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Centrient Pharmaceuticals is a global leader in the manufacturing of sustainable antibiotics, antimycotics, and statins, with a strong focus on reducing the environmental impact of…
This role involves managing quality assurance processes, including reviewing Certificates of Analysis, conducting internal audits, and overseeing GMP training.
Centrient Pharmaceuticals is a global leader in the manufacturing of sustainable antibiotics, antimycotics, and statins, with a strong focus on reducing the environmental impact of pharmaceutical production. The company operates as a business-to-business supplier, providing active pharmaceutical ingredients (APIs) and intermediates to pharmaceutical companies worldwide. With its global headquarters in Rijswijk, Netherlands, Centrient has production sites in Europe and Asia, employing over 2,000 people.
In Spain, Centrient has a significant manufacturing presence, particularly in Barcelona, where it operates a major production facility. The company is known for its commitment to sustainability and innovation, and it offers opportunities for professionals in quality assurance, production, and engineering. For international hires, Centrient provides a multicultural work environment and the chance to contribute to the production of essential medicines in a highly regulated industry.
Centrient Pharmaceuticals was established in 2015 when it was carved out of DSM's pharmaceutical products division. The company has since focused on sustainable production of antibiotics and other active ingredients, building on a legacy of pharmaceutical manufacturing that dates back decades. It has expanded its global footprint with production sites in the Netherlands, Spain, and India.