Job Vacancy: Regulatory Affairs & Quality Control (Q.C) Specialist
Location: Erbil, Iraq
Job Type: Full-time (9:00 AM – 5:00 PM)
Gender: Female
Salary: Determined after the interview
Job Overview
We are seeking a detail-oriented and organised Regulatory Affairs & Q.C Specialist to join our team in Erbil. The ideal candidate will handle product registrations, liaise with government authorities, and manage the logistics of imported products.
Key Responsibilities
Registration: Manage the registration process for both products and international manufacturers.
KMCA Representative: Act as the official authorised registration representative of the company at the Kurdistan Medical Control Agency (KMCA).
Document Review: Thoroughly review Q.C documents and ensure accurate submission into the KMCA system.
International Communication: Maintain professional communication and coordination with international manufacturers.
Importation & Logistics: Oversee the importation process and manage product logistics from end to end.
Requirements & Qualifications
Gender: Female.
Languages: Native Kurdish and fluent English (written and spoken) are mandatory.
Experience: Previous experience dealing with the KMCA system and regulatory affairs is highly preferred.
Skills: Strong communication, excellent organisational skills, and the ability to manage logistical workflows.
How to Apply
If you meet the criteria and are interested in this position, please send your CV to hr@daylightmed.com
with the subject line "Regulatory Affairs & Q.C Application".