|Investors:||Ben Franklin Technology Partners of Southeastern PA|
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Job ID41 OverviewAs a start pharmaceutical company employees are needed who are willing to perform any activity in their department and help support all other departments when needed. This position shall work in documentation and support cGMP compliance. As a member of the4/10/2015 East Windsor, NJ Save This Job
Job ID44 OverviewSupports the technical services department with execution of qualification and validation protocols and routine testing of drug product intermediates or in process samples. Will help generate procedures to acheive compliant sampling testing and reporting of4/10/2015 East Windsor, NJ Save This Job
Job ID38 OverviewThe Sr Product Development Scientist will have a high degree of technical and mechanical insight, perform tech transfer, troubleshooting and act as a liaison to the Tech Sending Group, in addition to responsibilities in pre-formulation, formulation, and process4/10/2015 East Windsor, NJ Save This Job
Job ID42 Overview As part of the Quality team, the Quality Systems Specialist supports and maintains site and corporate Quality Systems by performing the duties listed, which include, but are not limited to: Description of Duties Author, revise, and process standard operating4/10/2015 East Windsor, NJ Save This Job
Job ID43 Overview Responsible for control and status of identified pharmaceutical processes and drug product manufacturing, which includes all aspects of support for process control, validation and testing to maintain cGMP compliant drug product. Description of Duties4/10/2015 East Windsor, NJ Save This Job
Job ID38 OverviewThe Sr Product Development Scientist will perform tech transfer, troubleshooting and act as a liaison to the Tech Sending Group, in addition to responsibilities in pre-formulation, formulation, and process development aspects of pharmaceutical dosage form3/11/2015 East Windsor, NJ Save This Job
Aprecia Pharma Position TitleSenior Controls Automation Engineer Job ID25 Description of Duties1.Participate in, and coordinate activities regarding the development of automated equipment and control systems including the definition of specifications, risk assessments, design and3/11/2015 East Windsor, NJ Save This Job
Job ID40 Overview 1. Responsible for testing and release of finished products, stability samples, raw materials, registration, clinical and marketed products batches under GMP/GLP environment as per company's standard operating procedures and USP/FDA guidelines. 2. Performs3/11/2015 East Windsor, NJ Save This Job
Job ID15 OverviewResponsible for testing of raw materials, establishing impurity and degradation profiles for active bulk drug substance and release testing of drug product produced using Aprecia Pharmaceutical?s proprietary technology. Description of Duties Research, design and3/11/2015 Langhorne, PA Save This Job