| Resume alert | Resumes 11 - 20 of 1038 |
Program Management Gene Therapy
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
... 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
Precision Medicine Patient Care
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
... 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
Quality Assurance Medical Device
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
... 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
Clinical Research Associate
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
... 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
Customer Service Quality Assurance
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
... 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
Business Partner Financial Services
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
... 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
Supply Chain International Marketing
Queens, NY
... processes, integration flexibility, Supplier relationship management) Logistics management, Retail pricing, Process management, FDA Procedure handling, distribution process and marketing, Export import processing, Commercial Operations, Client ... - Feb 25
... processes, integration flexibility, Supplier relationship management) Logistics management, Retail pricing, Process management, FDA Procedure handling, distribution process and marketing, Export import processing, Commercial Operations, Client ... - Feb 25
Project Manager Management
Queens, NY
... • Provide in-depth data analysis on product performance to be submitted and reviewed by the FDA. Rutgers University, Student Financial Services. IT Systems Manager. (1998 - 2007) • Manage two direct reports, work-study students, and project ... - Feb 25
... • Provide in-depth data analysis on product performance to be submitted and reviewed by the FDA. Rutgers University, Student Financial Services. IT Systems Manager. (1998 - 2007) • Manage two direct reports, work-study students, and project ... - Feb 25
Sql Server Fp A
Teaneck, NJ
... approved by “Federal Drug Administrator (FDA)” to be used in drug manufacturing process. b) Chemical Hazard Information System: Application to record and produce Chemical Safety Data Sheet (CSDS) in PDF format. c) developed & implemented several ... - Feb 23
... approved by “Federal Drug Administrator (FDA)” to be used in drug manufacturing process. b) Chemical Hazard Information System: Application to record and produce Chemical Safety Data Sheet (CSDS) in PDF format. c) developed & implemented several ... - Feb 23
Quality Assurance Control
Jersey City, NJ
... of quality parameters during production (filling, crimping ) • Inspection of packaging procedures (labeling, packaging quality, ...) • Set up Packaging and production equipments In Quality Assurance • Solid knowledge of Health Canada and FDA GMPs. ... - Feb 22
... of quality parameters during production (filling, crimping ) • Inspection of packaging procedures (labeling, packaging quality, ...) • Set up Packaging and production equipments In Quality Assurance • Solid knowledge of Health Canada and FDA GMPs. ... - Feb 22