ForDoz Pharma Corp. Jobs in United States

Manages the daily work activities of the Quality Assurance group to ensure products manufactured by ForDoz Pharma comply with global/local regulations, guidelines and operating procedures. · ...

Job summary · Reporting to Vice President of Quality the QC Director provides leadership and support in all aspects of analytical testing. · The QC Director manages the analytical laboratory to meet testing requirements in support of site manufacturing and the development laborat ...

Job Brief · The person will perform validation activities associated with equipment, processes, facilities, and computer systems to ensure compliance with applicable current Good Manufacturing Practice (GMP) regulations, site Standard Operating Procedures (SOP), and corporate pol ...

The Senior Analytical Scientist is responsible for the development, validation, and transfer of analytical methods to support the development, manufacture, release, · and stability of injectable drug products. · Analytical Method Development & Validation · ...

Job Brief · The person will perform validation activities associated with equipment, processes, facilities, and computer systems to ensure compliance with applicable current Good Manufacturing Practice (GMP) regulations, site Standard Operating Procedures (SOP), and corporate pol ...

The QC Director provides leadership and support in all aspects of analytical testing. Provides strong leadership and guidance for laboratory operations and personnel. · ...

The Validation Specialist will be responsible for executing validation activities related to equipment, manufacturing processes, facilities, and computerized systems to ensure compliance with current Good Manufacturing Practice (cGMP) regulations, site Standard Operating Procedur ...

+Job summary · Senior Analytical Scientist I sought by ForDoz Pharma Corp. to develop and validate analytical methods,+ · ++ResponsibilitiesValidate and transfer analytical methods; · Prepare analytical method validation protocols, method validation reports, test methods, conduct ...

The Project Manager is responsible for planning, executing and closing cross-functional projects related to pharmaceutical development , technology transfer , GMP manufacturing facility upgrades etc. · ...

Company Description · ForDoz Pharma Corp. is a fully integrated pharmaceutical company specializing in addressing the unmet medical needs of sterile drug product development. Based in East Windsor, New Jersey, we focus on conventional sterile injectables and advanced technology p ...

Job Brief · The person will perform validation activities associated with equipment, processes, facilities, and computer systems to ensure compliance with applicable current Good Manufacturing Practice (GMP) regulations, site Standard Operating Procedures (SOP), and corporate pol ...

Job Brief · The person will perform validation activities associated with equipment, processes, facilities, and computer systems to ensure compliance with applicable current Good Manufacturing Practice (GMP) regulations, site Standard Operating Procedures (SOP), and corporate pol ...

Job Overview · The Validation Specialist will be responsible for executing validation activities related to equipment, manufacturing processes, facilities, and computerized systems to ensure compliance with current Good Manufacturing Practice (cGMP) regulations, site Standard Ope ...

The Project Manager is responsible for planning, executing, and closing cross-functional projects related to pharmaceutical development, technology transfer, GMP manufacturing, facility upgrades, etc. This role ensures projects are delivered on time, within scope and budget, and ...

The person will perform validation activities associated with equipment processes facilities and computer systems to ensure compliance with applicable current Good Manufacturing Practice GMP regulations site Standard Operating Procedures SOP and corporate policies. · Schedules co ...

The Project Manager is responsible for planning, executing, and closing cross-functional projects related to pharmaceutical development. · The role ensures projects are delivered on time, within scope and budget, and in compliance with applicable regulatory requirements. · This i ...

Job Brief · The person will perform validation activities associated with equipment, processes, facilities, and computer systems to ensure compliance with applicable current Good Manufacturing Practice (GMP) regulations, site Standard Operating Procedures (SOP), and corporate pol ...

The Senior Specialist, Regulatory Affairs will provide expertise to the organization in the development of regulatory compliance strategies and in ensuring its conformance to Health Authority requirements. · ...

Senior Analytical Scientist I sought by ForDoz Pharma Corp. · Develop and validate analytical methods · Conduct chemical/physical testing · ...