Eli Lilly and Company
Senior/Principal Scientist Tech Transfer (m/w/d)
Eli Lilly and Company, Germantown, Ohio, United States
Overview
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 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 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: Position
Senior Principal Scientist Tech Transfer (m/w/d) Responsibilities
Instruct and support the technical transfer as Molecule Steward of TS/MS; 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 accurate instructions (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 relevant technical documents, 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. Qualifications
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 leadership, project management, ability to influence and lead projects. 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 you can look forward to
Pioneering Spirit:
Be part of a groundbreaking team that will grow to up to 1,000 colleagues over the next three years. You’ll contribute to pharmaceutical innovation. Cutting-Edge Technology:
Work in a state-of-the-art medical high-tech production facility with advanced technology. Creative Freedom:
From day one, contribute ideas and collaborate with cross-functional teams. Personal and Professional Growth:
Access development opportunities through Corporate Lilly University to grow and advance your career globally. Attractive Benefits:
Competitive salary, strong pension plan, and benefits supporting well-being and financial security. Have we piqued your interest? 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 actively engage in the workforce, ensuring equal opportunities. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form for further assistance. 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. #WeAreLilly
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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 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 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: Position
Senior Principal Scientist Tech Transfer (m/w/d) Responsibilities
Instruct and support the technical transfer as Molecule Steward of TS/MS; 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 accurate instructions (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 relevant technical documents, 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. Qualifications
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 leadership, project management, ability to influence and lead projects. 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 you can look forward to
Pioneering Spirit:
Be part of a groundbreaking team that will grow to up to 1,000 colleagues over the next three years. You’ll contribute to pharmaceutical innovation. Cutting-Edge Technology:
Work in a state-of-the-art medical high-tech production facility with advanced technology. Creative Freedom:
From day one, contribute ideas and collaborate with cross-functional teams. Personal and Professional Growth:
Access development opportunities through Corporate Lilly University to grow and advance your career globally. Attractive Benefits:
Competitive salary, strong pension plan, and benefits supporting well-being and financial security. Have we piqued your interest? 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 actively engage in the workforce, ensuring equal opportunities. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form for further assistance. 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. #WeAreLilly
#J-18808-Ljbffr