About this role
Job Summary In this role, you will support all quality systems and functions for the respective site. Assists in establishing systems to support the facility to drive continuous improvement and minimize the costs of non-conformance. Plans, schedules, executes, and communicates all items regarding quality issues, complaints, validations, and other projects to the QA Manager and/or other interested parties. Performs all duties associated with compliance-related items for ISO standards and cGMPs. This role is the interface between the customers and site for supporting audits. Essential Duties and Responsibilities Lot/batch control and product release Technical document control (procedures, work instructions, technical specifications) Audits Knowledge of BPS and GMP (Anvisa’s Good Manufacturing Practices) Managing deviations Risk assessments / Risk analysis Change control Education Bachelor's degree in Farmacy, chemistry, engineering, Biology, or technician in these areas Preferred Knowledge, Skills and Abilities Advanced English Good Manufacturing pratices Experience or contact with the operations areas. Experience with Internal audit Nice to Have: Experience with External Audit and Knowledge of Good Manufacturing Practices (GMP)