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Metro location, mid-level (5 years) requirement, and recognizable global brand increase applicant competition.
Role requires regulated pharmaceutical/consumer-health experience, making cross-industry transferability limited.
Explicit 5 years regulated-industry experience and documentation/regulatory skills create strict filtering criteria.
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Manage and deliver assigned operational and documentation projects independently, ensuring quality and consistency from initiation to completion.
Conduct pre-approval quality checks of documentation to align with Written Standards and governance processes.
Collaborate cross-functionally to improve and maintain business processes, tools, and documentation, and support audit readiness and corrective action implementation.
College or university degree.
Minimum 5 years experience in a regulated industry, pharmaceutical or consumer healthcare business, or equivalent experience.
Experience in developing or maintaining written standards, procedures, or document management.
Strong written communication skills and confidence with digital tools and documentation platforms.
Experienced working in regulated, compliance-driven environments, preferably pharmaceutical or consumer healthcare sectors.
Capable of identifying and implementing process improvements and comfortable working independently with ownership of deliverables.
Experienced in supporting audit, assessment, or CAPA activities and collaborating with cross-functional or global stakeholders.