| Resume alert | Resumes 1 - 10 of 1509 |
Project Management Senior Business
Piscataway, NJ
... Make that biopharmaceutical firms are adhering to various regulated systems, such as FDA, SOX, GXP, CSV, 21 CFR Part 11, SOP, and other state and federal requirements. Worked with different lines of business to understand the ACA and HIX policies ... - May 06
... Make that biopharmaceutical firms are adhering to various regulated systems, such as FDA, SOX, GXP, CSV, 21 CFR Part 11, SOP, and other state and federal requirements. Worked with different lines of business to understand the ACA and HIX policies ... - May 06
Human Resources Talent Acquisition
Brooklyn, NY, 11201
... • Hiring for the following: FDA Compliance Engineers, FDA Compliance Analysts, Acoustic Engineers, Mechanical Engineers, Electrical Engineers, Network Engineers, Systems Engineers, Electronics Engineers as well as Procurement, Supply Chain and ... - May 06
... • Hiring for the following: FDA Compliance Engineers, FDA Compliance Analysts, Acoustic Engineers, Mechanical Engineers, Electrical Engineers, Network Engineers, Systems Engineers, Electronics Engineers as well as Procurement, Supply Chain and ... - May 06
Blockchain Engineer
Jersey City, NJ
... June 2015 to July 2017 Pharma DSCSA Project Pharma DSCSA project is the application provided for pharmaceutical companies for implementing pedigree and track and trace solution for pharmaceutical and cosmetic products as recommended by FDA. ... - May 02
... June 2015 to July 2017 Pharma DSCSA Project Pharma DSCSA project is the application provided for pharmaceutical companies for implementing pedigree and track and trace solution for pharmaceutical and cosmetic products as recommended by FDA. ... - May 02
Clinical Research Associate
Montville, NJ
... and site assessment Individual and large group training on EDC methods and best practices Liaison between sponsors, the FDA and research sites Responsibilities included a Phase III dermatology NDA, a pre-market maintenance study for a new ... - Apr 30
... and site assessment Individual and large group training on EDC methods and best practices Liaison between sponsors, the FDA and research sites Responsibilities included a Phase III dermatology NDA, a pre-market maintenance study for a new ... - Apr 30
Quality Assurance Regulatory Affairs
Kendall Park, NJ
... EDUCATION Master’s of Science in Regulatory Affairs & Health Policy MCPHS University Boston, MA Dec 2017 GPA:3.91/4.00 Bachelor’s of Science in Pharmacy Veer Narmad South Gujarat University India May 2005 GPA: 3.25/4.00 EDUCATION DETAILS • FDA ... - Apr 29
... EDUCATION Master’s of Science in Regulatory Affairs & Health Policy MCPHS University Boston, MA Dec 2017 GPA:3.91/4.00 Bachelor’s of Science in Pharmacy Veer Narmad South Gujarat University India May 2005 GPA: 3.25/4.00 EDUCATION DETAILS • FDA ... - Apr 29
Information Technology Supply Chain
Morristown, NJ
... Strong understanding of IT Governance (SOX ITGC) for FDA and global/global regulatory audits. Excellent interpersonal skills to manage multiple priorities in a dynamic environment. Experience in ITSM tools such as ServiceNow to manage global ... - Apr 22
... Strong understanding of IT Governance (SOX ITGC) for FDA and global/global regulatory audits. Excellent interpersonal skills to manage multiple priorities in a dynamic environment. Experience in ITSM tools such as ServiceNow to manage global ... - Apr 22
Case Manager Rn
Bayonne, NJ
... 2016 • Identify consumers of Johnson&Johnson bladder and hernia mesh recalls via medical charts for medical review to the FDA • Abstract patient information from medical charts such demographics, medical/surgical history and procedures before and ... - Apr 19
... 2016 • Identify consumers of Johnson&Johnson bladder and hernia mesh recalls via medical charts for medical review to the FDA • Abstract patient information from medical charts such demographics, medical/surgical history and procedures before and ... - Apr 19
Development Operations Clinical
Jersey City, NJ
... Skilled in leading cross-functional product development programs and Clinical trial team management, specifically developing and implementing strategic product development plans, and ensuring compliance with FDA regulations and ICH guidelines. ... - Apr 16
... Skilled in leading cross-functional product development programs and Clinical trial team management, specifically developing and implementing strategic product development plans, and ensuring compliance with FDA regulations and ICH guidelines. ... - Apr 16
Quality Assurance Medical Devices
Manhattan, NY, 10019
... Follow FDA, TUK- SUD AND ISO guidelines for build and test Medical Devices. Testing and fixing trouble shooting in Sub Assy. Refurbishing Instruments. Samblasting machine Sand blending, polsishing in to the machine shop Cycle Count with SAP System. ... - Apr 16
... Follow FDA, TUK- SUD AND ISO guidelines for build and test Medical Devices. Testing and fixing trouble shooting in Sub Assy. Refurbishing Instruments. Samblasting machine Sand blending, polsishing in to the machine shop Cycle Count with SAP System. ... - Apr 16
Customer Service Rep
North Plainfield, NJ
... Dayton, NJ • Managed arriving vessels for spice company overseeing and serving as the company’s liaison • Handled the compliance of Customs regulations, in addition to coordinating with FDA and clearing Customs with Brokers • Generated purchase ... - Apr 15
... Dayton, NJ • Managed arriving vessels for spice company overseeing and serving as the company’s liaison • Handled the compliance of Customs regulations, in addition to coordinating with FDA and clearing Customs with Brokers • Generated purchase ... - Apr 15