Associate Chemist

Integrated Resources Inc.; Edison (NJ); On-site; USD 50,000 - 70,000; Full time

Job summary

Integrated Resources Inc. is seeking a Chemist to join their team in Edison, NJ. The ideal candidate will perform QC testing to assess the quality of pharmaceutical materials, ensuring compliance with regulatory standards. This entry-level position is ideal for science graduates looking to start a career in the pharmaceutical industry, with opportunities to learn and grow in a dynamic lab environment.

Qualifications

• Recent graduate or up to 2 years experience in pharmaceuticals.
• Knowledge of regulatory guidelines (USP, ICH, FDA).
• Ability to perform QC testing using various instrumental techniques.

Responsibilities

• Perform QC testing on raw materials and finished products.
• Execute testing within established timelines and record data accurately.
• Ensure compliance with safety and regulatory standards.

Skills

Good Documentation Practices

Analytical Skills

Troubleshooting

Education

Bachelor's degree in Chemistry

Tools

HPLC

GC

UV-Vis

IR

Particle Size Analyzer

KF Auto titrator

Job description

A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

The 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 part of a team to effectively plan and execute QC analytical testing using established (official and/or in-house) test procedures. The Chemist may perform 90% - 100% of their work at the bench level.

Responsibilities include:

1. Perform sampling, physical, chemical tests, and assays 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) according to USP monograph, in-house, or other compendial standards.
2. Plan and maintain inventory of test reagents and solutions, ensuring supplies are ordered as needed.
3. Plan and execute testing within established timelines, including complex testing under supervisory guidance.
4. Record data and results accurately, ensuring clear documentation.
5. Prepare and review Test Procedures, SOPs, and Protocols as assigned.
6. Perform maintenance and calibration of laboratory instruments with supervisory support.
7. Conduct troubleshooting and investigations under supervisor direction.
8. Ensure compliance with all regulatory and in-house requirements, including safety, housekeeping, chemical waste disposal, cGMP, cGLP, and documentation standards.
9. Review analytical documents as required.

Qualifications

• Bachelor's degree in a scientific field, preferably Chemistry
• 0-2 years of experience in pharmaceuticals
• Experience in the generic pharmaceutical industry is a plus
• Knowledge of Good Documentation Practices and familiarity with USP, ICH, FDA guidelines
• Ability to learn quickly and make decisions effectively