Quality Control (Chemist)

NOTE:

Shift: Monday to Friday.

PURPOSE OF THE POSITION

Schedule, set-up and perform assays according to established protocols

· Review protocol and set-up assays according to priority level. Determine chemicals and quantities needed. Use appropriate equipment.

· Perform procedure independently, accurately, in a safe manner, according to an established protocol. Make minor adjustments to the protocol as needed.

· after completion of assay, appropriately discard waste; return reagents to proper location and clean area.

· accurately interpret results and prepare complete, accurate and legible records.

· Complete volume of work required to achieve group/departmental goals and meet the established deadlines.

· Prepare written procedures as needed.

Perform non-routine assays and assist in the troubleshooting process to resolve problems

· Carry out non-routine assays according to performance requirements for routine assays (see first essential responsibility).

· Use a logical approach to basic problem solving and demonstrate the ability and technical knowledge to develop a basic experimental design.

· Understand techniques and instrumentation to ensure accurate analysis

Contribute to support function of the Laboratory

· Ensure that lab supplies are adequately stocked.

· Prepare testing reagents (e.g. buffers, gels, standards, etc.) as needed.

· Maintain (clean, calibrate, etc.) equipment, properly document and notify appropriate individuals if calibration is overdue.

· maintain a clean work area and properly dispose of waste.

· Perform other group responsibilities thoroughly and in a timely manner.

Quality Expectations

· Ensure worksheets and other quality documents accurately reflect current procedure. Document procedures with appropriate technical detail in writing as directed by supervisor.

· Notify supervisor of any deviation from current procedure.

· Utilize system of quality documents for recording maintenance, calibration and usage of equipment and instruments as directed by supervisor.

· properly label chemicals and reagents with all needed quality documentation.

· properly label chemicals and reagents with all needed quality documentation.

· successfully complete required quality training.

· Write and review drafts of quality procedures as directed by supervisor

· Record quality observations in databases as directed by supervisor to aid in quality improvement efforts.

Feel free to forward my email to your friends/colleagues who might be available. We do offer referral Bonus.

Thank you.

Kind Regards,

Harris Kaushik

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

DIRECT # - (650)-399-0891

Gold Seal JCAHO Certified ™ for Health Care Staffing

“INC 5000’s FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)