| Resume alert | Resumes 61 - 70 of 75 |
Quality Assurance Manager
Plymouth, MA, 02360
... Conducted in-house GMP, Food Safety and OSHA safety audits. OCEAN SPRAY CRANBERRY CORPORATION Sept 2006 to Apr2007 Senior Manager Quality Assurance (cranberry juices, sauces and Craisins) Corporate Quality Assurance establishing direction for both ... - 2012 Sep 26
... Conducted in-house GMP, Food Safety and OSHA safety audits. OCEAN SPRAY CRANBERRY CORPORATION Sept 2006 to Apr2007 Senior Manager Quality Assurance (cranberry juices, sauces and Craisins) Corporate Quality Assurance establishing direction for both ... - 2012 Sep 26
Technician Maintenance
Brockton, MA, 02333
... BIOTECH • ASSISTED WITH ANNUAL EQUIPMENT MAINTENANCE FOR 200L BIOREACTORS UNDER IQ/OQ PROTOCOLS AND PREPARATION FOR FINAL GMP APPROVAL • C.I.P, AUTOCLAVING AND PARTS PREPARATION NOV 2006 – JUNE 2007 AEROTEK SCIENTIFIC LLC ROCKLAND, MA OSMETECH ... - 2012 Aug 10
... BIOTECH • ASSISTED WITH ANNUAL EQUIPMENT MAINTENANCE FOR 200L BIOREACTORS UNDER IQ/OQ PROTOCOLS AND PREPARATION FOR FINAL GMP APPROVAL • C.I.P, AUTOCLAVING AND PARTS PREPARATION NOV 2006 – JUNE 2007 AEROTEK SCIENTIFIC LLC ROCKLAND, MA OSMETECH ... - 2012 Aug 10
Regulatory Affairs Associate/Quality Assurance
Jamaica Plain, MA, 02130
... Quality Management System and Compliance, Design Controls, GCP, GLP, GMP standards, Advertisement and Labeling Regulations (SPL, PLR Format), Regulatory Compliance, Post Licensure Requirements • EU healthcare product regulatory environment and EU ... - 2012 Jul 16
... Quality Management System and Compliance, Design Controls, GCP, GLP, GMP standards, Advertisement and Labeling Regulations (SPL, PLR Format), Regulatory Compliance, Post Licensure Requirements • EU healthcare product regulatory environment and EU ... - 2012 Jul 16
Manager Quality
Somerset, MA, 02724
... **724 j0edhj@r.postjobfree.com Home: 508-***-**** Cell: 508-***-**** Summary Senior manager with twenty one years of experience in the Medical Device industry and full knowledge of ISO 13485, 21CFR 820, and GMP Guidelines. A demonstrated leader who ... - 2012 Jul 09
... **724 j0edhj@r.postjobfree.com Home: 508-***-**** Cell: 508-***-**** Summary Senior manager with twenty one years of experience in the Medical Device industry and full knowledge of ISO 13485, 21CFR 820, and GMP Guidelines. A demonstrated leader who ... - 2012 Jul 09
Quality Assurance Medical Device
Boston, MA, 02115
... • Filing a 510(k) Pre-market notification, Pre-Market Application processes and Investigational Device Exemption applications • GxPs(GMP, GCP, GLP) and cGMPs • Regulations of Europe, Canada, China, India , Australia and Japan • Good oral and written ... - 2012 Jun 26
... • Filing a 510(k) Pre-market notification, Pre-Market Application processes and Investigational Device Exemption applications • GxPs(GMP, GCP, GLP) and cGMPs • Regulations of Europe, Canada, China, India , Australia and Japan • Good oral and written ... - 2012 Jun 26
Quality Assurance Control
Boston, MA, 02120
... Intern QA Associate, Ydik Pharmaceuticals June 2009 - August 2009 • Maintained GMP while manufacturing Enteric Coated Aspirin tablets • Developed processes involved in unit operations (Batch Manufacturing) • Documented all the processes undertaken ... - 2012 May 02
... Intern QA Associate, Ydik Pharmaceuticals June 2009 - August 2009 • Maintained GMP while manufacturing Enteric Coated Aspirin tablets • Developed processes involved in unit operations (Batch Manufacturing) • Documented all the processes undertaken ... - 2012 May 02
Medical Device Project Management
Cumberland, RI
... Affairs in Pharmaceutical Manufacturing, Pharmaceutical Finishing and Packaging Systems–Solid Dosage, Regulatory in Pharmaceutical Industry, Contemporary Concepts In Validation, Quality in Pharmaceutical Industry, Designing of GMP Facilities. ... - 2012 May 01
... Affairs in Pharmaceutical Manufacturing, Pharmaceutical Finishing and Packaging Systems–Solid Dosage, Regulatory in Pharmaceutical Industry, Contemporary Concepts In Validation, Quality in Pharmaceutical Industry, Designing of GMP Facilities. ... - 2012 May 01
Project Manager
Boston, MA, 02120
... • Knowledge of GCP, GLP, GMP standards, Advertisement and Labeling regulations, Regulatory Compliance, Post Licensure Requirements, including CAPA, MedWatch, OOS, Auditing, Risk management. • A decent understanding of clinical protocol development, ... - 2012 Jan 23
... • Knowledge of GCP, GLP, GMP standards, Advertisement and Labeling regulations, Regulatory Compliance, Post Licensure Requirements, including CAPA, MedWatch, OOS, Auditing, Risk management. • A decent understanding of clinical protocol development, ... - 2012 Jan 23
Project Manager
Norwell, MA
... • Achieved superior testing results by following USP methods, GMP / GLP requirements, and Lot Release protocol, along with maintaining and monitoring state-of-the-art equipment to guarantee optimal product reliability rates. Education B.S., Food ... - 2011 Oct 11
... • Achieved superior testing results by following USP methods, GMP / GLP requirements, and Lot Release protocol, along with maintaining and monitoring state-of-the-art equipment to guarantee optimal product reliability rates. Education B.S., Food ... - 2011 Oct 11
Engineer Project
Boston, MA, 02115
... Training in Bacterial Vaccine Production, Viral Vaccine Production, SOP writing,GMP implementation,Quality Control and Packaging Departments. (Jun 2006- July 2006) Achievements Attended Intl. RSA (Research Society of Alcohol) conference 2010 at San ... - 2011 Aug 03
... Training in Bacterial Vaccine Production, Viral Vaccine Production, SOP writing,GMP implementation,Quality Control and Packaging Departments. (Jun 2006- July 2006) Achievements Attended Intl. RSA (Research Society of Alcohol) conference 2010 at San ... - 2011 Aug 03