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 : Green Card, US Citizen
Preferred years of experience : 1 years
Travel required : No travel required

Shift timings :