Title: Spec, QA, Brazil

Requisition ID: 75463

Date: Sep 15, 2026

Location:

Diadema, SP, BR

Department: Quality

Description:

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)