Analytical Development Scientist
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
Education:
- 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)