| Resume alert | Resumes 21 - 27 of 27 |
Manager Quality Assurance
Coventry, RI
... o Established written manufacturing procedures and routing system to comply with FDA & GMP guidelines, and a high level of quality and efficiency. o Well versed in Material Review Board decision making, pro-actively leading to product design change ... - 2012 Dec 03
... o Established written manufacturing procedures and routing system to comply with FDA & GMP guidelines, and a high level of quality and efficiency. o Well versed in Material Review Board decision making, pro-actively leading to product design change ... - 2012 Dec 03
High School Project Management
Plainfield, CT
... August 2009 to Current Coastal CT Research New London, CT Clinical Research Coordinator Drug Research Coordinator for pending FDA trials in full phase research, ensuring all clinical procedures are conducted by protocol and regulation. Daily ... - 2012 Dec 01
... August 2009 to Current Coastal CT Research New London, CT Clinical Research Coordinator Drug Research Coordinator for pending FDA trials in full phase research, ensuring all clinical procedures are conducted by protocol and regulation. Daily ... - 2012 Dec 01
Project Manager Quality Assurance
Norwich, CT
... presentations and conduct all ‘FDA Readiness’ and Ann Arbor GLP and annual refresher training • Member of the Pfizer Global educational Team and assisted in the development of the Global GLP refresher training to harmonize cross-site training. ... - 2012 Apr 22
... presentations and conduct all ‘FDA Readiness’ and Ann Arbor GLP and annual refresher training • Member of the Pfizer Global educational Team and assisted in the development of the Global GLP refresher training to harmonize cross-site training. ... - 2012 Apr 22
Project Manager Quality Assurance
New London, CT, 06320
... Assisted during various FDA/MHRA audits. Evaluated/reported on trending from audit findings and implemented any associated corrective actions. Facilitated the Connecticut GCP team, consisting of various pharmaceutical/biotech companies that met ... - 2012 Apr 19
... Assisted during various FDA/MHRA audits. Evaluated/reported on trending from audit findings and implemented any associated corrective actions. Facilitated the Connecticut GCP team, consisting of various pharmaceutical/biotech companies that met ... - 2012 Apr 19
Project Manager
Quaker Hill, CT, 06375
... requests to data management retention center and researched repository for specific applications investigated during FDA audits • Tracked weekly on-line multi-level Excel status worksheets of 80 plus applications in multiple process phases ... - 2012 Feb 08
... requests to data management retention center and researched repository for specific applications investigated during FDA audits • Tracked weekly on-line multi-level Excel status worksheets of 80 plus applications in multiple process phases ... - 2012 Feb 08
Chemist/Scientist
Gales Ferry, CT, 06335
... Possess solid background in MRA/FDA auditable laboratory along with proficiency in GMP laboratory practices. Reliable and solutions-focused leader, adept at conducting initial research, facilitating data analysis, as well as evaluating and ... - 2011 Sep 20
... Possess solid background in MRA/FDA auditable laboratory along with proficiency in GMP laboratory practices. Reliable and solutions-focused leader, adept at conducting initial research, facilitating data analysis, as well as evaluating and ... - 2011 Sep 20
Chemist/Project Manager
Lisbon, CT, 06351
... HPLC studies TECHNICAL WRITER Dec 2003-Mar 2005 - Accurately compiled data and prepared documents for IND submissions to the FDA - Served as information resource for the FDA - Managed and maintained organization of data using Documentum and Predict ... - 2010 May 05
... HPLC studies TECHNICAL WRITER Dec 2003-Mar 2005 - Accurately compiled data and prepared documents for IND submissions to the FDA - Served as information resource for the FDA - Managed and maintained organization of data using Documentum and Predict ... - 2010 May 05