Chemist

Tittle: Chemist 

Location: Dayton, NJ 

Duration: Fulltime Role 

Job Description: 

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. 

Responsibilities: 

1. Perform assigned sampling, physical, chemical tests and assay on raw 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 / In-house / any other Compendial 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 timelines. 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.laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity. 

9. Review of Analytical documents as required 

Qualifications - Skills & Requirements: 

Minimum BS with Scientific field 

BS with Chemistry is one of the subjects would be preferable 

Minimum 1-3 years’ experience in pharmaceuticals 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