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MSAT Process Specialist​/Expert – Formulation and Filling; m​/f​/d

in 55232, Alzey, Rheinland-Pfalz, Deutschland
Unternehmen: Eli Lilly and Company
Vollzeit position
Verfasst am 2026-10-13
Berufliche Spezialisierung:
  • Fertigung/Herstellung
    Compliance Analyst, Qualitätsingenieur, Validierungsingenieur, Pharmazeutische Produktion
  • Ingenieur
    Compliance Analyst, Qualitätsingenieur, Validierungsingenieur
Gehalts-/Lohnspanne oder Branchenbenchmark: 53000 - 121000 EUR pro Jahr EUR 53000.00 121000.00 YEAR
Stellenbeschreibung
Stellenbezeichnung: MSAT Process Specialist / Expert – Formulation and Filling (m/f/d)
Location: Alzey

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve.

This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

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."

In this role you will be part of the TS/MS (Technical Services / Manufacturing Science) team (also known as MSAT or MS&T). The TS/MS 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.

Key

Objectives / Deliverables
  • Responsible for maintaining a safe work environment, working safely and accountable to support all HSE corporate and site goals.
  • Act as TS/MS representative for the Formulation & Filling processes, addressing complex process issues in a structured manner and escalating as appropriate.
  • Act as link between operations, product team and local stakeholders for process related topics.
  • Ensure the preparation, formulation and filling process follow industry and authority expectation and are in full compliance with applicable regulations.
  • Provide technical guidance for formulation and aseptic filling processes to the whole site and serve as a source of knowledge to the operational staff.
  • Support validation and lifecycle management of filling processes, equipment, and control strategies to ensure robust and compliant commercial supply.
  • Own complex process deviations and drive change controls through in-depth understanding of critical process steps and process controls
  • Collaborate cross-functionally to drive continuous improvement and present responsible area during inspections and audits.
  • Ensure processes, procedures, and batch documentation are accurate, executable, and compliant with GMP and regulatory expectations.
Expected Qualifications
  • Degree as engineer, pharmacist, or equivalent qualifying certification/training.
  • At least 5 years of professional experience in the pharmaceutical industry.
  • Knowledge of GMP and operational skills.
  • Good knowledge of document and project management.
  • German language proficiency and basic English knowledge.
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