Scope: Quality Assurance Consultant – Life Sciences Industry
We are looking for a Quality Assurance (QA) Consultant to join our Consultancy Team in Lisbon. We seek professionals with talent, knowledge of quality systems and regulatory requirements, and the motivation to make a difference in the healthcare and life sciences sector.
As a QA Consultant, you will be part of a dynamic team supporting pharmaceutical companies in Portugal, contributing to challenging and high-impact projects. You will be involved in activities related to GMP compliance, quality systems implementation, validation activities, audits and inspections support.
Your role will focus on providing specialized technical support, ensuring that our clients meet the highest standards in regulated environments. This is an opportunity where you will deepen your expertise and actively contribute to meaningful projects from day one.
What we offer:
- A Market Leader in Pharma Consultancy: Join a highly skilled and experienced GMP consultancy team, recognized as a leader in its field.
- Exciting and Meaningful Projects: Work with top-tier pharmaceutical clients and contribute to projects that have a real impact on healthcare and patient safety.
- A Culture of Learning and Support: Gain hands-on experience through direct interaction with clients across Portugal. We provide a collaborative environment where you will be challenged and supported to develop your expertise in the field.
- A Purpose-Driven Career: Be part of a company that provides global solutions for the Life Sciences industry, with a worldwide presence.
Functions:
- Execute QA activities for pharmaceutical projects, following established strategies, methodologies, and best practices (e.g., Deviation Management, Batch Dossier Review, etc.).
- Prepare and review project-related documentation, including SOPs, RA documents, PQRs, Audit Reports, Manufacturing Instructions, Validation Protocols and Reports, Criticality Analyses, CPVs, Material Risk Analyses, and other QA deliverables.
- Ensure compliance with industry standards and regulatory requirements, including GMP and applicable pharmaceutical regulations.
- Contribute to continuous improvement initiatives within projects and QA processes.
- Stay updated with industry trends, technological advancements, and new methodologies in pharmaceutical QA.
