| Resume alert | Resumes 71 - 80 of 95 |
Mechanical Engineer Project Manager
Bartonsville, PA
... Reviewed all documentation related to the design and development of the project, and adherence to GMP (Good Manufacturing Practice). Participated in clinical studies; evaluate system performance. Transistor Devices Inc. Randolph NJ (Aug. 2000 - Dec. ... - 2013 May 13
... Reviewed all documentation related to the design and development of the project, and adherence to GMP (Good Manufacturing Practice). Participated in clinical studies; evaluate system performance. Transistor Devices Inc. Randolph NJ (Aug. 2000 - Dec. ... - 2013 May 13
Project Manager Quality Assurance
Allentown, PA, 18015
... Adherence to HIPPA/GMP/FDA/ Title 21 CFR Part 11 patient, healthcare, drug releases, and intellectual property. Provides technical solutions and training to all issues that include proactive notifications, mitigations, and resolutions. Adherence to ... - 2013 Apr 19
... Adherence to HIPPA/GMP/FDA/ Title 21 CFR Part 11 patient, healthcare, drug releases, and intellectual property. Provides technical solutions and training to all issues that include proactive notifications, mitigations, and resolutions. Adherence to ... - 2013 Apr 19
Development Training
Califon, NJ
... research publication expertise Enzyme analysis method development and optimization Expert in HPLC, UPLC and LCMS analysis and method development (Masslynx, Empower and Chem Station), training, GMP instrument validation and automation Preparative SFC ... - 2013 Feb 21
... research publication expertise Enzyme analysis method development and optimization Expert in HPLC, UPLC and LCMS analysis and method development (Masslynx, Empower and Chem Station), training, GMP instrument validation and automation Preparative SFC ... - 2013 Feb 21
Quality Control Assurance
Bethlehem, PA
... * Created Access database system to track documents, deviations, metrics, and terminology that was used in Drug Safety department at Merck * Knowledge of GMP/GLP and CFR regulations * Performed CAPA investigations on OOS intermediate and finished ... - 2013 Jan 29
... * Created Access database system to track documents, deviations, metrics, and terminology that was used in Drug Safety department at Merck * Knowledge of GMP/GLP and CFR regulations * Performed CAPA investigations on OOS intermediate and finished ... - 2013 Jan 29
Development Manager
Franklin, NJ
... Expertise in advanced HPLC method development and GMP method validation. Skilled in designing experiments, conducting analytical investigations, troubleshooting and resolving technical issues, and writing technical reports. Proficient in UPLC, HPLC, ... - 2012 Nov 29
... Expertise in advanced HPLC method development and GMP method validation. Skilled in designing experiments, conducting analytical investigations, troubleshooting and resolving technical issues, and writing technical reports. Proficient in UPLC, HPLC, ... - 2012 Nov 29
Quality Control Manager
Washington, NJ
... Solid State Electronics TRAINING CERTIFICATES Pharmaceutical Stability, Out of Specification Investigations (GMP), GMP (yearly), ISO Internal Auditor, Database Administrator, Novell Network Administration, Quality System Auditor - RAB certified. ... - 2012 Nov 15
... Solid State Electronics TRAINING CERTIFICATES Pharmaceutical Stability, Out of Specification Investigations (GMP), GMP (yearly), ISO Internal Auditor, Database Administrator, Novell Network Administration, Quality System Auditor - RAB certified. ... - 2012 Nov 15
Quality Assurance Control
Stewartsville, NJ, 08886
Experienced Pharmaceutical scientist with expertise in the GMP compliant handling and submission of samples submitted for Quality Control testing according to FDA, EU and JP testing requirements. Performs trending, tracking of testing records and ... - 2012 Jun 03
Experienced Pharmaceutical scientist with expertise in the GMP compliant handling and submission of samples submitted for Quality Control testing according to FDA, EU and JP testing requirements. Performs trending, tracking of testing records and ... - 2012 Jun 03
Quality Assurance Project
Perkasie, PA, 18944
... Over 40 years of experience in the Pharmaceutical Industry, 36+ years of those years are with GxP (GMP, GLP, GCP) systems compliance/QA and 21 CFR Part 11. Experience includes GxP system implementation projects, documentation/SOP writing/review. ... - 2012 May 31
... Over 40 years of experience in the Pharmaceutical Industry, 36+ years of those years are with GxP (GMP, GLP, GCP) systems compliance/QA and 21 CFR Part 11. Experience includes GxP system implementation projects, documentation/SOP writing/review. ... - 2012 May 31
Maintenance Cnc Machinist
Catasauqua, PA, 18032
... Received the training and instructions necessary for manufacturing processes that meet SOPs requirements in accordance with GMP guidelines. . Recorded completed tasks into equipment logs and material inventory logs. Drywall Hanger and Finisher ... - 2011 Aug 04
... Received the training and instructions necessary for manufacturing processes that meet SOPs requirements in accordance with GMP guidelines. . Recorded completed tasks into equipment logs and material inventory logs. Drywall Hanger and Finisher ... - 2011 Aug 04
Regulatory Affairs Manager
Allentown, PA, 18109
... Provide regulatory strategies for domestic and international markets, quality plans, assure GMP compliance with external manufacturers, FMEA, write and submit 510k’s, IDE’s, and develop Regulatory strategies for new indications and claims. Lead ... - 2011 Jun 24
... Provide regulatory strategies for domestic and international markets, quality plans, assure GMP compliance with external manufacturers, FMEA, write and submit 510k’s, IDE’s, and develop Regulatory strategies for new indications and claims. Lead ... - 2011 Jun 24