Chemist - II

Chemist - II

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 be expected to support and perform Laboratory activities that relate to finished good, bulk and raw material testing for use in production; testing of all in-coming bulk, finished goods or raw materials using USP and approved client methods, managing sample flow, standards, investigations for out of specification results, communicating with the supervisor on out of specification results, and maintaining laboratory note books and forms.

The Scientist must be familiar with using the following pieces of equipment: viscometer, pH meter, densitometer, potentiometric titrator, Karl Fischer, FT-IR, Conductivity meter, TOC Analyzer, HPLC and GC.

The Scientist will perform routine laboratory testing, non-routine testing, and compendia testing independently and with minimal direction.

Perform analytical chemical testing and organoleptic analysis of materials and products.

Perform HPLC & GC and routine instrumentation analysis with minimum supervision

Document and report results of analysis according to Good Laboratory Practices.

Initiate Non-Conformance Reports when an Out of specification result is confirmed.

Carry out timely OOS Investigations and Reporting of data.

Analyze the physical appearance of materials and report anomalies to the lab supervisor or manager.

Communicate with personnel in other departments as necessary.

Qualifications

Minimum 3-5 years working experience in a regulated QA lab environment is required.

Minimum 2 years working experience in routine HPLC analysis and sample preparation.

Broad-based experience or combination of experience, in Pharmaceutical Manufacturing, Quality Operations, Regulatory Compliance and/or Regulatory Affairs function is required.

Knowledge of FDA Regulations, specifically 21 CFR 210 and 211 is required.

Experience with current Good Manufacturing Practices and Good Laboratory Practices regulations is required.