Région
Brussels, BE
CordenPharma is a leading Contract Development & Manufacturing (CDMO) partner with approximately 2’000 employees across Europe and the United States and annual revenues > 500 M€, enabling pharmaceutical and biotechnology companies to link their requirements for product success with their patients’ healthier lives.
Founded in 1987, CordenPharma Brussels, formerly Peptisyntha, was a member of the Solvay group until being acquired by CordenPharma in October 2013. CordenPharma Brussels has built a 30-year track record of success in supplying pharmaceutical and biotech companies with clinical and commercial scale cGMP peptide APIs.
Through expertise and capabilities in all synthetic peptide-manufacturing technologies, CordenPharma Brussels assesses and customizes its manufacturing approach to achieve the most effective manufacturing process for its customers.
As QA Compliance Specialist you will participate in projects and activities that support the top and bottom line growth of the company through compliant improvement activities.
You will support quality compliance activities and initiatives through communication and interaction with key stakeholders including employees, customers, partners, vendors, and appropriate governmental and regulatory authorities.
We offer a permanent contract, a competitive salary package and varied and motivating responsibilities.
Then we should definitely get to know each other. We look forward to receiving your application via the button Apply or send it to jobs.[email protected]