Scientist II, Analytical Development

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Performs customary scientific/lab duties with minimal supervision. Participates/assists in the design and execution of non‑routine experiments to support vaccine development. Performs all work in conformance with applicable regulations. Performs all work in a safe manner. The scope of responsibility is primarily within the scientific/lab environment and immediate discipline. As an employee of 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 company’s 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, mobility, networking and work‑life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim’s high regard for our employees.

• Initiates and completes customary procedures in an independent and efficient manner, with minimal supervision; independently operates and is responsible for scientific/lab equipment; troubleshoots effectively.
• Demonstrates technical ability to assist in the design and execution of non‑routine experiments with supervision.
• Applies basic scientific principles with minimal guidance; performs literature searches and extracts relevant information from published protocols.
• Demonstrates the ability to correctly analyze data/results and interpret outcome of experiments and to propose appropriate follow‑up.
• Communicates own work effectively orally and in writing; contributes to writing protocols, procedures, and technical reports; provides input for scientific reports.
• Reports and treats data with a high level of integrity and ethics.
• Complies with applicable regulations, performing all work in a safe manner; maintains proper records in accordance with SOPs and policies.

• Bachelor’s Degree from an accredited institution with minimum of two (2) years of experience in a related scientific discipline or Master’s Degree from an accredited institution in a related scientific discipline with no experience.
• Research methodology experience and/or education.
• Expertise in the Biologicals/pharmaceutical life cycle process.
• Basic level of understanding of USDA and EMEA requirements of master seeds and raw materials is preferred.
• Demonstrate knowledge of field.
• Apply knowledge of basic theory and scientific principles.
• Able to draft portions of technical reports.
• 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.

With us, you can develop your own path in a company with a culture that knows our differences are our strengths – and break new ground in the drive to make millions of lives better. Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.

Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after - as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations.

• Mid-Senior level

• Full-time

• Research, Analyst, and Information Technology

• Pharmaceutical Manufacturing