Job Description:    General Description: Under the guidance of the Head of the Laboratory, perform routine laboratory operations within the CEUTICAL LABS Quality System.

Responsibilities:    Responsibilities include carrying out timely and safe execution of projects, completion of projects, presentation of data and production of concise, accurate, and professional laboratory report as directed by the Head of the Laboratory.  Responsible for reading, understanding, following and training CEUTICAL LABS SOPs, LAP’s, and LTM’s and performing them according to cGMP regulations.  In the absence of the Chemist II, responsible for the disposition of all samples and testing by-products.  Responsible for routine monitoring and recording of laboratory instrumentation (i.e., analytical balances, temperatures of refrigerators and ovens, pH meters, Karl Fisher) in accordance with procedures.  Responsible for cleaning and storage of laboratory glassware as needed.  Responsible for maintaining cleanliness and safety of the laboratory area in accordance to basic laboratory safety and housekeeping guidance’s.  Responsible for adhering to the Quality System and all that it implies and providing the example for other CEUTICAL LABS team members.

This position must have a basic understanding of the Industry regulations within drug laboratory requirements, including cGMP, cGLP, ICH, and FDA.  Must understand basic concepts of validation, calibration, standardization, cGMP, cQSR, standards and inventory control. Responsible for special projects as directed by the Head of the Laboratory.  Must meet the company goals as they apply to quality improvement within approved timelines and must work within a safe environment.  This position must be able to be multidisciplined to achieve company goals.

All applicants please contact Tiffany Smith in Human Resource at 972.241.8375