Research Associate, Analytical Development (Contract)

Are you a meticulous and driven Research Associate with a passion for cutting-edge cell and gene therapies? Our client, a leader in the biotechnology field, is seeking a talented individual to join their Technical Development team in Alameda, CA, on a contract basis.

In this role, you will be a critical contributor to analytical testing, supporting process development, and playing a key role in analytical method development and new technology evaluation. Your expertise will directly impact the successful development and manufacturing of innovative cell and gene therapy products.

What You Will Do:

• Sample Management and Testing:Assist in implementing sample management software and procedures.
• Receive, track, and manage samples from various process development projects.
• Perform routine in-process and final product testing to evaluate process performance and product quality.
• Ensure all testing is conducted according to established protocols and timelines.
• Data Analysis and Reporting:Independently analyze experimental data and identify trends or anomalies.
• Prepare clear, concise, and high-quality data reports for stakeholders.
• Maintain comprehensive and accurate records of all analyses.
• Proactively troubleshoot and resolve technical or procedural issues.
• Collaboration and Communication:Collaborate with process development teams to provide timely results.
• Work with the Analytical Development team to develop and optimize analytical methods.
• Support the preparation of technical reports, documentation, and presentations.
• Participate in cross-functional project teams.
• Additional Responsibilities:Maintain and calibrate analytical instruments and equipment.
• Ensure compliance with GMP and other relevant regulatory guidelines.
• Foster a culture of scientific excellence and continuous improvement.

What You Will Bring:

• Bachelor's or Master's degree in a relevant scientific discipline (e.g., Biochemistry, Chemistry, Molecular Biology).
• 2 - 5 years of experience in analytical development and testing in the biopharmaceutical or cell and gene therapy field (1 - 3 years with Masters).
• Exceptional organizational skills with the ability to manage multiple priorities and deadlines.
• Strong knowledge of analytical techniques, including Flow cytometry, qPCR, ELISA, and cell-based assays. Flow cytometry experience is required.
• Strong attention to detail, problem-solving skills, and the ability to work independently and collaboratively.
• Familiarity with regulatory guidelines (e.g., FDA, EMA) and GMP/GLP requirements is advantageous.