Scientist, Process and Analytical Development

General Responsibilities:

Contribute to the development, optimization, and execution of analytical assays and process methodologies in support of Castle Creek’s autologous cell therapy program. This role is primarily laboratory-based and requires strong technical skills, meticulous documentation, and clear communication of experimental results.

Responsibilities:

• Execute laboratory experiments involving primary cell culture, bioreactor operations, flow cytometry and ELISA in support of AD/PD objectives.
• Maintain detailed, accurate, and contemporaneous laboratory notebooks in accordance with internal documentation and data integrity standards.
• Analyze experimental data, prepare technical reports, and present findings to internal teams.
• Assist in the development and optimization of analytical methods and process parameters to improve product quality and process efficiency.
• Follow established SOPs, safety guidelines, and quality standards to ensure compliance with internal and external requirements.
• Collaborate with cross-functional teams to support technology transfer, scale-up activities, and troubleshooting efforts.
• Maintain laboratory equipment and inventory; identify and report maintenance needs.
• Perform weekend or off-hours work when necessary to support time-sensitive experiments.
• Effectively prioritize and execute multiple tasks in a dynamic environment. 
• Demonstrate integrity and professionalism in handling confidential information and contributing to a transparent, collaborative work culture.

Education:

• Bachelor’s degree (B.S.) in Biology, Biochemistry, Biotechnology, Immunology or a related scientific discipline.

Minimum Qualifications:

• Hands-on experience with aseptic primary cell culture techniques.
• Strong organizational skills and attention to detail.
• Demonstrated adaptability and flexibility in a fast-paced environment.
• Effective written and verbal communication skills.

Preferred Qualifications:

• Hands-on experience with bioreactor-based cell expansion and closed-system scale-up for cell therapy manufacturing.
• 2 years of experience in an analytical development or process development environment.
• Experience with at least one of the following techniques: flow cytometry, ELISA, or qPCR.
• Familiarity with data analysis software and statistical tools.
• Experience authoring technical reports or SOPs.
• Prior exposure to regulated environments (e.g., GMP, GLP).

Salary : $45 - $53