| Resume alert | Resumes 51 - 60 of 119 |
Medical Professional Experience
Providence, RI, 02908
... Play key role in implementing and using proper operational protocols, ensuring adherence to all AABB and FDA regulations and inspection procedures. Participated in researching and establishing new SOPs regarding proper use of cord tissue sterility ... - 2017 Oct 12
... Play key role in implementing and using proper operational protocols, ensuring adherence to all AABB and FDA regulations and inspection procedures. Participated in researching and establishing new SOPs regarding proper use of cord tissue sterility ... - 2017 Oct 12
Medical Marketing
Fall River, MA
... to be completed in accordance to the regulatory body standards and corporate compliance Manages all internal and external (FDA, BSi, TGA and PMDA) audits and the subject matter expert presenting on behalf of the post market surveillance team Trains ... - 2017 Sep 26
... to be completed in accordance to the regulatory body standards and corporate compliance Manages all internal and external (FDA, BSi, TGA and PMDA) audits and the subject matter expert presenting on behalf of the post market surveillance team Trains ... - 2017 Sep 26
Engineer Power Plant
Foxborough, MA
... Developed functional specifications, software test specifications (for FDA validation), Verification and Validation of the software including IQs, OQs, PQs, system configuration and Batch Unit Operations (i.e. Fermentation, reactor, centrifuge, ... - 2017 Sep 14
... Developed functional specifications, software test specifications (for FDA validation), Verification and Validation of the software including IQs, OQs, PQs, system configuration and Batch Unit Operations (i.e. Fermentation, reactor, centrifuge, ... - 2017 Sep 14
Medical Device Sales
Weymouth, MA, 02190
... Solid experience within regulatory affairs, medical device malfunctions and adverse event FDA submissions. Strong ability to effectively convey technical information to a general reader and to industry professionals. Resourceful administration of ... - 2017 Aug 02
... Solid experience within regulatory affairs, medical device malfunctions and adverse event FDA submissions. Strong ability to effectively convey technical information to a general reader and to industry professionals. Resourceful administration of ... - 2017 Aug 02
Management Quality
Walpole, MA
... Additional Areas of Expertise Strategic Planning Continuous Improvement Supply Chain Management P&L Management Inventory Control Statistical Process Control Safety Training Regulatory Compliance (FDA & DEP) Negotiation Project Management Process ... - 2017 May 10
... Additional Areas of Expertise Strategic Planning Continuous Improvement Supply Chain Management P&L Management Inventory Control Statistical Process Control Safety Training Regulatory Compliance (FDA & DEP) Negotiation Project Management Process ... - 2017 May 10
Human Resources Manager
North Attleborough, MA
... • Facilitated numerous performance and talent management workshops with all levels of the organization • Represented HR in all internal, inter-company, and external audits (FDA and ISO) • Facilitated corporate culture surveys; implemented programs ... - 2017 Apr 24
... • Facilitated numerous performance and talent management workshops with all levels of the organization • Represented HR in all internal, inter-company, and external audits (FDA and ISO) • Facilitated corporate culture surveys; implemented programs ... - 2017 Apr 24
Microsoft Office Computer Science
Bristol, RI, 02809
... oThe project also took into consideration the business aspect, FDA approval, intellectual property, and quality control. APPLICATIONS: Bioengineering Laboratory Work: oLab work included; the creation of a respiration measurement device using a ... - 2017 Apr 01
... oThe project also took into consideration the business aspect, FDA approval, intellectual property, and quality control. APPLICATIONS: Bioengineering Laboratory Work: oLab work included; the creation of a respiration measurement device using a ... - 2017 Apr 01
Sales Office Staff
Canton, MA, 02021
... – Ion Exchange, Affinity, Size Exclusion •( Protein Purification, TFF, Ultra filtration, DF •( Enzyme Kinetics •( cGMP, SOPs, FDA Regulations (21 CFR 210/211), Quality Assurance, Quality Control •( Validation and Calibration of Equipment (Autoclave, ... - 2017 Mar 16
... – Ion Exchange, Affinity, Size Exclusion •( Protein Purification, TFF, Ultra filtration, DF •( Enzyme Kinetics •( cGMP, SOPs, FDA Regulations (21 CFR 210/211), Quality Assurance, Quality Control •( Validation and Calibration of Equipment (Autoclave, ... - 2017 Mar 16
Quality Assurance Project Management
Brockton, MA
... ACADEMIC PROJECTS •Preparation of a Mock 510K Premarket Notification: Complied, analyzed and presented the viable regulatory paths for a new medical device using FDA guidance documents and regulations. Prepared extensive research reports. ... - 2017 Mar 15
... ACADEMIC PROJECTS •Preparation of a Mock 510K Premarket Notification: Complied, analyzed and presented the viable regulatory paths for a new medical device using FDA guidance documents and regulations. Prepared extensive research reports. ... - 2017 Mar 15
Regulatory Affairs executive
Brockton, MA
... Analytical with strong background in understanding of FDA, ICH and other regulatory CMC requirements through all phases of development, post-approval, and life-cycle of the product. Proven ability to effectively manage time, contribute effectively ... - 2017 Mar 02
... Analytical with strong background in understanding of FDA, ICH and other regulatory CMC requirements through all phases of development, post-approval, and life-cycle of the product. Proven ability to effectively manage time, contribute effectively ... - 2017 Mar 02