| Resume alert | Resumes 41 - 50 of 300 |
Technical Writer Regulatory Affairs
Ewing, NJ, 08618
... Edit/Write a variety of technical articles, reports, manuals, flow charts and other documentation for a wide range of uses, including GMP operations and validation activities. Assist in assembly of validation package documents for GMP libraries. ... - 2023 May 19
... Edit/Write a variety of technical articles, reports, manuals, flow charts and other documentation for a wide range of uses, including GMP operations and validation activities. Assist in assembly of validation package documents for GMP libraries. ... - 2023 May 19
Packaging Associate Machine
Hillsborough, NJ
... ● Responsible for accurately maintaining legible and accurate records, required logs, books, records, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating ... - 2023 May 14
... ● Responsible for accurately maintaining legible and accurate records, required logs, books, records, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating ... - 2023 May 14
Project Management Research and Development
Monmouth Junction, NJ
... against priorities according to business importance and impact Lead the overall execution of multiple technical projects regarding initiation, budgeting, scheduling, monitoring, and closure according to GMP, safety and environmental requirements. ... - 2023 Apr 15
... against priorities according to business importance and impact Lead the overall execution of multiple technical projects regarding initiation, budgeting, scheduling, monitoring, and closure according to GMP, safety and environmental requirements. ... - 2023 Apr 15
QA Director
Feasterville, PA
... Responsible for maintaining GxP (GCP, GLP and GMP) compliance. Implemented Electronic Document Management system and Learning Management System (Veeva) Knowledge of drug development process, US FDA Regulations, IND, NOA, ICH (Including Good Clinical ... - 2023 Apr 10
... Responsible for maintaining GxP (GCP, GLP and GMP) compliance. Implemented Electronic Document Management system and Learning Management System (Veeva) Knowledge of drug development process, US FDA Regulations, IND, NOA, ICH (Including Good Clinical ... - 2023 Apr 10
Scientist Data
East Brunswick, NJ
... e-mail: advzan@r.postjobfree.com PROFILE Analytical Scientist with wide experience of Research and Development and Quality Control in Pharmaceutical fields with a fully cGMP, GMP and GLP compliant environment. Expertise in complex products such as ... - 2023 Mar 17
... e-mail: advzan@r.postjobfree.com PROFILE Analytical Scientist with wide experience of Research and Development and Quality Control in Pharmaceutical fields with a fully cGMP, GMP and GLP compliant environment. Expertise in complex products such as ... - 2023 Mar 17
Document Control Packaging
Hightstown, NJ
... Mar-2020- Present Position: Quality Assurance Technician Responsibilities: • Monitor and verify product for defects per standard operating procedures and ensure compliance to all GMP, SQF and product safety practices. • Maintain accurate ... - 2023 Feb 22
... Mar-2020- Present Position: Quality Assurance Technician Responsibilities: • Monitor and verify product for defects per standard operating procedures and ensure compliance to all GMP, SQF and product safety practices. • Maintain accurate ... - 2023 Feb 22
Quality Manager Customer Service
Cherry Hill, NJ
... Defined, implement and Monitored the systems required to ensure compliance (GMP’s,required certifications, sanitation, and customer audit requirements). Worked as required with Engineering, Sales, and Customer Service in completing Customer ... - 2023 Jan 22
... Defined, implement and Monitored the systems required to ensure compliance (GMP’s,required certifications, sanitation, and customer audit requirements). Worked as required with Engineering, Sales, and Customer Service in completing Customer ... - 2023 Jan 22
works to analyze a variety of biological specimens.
Monmouth Junction, NJ, 08852
... experience with GMP and immunohematology procedures 2015 -Medical Diagnostic lab 2015 , Lab accessioning/ data entry/ consistently commended for the timely, high-quality completion of both routine and special laboratory assays of patient specimens. ... - 2022 Dec 28
... experience with GMP and immunohematology procedures 2015 -Medical Diagnostic lab 2015 , Lab accessioning/ data entry/ consistently commended for the timely, high-quality completion of both routine and special laboratory assays of patient specimens. ... - 2022 Dec 28
Laboratory Technician Mysore
East Brunswick, NJ
... Plant and animal tissue culture labs, good knowledge in the field of gene technology and molecular biology, cell biology and exceptionally good at bioprocessing technology and enzymology GMP documentation and record keeping Maintained excellent ... - 2022 Dec 17
... Plant and animal tissue culture labs, good knowledge in the field of gene technology and molecular biology, cell biology and exceptionally good at bioprocessing technology and enzymology GMP documentation and record keeping Maintained excellent ... - 2022 Dec 17
Plant Manager Construction
Hillsborough, NJ, 08844
... Instituted a GMP commissioning plan for the newly renovated space Upgraded and Validated cGMP HVAC systems to support manufacturing Operating and Capital budget management. ADDITIONAL EXPERIENCE ABM ENGINEERING SERVICES, Wilmington, Delaware, ... - 2022 Nov 21
... Instituted a GMP commissioning plan for the newly renovated space Upgraded and Validated cGMP HVAC systems to support manufacturing Operating and Capital budget management. ADDITIONAL EXPERIENCE ABM ENGINEERING SERVICES, Wilmington, Delaware, ... - 2022 Nov 21