Regulatory Affairs and Quality Management
We are seeking a seasoned professional to lead our compliance efforts in the pharmaceutical industry. As a Regulatory Affairs & Quality Manager, you will be responsible for ensuring product safety, quality, and market access by navigating local and global regulatory requirements.
Key Responsibilities:
* Strategic Submissions: Prepare and oversee all product registration submissions and variations across the territory.
* Market Access: Expedite applications and negotiate approvals with government regulatory authorities.
* Compliance: Manage import permits, license applications, and product labeling to ensure full government compliance.
You will own compliance across three core areas:
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