Job Description Purpose of Role Continue building the Quality Control (QC) GMP infrastructure for the Abzena, Bristol facility. Perform and/or oversee testing of raw materials, in-process samples, final testing of GMP intermediates and final bulk drug substance. In addition, establish/maintain stability program according to ICH guidelines, including testing of client stability samples. Also, monitor/execute/test retain […]
HR Business Partner
Job Description Overall Responsibilities: Serve as a link between management and employees by handling questions, interpreting and administering contracts and helping resolve work-related problems. Provide current and prospective employees with information about policies, job duties, working conditions, wages, opportunities for promotion and employee benefits. Analyze and modify compensation and benefits policies to establish competitive programs […]
Director of Quality Assurance / Quality Control (QA/QC)
Job Description The Quality Director will lead Abzena’s quality functions while promoting a culture of quality by collaborating across all departments and levels of management to accomplish company objectives. The Quality Director will oversee all quality activities supporting the development and manufacture of clients’ early-phase GMP novel cytotoxic and antibody drug conjugate (ADC) compounds. […]
Director of Quality Assurance / Quality Control (QA/QC)
Job Description The Quality Director will lead Abzena’s quality functions while promoting a culture of quality by collaborating across all departments and levels of management to accomplish company objectives. The Quality Director will oversee all quality activities supporting the development and manufacture of clients’ early-phase GMP novel cytotoxic and antibody drug conjugate (ADC) compounds. […]
Director of Quality Assurance / Quality Control (QA/QC)
Job Description The Quality Director will lead Abzena’s quality functions while promoting a culture of quality by collaborating across all departments and levels of management to accomplish company objectives. The Quality Director will oversee all quality activities supporting the development and manufacture of clients’ early-phase GMP novel cytotoxic and antibody drug conjugate (ADC) compounds. […]
Lead Manufacturing Associate (Upstream)
Job Description Typical Duties Include Perform work in a cGMP manufacturing environment. Operate in a Class 10,000 and Class 100,000 rooms. Perform cell vial thaw and flask expansion inside a Bio-Safety Cabinet (BSC) as well as generating Cell Banks for clients. Operate and maintain equipment designed for single-use technology as it relates to cell culture […]