Senior/Principal Scientist Validation Full-time

Senior Principal Scientist Validation

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.”

In this role you will be part of the TSMS (Technical Services / Manufacturing Science) team (also known as MSAT or MS&T). The TSMS team is the technical owner of the process — from tech transfer and validation through commercial lifecycle management. Our decisions on control strategy, lifecycle, and process robustness shape how this greenfield parenteral site runs for the next decades, with direct visibility to site leadership and Lilly's global technical network.

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

Requirements:

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!

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form for further assistance.

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.

Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is €52,500 – €110,000.

Full-time equivalent employees may also be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a pension plan; vacation benefits; eligibility for healthcare benefits; flexible benefits (if applicable) life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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