| Resume alert | Resumes 21 - 30 of 52 |
Biomedical engineering, biomechanics, medical devices, project mgmt
New Delhi, Delhi, India
... Other regulatory strategy exposure to FDA 510k, FDA QSR, CE, WHO guideline study, DICOM, HIPAA. Preparation of SOP for IC, IP and FG testing - 2018 Nov 25
... Other regulatory strategy exposure to FDA 510k, FDA QSR, CE, WHO guideline study, DICOM, HIPAA. Preparation of SOP for IC, IP and FG testing - 2018 Nov 25
Digital Marketing Sales
New Delhi, Delhi, India
... Coordination with other Inter Departments like FDA (for better Deals, DMS), Landing Page Team (for Landing pages, creative), Tech team (for DMS and other tech issues), Web Design Team (for design issues) etc. Team Training - Properly assign keywords ... - 2018 Sep 09
... Coordination with other Inter Departments like FDA (for better Deals, DMS), Landing Page Team (for Landing pages, creative), Tech team (for DMS and other tech issues), Web Design Team (for design issues) etc. Team Training - Properly assign keywords ... - 2018 Sep 09
Engineer Mechanical
Noida, UP, India
... Contributed to successful FDA (510(k)) approval of several anesthesia workstation systems and functional enhancements to existing equipment. Page 2 / 3 Other Hobbies Net Surfing Playing Outdoor Games Indoor Games Page 3 / 3 - 2018 May 03
... Contributed to successful FDA (510(k)) approval of several anesthesia workstation systems and functional enhancements to existing equipment. Page 2 / 3 Other Hobbies Net Surfing Playing Outdoor Games Indoor Games Page 3 / 3 - 2018 May 03
Electrical Engineer
New Delhi, DL, India
... It meets the IP / BP, USP, US FDA standards and is used for sterilization in fermentors, reactors, pipelines & autoclaves. It is also used for humidification of sterile area. 4.Ampule Filling 5.Heat Tunnel:-The technology of super heater steam ... - 2018 Mar 31
... It meets the IP / BP, USP, US FDA standards and is used for sterilization in fermentors, reactors, pipelines & autoclaves. It is also used for humidification of sterile area. 4.Ampule Filling 5.Heat Tunnel:-The technology of super heater steam ... - 2018 Mar 31
Secondary School Pharmacy
New Delhi, DL, India
... Job Profile: Handling Regulatory Affairs of company as well as ISO 9001-2004 Documentation, FDA Documentation, CE Documentation. Also active in licensing affairs of company. Duration:01/09/2010 to 31/01/2012 Eight month experience as Lecturer in ... - 2017 Oct 02
... Job Profile: Handling Regulatory Affairs of company as well as ISO 9001-2004 Documentation, FDA Documentation, CE Documentation. Also active in licensing affairs of company. Duration:01/09/2010 to 31/01/2012 Eight month experience as Lecturer in ... - 2017 Oct 02
Regulatory Affairs
Gurugram, HR, India
... Follow up with FDA for guidance, for queries related to dossiers or any updates on the filed submissions. Other activities involve filing of Controlled correspondences and Bio correspondence, Suitability Petitions with USFDA. Basic knowledge of ... - 2017 Sep 22
... Follow up with FDA for guidance, for queries related to dossiers or any updates on the filed submissions. Other activities involve filing of Controlled correspondences and Bio correspondence, Suitability Petitions with USFDA. Basic knowledge of ... - 2017 Sep 22
Management Project
DL, India
... Faced and replied to queries during Regulatory Audits FDA etc. Project: Pfizer IT ERP Quality & Compliance (Oct 2011 – Aug2013) Customer Name: Pfizer Inc Project Description: ERP SAP ECC 6.0 US Pharma Major's current ERP support framework to be ... - 2017 Jul 30
... Faced and replied to queries during Regulatory Audits FDA etc. Project: Pfizer IT ERP Quality & Compliance (Oct 2011 – Aug2013) Customer Name: Pfizer Inc Project Description: ERP SAP ECC 6.0 US Pharma Major's current ERP support framework to be ... - 2017 Jul 30
Manager Food Safety
Gurugram, HR, India
... Responsible to finalize and approve the labeling and nutritional value claim requirement for new as well as routine products as per FSSAI and FDA norms. Conducting regular vendor audit to maintain supply of quality materials. Responsible to take ... - 2017 Jun 20
... Responsible to finalize and approve the labeling and nutritional value claim requirement for new as well as routine products as per FSSAI and FDA norms. Conducting regular vendor audit to maintain supply of quality materials. Responsible to take ... - 2017 Jun 20
Project Management Clinical Research
DL, India
... Successful clearance of audits from ANVISA (Brazil), MHRA (UK), AFFSAPS (French & Danish), US FDA. Other interests include music, reading and Traveling. AREA OF INTEREST: Clinical Research and Project Management. SPECIFIC STRENGTHS: Good knowledge ... - 2017 May 15
... Successful clearance of audits from ANVISA (Brazil), MHRA (UK), AFFSAPS (French & Danish), US FDA. Other interests include music, reading and Traveling. AREA OF INTEREST: Clinical Research and Project Management. SPECIFIC STRENGTHS: Good knowledge ... - 2017 May 15
Clinical Research Management
New Delhi, DL, 110078, India
... In-depth Knowledge on ICH-GCP guidelines, Schedule Y and FDA regulations. ICF verification for GCP compliance Monitor the CRF completion and corrections as per the source data Monitoring the progress of the Clinical Trial with strict adherence to ... - 2017 Mar 06
... In-depth Knowledge on ICH-GCP guidelines, Schedule Y and FDA regulations. ICF verification for GCP compliance Monitor the CRF completion and corrections as per the source data Monitoring the progress of the Clinical Trial with strict adherence to ... - 2017 Mar 06