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, 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.

POSITION OVERVIEW:

Lilly is actively growing its manufacturing footprint globally to meet the needs of patients and deliver on our exciting future. As a result, Lilly is looking for experienced quality assurance associates to support our growth in Alzey, Germany. This is an outstanding opportunity to deliver on new manufacturing investments and new pioneering technologies.
The Senior Assistant, Quality Assurance – Document Control, is responsible for electronic documentation and records management oversight at the Alzey site. This role is responsible for execution, maintenance, and administration of document management systems. The Document Controller will aid in initial program startup and routine operation of the site, as well as support site inspection readiness and execution.

BASIC REQUIREMENTS:

• High school diploma or equivalent
• Minimum 3 years in the pharmaceutical industry with previous document management experience.
• On-site presence required.

ADDITIONAL SKILLS/PREFERENCES:

• Experience with Microsoft Office (e.g., Outlook, Word, Excel).
• Previous experience in records management, data entry, or similar experience.
• Demonstrated ability to work successfully in a team environment.
• Demonstrated Project Management skills.
• Strong written and verbal communication skills.
• Strong ability to solve problems and make decisions.
• Experience with documentation in a GMP environment and electronic tracking of documentation.
• Experience in quality systems such as Veeva Vault QualityDocs.

ADDITIONAL INFORMATION:

• Primary location is Alzey, Germany.
• Ability to work overtime as required.
  This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. For GMP purposes, the job description should be updated for significant changes. As always, you should consult with your supervisor regarding your actual job responsibilities and any related duties that may be required for the position.
  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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Please refer the Job description for details