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Resumes 1 - 10 of 1074 |
Jersey City, NJ
... ● Develop and maintain standard operating procedures (SOPs) and documentation related to Delta V systems, ensuring compliance with regulatory standards such as FDA regulations (e.g., 21 CFR Part 11). ● Perform system testing, validation, and ...
- May 16
Hasbrouck Heights, NJ
... Record keeping of incoming paperwork to FDA retention standards. Arranging Product transportation under consistently changing deadlines. Material Handling and Inventory Control, eliminating down time of Production Lines due to lack of materials. ...
- May 13
Manhattan, NY, 10019
... AWARDS & HOBBIES Nature Editorial Board member Good Clinical Practice (GCP), Clinical Coordinator Mandatory training, HIPAA, and Human Subjects Protection training (including minors and FDA), Radiation, Biological and Chemical Safety training. ...
- May 09
Cedar Grove, NJ
... Accurately completed all paperwork in accordance with FDA, ISO, and all company procedures and policies. Monitored Sterility of self, supplies, tissue, and environment as directed. Performed quality checks on the processed tissues and paperwork ...
- May 08
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
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
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
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
Hopatcong, NJ
... Supply Chain FDA inspection subject matter expert. • Created and optimized scheduling methodology for an immunotherapy product line. • Responsible for the development and maintenance of production schedules for both commercial and clinical products. ...
- Apr 21
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