The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast paced environment by effectively performing various activities at range of complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data,

The Associate Scientist is accountable for driving results in a fast paced environment by performing analytical routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. For this Associate Scientist position, HPLC, TOC, UV, osmolality, density, and pH are commonly employed in the described testing. Level II employs other key methodo

The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast paced environment by effectively performing various activities at range of complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data,

The Sr. Environmental Monitoring Technician is accountable for driving results in fast paced environment by performing monitoring of the pharmaceutical manufacturing environment and utilities in compliance with cGMP and internal SOPs. The Sr. Environmental Monitoring Technician must be detail oriented and possess organizational skills with a large quantity of data. On Sit

The Environmental Monitoring Technician is accountable for driving results in fast paced environment by performing monitoring of the pharmaceutical manufacturing environment and utilities in compliance with cGMP and internal SOPs. The Environmental Monitoring Technician must be detail oriented and possess organizational skills with a large quantity of data. On Site Expect

The Associate Scientist III is accountable for driving results in a fast paced environment by performing analytical routine and non routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also be required to work on method development/method validation projects. For this position, ICP methodologies are

The Associate Scientist I/II will perform microbiological routine and non routine testing in support of pharmaceutical product development or pharmaceutical manufacturing and stability bacterial endotoxins, sterility and microbial examination methodologies are commonly employed in the described testing. Other key methodologies applied include liquid particulate matter and