Description
Job Summary:
We are seeking an experienced professional from the pharmaceutical industry to join our Quality team, ensuring compliance with GACP/GMP and managing quality processes.
Key Highlights:
1. Experience in the pharmaceutical industry in QA, QC, or Production.
2. Ensure compliance with GACP/GMP and regulatory requirements.
3. Experience in good documentation practices and audits.
Location: **Rio de Mouro, Sintra**
We are looking for a professional with experience in the **pharmaceutical industry** to join our Quality team.
Key Responsibilities
* Ensure compliance with **GACP/GMP** and regulatory requirements
* Review **batch documentation**, analytical and manufacturing results
* Initiate, review, and approve **deviations, CAPAs, and change controls**
* Support **investigations**, audits, inspections, and on-the-floor activities
* Participate in **risk assessments**, continuous improvement, and document control
Desired Profile
* Bachelor's degree in **Health Sciences, Biological Sciences, or Chemistry**
* **3+ years** of experience in the pharmaceutical industry in **QA, QC, or Production**
* Knowledge of **GACP/GMP**
* Experience in **good documentation practices**, quality investigations, and audits
* Good command of **English**