Senior Scientific Regulatory Writer – Remote

HL Mando Corporation do Brasil; Abu Dhabi; Remote; AED 167,000 - 279,000; Full time

Job summary

HL Mando Corporation do Brasil in UAE seeks a Senior Scientific Regulatory Documentation Specialist to prepare and review scientific documents for regulatory submissions across pharma, biotech, medical devices, and chemicals. The role is fully remote in the United Arab Emirates, requiring coordination with QA, regulatory affairs, manufacturing, and legal teams to ensure traceability and compliance.

Responsibilities include maintaining document control, addressing data gaps, and tracking

Qualifications

• Bachelor degree in a scientific discipline related to regulatory work.
• Postgraduate qualification in Regulatory Affairs or Scientific Documentation is an advantage.
• Experience in scientific documentation, regulatory affairs, technical writing, or regulated product compliance.
• Knowledge of document control, change management, data integrity and quality management principles.

Responsibilities

• Prepare, review, and coordinate scientific and technical documents for regulatory submissions and product compliance.
• Compile information from research reports, lab records, and manufacturing data.
• Review reports, specifications, validation records, and data for accuracy and consistency.
• Develop and maintain regulatory document packages and submission sections.
• Track regulatory changes and assess impact on documentation and submissions.
• Maintain document version control, approval records, and traceability.
• Coordinate responses to regulatory questions and requests for information.
• Ensure alignment between regulatory submissions and quality records.
• Manage submission calendars, trackers, and inventories.

Skills

Scientific writing

Regulatory writing

Documentation management

Stakeholder coordination

Microsoft Office

Regulatory information management

Data interpretation

Quality management principles

Technical editing

Attention to detail

Education

Bachelor's degree in Pharmaceutical Sciences, Chemistry, Biology, Biotechnology, Biomedical Science, Regulatory Affairs, or related

Postgraduate qualification or professional certification in Regulatory Affairs or Scientific Documentation

Tools

Microsoft Office

Electronic Document Management Systems (EDMS)

Job description

HL Mando Corporation do Brasil in UAE seeks a Senior Scientific Regulatory Documentation Specialist to prepare and review scientific documents for regulatory submissions across pharma, biotech, medical devices, and chemicals. The role is fully remote in the United Arab Emirates, requiring coordination with QA, regulatory affairs, manufacturing, and legal teams to ensure traceability and compliance.

Responsibilities include maintaining document control, addressing data gaps, and tracking