Senior/Principal Scientist Validation

Eli Lilly and Company; Alzey; Vor Ort; EUR 80.000 - 100.000; Vollzeit

Zusammenfassung

A global healthcare leader is seeking a Senior Principal Scientist Validation to instruct and support the validation of production equipment and systems. The ideal candidate will have a degree in Engineering or Pharmacy with at least 5 years of industry experience, knowledge of GMP, as well as strong analytical and interpersonal skills. This position offers cutting-edge technology, competitive salary, and opportunities for personal and professional growth.

Leistungen

Competitive salary

Excellent pension plan

Professional development opportunities

Dynamic work environment

Qualifikationen

• At least 5 years of professional experience in the pharmaceutical industry.
• Knowledge of GMP.
• Ability to work independently and in a team.

Aufgaben

• Instruct and support the validation of production equipment and systems.
• Prepare and review relevant technical documents.
• Coordinate validation-related activities.

Kenntnisse

German language proficiency

Basic English knowledge

Good document management skills

Strong analytical skills

Interpersonal skills

Ausbildung

Degree in Engineering or Pharmacy

Jobbeschreibung

Overview

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader with a presence in Germany and worldwide. We aim 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 seek people who are determined to make life better for people around the world.

Position

Senior Principal Scientist Validation (m/w/d)

What tasks await you?

As Principal Scientist Validation, you will 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 a 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.

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?

• 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.

Application

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

EEO and Accommodation

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.

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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