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Chemistry Jobs in New Jersey

Chemist

Integrated Resources, Inc

New Brunswick, New Jersey

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Active Pharmaceutical Ingredient (API), Analysis Skills, Assays, Biotech and Pharmaceutical, Chemistry, Current Good Manufacturing Practice (cGMP), Documentation, FDA (Food and Drug Administration), GLP (Good Laboratory Practices), High Performance Liquid Chromatography (HPLC), Housekeeping/Cleaning, ICH Regulations, IR (Infrared), Identify Issues, Laboratory Equipment, Order Supplies, Physical Chemistry, Quality Control, Regulations, Standard Operating Procedures (SOP), Team Player, Testing, Titration, UV/VIS (Ultraviolet-Visible Spectroscopy)
LOCATION
New Brunswick, New Jersey
POSTED
1 day ago
ChemistChemist 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, 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 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, housekeeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity.9. Review of Analytical documents as requiredQualifications:• 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

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Integrated Resources, Inc

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