US - High Point North Carolina / United States

Pay Rate: XXX

Bill Rate: XXX

Shift: 8am-5pm

SUMMARY OF POSITION

The Analyst I is responsible for the complete testing and results documentation of any of the following: Raw Materials, In-Process, Finished Product, Stability, Technical Service samples or projects within the QC Chemistry or Microbiology Laboratory, in a manner consistent with established standards.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Up to 10% Standardizations/ Preparatory Set Up

Perform daily verifications of instruments such as balances, pH meters and IR as required by work instructions.

Performs standardizations of volumetric/titrimetric solutions, and prepares dissolution media and HPLC mobile phase, among other solutions including microbiological solutions.

Prepare media, collect purified water for testing and use the Autoclave for waste disposal.

Up to 80% Testing/Documentation:

Perform core techniques or methods as assigned for testing on raw materials, in-process, release, stability, environmental or technical service samples or projects as assigned.

May require guidance until proficient in analytical instrumentation such as HPLC and GC.
Ensure that the calibration of critical laboratory equipment is current before use.

Up to 5% Housekeeping:

Clean and organize all laboratory areas including bench, sinks, drawers, cabinets, solvent cabinets, fume hoods, refrigerators, freezers, desiccators and storage areas.

Occasionally clean laboratory pipettes and other glassware.

Maintain laboratory instruments disposing of wastes, cleaning them and replacing consumable parts as required.

Dispose of solvent, acids and other wastes according to procedures and local regulations.
Clean HPLC and dissolution systems after use.

Up to 5% Training and Development

Participate in ongoing training for the development of skills and responsibility with an emphasis on technology.

Assist training of other analysts in areas of expertise.

EDUCATION AND EXPERIENCE:

Bachelor s Degree in Chemistry, Microbiology, Biology, Biochemistry or related field and 0-5 years of related experience in an analytical laboratory setting, preferably in a Quality Control Laboratory in a GMP facility; or an Associate degree in Chemistry, Microbiology, Biology, Biochemistry or related field with at least 5 years of experience in a Quality Control

Laboratory in a GMP facility.