| Resume alert | Resumes 41 - 50 of 611 |
Data Analyst Accounts Payable
Edison, NJ
... Sample products examine for FDA Validation of bulk & finished products manufactured by contractors prior to release. Performed the review and disposition of batch manufacturing and packaging records. Reviewed Certificates of Analysis and Compliance ... - Jan 18
... Sample products examine for FDA Validation of bulk & finished products manufactured by contractors prior to release. Performed the review and disposition of batch manufacturing and packaging records. Reviewed Certificates of Analysis and Compliance ... - Jan 18
Customer Service Quality Assurance
Plainsboro Center, NJ, 08536
... skills Courteous demeanor Adaptive team player Energetic work attitude Opening/closing procedures Staff Development FDA Compliance Problem-Solving Skills Regulatory Compliance Quality Assurance and Control Patient Education and Counseling ... - Jan 17
... skills Courteous demeanor Adaptive team player Energetic work attitude Opening/closing procedures Staff Development FDA Compliance Problem-Solving Skills Regulatory Compliance Quality Assurance and Control Patient Education and Counseling ... - Jan 17
Clinical Research Business Development
Trenton, NJ
... specified market share in selected therapeutic areas with great emphasis in being competitive in drug labeling and promotion activities within FDA guidelines and industry standard with investigative activities to ensure compliance in all functions. ... - Jan 15
... specified market share in selected therapeutic areas with great emphasis in being competitive in drug labeling and promotion activities within FDA guidelines and industry standard with investigative activities to ensure compliance in all functions. ... - Jan 15
Software Development Health Care
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
... 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
Inventory Specialist Medical Device
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
... 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
Senior Accountant Customer Service
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
... 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
Senior Director Quality Control
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
... 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
Vice President Executive Director
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
... 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
Statistical Programmer Customer Service
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
... • 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
Drug Safety Team Leader
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
... 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