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Resume alert |
Resumes 51 - 60 of 619 |
Princeton, NJ
... (KOL) as aligned with medical strategy ● Experienced in promotional review committees to ensure medically supported data through commenting, improving, approving, or rejecting material based on established company practice and FDA regulation. ...
- Jan 22
Chalfont, PA
... Management, Validation and FDA Compliance, Leading High Performance Teams, CTFA Cleaning/Sanitizing validation, P&G Auditor training, cGMP seminar, PMI (project management Institute) and Lean manufacturing seminars, 6 Sigma, Veeva Vault seminars. ...
- Jan 19
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
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
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
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
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
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