| Resume alert | Resumes 51 - 60 of 180 |
Manager Project
Wilmington, DE
... established deadlines • Worked collaboratively to establish and enforce labeling standards • Stabilized project workflow to FDA guidelines to gain Medical, Legal, and Regulatory approvals DAY ONE MARKETING, LLC, Skippack, PA Proposal Editor / Writer ... - 2018 Sep 30
... established deadlines • Worked collaboratively to establish and enforce labeling standards • Stabilized project workflow to FDA guidelines to gain Medical, Legal, and Regulatory approvals DAY ONE MARKETING, LLC, Skippack, PA Proposal Editor / Writer ... - 2018 Sep 30
Medical Device
Media, PA
... Recommended remediations to FDA, ensuring compliance with current FDA/QSR, ISO13485, CE Marking, and other appropriate product guidelines. Key Accomplishments: Led continuous process improvements to quality management activities, implementing and ... - 2018 Sep 28
... Recommended remediations to FDA, ensuring compliance with current FDA/QSR, ISO13485, CE Marking, and other appropriate product guidelines. Key Accomplishments: Led continuous process improvements to quality management activities, implementing and ... - 2018 Sep 28
Engineer Software
Newark, DE
... Professional experience and problem-solving concepts Utilized time in making webpages Worked with HTML with Wiki Source (Troubleshooting of Atellica) Utilized the Software: TFS – FDA – R&D - SAP – JIRA Oberthur Technologies Software Engineer ... - 2018 Jul 24
... Professional experience and problem-solving concepts Utilized time in making webpages Worked with HTML with Wiki Source (Troubleshooting of Atellica) Utilized the Software: TFS – FDA – R&D - SAP – JIRA Oberthur Technologies Software Engineer ... - 2018 Jul 24
Medical Pharmacy
Downingtown, PA
... Knowledgeable of the FDA, OIG, ICH, HIPAA and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers. Skills: Have demonstrated; Experience as Medical Affairs Associate. Experience in meetings ... - 2018 Jun 29
... Knowledgeable of the FDA, OIG, ICH, HIPAA and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers. Skills: Have demonstrated; Experience as Medical Affairs Associate. Experience in meetings ... - 2018 Jun 29
Desktop Support Technician
Broomall, PA
... This group consisted of top executives, who were involved in projects concerning FDA submissions for developing drugs. Provide IBM laptops/desktop support, running Windows 2000 and Windows XP. Provide email support for Outlook 2000/2002/2007. ... - 2018 Jun 25
... This group consisted of top executives, who were involved in projects concerning FDA submissions for developing drugs. Provide IBM laptops/desktop support, running Windows 2000 and Windows XP. Provide email support for Outlook 2000/2002/2007. ... - 2018 Jun 25
Sales Representative
West Chester, PA
... Washington, PA Laboratory Technician, Quality Control/Quality Assurance, Microbiology Routine QC compliance testing of OTC pharmaceuticals per FDA regulations. Responsible for lab maintenance of routine stock cultures and supplies. Responsible for ... - 2018 Jun 08
... Washington, PA Laboratory Technician, Quality Control/Quality Assurance, Microbiology Routine QC compliance testing of OTC pharmaceuticals per FDA regulations. Responsible for lab maintenance of routine stock cultures and supplies. Responsible for ... - 2018 Jun 08
Quality Engineer
Newtown Square, PA, 19073
... regulatory compliance operating procedures to meet FDA and ISO 13485 requirements ● Review the adequacy and correctness of changes to Bill of Materials (BOM’s), Assembly Procedures, Drawings, Component Specification, FMEAs, Control Plans, etc. ... - 2018 Apr 30
... regulatory compliance operating procedures to meet FDA and ISO 13485 requirements ● Review the adequacy and correctness of changes to Bill of Materials (BOM’s), Assembly Procedures, Drawings, Component Specification, FMEAs, Control Plans, etc. ... - 2018 Apr 30
Manager Engineering
Bear, DE, 19701
... FARMERS FRIDGE, Chicago, IL Sep 2016 - Dec 2016 Plant Manager Overall P&L responsibility including the daily operations regarding inventory, staffing, machine efficiency, maintenance, quality and safety at an FDA regulated facility producing goods ... - 2018 Apr 05
... FARMERS FRIDGE, Chicago, IL Sep 2016 - Dec 2016 Plant Manager Overall P&L responsibility including the daily operations regarding inventory, staffing, machine efficiency, maintenance, quality and safety at an FDA regulated facility producing goods ... - 2018 Apr 05
Sales Medical
Downingtown, PA, 19335
... Discussed pharmaceutical life cycles, sales staff needs, FDA regulatory needs, and assisted multiple simultaneous projects accordingly. HMP Communications, Inc. Special Projects Editor, July 2016-February 2017 Proofread, copyedited, and fact checked ... - 2018 Mar 19
... Discussed pharmaceutical life cycles, sales staff needs, FDA regulatory needs, and assisted multiple simultaneous projects accordingly. HMP Communications, Inc. Special Projects Editor, July 2016-February 2017 Proofread, copyedited, and fact checked ... - 2018 Mar 19
Customer Service Sales
Clifton Heights, PA
... CORE QUALIFICATIONS • Customer / Field Service Management • Policy/Program development • Quality and Regulatory Affairs • FDA / TUV experience • Standards utilization • 510K Submissions • CAPA and Complaint Surveillance • Quality Management • ... - 2018 Mar 15
... CORE QUALIFICATIONS • Customer / Field Service Management • Policy/Program development • Quality and Regulatory Affairs • FDA / TUV experience • Standards utilization • 510K Submissions • CAPA and Complaint Surveillance • Quality Management • ... - 2018 Mar 15