
Job description
Join Hovione, a global Contract Development and Manufacturing Organization (CDMO), as a Process Engineer. You will be responsible for enabling efficient manufacture of pharmaceutical products, defining and implementing manufacturing processes, and ensuring compliance with cGMP and HSE regulations.
Your day-to-day responsibilities will include planning and designing manufacturing processes, preparing and reviewing documentation, participating in risk assessments, and reporting potential risks and discrepancies.
We are looking for a candidate with a degree in Science or Engineering, experience in regulated industry, and strong interpersonal skills. You will have the opportunity to develop and accumulate engineering expertise, share knowledge of state-of-the-art technologies, and contribute to the increase of productivity.
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Healthcare • Manufacturing
Hovione is an international pharmaceutical CDMO with over 60 years of experience, offering a wide range of services including contract manufacturing, generic API products, and inhalation drug development. With FDA-inspected sites globally and a focus on innovation, quality, and dependability, Hovione provides customized solutions across the entire drug life cycle and is a leader in industry quality improvement initiatives.