Associate Scientist

Overview

• Contribute to the development of oligonucleotide manufacturing processes for siRNA therapeutics in a dynamic environment.
• Collaborate with senior scientists and engineers to support process optimization and technology transfer activities.
• Gain hands-on experience in laboratory operations, data collection, and documentation within a cGLP setting.
• Perform routine analytical tests and support the execution of laboratory-scale and pilot-scale processes.
• Engage in drafting and revising technical documentation, SOPs, and batch records.
• Maintain a safe and organized laboratory workspace while adhering to compliance standards.
• Collaborate across teams including Process Development, Analytical Sciences, and Manufacturing.
• Ideal for recent graduates or early-career scientists seeking professional growth in process sciences.

Key Responsibilities & Duties

• Support oligonucleotide manufacturing processes under guidance from senior staff.
• Execute laboratory-scale and pilot-scale processes to meet research and material needs.
• Perform routine analytical tests such as pH, conductivity, and UV spectroscopy.
• Assist in the preparation and documentation of non-GMP manufacturing runs.
• Operate laboratory and analytical equipment following proper training protocols.
• Draft and revise SOPs, batch records, and technical documentation.
• Document experimental work accurately following good documentation practices.
• Collaborate with cross-functional teams to ensure process development success.
• Maintain inventory and ensure laboratory compliance with safety standards.

Job Requirements

• Bachelor's degree in Chemistry, Chemical Engineering, Biochemistry, or a related field.
• 0–2 years of laboratory experience, including academic, co-op, internship, or industrial settings.
• Basic familiarity with analytical techniques such as pH, conductivity, HPLC, or LC-MS preferred.
• Strong attention to detail and commitment to high-quality documentation practices.
• Willingness to learn regulated laboratory practices and manufacturing workflows.
• Ability to work collaboratively in a team-oriented environment.
• Effective time management skills to meet project deadlines.
• Proficiency in maintaining a safe and compliant laboratory workspace.
• Experience in inventory management and laboratory organization is advantageous.