Glassboro, NJ
... • Produced quality products and adhered to safety policies and procedures to ensure cGMPs as required by FDA and other regulatory compliance agencies. • Performed all Production Assistant (group leader) duties, accurately and with minimal ...
- May 02
San Diego, CA
... pulse generator devices • Identified root cause and troubleshoot defective electroporation medical devices • Complied with the FDA policies, guidelines and regulatory requirements • Performed and documented all activities in compliance with Good ...
- May 02
Memphis, TN
... ●Organizational Skills EDUCATION Rust College Holly Springs, MS • 04/1998 Bachelor's of Science Degree CERTIFICATIONS FDA Food Defense Certified PROFESSIONAL SUMMARY Industrious Chemist with 25 years of laboratory experience in Quality Control. ...
- May 02
Los Angeles, CA
... At times acted as a lead for technology development documents Organized, edited, standardized, materials from cross functional teams for FDA application for a new product (product was approved). Edited over 10,000 pages. Supported SMEs working on ...
- May 02
Jersey City, NJ
... June 2015 to July 2017 Pharma DSCSA Project Pharma DSCSA project is the application provided for pharmaceutical companies for implementing pedigree and track and trace solution for pharmaceutical and cosmetic products as recommended by FDA. ...
- May 02
Herndon, VA
... ●Supported the FDA CBER Lot Release System (LRS) contract, an Oracle client-server application used by CBER's Product Release Branch that supports the processing and release of lots of licensed biological products. Included creating and editing ...
- May 02
Lake Elsinore, CA
... California, USA – 11/2023 Travel Nursing: RN activities at acute rehabilitation(LTC) HACU/FDA, St Antonio(TX); Maryland (D.C.) -05/22 - 08/2022 Molecular epidemiology for the reviewing process. Studies on molecules used in pharmaceutics, biologics, ...
- May 02
Houston, TX
... ● Strong knowledge on ISO 9001:2015, API-Q1 Quality Management Systems, ISO13485, ISO14971 and FDA part 21 CFR Part820, Part11, Part210, Part211 focused guidelines and regulations for medical devices. ● Performed SCR, CAPA, RCA, NCR Issues, supplier ...
- May 01
El Paso, TX
... Work closely with Sanitation, Quality Control and FDA. Six consecutive years of AIB honors and recognition. Head of safety committee, Emergency Action Plan and conducted all investigations. Coca-Cola Enterprises, El Paso, Texas Assistant Inventory ...
- May 01
Hampstead, NH
... center, responsible for total quality management, enhancement of performance in all areas Ensured compliance of all policies and procedures by staff Negotiated contracts for research studies involving MRI imaging and drug research and FDA approval. ...
- May 01