In life sciences, Quality Assurance is one of the most central roles, acting as the glue that connects all activities and divisions.

Quality management ensures consistency across an organization, its products, and services, covering everything from quality planning and assurance to control and continuous improvement.

At QbD Group, we offer a full range of QA services to ensure your product reaches the market safely and compliantly. This includes setting up quality systems, maintaining operations, certified audits, and QP/RP responsibilities.

It’s not just a legal requirement, it’s about having a direct impact on the quality of products delivered to patients.

As part of QA, you play a crucial role in deciding whether to release a product or withhold a defective one from the market. This responsibility involves conducting investigations, making assessments, and collaborating with colleagues across different departments. While there’s more to it, that’s the core of the role.

QA is also the key department liaising with regulatory authorities like the FDA, EMA, FAHMP, and IGJ. You’re the first point of contact during inspections, ensuring that the quality delivered meets all standards.

As a Quality Assurance consultant, you’ll be involved in every aspect of pharmaceutical or medical device production and quality control. This includes investigating quality issues, defining corrective actions, reviewing production records, and analyzing validation dossiers.

Through this role, you’ll gain deep insights into the daily operations of the pharmaceutical industry, building a comprehensive understanding of the sector and its diverse processes.

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