Chemist

Dexian; Melrose Park (IL); On-site; USD 65,000 - 90,000; Full time

Job summary

Dexian is seeking an analytical chemist in Melrose Park, IL, to perform routine analytical testing using HPLC, GC, FTIR, UV-Vis and ICP-MS, ensuring USP compliance and GDP documentation. The role includes method validation support, training, and peer data reviews.

The ideal candidate holds a chemistry-related degree with 1–4 years in pharma, proficiency in Empower, and strong communication and problem-solving skills. This is an on-site position requiring strict adherence to GMP standards.

Qualifications

• Bachelor's degree in chemistry, biology or related physical science.
• 1–4 years pharma experience; familiar with cGMP and FDA regulations.
• Hands-on chromatography experience and data systems (e.g., Empower).
• Proficiency in Microsoft Office applications.
• Strong analytical, troubleshooting, communication, and documentation skills.

Responsibilities

• Communicate work-related issues clearly and effectively to management and peers.
• Perform routine testing using instrumental methods (HPLC, GC, FTIR, UV-Vis, ICP-MS) with emphasis on chromatography to meet objectives.
• Update and revise SOPs and MOAs through Documentum to support USP compliance.
• Provide technical support for method validation, verification, transfers, and evaluations.
• Troubleshoot analytical instruments by applying problem-solving skills and consulting literature or vendors.
• Provide technical guidance and support to Associate Scientists as needed.
• Assist with the formal training of laboratory personnel on GMP, laboratory safety, and onboarding.
• Maintain accurate records of all work and document testing activities in GDP compliance.
• Manage workload and time effectively based on department priorities with sound judgment.
• Perform peer reviews of analytical data to ensure accuracy and compliance.

Skills

Analytical skills

Troubleshooting

Documentation

Communication

Team collaboration

Education

Bachelor’s degree in chemistry, biology, or related science

Familiarity with cGMP and FDA regulations

Tools

Empower

Job description

• Communicate work-related issues clearly and effectively to management and peers.
• Perform accurate routine testing using instrumental analytical methods, including HPLC, GC, FTIR, UV-Vis, and ICP-MS, with an emphasis on chromatography to meet departmental objectives.
• Update and revise SOPs and MOAs through Documentum, as directed by the supervisor, to support USP compliance.
• Provide technical support for method validation, verification, transfers, and evaluations.
• Troubleshoot analytical instruments by applying problem-solving skills and consulting technical literature or vendors when necessary.
• Provide technical guidance and support to Associate Scientists as needed.
• Assist with the formal training of laboratory personnel on topics such as GMP, laboratory safety, and new employee onboarding.
• Maintain accurate records of all work performed for assigned projects and document testing activities in compliance with Good Documentation Practices (GDP).
• Manage workload and time effectively based on departmental priorities, using sound judgment and objective reasoning.
• Perform peer reviews of analytical data to ensure accuracy, completeness, and compliance with applicable requirements.

• Bachelor’s degree in chemistry, Biology, or an equivalent physical science discipline.
• Typically, 1–4 years of relevant experience in the pharmaceutical industry, along with familiarity with cGMP and FDA regulations.
• Hands-on experience and knowledge of chromatographic methods and related chromatography data systems, such as Empower.
• Proficiency in Microsoft Office applications.
• Strong analytical, troubleshooting, communication, and documentation skills.

Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status.