| Resume alert | Resumes 1 - 10 of 611 |
Social Media Digital Marketing
East Brunswick, NJ, 08816
... across the overall umbrella of products within the portfolio • Collaborated with medical and regulatory agencies in assembling FDA review packages, as well as formulating answers to FDA product queries • Maintained all project timelines, managed and ... - May 22
... across the overall umbrella of products within the portfolio • Collaborated with medical and regulatory agencies in assembling FDA review packages, as well as formulating answers to FDA product queries • Maintained all project timelines, managed and ... - May 22
Quality Assurance Software Testing
Piscataway, NJ
... Executed manual test cases using JAMA, focusing on FDA rules and IES code of conduct standards, and documented results. Logged defects and Change Control Requests in JIRA and tracked the bug resolution cycle. Conducted regression testing after ... - May 21
... Executed manual test cases using JAMA, focusing on FDA rules and IES code of conduct standards, and documented results. Logged defects and Change Control Requests in JIRA and tracked the bug resolution cycle. Conducted regression testing after ... - May 21
Quality Assurance Software Testing
Piscataway, NJ
... Executed manual test cases using JAMA, focusing on FDA rules and IES code of conduct standards, and documented results. Logged defects and Change Control Requests in JIRA and tracked the bug resolution cycle. Conducted regression testing after ... - May 21
... Executed manual test cases using JAMA, focusing on FDA rules and IES code of conduct standards, and documented results. Logged defects and Change Control Requests in JIRA and tracked the bug resolution cycle. Conducted regression testing after ... - May 21
Clinical Research Trial
Ringoes, NJ, 08551
Amjad Khan, BS ad5uvt@r.postjobfree.com 215-***-**** LinkedIn Clinical Research Training: Clinical Research Fastrack July 2022 Clinical Research Training covering Core Competencies including: ●ICH GCP E6 R (2) ●FDA Regulations 21CFR 11, 50, 54, 56 ... - May 21
Amjad Khan, BS ad5uvt@r.postjobfree.com 215-***-**** LinkedIn Clinical Research Training: Clinical Research Fastrack July 2022 Clinical Research Training covering Core Competencies including: ●ICH GCP E6 R (2) ●FDA Regulations 21CFR 11, 50, 54, 56 ... - May 21
Project Management Assay Development
Piscataway, NJ
... Improved Quality Operation of the team for GMP audit, FDA, and Health Canada site inspection. SGS, North America, Mississauga, ON, Canada August 2019 – April 2021 Scientist, QC Analytical Cell Biology Department Led and executed test development, ... - May 14
... Improved Quality Operation of the team for GMP audit, FDA, and Health Canada site inspection. SGS, North America, Mississauga, ON, Canada August 2019 – April 2021 Scientist, QC Analytical Cell Biology Department Led and executed test development, ... - May 14
Software Development Management Process
Edison, NJ
... • Compliance – Ensured compliance with all CCT standards, SOX, FDA, GXP, CSV, 21 CFR part 11, SDLC, SOP and other regulatory requirements. Celgene Inc. – Summit, NJ (http://www.celgene.com) IT Consultant February 2005 – April 2006 • IT Projects – ... - May 13
... • Compliance – Ensured compliance with all CCT standards, SOX, FDA, GXP, CSV, 21 CFR part 11, SDLC, SOP and other regulatory requirements. Celgene Inc. – Summit, NJ (http://www.celgene.com) IT Consultant February 2005 – April 2006 • IT Projects – ... - May 13
Risk Assessment 3Rd Party
Levittown, PA
... (US-FDA) Engaged and accomplished 3rd party Batch Review & System Assessment / Certification / GAP Assessment projects for both API and Formulations manufacturing unit. Hands on as quality professional for Bio-pharmaceutical manufacturing & testing ... - May 11
... (US-FDA) Engaged and accomplished 3rd party Batch Review & System Assessment / Certification / GAP Assessment projects for both API and Formulations manufacturing unit. Hands on as quality professional for Bio-pharmaceutical manufacturing & testing ... - May 11
Quality Assurance Control
Piscataway, NJ
... Reviewed and approved Batch documentations for FDA regulated products. Document control coordinator for the organization, keeping track of procedures and their lifecycle, issue new procedures and archive old when no longer needed. Installed a QMS ... - May 10
... Reviewed and approved Batch documentations for FDA regulated products. Document control coordinator for the organization, keeping track of procedures and their lifecycle, issue new procedures and archive old when no longer needed. Installed a QMS ... - May 10
Medical Editor Copy
Belvidere, NJ, 07823
... able to meet multiple tight deadlines In-depth understanding of routing and production processes, OPDP guidelines, and FDA advertising regulations for fair balance, safety information, and branding placement Expert user of PowerPoint, Word, and ... - May 08
... able to meet multiple tight deadlines In-depth understanding of routing and production processes, OPDP guidelines, and FDA advertising regulations for fair balance, safety information, and branding placement Expert user of PowerPoint, Word, and ... - May 08
Copy Editor Quality Assurance
Ewing, NJ
... physician prescribing information, patient information inserts, and drug labeling according to FDA guidelines; regulatory compliance; slide kits Technology: Aviation reports; biotechnology, communications technology, computer literature, and ... - May 07
... physician prescribing information, patient information inserts, and drug labeling according to FDA guidelines; regulatory compliance; slide kits Technology: Aviation reports; biotechnology, communications technology, computer literature, and ... - May 07