Regulatory Affairs & Registration Specialist - Oman

Tawteen; Muscat; On-site; OMR 6,000 - 12,000; Full time

Job summary

Tawteen is seeking a Regulatory Affairs and Registration Officer in Muscat to manage product registrations and regulatory submissions. You will ensure compliance with MOH Oman regulations, review licenses and technical documents, and coordinate with MOH and other authorities.

The role requires a Bachelor’s in Pharmacy or related field, familiarity with CTD/eCTD, and strong command of English, with attention to detail and deadlines being essential.

Qualifications

• Bachelor's degree in Pharmacy or related field.
• Experience in Regulatory Affairs and Product Registration is preferred.
• Knowledge of MOH Oman regulations and CTD/eCTD dossier preparation is an advantage.
• Familiarity with CTD/eCTD dossier preparation and regulatory documentation is an advantage.
• Strong understanding of pharmaceutical regulations, guidelines and compliance requirements.

Responsibilities

• Prepare, compile and submit regulatory dossiers for pharmaceutical and medical products.
• Manage new product registrations, renewals, variations and post-registration activities.
• Coordinate with MOH and other regulatory authorities.
• Review product documentation including licenses, product information and technical documents.
• Follow up on submissions and respond to queries from authorities.

Skills

CTD/eCTD

Regulatory submissions

MS Office

English

Detail-oriented

Deadline-driven

Education

Bachelor's degree in Pharmacy or related field

Job description

Tawteen is seeking a Regulatory Affairs and Registration Officer in Muscat to manage product registrations and regulatory submissions. You will ensure compliance with MOH Oman regulations, review licenses and technical documents, and coordinate with MOH and other authorities.

The role requires a Bachelor’s in Pharmacy or related field, familiarity with CTD/eCTD, and strong command of English, with attention to detail and deadlines being essential.