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Title

Scientist II 

EOE StatementWe are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.
 
Full-Time/Part-Time Full-Time  
Description

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.

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.

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

 
Location St. Joseph, MO  

This position is currently accepting applications.

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