| Resume alert | Resumes 81 - 90 of 91 |
Service Engineer
MA, 01581
... Revise outdated standard operating procedures and work instructions following the standards of good manufacturing practice (GMP). On the Job Trainee IBM Solutions Delivery Inc (4/2008 - 6/2008) Provide first level support/assistance to IBM ... - 2012 Jul 29
... Revise outdated standard operating procedures and work instructions following the standards of good manufacturing practice (GMP). On the Job Trainee IBM Solutions Delivery Inc (4/2008 - 6/2008) Provide first level support/assistance to IBM ... - 2012 Jul 29
Engineer Manager
Southborough, MA, 01772
... Skills: Statistical Process Control, OOD, Data Structures, Computer Architectures, LEAN, 6 sigma, Project Management, FDA GMP, QSR, ISO 13485, IEC 60601-1 & 60601-2 Certifications: Informix DBSA and Level 1 HP-UX administrator Protocols: PCIe, QPI ... - 2012 Jun 12
... Skills: Statistical Process Control, OOD, Data Structures, Computer Architectures, LEAN, 6 sigma, Project Management, FDA GMP, QSR, ISO 13485, IEC 60601-1 & 60601-2 Certifications: Informix DBSA and Level 1 HP-UX administrator Protocols: PCIe, QPI ... - 2012 Jun 12
High School Maintenance
Worcester, MA, 01603
... •Familiar with Environmental Monitoring (EM) Sampling, Aseptic Sterile Filling Process, Product Inspection and Good Manufacturing Practices (GMP) and Good Documentation Practices /Five "S" and Standard Operating Procedures (SOP). •Tested Vero cells ... - 2012 May 09
... •Familiar with Environmental Monitoring (EM) Sampling, Aseptic Sterile Filling Process, Product Inspection and Good Manufacturing Practices (GMP) and Good Documentation Practices /Five "S" and Standard Operating Procedures (SOP). •Tested Vero cells ... - 2012 May 09
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
Building Services Technician
Worcester, MA, 01605
... • Practiced all clean room principles and techniques, contamination prevention and clean room sanitization dictated by GMP’s and SOP’s to assure product integrity. • Interacted with production to assure all rejected product is removed and properly ... - 2012 Jan 31
... • Practiced all clean room principles and techniques, contamination prevention and clean room sanitization dictated by GMP’s and SOP’s to assure product integrity. • Interacted with production to assure all rejected product is removed and properly ... - 2012 Jan 31
Regulatory Affairs
Westborough, MA, 01581
... Comprehensive understanding about medical device and drug regulations, proficient in regulatory submissions including 510(k), PMA, IND, NDA along with fluency in GMP’s and Quality Systems. Thorough understanding of product development process. ... - 2011 Sep 14
... Comprehensive understanding about medical device and drug regulations, proficient in regulatory submissions including 510(k), PMA, IND, NDA along with fluency in GMP’s and Quality Systems. Thorough understanding of product development process. ... - 2011 Sep 14
Procurement Specialist
Marlborough, MA, 01752
... cost reduction solutions • Working knowledge of ISO, GMP, JIT and ERP practices, MRP and production processes • Experienced in vendor selections; building relationships; negotiations; vendor rating/performance system • Maintained standard purchase ... - 2011 Sep 08
... cost reduction solutions • Working knowledge of ISO, GMP, JIT and ERP practices, MRP and production processes • Experienced in vendor selections; building relationships; negotiations; vendor rating/performance system • Maintained standard purchase ... - 2011 Sep 08
Research scientist, chemist, manager, cordinator
Johnston, RI, 02919
... starting materials, reference standards, active ingredients, related substances, excipients and impurities Performed GMP release and stability testing of drug substances and products intended to be used in clinical studies Wrote technical ... - 2011 Apr 21
... starting materials, reference standards, active ingredients, related substances, excipients and impurities Performed GMP release and stability testing of drug substances and products intended to be used in clinical studies Wrote technical ... - 2011 Apr 21
Sales Manager
Sterling, MA, 01564
... Quality Control / Quality Assurance Supervisor Responsible for new product development, competitor’s analysis, budgeting/cost control, supervision, implementation of FDA/GMP rules and regulations. Education: w American College - Financial & ... - 2011 Feb 08
... Quality Control / Quality Assurance Supervisor Responsible for new product development, competitor’s analysis, budgeting/cost control, supervision, implementation of FDA/GMP rules and regulations. Education: w American College - Financial & ... - 2011 Feb 08
Operations Manager
North Attleboro, MA, 02760
... Areas of Strength ▪ Planning/Scheduling/Forecasting ▪ Quality Assurance and TQM ▪ Cost Management ▪ Bill of Materials (BOM) ▪ ISO Compliance ▪ SAP ▪ Procurement/Buying ▪ FDA Regulatory Compliance ▪ CAPA and GMP ▪ MRP and SYSPRO ERP ▪ Audit (Software ... - 2010 Sep 30
... Areas of Strength ▪ Planning/Scheduling/Forecasting ▪ Quality Assurance and TQM ▪ Cost Management ▪ Bill of Materials (BOM) ▪ ISO Compliance ▪ SAP ▪ Procurement/Buying ▪ FDA Regulatory Compliance ▪ CAPA and GMP ▪ MRP and SYSPRO ERP ▪ Audit (Software ... - 2010 Sep 30