Frontage Laboratories Visa Sponsorship Jobs USA
Frontage Laboratories is a contract research organization known for supporting scientists and researchers at every stage of drug development. It has a consistent track record of sponsoring work visas, making it a reliable option for international candidates pursuing careers in pharmaceutical and biomedical research in the U.S.
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Get Access To All JobsAnalytical Chemist
Location: Chicago, IL (on-site)
Reports to: Director Laboratory Operations
Job Type: Full-time
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.
Position/Job Summary:
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.
Roles and Responsibilities:
Frontage Laboratories is seeking a highly motivated and experienced Chemist/Scientist for the Dose Formulation Analysis (DFA) group supporting non-clinical toxicology studies conducted under GLP regulations.
Key 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 troubleshoot method/instrument-related issues.
- Collaborate with toxicology, formulation, and study management teams to support study timelines.
- Prepare SOPs and study-specific methodologies.
- Lead and coordinate activities of less experienced staff in specific assignments.
- Interact with Study Directors and help define study priorities and schedules.
- Implement and enforce the use of safety procedures.
- Complete tasks within time and budget constraints.
- Demonstrate the ability to contribute to the success of assignments.
- Perform other duties as assigned.
Qualifications and Experience:
- BS, MS, or PhD in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field.
- Hands-on experience with HPLC and UPLC systems.
- Experience with Mass Spectrometry will be preferred.
- 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.
Salary: $65-80k, negotiable based on experience.
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
Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.
Analytical Chemist
Location: Chicago, IL (on-site)
Reports to: Director Laboratory Operations
Job Type: Full-time
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.
Position/Job Summary:
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.
Roles and Responsibilities:
Frontage Laboratories is seeking a highly motivated and experienced Chemist/Scientist for the Dose Formulation Analysis (DFA) group supporting non-clinical toxicology studies conducted under GLP regulations.
Key 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 troubleshoot method/instrument-related issues.
- Collaborate with toxicology, formulation, and study management teams to support study timelines.
- Prepare SOPs and study-specific methodologies.
- Lead and coordinate activities of less experienced staff in specific assignments.
- Interact with Study Directors and help define study priorities and schedules.
- Implement and enforce the use of safety procedures.
- Complete tasks within time and budget constraints.
- Demonstrate the ability to contribute to the success of assignments.
- Perform other duties as assigned.
Qualifications and Experience:
- BS, MS, or PhD in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related field.
- Hands-on experience with HPLC and UPLC systems.
- Experience with Mass Spectrometry will be preferred.
- 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.
Salary: $65-80k, negotiable based on experience.
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
Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.
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Get Access To All JobsTips for Finding Frontage Laboratories Visa Sponsorship Jobs USA
Target scientific and research roles directly
Frontage's sponsorship activity is concentrated in laboratory, analytical chemistry, and pharmacokinetics roles. Focus your applications on positions that align with your scientific background rather than administrative or support functions, which are less likely to attract sponsorship consideration.
Understand which visa types Frontage supports
Frontage Laboratories sponsors H-1B, TN, F-1 OPT, and F-1 CPT visas, as well as Green Card pathways. If you're on OPT or CPT, you may have an entry point before pursuing long-term H-1B sponsorship, which is their most active visa category.
Highlight your CRO or pharma lab experience
Frontage works across drug metabolism, bioanalytical testing, and formulation development. Candidates who can demonstrate hands-on contract research organization experience or relevant pharmaceutical lab skills are better positioned to advance through their hiring process.
Apply early in hiring cycles
Because Frontage has a consistent sponsorship track record in Science and Research, their roles with visa support tend to attract competitive applicant pools. Applying early when a position is posted improves your chances before headcount decisions are finalized.
Use a platform built for sponsored job searches
Finding roles at verified sponsors like Frontage is faster when you filter by real sponsorship history. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history and identify open Frontage positions without sorting through unverified listings.
Prepare for a technically rigorous interview process
Frontage evaluates candidates on domain-specific scientific knowledge, not just general qualifications. Be ready to discuss your expertise in areas like bioanalysis, DMPK, or formulation science in depth, since hiring managers are typically senior scientists assessing technical fit.
Frequently Asked Questions
Does Frontage Laboratories sponsor H-1B visas?
Yes, Frontage Laboratories sponsors H-1B visas and has done so consistently, making it one of the more active sponsors in the contract research organization space. Sponsorship is typically tied to scientific and research roles requiring specialized qualifications. If you're targeting an H-1B, focus your application on laboratory-based positions that directly match your degree and technical background.
Which visa types does Frontage Laboratories sponsor?
Frontage Laboratories sponsors H-1B visas, TN visas for Canadian and Mexican nationals, F-1 OPT, and F-1 CPT for students in qualifying STEM programs. They also support Green Card sponsorship through the EB-2 and EB-3 employment-based immigrant visa categories, which is particularly relevant for candidates looking to build a long-term career in U.S. pharmaceutical research.
Which departments or roles at Frontage Laboratories are most likely to be sponsored?
Sponsorship at Frontage is concentrated in scientific and laboratory roles. Positions in bioanalytical chemistry, drug metabolism and pharmacokinetics, formulation development, and regulatory affairs have historically been the strongest areas for visa sponsorship. Roles that require a graduate degree in chemistry, biology, pharmacology, or a related life sciences field are the most consistent candidates for H-1B and Green Card support.
How do I find open visa-sponsored jobs at Frontage Laboratories?
Migrate Mate is the most efficient way to find open positions at Frontage Laboratories that come with verified visa sponsorship. You can filter by company and sponsorship type to see current Frontage listings, rather than manually searching and trying to determine whether sponsorship is available. This is especially useful if you're targeting multiple CROs alongside Frontage.
How do I approach the application timeline when targeting Frontage Laboratories for H-1B sponsorship?
If your goal is H-1B sponsorship through Frontage, timing your job search matters. The H-1B cap lottery opens each March for an October 1 start date. Ideally, you'd secure an offer with enough lead time for Frontage to complete the Labor Condition Application and file your petition before the registration window closes. Starting your search in the prior fall or winter gives you the best runway.