Scientist I

Scientist I

Requirements

• Ph.D. and 0-2 years directly related experience or Master’s and 5 years related experience or Bachelor’s and 7 years related experience in biotechnology or pharmaceutical industries.
• Experience in plate-based assay techniques are required.
• Good oral presentation and technical writing skills are required.
• Records (accurately, clearly, and consistently) information, facts, and measurements that are required by cGMP, GLP, GCP, and/or by co-workers to understand situations and to perform their assignments.
• Understanding of biotherapeutic regulatory requirements and expectations.
• Strong communication skills.

Responsibilities

• Design and execute product development efforts in the process, formulations, and analytical development areas.
• Conceptualizes and proposes process development, formulations development and analytical development strategies based on bio-pharmaceutic data.
• Responsible for producing high quality documentation, client reports, etc. suitable for publication and regulatory requirements.
• Review and analyze data for the experiments performed by self and by other analysts.
• Responsible for the equipment within the AFS team and ensure operational status of instruments and equipment.
• Responsible for developing/maintaining a current understanding of cGMP and other regulatory requirements.
• Maintain broad knowledge of state-of-the-art principles and theory; provides technical leadership in the group, serves as in-house advisor on key scientific discipline areas.
• Build collaborative relationships with customers and provide scientific presentations to clients.
• React to change productively and handle other essential tasks as assigned.

Preferred Qualifications

• Experience in chromatographic and electrophoretic analytical techniques are preferred.