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Pharmaceutical document control specialist

Torres Vedras
beBeeCompliance
Documentação
Anunciada dia 6 agosto
Descrição

Batch Record Reviewer Technician Job Description

We are a multinational company with over 40 years of history in the life cycle of drug products for human use.

Our mission is to improve and preserve human life and health.

We are present in multiple countries across Europe, Africa, and South America.

We export to numerous countries worldwide and have a strong focus on international expansion and strategic partnerships.

In our office, we are looking for a Batch Record Reviewer Technician to join our team.

Your key responsibilities will include:

* Reviewing and assessing manufacturing and packaging batch records for accuracy, completeness, and compliance with GMP guidelines and company standards.
* Identifying and documenting discrepancies, deviations, or non-conformities, ensuring timely resolution and escalation as needed.
* Collaborating with production, quality assurance, and regulatory teams to ensure proper documentation practices.
* Supporting continuous improvement initiatives related to batch documentation and quality processes.
* Maintaining up-to-date knowledge of regulatory requirements and company SOPs.
* Assisting in audits and inspections by providing relevant documentation and explanations.

To be successful in this role, you will need:

* Previous experience (minimum 1 year) in batch record review within the pharmaceutical industry.
* Solid understanding of GMP guidelines and pharmaceutical manufacturing processes.
* Attention to detail and strong organizational skills.
* Proficiency in English (written and spoken).

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