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Resumes 81 - 90 of 1036 |
Irvington, NJ
... Develop and maintain an excel spreadsheet or other mechanism to track corporate compliance Prepared procurement documentation including purchase orders, contracts and amendments Knowledge of cGMP/compliance/FDA Excellent organization and team ...
- 2023 Sep 06
Yonkers, NY
... - first FDA approved detection tests for lyme disease and anthrax infections, Can-Am Care, Inc. - OneTouch diabetes kit and HUGO mobility assistance devices, ReliOn – first blood pressure monitor designed for women, Inverness – SoyCare HRT ...
- 2023 Aug 16
Queens, NY
... review, and submit high-quality regulatory submissions, including ANDAs, amendments, supplements, annual reports, and additional documents as needed to the FDA within company timelines and per regulatory guidelines and applicable federal laws. ...
- 2023 Aug 14
New Milford, NJ
... ● Assisted in the documentation of interpretation of new Federal (FDA) and state regulations. ● Collaborated with team members to troubleshoot and resolve database-related issues, ensuring smooth system operations. Assistant Office Manager Aug 2015 ...
- 2023 Aug 12
New York, NY
... SCOTT 848-***-**** adyp0s@r.postjobfree.com LinkedIn New York, NY Certified Quality Engineer Over 11 years of experience in the Medical Device and Pharmaceutical industries with in-depth knowledge of FDA compliance ensuring current good ...
- 2023 Aug 04
Flushing, NY
... in Macy’s Valley Stream ●Proficient in working with Current Good Manufacturing Practices (cGMP), FDA, OPDP, and PDUFA ●Served clients such as, Astra Zeneca, DuPont Pharma, GlaxoSmithkline, Merck, Pfizer, Dey, Acorda, Actavis, Stiefel Pharma, Eisai, ...
- 2023 Aug 01
Newark, NJ
... ●Maintain GMP and cGMP compliance to meet regulatory requirements of the FDA. ●Document processes and SAP functionality – processes, flowcharts, procedures, work instructions, configurations. Support SAP Core Model ●Review master batch records, ...
- 2023 Jul 27
Teaneck, NJ
... ● Aided Quality Assurance department with generating graphic supporting material for FDA product submissions. ● Coordinated product mockups and graphics for investor presentations. ● Responsible for CAD software upgrades and maintenance. JCDecaux ...
- 2023 Jul 21
West New York, NJ
... Good working knowledge of FDA, and GCP regulations and guidelines and hands on experience in implementing CDISC/SDTM standards and Define.xml, along with efficacy. Developed and used SAS MACROS programs and modified existing SAS programs to make ...
- 2023 Jul 20
The Bronx, NY
... Research Study Participant Self-employed Jul 2018 – Aug 2019 ● Participated in research medical studies about not approved FDA drugs Certified Nursing Assistant Bronx Gardens Rehabilitation Center, Bronx, NY Jan 2018 – Jun 2018 ● Observed and ...
- 2023 Jul 14