Senior/Principal Scientist Validation

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Germany, Alzeytime type

Full timeposted on

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R- At Lilly, we unite caring with discovery to make life better for people around the world.

We are a global healthcare leader headquartered in Indianapolis, Indiana.

Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.

We give our best effort to our work, and we put people first.

We’re looking for people who are determined to make life better for people around the world.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

Senior Principal Scientist Validation (m/w/d) 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 remoteDegree/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

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: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.

Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. #WeAreLillyLilly 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.

Please note this is for individuals to request an accommodation as part of the application process and any 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.#WeAreLillyAt Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world.

We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!#J-18808-Ljbffr