Compliance Specialist III
Core
Author, review, and approve technical and regulatory documentation to ensure compliance with Good Manufacturing Practices (GMP) and internal procedures for pharmaceutical operations.
Role type
Compliance Specialist
Builds
Technical documents, batch records, and Standard Operating Procedures (SOPs) for pharmaceutics and operations teams.
Domain
Pharmaceutical manufacturing / Quality Compliance
Required skills
GMP knowledge, document authoring and review, batch record management, SOP drafting, spot-checking experimental areas, data tracking and trending, Microsoft Word/Excel proficiency
Responsibilities
Author and approve technical documents (protocols, reports, SOPs); Review executed batch records for GMP conformance; Perform spot-checks of experimental areas and track laboratory notebooks; Track and trend batch record initiation, approvals, and feedback; Maintain readiness for on-site clients.
Seniority
Mid-level individual contributor
