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QC Chemist in the Pharmaceutical Industry!

Currently seeking an experienced QC Chemist in the Greenville, SC area. We are looking for someone who has a Bachelor's Degree in Chemistry, or related science. Also, we are looking for an individual who has no less than 2 years of HPLC and/or GC experience, preferably in a cGMP facility. This position will be a permanent, daylight position! 

The primary responsibility of this position is to analyze drug substances, drug products, and/or stability samples using approved laboratory monographs/specifications, Standard Operating Procedures, and USP/NF methodologies to ensure drug products manufactured at and distributed meet all quality and compliance requirements.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following.  Other duties may be assigned.

HPLC/GC Chemists: Shall have an emphasis in HPLC and/or GC methodology and analyses including all applicable preparations (extractions, dissolution, ISE separation, etc.), and training or experience in chromatographic software and instrument troubleshooting.

 

Wet Chemists: Shall have an emphasis in wet chemistry methodology and analyses such as various titrations, dissolution, USP/NF limit tests, Identifications, TLC, etc.

 

  1. Responsible for performing analysis of raw materials, bulk, finished product, and stability samples in a timely and compliant manner, as instructed by QC Supervisor, per applicable SOPs, monographs/specifications, and USP methodology to ensure finished goods are acceptable for distribution.
  2. Responsible for documentation of all analyses per applicable SOPs.
  3. Responsible for performance of routine laboratory functions to support manufacturing/production and assure that production schedule is met.
  4. Responsible for the timely testing and release of manufactured bulk drug products for packaging.
  5. Responsible for maintaining clean and organized laboratories.  Wash labware and pipettes by loading/unloading dishwasher/pipette washer.
  6. Notify Laboratory Coordinator when reagents, standards, and other materials need to be ordered to ensure all resources available for testing.
  7. Assist in training and evaluating laboratory personnel to run laboratory equipment for established methods.
  8.  Assist in documentation review of laboratory notebooks
  9. Additional duties and responsibilities as required.

ACCOUNTABILITY

For accuracy and timeliness of work, attention to detail, and adherence to test method monograph/specifications.  For following applicable Standard Operating Procedures, including all safety procedures and policies.  For working safely in an effective work team. 

QUALIFICATIONS

A 4-year degree in chemistry, or related science, from an accredited college program.  Applicable experience in an analytical laboratory preferred, experience in GMP laboratory is ideal.

EQUIPMENT AND MACHINES

Standard laboratory equipment, including viscometer, centrifuge, analytical balance, , conductivity meter, dissolution apparatus, Karl Fischer, density meter, pH meter, HPLC, GC/FID, GC/Headspace, IR, UV-Vis, AA, polarimeter, particle size analyzer, and refractomer.

WORKING CONDITIONS

 Laboratory environment using required Personal Protective Equipment.

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