What are the responsibilities and job description for the Associate Scientist II position at Abzena?
With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing. Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely. We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services. We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient. The Associate II will conduct research, troubleshoot, and solve problems arising during synthetic route/process development. The associate II will safely execute synthetic processes adhering to EHS and regulatory guidelines. Responsibilities
- Set up organic chemical reactions, monitor and isolate organic compounds in desired purity.
- Perform the column purification, crystallization and characterization of organic compounds.
- Execute reactors cleaning, set-up and handling of reactor related process operations.
- Maintaining clear and current records of your daily work within a laboratory notebook and batch records as needed.
- Performing analytical work, attending and contributing to meetings, writing comprehensive reports and purchasing all necessary supplies and equipment.
- Follow safety procedures as per organizational policies.
- Communicate effectively with supervisors, colleagues, and staff.
- Participate effectively as a team player in all aspects of Abzena's business.
- Adhere to quality standards set by regulations and Abzena policies, procedures, and mission.
- B.Sc. or Associate degree in Chemistry or Chemical Engineering.
- 1-2 years of work experience as a process chemist will be preferred but not mandatory.
- Experience in a GMP environment preferred.
- Basic knowledge of analytical techniques and compound characterization.
- Strong capability in MS Office.
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