Associate Scientist

Summary:

Summary:

BioPharma Consulting JAD Group is looking for a motivated Associate Scientist to join our dynamic team. The successful candidate will be a part of the CMC - DS Process Development Group, responsible for the process development to incorporate novel chemistries into our manufacturing platform.

Key Responsibilities:

• Support oligonucleotide synthesis method development, optimization and scale-up
• Support downstream processing method development
• Execution of in-process analytical testing
• Working with research and process scientists to develop robust processes for novel chemistries
• Conduct laboratory experiments and research to support ongoing projects, following established protocols and methodologies.
• Compile and analyze experimental data, generating reports and summaries for senior scientists and project teams.
• Develop and optimize assay methods, providing technical insights for process improvements and innovative approaches.

• Maintain accurate and detailed laboratory records, ensuring compliance with GLP and GMP standards.
• Collaborate with cross-functional teams to achieve project milestones and objectives.
• Contribute to the preparation of scientific presentations, documentation, and technical reports.
• Participate in the maintenance of laboratory equipment and inventory management, ensuring a safe and efficient laboratory environment.

Skills:

• Basic understanding of analytical techniques (pH, osmolality, conductivity measurement, HPLC, LC-MS etc.).
• Knowledge of oligonucleotide manufacture process including phosphoramidite chemistry, chromatography, ultrafiltration etc.
• Record-keeping and excellent laboratory documentation practice.
• Ability to maintain a safe, clean, and orderly laboratory work environment.
• Good communication skills.

Requirements

Qualifications:

• Bachelor's degree in Chemistry or Chemical Engineering with 0-3 years of lab experience.

Preferred Qualifications:

• Familiarity with laboratory techniques such as PCR, chromatography, and electrophoresis.
• Experience in data analysis software and scientific reporting tools.
• Knowledge of GLP/GMP regulations and practices.
• Basic understanding of biopharmaceutical processes and drug development lifecycle.
• Hands-on experience with assay development and optimization is a plus.