Regulatory Information Management (RIM) Administrator

Why REMEDICA:

Remedica is a leading pharmaceutical company with a vision for a healthier world through high quality, safe and efficacious products at affordable prices

As a RIM Administrator you will:

• Generating reports and ensuring that product lifecycle information is communicated to interested stakeholders.
• Ensuring that tasks and processes are executed according to established regulations and guidelines such as Standard Operating Procedures (SOPs) and the current Good Manufacturing Practices (cGMP).
• Identify and implement improvements to RIM processes, workflows, and system functionalities.
• Generate and distribute regulatory data reports for internal stakeholders and external regulatory bodies.
• Basic understanding of relevant country-specific regulatory regulations to ensure data governance policies align with these standards.

What you will bring:

• Excellent oral and written knowledge of English language.
• Highly Competent in Microsoft Office.
• Previous Experience in data entry / management in company systems is preferred.
• Strong attention to detail.
• Effective communication and interpersonal skills.
• Organisational, multitasking and prioritization skills, good time-task allocation, and ability to meet project deadlines.

What’s in it for you?

• 13th and 14th Salary
• Provident Fund
• Group Medical Plan
• Discount Scheme
• Gym access

If you are interested you can apply via email : [email protected]