Shift     flexible 6:00 a.m. through 6:00 p.m.

• Contributes to and assists in data handling and processing to support the biological development of vaccines, therapeutics, and other related products.
• Integrates Analytical Development with BioProcess and Formulations workflows 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 Client, 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 Client's high regard for our employees.

Duties & Responsibilities

• To assure Analytical Development missions:
• To set up and execute digital processing, transfer, and retrieval of Analytical Development data to support efficient use and analysis among CMC Development Functios
• 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 are retrievable/searchable
• To help maintain the Analytical lab
• Assist in the execution of non-routine experiments with supervision collaboratively with CMC Development and Global MSAT colleagues
• To contribute to project advancement:
• To follow protocols, complete results, and provide data compilation for reports
• To correctly analyze, process, and transfer data from relevant 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 data packages 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

Skills:    

• 2 years experience
• General knowledge of bioanalytical techniques
• Expeience in computer science disciplines related to pharmaceutical/biological life science industry is highly preferred.
• Academic knowledge and experience with: C#, SQL, Graph, GO, Javascript, NoSQL,
• Recommended software experience:  OSIsoft PI, PI AF, Libre, ETL Data Warehouse Design and Implementation, Grafana, SIMCA, SIMCA-online, SAS JMP, Visual Studio, MS DB Mgmnt Studio, MongoDB, PostgreSQL, Kubernetes, RedHat OpenShift, Task Scheduler.
• Desired Proficiency:  R, Python, Rust, Swift
• 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

• Bachelor's Degree from an accredited institution with minimum of two (2) years of experience in Biology or related scientific discipline is preferred, or Master’s Degree in Data Analytics (e.g., Bioinformatics)