Scientist, Analytical Development

The Scientist, Analytical Development will lead and evolve the Analytical Development and Quality Control function within a Contract Development and Manufacturing Organization (CDMO) business, supporting a broad portfolio and advancing manufacturing capabilities to deliver life-changing medicines.

Requirements

• Master's degree with 2+ years of relevant industry experience, or Bachelor's degree with 5+ years, or Ph.D. with relevant experience.
• Degree in Chemistry, Biochemistry, Molecular Biology, or related scientific field; experience in gene and cell therapy is a plus.
• Hands-on experience with analytical techniques such as UPLC/HPLC, CE-SDS and/or AUC; experience working with MALS and/or CAD detectors is a plus.
• Experience executing assays in accordance with Standard Operating Procedures and protocols in a regulated or controlled environment.
• Strong problem-solving skills with the ability to work independently and collaboratively in a fast-paced environment.
• Familiar with principles of Good Documentation Practices, Data Integrity, and ALCOA+.
• Strong interpersonal, verbal, and written communication skills.
• Experience with Next-Generation Sequencing (NGS) is a plus.
• Experience with Microsoft Office tools.
• Experience with statistics, coding, programming, troubleshooting, and/or data management software is a plus.

Benefits

• Paid Time Off
• 401k Matching