| Resume alert | Resumes 31 - 40 of 623 |
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
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
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
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
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
Clinical Research Business Development
Plainsboro, NJ
... sales and marketing and opinion leaders to develop and implement products labelling strategy to meet the requirements of the FDA and other regulatory agencies to achieve enhanced FDA’s agreements to company’s approval desires based on products ... - Apr 21
... sales and marketing and opinion leaders to develop and implement products labelling strategy to meet the requirements of the FDA and other regulatory agencies to achieve enhanced FDA’s agreements to company’s approval desires based on products ... - Apr 21
Senior Manager / Associate Director
Lawrence Township, NJ
... Maintained rigorous compliance in clinical trial operations, meticulously ensuring that all patient-related content aligned with FDA regulations and Bristol-Myers Squibb (BMS) guidelines. As well as ensuring that all CMC practices were updated ... - Apr 18
... Maintained rigorous compliance in clinical trial operations, meticulously ensuring that all patient-related content aligned with FDA regulations and Bristol-Myers Squibb (BMS) guidelines. As well as ensuring that all CMC practices were updated ... - Apr 18