Quality Intern

Lilly İlaç

QUALIFICATIONS AND JOB DESCRIPTION 

Lilly started its operations in Turkey in 1950’s by having its products manufactured and distributed through partnership with a Turkish company. In 1993, its operations were gathered under Lilly İlaç Ticaret Ltd. Şti. Since then, Lilly has been providing various products in the therapeutic areas of diabetes, endocrinology, osteoporosis, central nervous system diseases, oncology, psoriasis and men’s health in Turkey.

Recognitions

Lilly İlaç has been awarded Top Employers Turkey 2018 and Top Employers Turkey 2019 Certifications two years in a row for its exceptional employee offerings.

Lilly İlaç has been among Turkey’s best employers in Aon Hewitt’s Best Employer Surveys two times.

Lilly İlaç has been recognized by EDMER (Etik Değerler Merkezi) with “ETIKA Turkey Ethics Awards” seven times in a row.

Explore a great opportunity at Lilly by applying to join our team as a Quality Intern where we unite caring with discovery to make life better.

Quality Intern will be responsible for;supporting Quality activities in our Affiliate.

We are looking for a Quality intern to be part of our QualityTeam affiliated to the Quality Department who;

·         4th or 5th grade Pharmacy student or new graduate

·         can continue for at least 4 days a week for 6 months,

·         Good command of English,

·         Good use of MS Office programs,

·         Has planning and organizing, job tracking and effective communication skills,

·         Prone to team work.

JOB DESCRIPTION

·         Enter trackwise system and perform translation of complaints and assign it to regional center.

·         Prepare complaint closure letters according to the templates

·         Perform sample requests from the patients

·         Separate and check the incoming complaint samples and package them accordingly.

·         Manage the DHL complaint sample shipment to complaint regional center per the defined process

·         Prepare letters for importation permit

·         Archive and prepare commercial batch release documents

·         Archive and prepare clinical trial release documents

·         Perform the calls to the reporter according to our aberrant temperature excursion assessment result.