Scientist II Position Available In Clarke, Georgia
Tallo's Job Summary: The Scientist II role at Boehringer Ingelheim in Athens, GA involves conducting analytical testing methods to support vaccine and therapeutics development. Responsibilities include method development, sample testing, troubleshooting, and ensuring compliance with regulations. The position requires a Bachelor's Degree and at least two years of related scientific experience, with a background in microbiology, immunology, or molecular biology preferred.
Job Description
Scientist
II 4.0 4.0
out of 5 stars Athens, GA Contributes to and assists in the execution of analytical testing methods to support the biological development of vaccines, therapeutics, and other related products. Conducts sample testing for process and analytical development as dictated by project requirements. Actively engages in learning new techniques through expert-led training and self-motivation, enabling independent performance of standard scientific and laboratory duties with minimal supervision. Ensures compliance with all applicable regulations, maintaining a safe working environment. While working at Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies’ success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our employees. Duties & Responsibilities To assure Analytical Development missions: To set up, execute studies, and support development of robust and reliable methods for analytical testing To carry out and assure the testing of submitted samples with the appropriate methods To troubleshoot technical issues and provide recommendations to increase efficiency To ensure compliance with Good Documentation Practices (GDP) or other requirements; making sure that all data are recorded and other documentation and files are checked, secured, and approved To help maintain the Analytical lab To apply basic scientific principles with minimal guidance. Assist in the execution of non-routine experiments with supervision To contribute to project advancement: To follow protocols, complete results, and provide data compilation for reports To correctly analyze data/results and interpret outcome of experiments under supervision To develop and maintain interfaces with Analytical team members, internal partners, and customers (Clinical Analytical, Process Development, and other Global Innovation teams) To ensure all information and documentation necessary to meet project timelines is available in the agreed upon time Complies with applicable regulations, performing all work in a safe manner; maintains proper records in accordance with Standard Operating Procedures (SOPs) and policies Willingness to learn from and and actively engage in work with other colleagues to supprt a collaborative team environment Must be able to work cross-functionally Demonstrate willingness to advance knowledge of analytical development and vaccinology Apply knowledge of basic theory and scientific principles Ability to learn new technology and concepts and apply appropriately with minimal supervision Concise and accurate reporting of technical data and information Ability to troubleshoot Written and verbal communication skills Appropriate level of understanding of applicable regulations Bachelor’s Degree from an accredited institution with minimum of two (2) years of experience in related scientific discipline is preferred Background in microbiology, immunology, cellular and molecular biology, virolology General knowledge of bioanalytical techniques Basic level of understanding of USDA and EMA requirements
QUALIFICATION/LICENSURE
Work Authorization :
US Citizen Preferred years of experience : 1 years Travel required : No travel required Shift timings :