A position is open for a contract opportunity in the Process Analytical Sciences routine testing labs. This role supports the development of a wide variety of therapeutic biologics that include monoclonal antibodies, bi-specific antibodies, fusions, and gene therapies. A broad skill set is preferred for various protein analytical technologies including chromatography, electrophoresis, mass spectrometry, and spectroscopy applications.
Responsibilities:
Hands-on development, validation and transfer biochemical methods such as capillary electrophoresis (CE) and HPLC methods for characterization and quality control of biological products.
Lead or contribute to improvement in laboratory operations to increase efficiency and throughput for non-GMP methods.
Performs routine analytical testing under both GMP and non-GMP guidelines.
Demonstrate excellent communication and strong interpersonal skills combined with technical, writing, and organizational skills as well as demonstrated attention to detail and record keeping.
Complete all electronic lab notebooks and safety trainings as required in a timely fashion
Contribute to lab coordination activities such as logbook signoff, scheduling maintenance and repairs, and instrument troubleshooting
Qualifications:
A minimum of a bachelor's degree in chemistry, biological sciences, or Engineering.
A strong background in chromatography technologies (e.g., HPLC and other chromatography-based applications) is preferred/required.
Experience in analytical method development/qualification/validation by chromatography and electrophoresis is preferred.
Strong planning and tracking skills, well -organized, results oriented, capable of managing multiple projects
Ability to quickly learn new techniques and excellent in problem solving skills
Ability to work with limited guidance to plan, execute, and follow through with studies is preferred.
Demonstrated ability to work collaboratively in a fast-paced team environment