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Resume alert |
Resumes 11 - 20 of 619 |
Somerset, NJ, 08873
... •I was very much involved and supported business in periodic review process for all GMP applications for Site and GxP System Audit Trail Review Summary Report, FDA audit,HER. •I helped business to document functional requirement, validation process ...
- May 28
Hillsborough, NJ
... ● Performed quantitative analysis for pharmaceutical drug-substances, excipients and drug products using USP/NF, EP, in-house test methods and standard protocols, maintaining full compliance with all applicable US FDA - cGMP regulations and internal ...
- May 27
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
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
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
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
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
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
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
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