Analytical Chemist
About The Position
Frontage Laboratories Inc. is an award-winning, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China. Our core competencies include drug metabolism, pharmacokinetics/pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Our Chicago, IL site provides toxicology testing and research laboratory services and specialized pre-clinical studies in support of pharmaceutical and biotechnology products. The individual in this position is involved in studies that evaluate the safety and/or toxicity of various materials (e.g., pharmaceuticals, chemicals, etc.). This position involves formulating, developing and validating methodologies for dose formulation analysis. As needed, the Analytical Chemist supervises support personnel and reports to the Director of Laboratory Operations. This is a full-time on-site position at our Chicago facility with no provisions for working remotely.
Requirements
- BS, MS, or PhD in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field.
- Hands-on experience with HPLC and UPLC systems.
- Strong experience in analytical method development and validation.
- Experience supporting Non-GLP and GLP non-clinical toxicology studies is preferred.
- Excellent scientific writing and documentation skills.
- Ability to work independently and in a fast-paced CRO environment.
- Experience in dose formulation analysis for toxicology studies.
- Familiarity with FDA, OECD, and GLP regulatory requirements.
- Experience with Agilent Open Lab software.
Nice To Haves
- Experience with Mass Spectrometry will be preferred.
Responsibilities
- Develop, optimize, and validate analytical test methods for dose formulation analysis.
- Preparation of formulations (e.g., solutions, suspensions, etc.) to be used in toxicology studies
- Perform analysis of dose formulation samples using HPLC/UPLC
- Analyze and interpret analytical data with high accuracy and scientific rigor
- Prepare and review Method Development/Validation and Dose Formulation Analysis (DFA) reports for GLP toxicology studies
- Function as Study Director on analytical validation studies
- Ensure compliance with GLP, SOPs, and regulatory guidelines
- Maintain analytical instruments and troubleshooting method/instrument-related issues
- Collaborate with toxicology, formulation, and study management teams to support study timelines
- Prepares SOPs and study specific methodologies
- Leads and coordinates activities of less experienced staff in specific assignments
- Interact with Study Directors and help define study priorities and schedules
- Implements and enforce the use of safety procedures
- Completes tasks within time and budget constraints
- Demonstrates the ability to contribute to the success of assignments
- Performs other duties as assigned
Benefits
- 401k Employer Match with immediate vesting
- Vision Insurance
- Medical and Dental Insurance with multiple coverage options
- FSA (Medical, Dependent Care, and Commuter)
- Short Term Disability
- Long Term Disability
- Life Insurance
- Generous Paid Holidays and PTO
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
