Full-time
Hiregulf
Licensed Pharmacist wanted at a leading Medical Devices Trading Company in Sharjah, UAE with the following:
Job Responsibilities
- Manage and coordinate all regulatory approvals with the Ministry of Health (MOH UAE) for medical devices and equipment.
- Handle product registration, classification, and listing processes in compliance with UAE regulatory guidelines.
- Prepare, review, and submit technical documentation, dossiers, and regulatory files for new product approvals.
- Liaise with government authorities, including MOH and other regulatory bodies, to ensure smooth approval processes Licensed Pharmacist.
- Ensure all products meet UAE medical device regulations, safety standards, and quality requirements.
- Maintain accurate records of product registrations, approvals, renewals, and regulatory correspondence.
- Monitor updates in healthcare regulations, compliance standards, and medical device laws in the UAE.
- Coordinate with suppliers and manufacturers to obtain required documentation such as Free Sale Certificates, CE certificates, and ISO certifications.
- Support internal teams (sales, procurement, logistics) with regulatory guidance and product compliance requirements.
- Ensure timely renewal of licenses, product registrations, and regulatory approvals.
- Conduct internal audits to ensure compliance with quality management systems and regulatory standards.
- Provide training and guidance to staff on regulatory procedures and compliance requirements.
Job Qualifications – Pharamcist
- Bachelor’s Degree in Pharmacy (B.Pharm) or a related field.
- Valid MOH Pharmacist License (UAE) is mandatory.
- Minimum 1–3 years of experience in regulatory affairs, preferably in the medical devices or healthcare industry.
- Strong knowledge of UAE MOH regulations, product registration, and classification processes.
- Familiarity with medical device documentation, CE marking, and international regulatory standards.
- Excellent understanding of quality assurance and compliance requirements in the healthcare sector.
- Strong communication and coordination skills to interact with regulatory authorities and internal teams.
- Proficiency in documentation, report writing, and regulatory submissions.
- Ability to manage multiple approvals and deadlines efficiently.
- Knowledge of ISO standards and Good Distribution Practices (GDP) is an added advantage.
- Fluency in English; knowledge of Arabic is a plus.