Chemist
Integrated Resources, Inc ( IRI )
East Windsor, NJ
See who Integrated Resources, Inc ( IRI ) has hired for this role
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:
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
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:
- 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.
- Independently plan and make adequate inventory of test reagents and solutions to perform work, assure supplies are ordered as needed to perform assigned work.
- Independently plan and execute testing to meet established timelines. Perform complicated testing with supervisory direction.
- Record data and results as specified in documentation procedures. Document work clearly and perform tests accurately.
- Prepare and/or Review Test Procedures, SOPs, and Protocols as assigned.
- Perform maintenance and calibrations of laboratory instruments/equipments with supervisory direction/training.
- Perform troubleshooting and investigations under the direction of a supervisor.
- laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity.
- Review of Analytical documents as required
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
-
Seniority level
Mid-Senior level -
Employment type
Full-time -
Job function
Research, Analyst, and Information Technology -
Industries
IT Services and IT Consulting, Software Development, and Financial Services
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