Intern – Global Regulatory Labeling

Intern – Global Regulatory Labeling  

Positions: 1  

Start date: January or  March or April  2027 

Duration:  6 months 

Salary: €30,500 

Location: Lilly GBS, Little Island Cork 

Type: Hybrid role requiring the successful candidate to be on site 50% of the month in Little Island, Cork and 50% working remotely.  

Course Eligibility: BSc or Msc in Sciences, pharmaceutical or similar  

Eli Lilly Cork is made up of a talented diverse team of over 2000 employees across 60 nationalities who deliver innovative solutions that add value across a variety of Business Service functions including Finance, Information Technology, Medical, Clinical Trials and more. Eli Lilly Cork offers a premium workspace across our campus in Little Island, complete with flexible hybrid working options, healthcare, pension and life assurance benefits, subsidised canteen, onsite gym, travel subsidies and on-site parking. Inhouse People Development services, Educational Assistance, and our ‘Live Your BEST Life’ 

wellbeing initiatives are just some of the holistic benefits that enhance the career experience for our colleagues. 

Eli Lilly Cork is committed to diversity, equity and inclusion (DEI). We cater for all dimensions ensuring inclusion of all ethnicities, nationalities, cultural backgrounds, generations, sexuality, visible and invisible disabilities and gender, with four pillars: EnAble, embRACE, LGBTQ+ & Ally and GIN-Gender Inclusion Network. EnAble, our pillar for people with disabilities and those that care for them, partners with the Access Lilly initiative to make our physical and digital environment accessible and inclusive for all. Together they are committed to promoting awareness to create a disability confident culture both at Eli Lilly Cork and beyond. 

Come join our team - Be Creative, Be an Innovator, and most of all, Be Yourself! 

The Global regulatory labeling team leads the development and maintenance of Core labeling and packaging for US and Canada. The team manages the labeling updates for US/CA submissions for post-marketed products. 

Responsibilities:  

• Main responsibilities will include administration with some labeling system tasks. 

• Document formatting which may include any process updates, updating job aids, updating submission documents and sending documents for review. 

• Quality checking of artwork components 

• System – this may include RIM updates, assigning document owners, creating RIM binders etc. 

• Special projects such as presentations on Labeling requirements, team presentations to other functions etc. 

Requirements: 

• Currently enrolled in 3rd level education and ready to pursue student placement as part of an undergraduate/masters program. 

• Studies include regulatory, Labeling not required but desired. 

• Drug development process – understanding of the process. 

• Good communication skills, technical ability, and presentation skills. 

• Good teamwork and collaboration skills. 

• Excellent attention to detail and quality focused.