Compliance with international regulations is essential and non-negotiable for health authorities such as MedSafe, the US FDA, the EMA, and others across the markets where Douglas products are sold.
QA operate across several teams including – Batch Release, QA Systems and Technical. They work closely with teams across the business including QC, Validation, Production, Supply Chain, and Engineering to ensure our products consistently meet regulatory expectations and deliver a positive impact for customers and patients around the world.
We regularly recruit:
QA Officers review manufacturing and packaging documentation to support batch release and ensure every product is fit for purpose. All QA activities uphold GMP compliance, so attention to detail, a passion for quality, and strong documentation skills are essential. We look for science-qualified candidates with solid knowledge of GMP and validation principles who enjoy working in a structured, process-driven environment.
Senior QA Officers bring experience in managing projects, engaging key stakeholders, improving processes, and overseeing quality investigations. Their work includes reviewing validation documentation for processes, equipment and installations, handling customer complaints, following up on root-cause analyses related to Quality Events, and performing periodic product reviews. To thrive here, you’ll need proven experience in QA — ideally within a GMP-regulated setting.
We look for QA professionals who bring a strong scientific foundation and experience in pharmaceuticals or manufacturing. Our ideal team members understand GMP and robust quality systems, and can communicate clearly through strong technical writing. Above all, we value adaptability, teamwork, and a commitment to maintaining the highest standards of product quality and safety.
