|
Resume alert |
Resumes 31 - 40 of 594 |
Atco, NJ, 08004
... Conducted extensive walk downs for as-built conditions, and construction support of process and utility piping systems in support of a FDA pre-approval pharmaceutical facility. Fluor Daniel Inc. - Marlton, N.J. (July 1989 – March 2000) Senior Piping ...
- 2023 Dec 28
Pennsauken, NJ
... Certificate in Pharmacy Technology School Of Health Care Sciences - Falls, TX, US Skills • DRUG SAFETY (10+ years) • ETIQUETTE (Less than 1 year) • FDA (10+ years) • MEDICAID (10+ years) • MEDICARE (10+ years) • PTCB (10+ years) • Pharmacy Tech (10+ ...
- 2023 Dec 26
Willingboro, NJ
... Patents and a robust consultancy background managing IND-Enabling Studies and drug supply, CMC management (Phase 1-2a), and recognized expert Credited with discovering DPP4 inhibitor saxagliptin (Onglyza) at BMS for T2DM, FDA 2009 and credited with ...
- 2023 Dec 18
Lansdale, PA
... Piramal Pharmaceuticals (Teva supplier) - Pennsylvania QAIT Architect 07-2022 to 02-2023 In less than six months, I built a new, highly efficient risk-based CSV program in preparation for an FDA audit and product release. I Developed twenty-seven ...
- 2023 Dec 18
Wilmington, DE
... (The above job was a transfer still within DuPont) OTHER EXPERIENCE: FDA, CGMP, Six Sigma, Safety Committee, SAP, JD Edwards, Certified in Tech Drafting, Certified in First Aid and CPR, ISO Audit Training, Implemented TMS, CMM Training. TOOL AND ...
- 2023 Dec 15
Cherry Hill, NJ
... Documented product complaints into Quality Management Systems database for trending and responsible for investigating, completing, and maintaining Complaint Records in timely and accurate manner in accordance with the FDA's QSR Regulations, ISO ...
- 2023 Dec 11
Wilmington, DE
... 01/2014 – 03/2014 Cura Scripts/Express Scripts, New Castle, DE Administrative Assistant (temporary assignment) Input prescription numbers into RX Home System, print out prescription & label and attach for FDA auditing purposes, filing, and train new ...
- 2023 Dec 10
Swedesboro, NJ
... Advance knowledge in FDA, EMA and PMDA regulatory compliance. Well versed in 21 CFR Part 803. Proficient in global GMP and Regulatory requirements. Working knowledge in CAPAs, INDs, recalls, QA, JDE, Literature, legal (litigations), clinical trials ...
- 2023 Dec 08
Norristown, PA
... Assisted with FDA submissions of ISE and ISS with extensive graphs, tables, and listings. Led validation of TLF and analysis data . Worked in therapeutic areas of oncology, cardiovascular, diabetics studies, and blood pressure reductions. AUXILIUM ...
- 2023 Dec 06
Philadelphia, PA
... Responsibility for clinical and operational compliance with USP 797, FDA, DEA, and PA BoP regulations Performed benefit appeals or other reimbursement/payer research, responded to CMS and PBM audits Took reports of and responded to: Assisted ...
- 2023 Dec 05