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Resume alert |
Resumes 11 - 20 of 1092 |
North Bergen, NJ
... The entire software followed FDA regulations like PDMA and 21 CFR for sample validations rules. Environment: Oracle PL/SQL, C++, VB6, ASP, Sybase, HTML, JavaScript, XML, Perl Scripting, UNIX Shell Scripting. Sample Management as per CFR 21 Oct 1998 ...
- Mar 31
New York, NY
... & Safety Medication Inventory Management FDA Compliance Customer Service/Customer Relations Good communication and interpersonal skills Notary Public (New York) Ability to operate devices such as scan guns, tablet counters, and cash registers
- Mar 28
Newark, NJ
... Lupin Pharmaceuticals Somerset, NJ 01/2022 - 11/2022 Warehouse associate/Material Handler Current good manufacturing Practice regulation enforced by the FDA. Performed cycle counts and inventory control to accurately track product levels. Fastened ...
- Mar 28
Newark, NJ
... • Knowledge of cGMP/FDA regulated industry Education High school diploma Piscataway High School - Piscataway, NJ Baskerville Institute Skills • Forklift • Ups/fedex • Operator certification • Time Management • Manufacturing • Warehouse management ...
- Mar 26
Wood Ridge, NJ
... company from Discovery through multiple IND approvals, IPO and M&A • Experience with implementing CMC strategies based on FDA/EMA guidance in Neurodegenerative and Pain diseases • Leader for technical teams in various departments including CMC, ...
- Mar 11
Stamford, CT
... Mechanisms for matching drug treatment with genomic aberrations (mutations, amplifications, translocations, etc.) with targeted therapy include participation in clinical trials, single patient INDs and utilizing FDA drugs for non-FDA approved ...
- Mar 11
Brooklyn, NY
... Basic understanding of regulatory guidance documents of ICH, FDA and EMEA PROFESSIONAL WORK EXPERIENCE: JANSEEN BIOTECH (JOHNSON & JOHNSON PHARMACEUTICAL)- MALVERN- PA- USA Jan 2024- Present, Operation Co-Op, Full-Time. Contribute to the overall ...
- Mar 08
Belleville, NJ
... Possesses a profound understanding of ICH-GCP guidelines, FDA regulations, and ALCOA principles. Strong communication and ICT skills, combined with a meticulous eye for detail. THERAPEUTIC EXPERIENCE oMEDICAL DEVICES/IVD: Cardiovascular Devices, ...
- Mar 08
Newark, NJ
... Verify that all entries we’re received from suppliers with required data and FDA release for customs audit regulations reports and graphs. Identify to which internal business the invoices/purchase order belonged to and provide data to the finance ...
- Mar 05
Queens, NY
... Accomplishment lowered mean time to resolve support tickets by 50% Built an enhanced Cybersecurity framework to support the Department of Defense compliance requirements for both NIST and CMMC, as well as the FDA, ISO, GDPR, and others. This new ...
- Feb 28