Senior/Principal Scientist Tech Transfer (m/w/d)

Eli Lilly and; Alzey; Vor Ort; EUR 75.000 - 95.000; Vollzeit

Zusammenfassung

A leading pharmaceutical firm is seeking a Senior Principal Scientist Tech Transfer in Alzey, responsible for providing technical support for an insulin cartridge project. Candidates should have significant experience in the industry, knowledge of GMP, and skills in leadership and project management. The role offers competitive benefits and the chance to work in a cutting-edge production facility.

Leistungen

Competitive salary

Excellent company pension plan

Professional development opportunities

Qualifikationen

• Minimum 5 years of industry experience.
• Knowledge of GMP and parenteral manufacturing.
• Fluent in German and basic English.

Aufgaben

• Provide technical support for insulin cartridge filling project.
• Prepare and approve technical documents.
• Support and lead technical projects to improve process control.

Kenntnisse

Leadership skills

Analytical thinking

Communication skills

Project management

Problem-solving

Ausbildung

Degree in engineering, pharmacy, or equivalent

Jobbeschreibung

Overview

At Lilly in Germany, we are planning and building a high-tech production facility in Alzey (Rhineland-Palatinate) to expand our injectable drug production from 2027 and employ up to 1,000 specialists. We aim to ensure the supply of Lilly medicines in Germany, Europe, and worldwide, guided by the Lilly values of Excellence, Integrity, and Respect for People.

Senior Principal Scientist Tech Transfer (m/w/d)

What tasks await you?

• Serve as Molecule Steward of TS/MS and provide technical support for the delivery of the new insulin cartridge filling project at the Alzey site.
• Provide technical support on warehouse shipping study at the Alzey site.
• Understand the scientific principles required for manufacturing insulin products, including the interactions between chemistry, equipment and container closure systems.
• Ensure that an accurate instruction set (batch records and procedures) and PFD describe the process as performed and the control strategy for the discrete manufacturing steps.
• Develop, monitor and appropriately react to established statistically based metrics in real-time to assess process variability and capability.

Key Objectives/Deliverables:

• Prepare, review, approve and provide technical support for preparation of relevant technical documents, as required, such as change controls, regulatory submissions, deviation investigations, validation protocols and summary reports, processing records, procedures, PFDs, VMPs, and APRs.
• Support and/or lead technical projects (experimental, modeling and/or production data analysis) to improve process control, yield and productivity. Execute validation related activities.

How do you convince us?

• Degree/qualifying certifications/training/experience: Engineer, pharmacist, or equivalent with professional experience (at least 5 years) in the industry.
• Knowledge of GMP and experience in parenteral manufacturing.
• Good skills in leadership, project management, ability to influence and lead projects.
• You have German and basic English knowledge.

Additional Skills/Preferences:

• Parenteral manufacturing
• Analytical thinking, multi-tasking, decision-making and problem-solving
• Excellent interpersonal and communication skills
• Ability to work independently and in a team
• Ability to coordinate teams without direct hierarchical power

What can you look forward to with us?

At Lilly, we believe in creating an environment where innovation thrives and every team member can shine. Here's what you can expect when you join our team:

• Pioneering Spirit: Be part of a groundbreaking team of specialized professionals that will grow to up to 1,000 colleagues over the next three years. You’ll contribute to life-changing pharmaceutical innovations.
• Cutting-Edge Technology: Work in a state-of-the-art medical high-tech production facility with the latest technologies to excel in your role.
• Creative Freedom: From day one, bring your ideas to life and collaborate with cross-functional teams in a dynamic, supportive environment.
• Personal and Professional Growth: Through our Corporate Lilly University, access professional development opportunities to grow and advance your career globally.
• Attractive Benefits: Competitive salary, excellent company pension plan, and benefits to support well-being and financial security.

Application and Equal Opportunity

Have we piqued your interest? Please apply online with your complete application documents through our applicant portal. Lilly is dedicated to helping individuals with disabilities participate in the workforce and ensuring equal opportunities for all applicants. If you require accommodation to submit a resume, please complete the accommodation request form: https://careers.lilly.com/us/en/workplace-accommodation. This request is for accommodation during the application process only; other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

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