Industry: Pharmaceutical

Duration: 12  Months (++Possibility of Extension)
Position Overview

Client’s Product Development Science and Technology (PDS&T) Analytical Development – Lake County (AD-LC) group is seeking a motivated Chemist I/II contractor to support analytical method development, robustness, and validation studies. The successful candidate will contribute to the development and optimization of analytical methods for biologic products, ensuring readiness for commercial manufacturing and regulatory submissions.

The AD-LC team plays a critical role in advancing Client’s biologics pipeline including monoclonal antibodies, antibody-drug conjugates (ADCs), and other novel therapeutic modalities, from clinical proof of concept through commercial launch.

Key Responsibilities

• Perform analytical testing to support method development, robustness, and validation for biologic drug products.
• Conduct hands-on laboratory work involving protein characterization and separation techniques.
• Prepare and analyze samples using established methods; document results accurately in accordance with GMP/GLP requirements.
• Support process and formulation development through analytical data generation and interpretation.
• Contribute to method transfer and optimization for commercial QC implementation.
• Maintain laboratory instruments and ensure compliance with safety and quality procedures.
• Collaborate with cross-functional teams including formulation, process development, and quality operations.

Required Qualifications:

• Bachelor’s degree in Chemistry, Biochemistry, or related field with 3–5 years of laboratory experience, or a Master’s degree with 0 years of experience.
• Strong understanding of analytical techniques and scientific principles.
• Demonstrated ability to work independently and manage multiple priorities.
• Excellent documentation and communication skills with attention to detail.
• Experience maintaining laboratory notebooks in compliance with GLP/GMP requirements.
• Familiarity with data analysis and relevant laboratory software.

Nice-to-Have (Preferred) Qualifications:

• Hands-on experience with protein HPLC techniques such as SEC, IEX, HIC, and capillary electrophoresis.
• Familiarity with other protein separation and characterization methods.
• Prior experience in a biopharmaceutical analytical development or QC environment.
• Proficiency in routine laboratory operations (sample prep, solution formulation, pH measurement, etc.).
• Understanding of method validation and tech transfer in a GMP setting.

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable)