISO 9001, FDA, and current Good Manufacturing Practices (cGMPs) as they pertain to the industrial gases industry Proven ... - 2017 Oct 07
Lab Technician
Great Meadows, NJ, 07838
... Skills Laboratory/Technical: FDA GMP, CAPA, GDP, ISO-compliant, cryopreservation, general aseptic technique, pipetting, data entry, PhRMA code, biomaterials processing, equipment management. Proficient in Oracle, PACS, MS Office (Word, Excel, & ... - 2017 Sep 18
... Skills Laboratory/Technical: FDA GMP, CAPA, GDP, ISO-compliant, cryopreservation, general aseptic technique, pipetting, data entry, PhRMA code, biomaterials processing, equipment management. Proficient in Oracle, PACS, MS Office (Word, Excel, & ... - 2017 Sep 18
Medical Device Quality
Andover, NJ
... Knowledge of FDA and CE medical device requirements related to post market medical device reporting (MDR) to improve product quality, reliability, and safety. EXPERIENCE GE (General Electrics) Healthcare April 2017- Present Biomedical Technician II ... - 2017 Aug 16
... Knowledge of FDA and CE medical device requirements related to post market medical device reporting (MDR) to improve product quality, reliability, and safety. EXPERIENCE GE (General Electrics) Healthcare April 2017- Present Biomedical Technician II ... - 2017 Aug 16
Microsoft Office Quality Control
Phillipsburg, NJ, 08865
... ahead of any areas of potential problems Supervisor 2004 - 2006 Maintained proper documentation in accordance with: DDD, FDA, GDP Responsible for regulating cold storage of vials and controlled medication counts: Calcitonin, Phenobarbital, Lyrica ... - 2017 Aug 05
... ahead of any areas of potential problems Supervisor 2004 - 2006 Maintained proper documentation in accordance with: DDD, FDA, GDP Responsible for regulating cold storage of vials and controlled medication counts: Calcitonin, Phenobarbital, Lyrica ... - 2017 Aug 05
Production Technician
East Stroudsburg, PA, 18301
... Learned FDA regulations and guidelines. Reviewed and interpreted analysis of data. Microbiology Studied microscopic life forms. Learned growth, metabolism, and control of microorganisms. Applied laboratory techniques of isolation, staining, ... - 2017 Aug 02
... Learned FDA regulations and guidelines. Reviewed and interpreted analysis of data. Microbiology Studied microscopic life forms. Learned growth, metabolism, and control of microorganisms. Applied laboratory techniques of isolation, staining, ... - 2017 Aug 02
Quality Assurance Medical
Easton, PA
... Acquired during my jobs and Biotech Graduate courses: Followed Standard Operating Procedures (SOPs), Good Laboratory Practices (GLP), Good Clinical Practice (GCP), and current Good Manufacturing Practices (cGMP) established by the FDA, ICH, and WHO. ... - 2017 Jul 21
... Acquired during my jobs and Biotech Graduate courses: Followed Standard Operating Procedures (SOPs), Good Laboratory Practices (GLP), Good Clinical Practice (GCP), and current Good Manufacturing Practices (cGMP) established by the FDA, ICH, and WHO. ... - 2017 Jul 21
Manager Chemical Engineering
Easton, PA
... $1M + cGMP/FDA BUSINESS EXPERIENCE Honeywell, Morris Plaines NJ 2015 to Present Performance Materials Technology Business Implementation Leader – PSM Led cross functional team, which brought to zero occurrences costly and serious PSM incidents. ... - 2017 Jul 18
... $1M + cGMP/FDA BUSINESS EXPERIENCE Honeywell, Morris Plaines NJ 2015 to Present Performance Materials Technology Business Implementation Leader – PSM Led cross functional team, which brought to zero occurrences costly and serious PSM incidents. ... - 2017 Jul 18
Customer Service Management
Cresco, PA, 18326
... This is a key initiative for Sanofi from 2014 – 2105 with successful completion imperative to meet FDA requirements. Key Tasks and Achievements: Review contracts and agreements for compliance with company requirements Participated on multi ... - 2017 Jul 13
... This is a key initiative for Sanofi from 2014 – 2105 with successful completion imperative to meet FDA requirements. Key Tasks and Achievements: Review contracts and agreements for compliance with company requirements Participated on multi ... - 2017 Jul 13
Medical Professional Experience
Hackettstown, NJ, 07840
... My responsibilities included proofreading all documents that were required for clinical trials and blinded/unblinded medical studies, which adhered to strict FDA regulations. The position required concentration, strict attention to detail, and ... - 2017 Jun 06
... My responsibilities included proofreading all documents that were required for clinical trials and blinded/unblinded medical studies, which adhered to strict FDA regulations. The position required concentration, strict attention to detail, and ... - 2017 Jun 06
Process Engineer Product Development Engineer Coatings Specialist
Newton, NJ, 07860
... *Familiar with cGMP, FDA Quality and Documentation procedures, FMECA for product and process, and Stage Gate product development process for medical device products. *Compounded temperature sensitive components into dispersions that could be applied ... - 2017 Feb 02
... *Familiar with cGMP, FDA Quality and Documentation procedures, FMECA for product and process, and Stage Gate product development process for medical device products. *Compounded temperature sensitive components into dispersions that could be applied ... - 2017 Feb 02