Chipton-Ross is seeking an Associate Scientist l - R&D for a contract opportunity in High Point, NC.

RESPONSIBILITIES:
The Associate Scientist - is responsible for the complete testing and results documentation of any finished goods, stability and in-process samples within the QC Chemistry Laboratory, in a manner consistent with established standards.

Up to 50% Calibrations/ Standardizations/ Preparatory Set Up
o Perform calibrations/standardizations of instruments such as balances and pH meters
o Perform standardizations of volumetric/titrimetric solutions, and prepares buffers and HPLC mobile phase, among other solutions.
o Prepare and stage the solution for testing by senior analysts
o Understand and follow the Data integrity
Up to 20% Testing/Documentation/Data Review
o Independently perform core techniques or methods as assigned for testing on raw materials and in-process samples.
o Perform testing that has the highest level of difficulty compared to other testing methods.
o Demonstrate ability to troubleshoot and provide technical assistance to other analysts in the area of analytical instrumentation such as HPLC, GC, FTIR, and UV.
o Ensure that the calibration of critical laboratory equipment is current before use.
Up to 25% Housekeeping
o Clean and organize all laboratory areas including bench, sinks, drawers, cabinets, solvent cabinets, fume hoods, refrigerators, freezers, desiccators and storage areas.
o Occasionally clean laboratory pipettes and other glassware.
o Maintain laboratory instruments disposing of wastes, cleaning them and replacing consumable parts as required.
o Ensure the lab areas are audit ready at all times

REQUIRED EXPERIENCE:
Up to 5% Training and Development
o Participate in ongoing training for the development of skills and responsibility with an emphasis on technology.
o Perform training of other analysts in areas of expertise, such as but not limited to chromatographic techniques, laboratory documentation, and documentation review.
o Ability to actively participate on various and/or lead laboratory projects or teams and propose solutions to problems encountered by such teams.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Additionally, an individual must uphold the standards of conduct of the company, which include confidentiality, cooperation, and respect for people and property. The requirements listed above are representative of the knowledge, skill, and/or ability required.

EDUCATION:
Accredited Bachelor's Degree in Chemistry, Microbiology, Biology, Biochemistry or related field, Experience in a Quality Control Laboratory in GMP Pharmaceutical facility preferred.

WORK HOURS:
Full-Time; Days, 8:00 AM - 5:00 PM