| Resume alert | Resumes 121 - 130 of 527 |
Associate Director
Acton, MA
... Evaluates, trends and reports stability data for internal use and for FDA via required periodic reports. Conduct QC review of data associated with these drug product Development activities. Coordinate the activities at various contractors to insure ... - 2020 May 06
... Evaluates, trends and reports stability data for internal use and for FDA via required periodic reports. Conduct QC review of data associated with these drug product Development activities. Coordinate the activities at various contractors to insure ... - 2020 May 06
Accountant
Boston, MA
... and field calls to provide assistance regarding returns, exchanges and warranty information Process product complaints received from customers and sales force, including all required quality data which strongly impacts FDA reporting requirements - 2020 Apr 04
... and field calls to provide assistance regarding returns, exchanges and warranty information Process product complaints received from customers and sales force, including all required quality data which strongly impacts FDA reporting requirements - 2020 Apr 04
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
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
Pharmacy Manager
Roslindale, MA
... to clinicians based on patient parameters Shamrock Medical Solution Group, Taunton, MA 08/2010 – 07/2011 Staff Pharmacist A FDA registered state of the art repackaging manufacturer providing unit dose medications for hospitals, doctor’s offices and ... - 2020 Jan 07
... to clinicians based on patient parameters Shamrock Medical Solution Group, Taunton, MA 08/2010 – 07/2011 Staff Pharmacist A FDA registered state of the art repackaging manufacturer providing unit dose medications for hospitals, doctor’s offices and ... - 2020 Jan 07