Other Specification

• Bachelor's degree in a relevant field (e.g., Health Sciences, Pharmacy, Regulatory Affairs).
• Experience in documentation management within the pharmaceutical or healthcare industry.
• Knowledge of regulatory requirements and quality standards (e.g., FDA, EMA, GMP).
• Strong attention to detail and organizational skills.
• Excellent communication and interpersonal skills.
• Familiarity with electronic document management systems.
• Ability to work collaboratively in a cross-functional team environment.
• Knowledge of pharmaceutical development processes and clinical trial documentation is a plus.

Note

• Should have experience with bidding tenders and using PPMO.

Source: Merojob

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