Cosmetic Otc Compliance Technical Writer

Cosmetic, OTC, and natural products experience meets technical documentation expertise at Apollo Health & Beauty Care. The full-time role supports North American compliance.This mid-senior Technical Writer prepares documentation aligned with internal Quality Management System requirements and regulatory expectations. The position supports laboratory development through commercial batch production across FDA and Health Canada contexts. You will author reports, risk evaluations, change controls, SOPs, and transfer records while collaborating with R&D, Regulatory, Quality Assurance, and Manufacturing.Key Responsibilities:
Author and manage deviation, OOS, and OOT investigationsFacilitate root cause analysis using 5 Whys and FishboneDraft documentation supporting formulation and process changesSupport transfer of R&D products to commercial manufacturingCollaborate with technical and regulatory teamsRequirements:
Bachelor’s degree in chemistry, cosmetic science, or related fieldThree to five years’ North American industry experienceKnowledge of FDA and Health Canada expectationsStrong understanding of cGMP-regulated manufacturing environmentsMicrosoft Word, Excel, and PowerPoint proficiencyUse compliant technical writing, investigation expertise, and regulatory knowledge to support Apollo’s cosmetic and OTC manufacturing documentation.
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