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Mid-level metro operations role with generalist documentation scope and known consumer-health brand increases applicant density.
Requires regulated pharma/consumer-health documentation experience limiting cross-industry transferability.
Mandatory five years in regulated pharmaceutical/documentation roles and audit/CAPA exposure enforces stringent shortlisting.
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Own and deliver defined operational activities and documentation projects from initiation through completion with minimal supervision.
Ensure quality and consistency of documentation aligned with Written Standards and governance processes, including pre-approval quality checks.
Support the development, enhancement, and adoption of business processes and tools, collaborate with stakeholders, and aid audit and inspection readiness activities.
College/university degree required.
5 years’ experience in regulated industry, pharmaceutical or consumer healthcare business or equivalent.
Experience developing or maintaining written standards, procedures, or document management.
Strong written communication skills and confidence with digital tools/documentation platforms.
Experienced in regulated or compliance-driven environments, preferably pharmaceutical or consumer healthcare sectors.
Capable of independent work with ownership of deliverables, critical thinking, and identifying improvement opportunities.
Experienced in cross-functional collaboration, audit support including CAPA activities, and agile or continuous improvement methodologies.