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.
Job Title: Associate Director – Sterility Assurance
Location: Alzey, Rheinland-Pfalz, Germany
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 professionals who, together with us, will ensure the supply of Lilly medicines in Germany, Europe, and worldwide. We are dedicated to producing medicine with an unwavering commitment to safety and a relentless focus on quality
Join our Lilly team in Alzey and start as soon as possible as:
Associate Director – Sterility Assurance
Key Objectives/Deliverables:
- The Associate Director Sterility Assurance develops and maintains up-to-date technical/scientific knowledge and expertise in sterility assurance (QA/QC, microbiology, environmental monitoring , TS/MS, engineering, sterile manufacturing, etc.)
- Is responsible for technical investigations or evaluations, and sterility assurance improvement projects
- Evaluates, suggests, and makes decisions on technical solutions during project activities or change controls, including approving or rejecting them
- Defines, develops, evaluates, and validates on-site sterility assurance strategies to ensure compliance with current regulations and Lilly Global Quality Policies and Common Quality Practices
- Reports sterility assurance quality issues and inspection risks to site leadership as part of site reviews and in global forums as appropriate.
- Actively participates in regulatory inspections, internal audits, or global audits as a key contact for sterility assurance.
- Serves as a primary contact for all matters related to sterility assurance during Health Authority inspections, internal audits and as needed external audits of business partners/suppliers/etc.
- Develops and Implements EM sampling strategy and execution
- Responsible for site CCS (Contamination Control Strategy)
How do you convince us?
- Bachelor’s degree in science, Engineering, Management, Pharmacist PHD or a related field. A Master's degree in any of these disciplines is desirable.
- Proven 7+ years of experience working in the medical device industry, with preferred experience in assembly and packaging and a minimum of 3 years of leadership experience.
- Possess a solid understanding of the basic requirements of regulatory agencies such as the FDA and EMEA.
- Demonstrate strong leadership, work well within a team, and are passionate about people development
- Adept at problem-solving and eager to lead your team, equally passionate about the opportunity to be part of the site start-up.
- Adaptability and passion are critical. Your leadership will inspire your team and foster growth opportunities at the site. You are ready to take on new challenges and drive success.
- Open to international travel, proficient in German and English, and willing to work at the Alzey site.
What can you look forward to with us?
Pioneering spirit: Become part of a team of specialized professionals that will grow to up to 1,000 colleagues over the next three years.
Innovation: You will work in a medical high-tech production facility equipped with the most advanced technology.
Creative freedom: From the beginning, you will have the freedom to contribute your ideas and implement them in cross-functional teams.
Development: We value the individual career development of our employees and ensure fair access to professional development worldwide through our " Lilly University."
Financial benefits: In addition to your attractive salary, we offer you the option of an excellent company pension plan and other individual benefits.
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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 (https://careers.lilly.com/us/en/workplace-accommodation) 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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Eli Lilly and Company engages in the discovery, development, manufacture, and sale of products in pharmaceutical products business segment.
For more than a century, we have stayed true to a core set of values – excellence, integrity, and respect for people – that guide us in all we do: discovering medicines that meet real needs, improving the understanding and management of disease, and giving back to communities through philanthropy and volunteerism.
