Overview In this role you support the pharmaceutical manufacturer by preparing and reviewing regulatory dossiers, ensuring compliance, and coordinating documentation for health authority submissions. You will liaise with authorities and clients on changes to manufacturing or control processes, and help implement and train staff on regulatory policies. You will oversee ongoing registration activities, including certificates and permits, contributing to a compliant, transparent operation.

This role offers professional development in a high-quality pharmaceutical environment and a hybrid work setup.

Compensaciones / Incentivos Job stability comprehensive benefits package professional development continuous digital training flexible working hours hybrid work model

Responsabilidades Prepare and review product registration dossiers and ensure regulatory compliance for submissions

Coordinate collection and organization of technical documentation to meet regulations





Respond to inquiries and deficiency letters from health authorities and implement required changes

Communicate changes in products or facilities to clients and authorities for transparency

Implement internal policies related to registration processes and provide staff training

Oversee registration activities including updating certificates and issuing permits

Requisitos principales Bachelor in Health Sciences (Pharmacy, Biology or Chemistry)

2 years of experience in a similar role

Proficient level of English

MSc in Pharmaceutical Industry, Regulatory or related field is highly valued strong communication attention to detail proactive problem solving regulatory affairs dossier preparation and submission knowledge of health authority requirements

📌 Medical Device Regulatory Affairs (Rubí)
🏢 Marlex Human Capital
📍 Rubí