Job ID 17-00121

Industry Pharma

Job Type Permanent

Location Lawrenceville, NJ


Want to work for a top Generic Pharma company with lots of growth potential? How about a company that you can be promoted quickly and be recognized for your work? We have a direct relationship with our Hiring Managers and can get you in for the interview! This client provides great benefits and bonus structure as well. Apply with us today!

Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Chemist will work as a member of team to effectively plan and QC analytical testing using established (official and/or in-house)
test procedures. The Chemist may execute 90% - 100% of their work at the bench level.
1. Perform assigned sampling, physical, chemical tests and assay on raw materials, packaging materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemicals, physical and instrumental techniques (HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments) as per as per USP monograph I In-house I any other Compendia! monographs.
2. Independently plan and make adequate inventory of test reagents and solutions to perform work, assure supplies are ordered as needed to perform assigned work.
3. Independently plan and execute testing to meet established time lines. Perform complicated testing with supervisory direction.
4. Record data and results as specified in documentation procedures. Document work clearly and perform tests accurately.
5. Prepare and/or Review Test Procedures, SOPs, and Protocols as assigned.
6. Perform maintenance and calibrations of laboratory instruments/equipments with supervisory direction/training.
7. Perform troubleshooting and investigations under the direction of a supervisor.
8. Comply with all regulatory/in-house requirements (may include but not limited to safety, house keeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity.
9. Review of Analytical documents as required
10% Daily Review of day-to-day analytical data generated in the laboratory
90% Daily Analyze finished product and raw material samples


- Minimum BS with Scientific field
- BS with Chemistry would be preferable
- Minimum 1-3 year experience in pharmaceuticals (OTC, Brand, or Generic) and 1-2 year experience in Analytical testing desirable
- QC experience in Generic Pharmaceutical industries would be preferable
- Knowledge in Good Documentation practices. Knowledge in USP/ICH/FDA
- Ability to learn quickly and decision making skills