Lilly is a global healthcare leader that unites caring with discovery to make life better for people around the world.
We are headquartered in Indianapolis, Indiana, and our employees work together 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.
Job Description
We are looking for a Technical Writer to support the Medicines Quality Organization (MQO) Quality Systems team at Eli Lilly Cork. The successful candidate will be responsible for delivering high-quality documents in the Safety and Efficacy Quality System (SEQS).
Main Responsibilities
* Ensure timely delivery of error-free, high-quality documents that meet international standards of written English.
* Develop and maintain accurate, clear, and concise procedures, required tools, and resource documents using appropriate technical writing standards, templates, and style guides.
* Verify quality system architecture accuracy and consistency of content within and between related documents.
Requirements
* Bachelor's degree (or equivalent work experience) in a scientific, health, communications, technology health-related field.
* Minimum 3 years of experience in technical/medical writing.
* Experience using Veeva QualityDocs or other electronic document management systems (EDMS).
Preferred Qualifications
* Experience in a regulated environment.
* Specialized knowledge of editing & proofreading techniques.
* Excellent attention to detail and organizational skills.
Eli Lilly Cork is committed to diversity, equity, and inclusion. We cater for all dimensions ensuring inclusion of all ethnicities, nationalities, cultural backgrounds, generations, sexuality, visible and invisible disabilities, and gender.
This role offers a premium workspace, flexible hybrid working options, healthcare, pension, and life assurance benefits, and more.