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Resumes 41 - 50 of 731 |
East Windsor, NJ
... Strong knowledge about Pharmaceutical/Medical device regulations like FDA: 21 CFR Part 210, 21 CFR Part 211 and 21 CFR Part 820 and involved in implementation of CFR Part 11 rules (Electronic Records, Electronic Signatures, Audit Trails, and ...
- Jan 06
Elizabeth, NJ
... approach Strong Knowledge of GCPs, FDA, and ICH requirements Superior work ethics Excellent interpersonal and leadership skills with an eye for detail Excellent knowledge of MS Word, Access, Excel, Teams, Skype, One Note, Zoom, and Share drives. ...
- Jan 05
Somerset, NJ, 08873
... Possessed in-depth knowledge of FDA, DEA, cGMP, GLP, OSHA, EHS, SOP, Parts 210 & 211, and Federal regulations. Professional Experience Ethicon - Med-Tech, Raritan, NJ 08/2022 – Present Sample Management – Global Product Stability, R & D - Biosurgery ...
- Jan 04
Keyport, NJ
... Central Storage Picked orders and served as a Receiving Clerk EDUCATION High School Graduate RELATED TRAINING FDA Good Manufacturing Practice Powered Industrial Lift Truck Training OSHA related training CERTIFICATIONS Certified Forklift Operator ...
- Jan 03
Hillsborough, NJ
... brokers which included manufacturing info,repair and supply values,Lacey Act,fish and wildlife,FDA Wrote some of the standard operating procedures, provided support and worked with other departments such as customer service and inventory control. ...
- Jan 02
Piscataway, NJ
... all processes and documents for digital FDA review remotely. •Developed company expansion capacity models and execute resourcing strategies to ensure delivery of activities and scopes of work from various internal teams and external consultants ...
- Jan 02
Trenton, NJ
... Assisted in the preparation of FDA filing for Vanlev preparing articles and references to meet the FDA standards. TAS Coordinator for time allocation for the exempt employees. *Responsible for overseeing administrative staff of eight (8); ...
- Jan 02
Edison, NJ
... • Provided further analysis as requested by FDA after submission. Carried out new analyses on past studies and designed tables to display information. • • Produced patient profiles listings for oncology studies. Created standard and custom reports ...
- Jan 02
North Brunswick, NJ, 08902
... Proficient in performing causality assessment, writing case summaries and assisting in preparing reports for FDA, EMA and EU submissions. High-energy result-driven dedicated, team player, multi-tasking experienced professional with strong ...
- 2023 Dec 22
Edison, NJ
... I understand the rigors of not only performing a task/project correctly but also documenting work in a fashion that is clear and concise since it is subject to FDA inspections. Realize the critical importance of developing relationships both inside ...
- 2023 Dec 20