| Resume alert | Resumes 101 - 110 of 460 |
Clinical Research
Boston, MA
... • Drafted a Pre-IND Meeting Request for including a brief product review, purpose and objectives of the meetings and questions for the FDA. • Provided a regulatory review of a non-clinical data and helped to prepare a Briefing package to support the ... - 2020 Apr 02
... • Drafted a Pre-IND Meeting Request for including a brief product review, purpose and objectives of the meetings and questions for the FDA. • Provided a regulatory review of a non-clinical data and helped to prepare a Briefing package to support the ... - 2020 Apr 02
Quality Engineer Chemical Engineering
Medford, MA
Snehal Rajesh Rane, CQE Medford, MA ***** adcji9@r.postjobfree.com 716-***-**** www.linkedin.com/in/snehalr SUMMARY Quality Engineer with 5 years of experience in Product Development Life Cycle, ISO and FDA Audits, Risk Management, and ... - 2020 Mar 30
Snehal Rajesh Rane, CQE Medford, MA ***** adcji9@r.postjobfree.com 716-***-**** www.linkedin.com/in/snehalr SUMMARY Quality Engineer with 5 years of experience in Product Development Life Cycle, ISO and FDA Audits, Risk Management, and ... - 2020 Mar 30
Medical Device Manager
Watertown, MA
... Adept at building credibility and working effectively with senior management, engineers, quality managers, manufacturers, FDA, EU and other global regulators to identify and manage the most optimal regulatory path to market for the organization(s). ... - 2020 Mar 06
... Adept at building credibility and working effectively with senior management, engineers, quality managers, manufacturers, FDA, EU and other global regulators to identify and manage the most optimal regulatory path to market for the organization(s). ... - 2020 Mar 06
Content and Digital Marketing Manager
Chelmsford, MA
... Represented the marketing team’s interests as part of weekly review process for regulatory/medical/legal approvals of digital marketing content before FDA submission. Interfaced with 5 different agencies to create more than 40 digital ads, three ... - 2020 Mar 05
... Represented the marketing team’s interests as part of weekly review process for regulatory/medical/legal approvals of digital marketing content before FDA submission. Interfaced with 5 different agencies to create more than 40 digital ads, three ... - 2020 Mar 05
Biomedical Engineer
Watertown, MA
... August- December 2017 Development Co-op: Packaging and Case Development (Zimmer Biomet, Warsaw, IN) ● Responsible for complying with FDA requirements for case functionality and new product development. ● Performed risk analysis through FMEA ... - 2020 Feb 25
... August- December 2017 Development Co-op: Packaging and Case Development (Zimmer Biomet, Warsaw, IN) ● Responsible for complying with FDA requirements for case functionality and new product development. ● Performed risk analysis through FMEA ... - 2020 Feb 25
Customer Service Sales
Newton, NH
... Established services agreements, tolling manufacturing, contract manufacturing, and built new manufacturing locations among 13 shared locations supporting the FDA process validation for food packaging products and class 2 medical devices “sodasorb”. ... - 2020 Feb 06
... Established services agreements, tolling manufacturing, contract manufacturing, and built new manufacturing locations among 13 shared locations supporting the FDA process validation for food packaging products and class 2 medical devices “sodasorb”. ... - 2020 Feb 06
Executive Assistant Administrative
Billerica, MA
... Played a vital communication role in assisting all teams within the department to ensure timely FDA submissions. Welcoming all guests and or candidates. EXPERIENCE 2005 – 2007 LINBECK GROUP, DESIGN AND CONSTRUCTION FIRM EXECUTIVE ASSISTANT Served as ... - 2020 Jan 26
... Played a vital communication role in assisting all teams within the department to ensure timely FDA submissions. Welcoming all guests and or candidates. EXPERIENCE 2005 – 2007 LINBECK GROUP, DESIGN AND CONSTRUCTION FIRM EXECUTIVE ASSISTANT Served as ... - 2020 Jan 26
Engineering Quality Assurance
Arlington, MA
... • Performed Internal and Supplier Audits per ISO 9001and per FDA requirements. EXPERIENCE: MedSource Technologies, Norwell, MA 020**-****-**** - 2004 Quality Assurance Systems Administrator/Supervisor • Successfully streamlined inspection criteria ... - 2020 Jan 21
... • Performed Internal and Supplier Audits per ISO 9001and per FDA requirements. EXPERIENCE: MedSource Technologies, Norwell, MA 020**-****-**** - 2004 Quality Assurance Systems Administrator/Supervisor • Successfully streamlined inspection criteria ... - 2020 Jan 21
Graphic Designer/Technical Illustrator
Westford, MA, 01886
... Followed the corporate master brand guidelines, work instructions, SOP/SAP, and FDA specifications, while collaborating with teams consisting of legal, regulatory, quality, marketing, packaging engineering, manufacturing, and R&D. Managed multiple ... - 2020 Jan 02
... Followed the corporate master brand guidelines, work instructions, SOP/SAP, and FDA specifications, while collaborating with teams consisting of legal, regulatory, quality, marketing, packaging engineering, manufacturing, and R&D. Managed multiple ... - 2020 Jan 02
Quality Engineer Training
Chelmsford, MA
... Non-normal data oSample size selection oStatistical process control techniques FDA 13485 2016 trained (Stat-O-Matrix) Edmund Foley Page 2 Smith-Nephew Lean Sigma Master Blackbelt (09/15 to 01/17) Provide Lean and Six Sigma training globally for SN. ... - 2019 Dec 16
... Non-normal data oSample size selection oStatistical process control techniques FDA 13485 2016 trained (Stat-O-Matrix) Edmund Foley Page 2 Smith-Nephew Lean Sigma Master Blackbelt (09/15 to 01/17) Provide Lean and Six Sigma training globally for SN. ... - 2019 Dec 16