Senior/Principal Scientist Validation Full-time

Senior Principal Scientist Validation (M/W/D)

At Lilly in Germany, we are currently planning and building a high-tech production facility in Alzey (Rhineland-Palatinate), which will expand our production of injectable drugs from 2027 and employ up to 1,000 specialists. To make the most of our innovative production site, we are looking for motivated reinforcements who, together with us, will ensure the supply of Lilly medicines in Germany, Europe, and worldwide, in line with the three Lilly values of “Excellence,” “Integrity,” and “Respect for People.”

Join our Lilly team in Alzey and start as soon as possible as:

What tasks await you?

As Principal Scientist Validation, you will be expected to instruct and support the validation of production equipment and systems. Your responsibilities will include:

• Sterilization validation, cleaning validation, filter validation, shipping validation, process validation, and other TS/MS related activity.
• Prepare, review relevant technical documents, as required, such as: change controls, regulatory submissions, deviation investigations, validation protocols and summary reports, processing records, procedures.
• Participate in development and implementation of process functional teams in positive fashion to implement TS/MS objectives and deliver on business and quality objectives.
• Initiate related validation protocols and reports, and coordinate validation related activities Complete required and assigned trainings on-time.

Key Objectives/Deliverables:

• Instruct and support validation of production equipment and systems.
• Prepare, review and support relevant technical documents.
• Execute validation related activities.
• Ensure compliance with the final objective and coordinate with local project team.
• English fluent, additional German is preferred
• The position is onsite, not hybrid, not remote

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 Operation skills Good knowledge of document and project management. You have German and basic English knowledge. Additional Skills/Preferences:Parenteral manufacturing Strong analytical and synthesis skills. 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 be at the forefront of pharmaceutical innovation, contributing to life-changing advancements.
• Cutting-Edge Technology: Work in a state-of-the-art medical high-tech production facility equipped with the latest and most advanced technology. You'll have the tools and resources to excel in your role and push the boundaries of what's possible.
• Creative Freedom: From day one, you'll have the freedom to bring your ideas to life and make a real impact. Collaborate with cross-functional teams and see your innovative solutions implemented in a dynamic and supportive environment.
• Personal and Professional Growth: We are committed to your development. Through our “Corporate Lilly University,” you'll have access to a wealth of professional development opportunities, ensuring you can grow and advance your career on a global scale.
• Attractive Benefits: Enjoy a competitive salary, an excellent company pension plan, and a range of individual benefits designed to support your well-being and financial security. We value your contributions and reward your dedication.

Have we piqued your interest? Then please apply online with your complete application documents through our applicant portal. We look forward to your application!

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