JOB DESCRIPTION:

The Chemist I/II contractor will support method development, robustness studies, validation activities, and general laboratory testing. The role requires hands-on laboratory skills, strong attention to detail, and the ability to work under established practices while maintaining compliance with GLP/GMP requirements.

Responsibilities:

• Perform routine laboratory activities, including sample preparation, weighing, pipetting, pH measurement, and solution preparation.
• Execute analytical methods independently and operate relevant analytical software.
• Maintain laboratory notebooks and records in compliance with GLP/GMP standards.
• Support method development, optimization, and validation studies for protein-based therapeutics.
• Collaborate with cross-functional teams to support formulation and process development studies.
• Assist in tech transfer of methods to commercial QC laboratories.
• Manage multiple tasks and meet project timelines in a fast-paced environment.

Requirements:

• BS in Chemistry (or related field) with 3–5 years of laboratory experience or MS in Chemistry (or related field) with 0 years of experience.
• Strong hands-on experience with core laboratory techniques (sample preparation, weighing, pipetting, pH measurement, solution preparation, etc.).
• Ability to maintain compliance with GLP/GMP practices.
• Demonstrated ability to multitask and meet deadlines.
• Practical experience and knowledge of protein HPLC (e.g., SEC, IEX, HIC), capillary electrophoresis, and other separation techniques as applied to protein analysis preferred.
• Experience supporting method development, robustness, and validation studies.
• Familiarity with documentation and data integrity requirements for regulatory submissions.

• Perform routine laboratory activities, including sample preparation, weighing, pipetting, pH measurement, and solution preparation.
• Execute analytical methods independently and operate relevant analytical software.
• Maintain laboratory notebooks and records in compliance with GLP/GMP standards.
• Support method development, optimization, and validation studies for protein-based therapeutics.
• Collaborate with cross-functional teams to support formulation and process development studies.
• Assist in tech transfer of methods to commercial QC laboratories.
• Manage multiple tasks and meet project timelines in a fast-paced environment