Senior Documentation Analyst

Strong knowledge of documentation standards, quality assurance processes, and regulatory requirements. Excellent written and verbal communication skills, with attention to detail and accuracy. Ability to work independently and as part of a team, with strong organizational and time management skills.

• Documentation Management:
  Develop, implement, and maintain documentation procedures and standards for R&D projects.
• Create, review, and update technical documents, research reports, and project records.
• Ensure all documentation meets regulatory requirements and industry standards.

• Organize and maintain electronic and physical document storage systems.
• Manage version control to track changes and revisions in documents.
• Ensure proper archiving of completed projects and historical data.

• Work closely with R&D teams to understand documentation needs and provide support in creating and formatting documents.
• Facilitate communication between departments to ensure accuracy and consistency of information.
• Assist in preparing presentations, technical papers, and reports for internal and external stakeholders.

• Review documentation for accuracy, completeness, and adherence to quality standards.
• Create and ensure compliance with relevant regulatory requirements (e.g., FDA, ISO) and internal policies.

• Provide training and support to R&D staff on documentation procedures and best practices.
• Develop and maintain documentation guidelines and training materials.

• Assist in the preparation of documentation for grant proposals, patent applications, and other external submissions.
• Support project managers by tracking documentation milestones and deadlines.

M. Sc. /

B. Sc. / M. Pharm/

B. pharm (Chemistry) with 2 - 5 years of relevant experience Proven experience (3+ years)

At SVAK Life Sciences, our strength lies within our team who are adaptable to the growing challenges faced by the industry.

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