| Resume alert | Resumes 21 - 30 of 304 |
High School Teacher Hazardous Materials Manufacturing
Trenton, NJ, 08611
... Helped build this company from the ground, using analytical skills in the QC department and GMP on the production floor. Americhem Inc., Salisbury, Maryland Color Design Technician, Jul 1999 – Dec 2000 Matched custom colors under various light ... - Jan 14
... Helped build this company from the ground, using analytical skills in the QC department and GMP on the production floor. Americhem Inc., Salisbury, Maryland Color Design Technician, Jul 1999 – Dec 2000 Matched custom colors under various light ... - Jan 14
Software Development Health Care
East Windsor, NJ
... Extensive validating experience in FDA regulated environment with good understanding of cGxP (GMP, GDP, GCP and GLP). Experienced in Software Development Life Cycle (SDLC) and Software Testing Life Cycle (STLC) and software development methodologies ... - Jan 06
... Extensive validating experience in FDA regulated environment with good understanding of cGxP (GMP, GDP, GCP and GLP). Experienced in Software Development Life Cycle (SDLC) and Software Testing Life Cycle (STLC) and software development methodologies ... - Jan 06
Synthetic Organic Continuous Improvement
Willingboro, NJ
... Career Experience DJ Augeri Pharma Consulting, LLC 2012 – Present Synthetic-Organic & Medicinal Chemist/Consultant Biotech Preclinical/IND Enabling/CMC Management GLP/GMP API, Regulatory/FDA Head operations associated with setup and management of ... - 2023 Dec 18
... Career Experience DJ Augeri Pharma Consulting, LLC 2012 – Present Synthetic-Organic & Medicinal Chemist/Consultant Biotech Preclinical/IND Enabling/CMC Management GLP/GMP API, Regulatory/FDA Head operations associated with setup and management of ... - 2023 Dec 18
Quality Assurance Control
Trenton, NJ
... Performing weekly GMP walk, environmental monitoring and maintain EMP reports (21 CFR 111 and 117) To perform microbial testing on raw material through M3 system. Testing of cleaning and sanitizing agents (Chem station) and RO water. FTIR and micro ... - 2023 Dec 11
... Performing weekly GMP walk, environmental monitoring and maintain EMP reports (21 CFR 111 and 117) To perform microbial testing on raw material through M3 system. Testing of cleaning and sanitizing agents (Chem station) and RO water. FTIR and micro ... - 2023 Dec 11
Quality Management System
Cherry Hill, NJ
... Built and maintained capability within the assigned sub-system for compliance with QMS, ISO, and FDA GMP's. Ensured activities and items were in compliance with both company quality assurance standards and applicable government regulations, such as ... - 2023 Dec 11
... Built and maintained capability within the assigned sub-system for compliance with QMS, ISO, and FDA GMP's. Ensured activities and items were in compliance with both company quality assurance standards and applicable government regulations, such as ... - 2023 Dec 11
Quality Control Specialist
Somerset, NJ, 08873
... Knowledge of GMP, ISO, and FDA regulations and audit Experience with environmental monitoring, air and water sampling with GMP regulations. Performed Cross Functional Lab audits for FDA Inspection. Worked according to the approved validation ... - 2023 Dec 07
... Knowledge of GMP, ISO, and FDA regulations and audit Experience with environmental monitoring, air and water sampling with GMP regulations. Performed Cross Functional Lab audits for FDA Inspection. Worked according to the approved validation ... - 2023 Dec 07
Human Resources Production Line
Skillman, NJ
... Knowledge of health and safety procedures including OSHA, SOP, GMP regulations. Extensive knowledge of the inner workings of production line companies from human resources down to production line workers. EDUCATION 2009 - Paraprofessional ... - 2023 Dec 04
... Knowledge of health and safety procedures including OSHA, SOP, GMP regulations. Extensive knowledge of the inner workings of production line companies from human resources down to production line workers. EDUCATION 2009 - Paraprofessional ... - 2023 Dec 04
Regulatory Affairs United States
Mount Laurel, NJ, 08054
... Job Title Manager CMC Regulatory CATALENT Dates Position Held March 2018 June 2018 Responsibilities As Regulatory Affairs Manager it was my primary duty to support: ●Product development ●Manufacturing activities ●Compliance with GMP regulations. ... - 2023 Nov 29
... Job Title Manager CMC Regulatory CATALENT Dates Position Held March 2018 June 2018 Responsibilities As Regulatory Affairs Manager it was my primary duty to support: ●Product development ●Manufacturing activities ●Compliance with GMP regulations. ... - 2023 Nov 29
CSV Specialist, Compliance Specialist, Quality Control and AR&D Lab
Hillsborough, NJ
... Summary of Qualifications • 12 years of analytical experience in Quality Control and R&D Laboratory • 11 years of Computerized System validation/qualification experience in the Validation Department • 2 years of GMP quality compliance/quality ... - 2023 Nov 17
... Summary of Qualifications • 12 years of analytical experience in Quality Control and R&D Laboratory • 11 years of Computerized System validation/qualification experience in the Validation Department • 2 years of GMP quality compliance/quality ... - 2023 Nov 17
Quality Assurance Business Development
Somerset, NJ
... Highly effective at contributing to drug development and technology transfer, facilitating GMP audits, CAPA, and root cause analysis, and clearly and concisely liaising with agencies and clients. Encouraging mentor, excellent team leader and ... - 2023 Nov 16
... Highly effective at contributing to drug development and technology transfer, facilitating GMP audits, CAPA, and root cause analysis, and clearly and concisely liaising with agencies and clients. Encouraging mentor, excellent team leader and ... - 2023 Nov 16