
Job description
Join Hovione, a global Contract Development and Manufacturing Organization (CDMO), as a Quality Control Supervisor. You will be responsible for defining and implementing quality control techniques, managing Quality Control activities, and contributing to area planning and methodology definition.
Your day-to-day responsibilities will include defining quality control techniques, managing Quality Control activities, contributing to area planning, proposing new methodologies, and ensuring the fulfillment of tasks assigned to the team.
This role requires a degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a similar field, with previous relevant experience in an Analytical Chemistry / Quality Control laboratory. You should have proven experience in training and leading others, knowledge of GMP and ICH guidelines, and good communication skills.
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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.